2023N10 - prova di preselezione con correttore

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2023N10 - criteri di valutazione prove d'esame

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All'Istituto Italiano di Cultura di Amburgo si discute del fascismo in Europa

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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Giovedì 30 novembre alle ore 19, l'Istituto Italiano di Cultura di Amburgo (Hansastrasse, 6 -20149 Hamburg) ospiterà una conferenza del professore Unipd Marco Mondini sull'ascesa del fascismo in Italia, a partire dai contenuti del proprio libro, "Roma 1922. Il fascismo e la guerra mai finita".

Nel corso dell'incontro, che rientra nell'ambito del ciclo di conferenze "L'anno di crisi 1923 e il fascismo in Europa", si discute anche della traduzione tedesca di "Marcia su Roma e dintorni" di Emilio Lussu, di cui l’attrice Annalena Schmidt leggerà alcuni brani.

L’ascesa al potere del fascismo e il suo atto culminante, la cosiddetta marcia su Roma, possono essere capiti solo all’interno di un quadro più vasto, quello di un’Europa incapace di chiudere i conti con la Grande guerra. E se furono soprattutto i paesi sconfitti a scoprire che uscire dalla cultura dell’odio e della violenza quotidiana non era facile, frustrazione, scontento e desiderio di rivalsa si impossessarono anche degli italiani che pure – almeno formalmente – la guerra l’avevano vinta. Marco Mondini compone la storia corale e implacabile di un’Italia in cui la lotta politica si trasforma in guerra civile e che scivola via via verso il lungo ventennio della dittatura fascista.

La partecipazione all'incontro è libera, su registrazione.

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2023T52 - Esito prova scritta - candidati ammessi al colloquio

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candidati ammessi al colloquio [format] => [safe_value] => Esito prova scritta - candidati ammessi al colloquio ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 125331 [uid] => 32 [filename] => 17 esito prova scritta web 2023T52.pdf [uri] => public://2023/17 esito prova scritta web 2023T52.pdf [filemime] => application/pdf [filesize] => 105203 [status] => 1 [timestamp] => 1701263014 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => stefano.zampieri [picture] => 0 [data] => a:2:{s:13:"form_build_id";s:48:"form-WsCySmos4vAVlyFhG6gU5T7knfAyqco8LxlocSU_yIA";s:14:"wysiwyg_status";a:1:{i:1;i:1;}} [num_revisions] => 1 [current_revision_id] => 443457 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [fid] => 125331 [uid] => 32 [filename] => 17 esito prova scritta web 2023T52.pdf [uri] => public://2023/17 esito prova scritta web 2023T52.pdf [filemime] => application/pdf [filesize] => 105203 [status] => 1 [timestamp] => 1701263014 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) [#formatter] => file_default [0] => Array ( [#theme] => file_link [#file] => stdClass Object ( [fid] => 125331 [uid] => 32 [filename] => 17 esito prova scritta web 2023T52.pdf [uri] => public://2023/17 esito prova scritta web 2023T52.pdf [filemime] => application/pdf [filesize] => 105203 [status] => 1 [timestamp] => 1701263014 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [links] => Array ( [#theme] => links__node [#pre_render] => Array ( [0] => drupal_pre_render_links ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) [node] => Array ( [#theme] => links__node__node [#links] => Array ( [node-readmore] => Array ( [title] => Read more about 2023T52 - Esito prova scritta - candidati ammessi al colloquio [href] => node/105848 [html] => 1 [attributes] => Array ( [rel] => tag [title] => 2023T52 - Esito prova scritta - candidati ammessi al colloquio ) ) ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) ) ) )

Procedure valutative per professori di seconda fascia

Array ( [body] => Array ( [#theme] => field [#weight] => -4 [#title] => Body [#access] => 1 [#label_display] => hidden [#view_mode] => teaser [#language] => und [#field_name] => body [#field_type] => text_with_summary [#field_translatable] => 0 [#entity_type] => node [#bundle] => foglia_complessa [#object] => stdClass Object ( [vid] => 447050 [uid] => 32 [title] => Procedure valutative per professori di seconda fascia [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105847 [type] => foglia_complessa [language] => it [created] => 1701262387 [changed] => 1705917962 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917962 [revision_uid] => 32 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_3] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[summary] => [format] => 2 [safe_value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[safe_summary] => ) ) ) [field_foglia_complessa_accordion] => Array ( [und] => Array ( [0] => Array ( [nid] => 105846 [access] => 1 [node] => stdClass Object ( [vid] => 447049 [uid] => 8831 [title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105846 [type] => accordion [language] => it [created] => 1701262371 [changed] => 1705917950 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917950 [revision_uid] => 32 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 105844 [access] => 1 ) [1] => Array ( [nid] => 105845 [access] => 1 ) [2] => Array ( [nid] => 106602 [access] => 1 ) [3] => Array ( [nid] => 106837 [access] => 1 ) [4] => Array ( [nid] => 106959 [access] => 1 ) [5] => Array ( [nid] => 106960 [access] => 1 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 5 [current_revision_id] => 447049 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) [1] => Array ( [nid] => 58783 [access] => 1 [node] => stdClass Object ( [vid] => 438805 [uid] => 8831 [title] => Concorsi docenti altre informazioni [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 58783 [type] => accordion [language] => it [created] => 1559112888 [changed] => 1697443786 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697443786 [revision_uid] => 4 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[summary] => [format] => 2 [safe_value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[safe_summary] => ) ) ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( [und] => Array ( [0] => Array ( [value] =>

Altre informazioni

[format] => 1 [safe_value] =>

Altre informazioni

) ) ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 58782 ) [1] => Array ( [nid] => 82541 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 18 [current_revision_id] => 438805 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_foglia_complessa_allegato] => Array ( ) [field_image_fc] => Array ( ) [field_testo_opzionale_fc] => Array ( [und] => Array ( [0] => Array ( [nid] => 8456 [access] => 1 [node] => stdClass Object ( [vid] => 443433 [uid] => 4 [title] => Ufficio Personale docente - Settore Reclutamento [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 8456 [type] => testo_opzionale [language] => und [created] => 1341050862 [changed] => 1701255566 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1701255566 [revision_uid] => 4 [field_testo_opz] => Array ( [und] => Array ( [0] => Array ( [value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

[format] => 1 [safe_value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

) ) ) [name] => simonetta.capparotto [picture] => 0 [data] => a:2:{s:13:"form_build_id";s:37:"form-fe5ebd9e5e240c4294455b6b42fa6a76";s:14:"wysiwyg_status";a:1:{i:1;i:1;}} [num_revisions] => 21 [current_revision_id] => 443433 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_immagine_top] => Array ( ) [field_immagine_bottom] => Array ( ) [field_immagine_decorativa_latera] => Array ( [und] => Array ( [0] => Array ( [fid] => 72106 [uid] => 4 [filename] => selezioni.png [uri] => public://selezioni.png [filemime] => image/png [filesize] => 67347 [status] => 1 [timestamp] => 1634297584 [type] => image [field_file_image_alt_text] => Array ( [und] => Array ( [0] => Array ( [value] => Immagine decorativa [format] => [safe_value] => Immagine decorativa ) ) ) [field_file_image_title_text] => Array ( ) [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2048 ) ) ) [metatags] => Array ( [und] => Array ( [title] => Array ( [value] => [current-page:title] | [current-page:pager][site:name] [default] => [current-page:title] | [current-page:pager][site:name] ) [description] => Array ( [value] => ) [abstract] => Array ( [value] => ) [keywords] => Array ( [value] => ) [robots] => Array ( [value] => Array ( [index] => 0 [follow] => 0 [noindex] => 0 [nofollow] => 0 [noarchive] => 0 [nosnippet] => 0 [noodp] => 0 [noydir] => 0 [noimageindex] => 0 [notranslate] => 0 ) ) [news_keywords] => Array ( [value] => ) [standout] => Array ( [value] => ) [rating] => Array ( [value] => ) [referrer] => Array ( [value] => ) [rights] => Array ( [value] => ) [image_src] => Array ( [value] => ) [canonical] => Array ( [value] => [current-page:url:absolute] [default] => [current-page:url:absolute] ) [set_cookie] => Array ( [value] => ) [shortlink] => Array ( [value] => [current-page:url:unaliased] [default] => [current-page:url:unaliased] ) [original-source] => Array ( [value] => ) [prev] => Array ( [value] => ) [next] => Array ( [value] => ) [content-language] => Array ( [value] => ) [geo.position] => Array ( [value] => ) [geo.placename] => Array ( [value] => ) [geo.region] => Array ( [value] => ) [icbm] => Array ( [value] => ) [refresh] => Array ( [value] => ) [revisit-after] => Array ( [value] => [period] => ) [pragma] => Array ( [value] => ) [cache-control] => Array ( [value] => ) [expires] => Array ( [value] => ) [og:type] => Array ( [value] => article [default] => article ) [og:url] => Array ( [value] => [current-page:url:absolute] [default] => [current-page:url:absolute] ) [og:title] => Array ( [value] => [current-page:title] [default] => [current-page:title] ) [og:determiner] => Array ( [value] => ) [og:description] => Array ( [value] => ) [og:updated_time] => Array ( [value] => ) [og:see_also] => Array ( [value] => ) [og:image] => Array ( [value] => ) [og:image:url] => Array ( [value] => ) [og:image:secure_url] => Array ( [value] => ) [og:image:type] => Array ( [value] => ) [og:image:width] => Array ( [value] => ) [og:image:height] => Array ( [value] => ) [og:latitude] => Array ( [value] => ) [og:longitude] => Array ( [value] => ) [og:street_address] => Array ( [value] => ) [og:locality] => Array ( [value] => ) [og:region] => Array ( [value] => ) [og:postal_code] => Array ( [value] => ) [og:country_name] => Array ( [value] => ) [og:email] => Array ( [value] => ) [og:phone_number] => Array ( [value] => ) [og:fax_number] => Array ( [value] => ) [og:locale] => Array ( [value] => ) [og:locale:alternate] => Array ( [value] => ) [article:author] => Array ( [value] => ) [article:publisher] => Array ( [value] => ) [article:section] => Array ( [value] => ) [article:tag] => Array ( [value] => ) [article:published_time] => Array ( [value] => ) [article:modified_time] => Array ( [value] => ) [article:expiration_time] => Array ( [value] => ) [profile:first_name] => Array ( [value] => ) [profile:last_name] => Array ( [value] => ) [profile:username] => Array ( [value] => ) [profile:gender] => Array ( [value] => ) [og:audio] => Array ( [value] => ) [og:audio:secure_url] => Array ( [value] => ) [og:audio:type] => Array ( [value] => ) [book:author] => Array ( [value] => ) [book:isbn] => Array ( [value] => ) [book:release_date] => Array ( [value] => ) [book:tag] => Array ( [value] => ) [og:video:url] => Array ( [value] => ) [og:video:secure_url] => Array ( [value] => ) [og:video:width] => Array ( [value] => ) [og:video:height] => Array ( [value] => ) [og:video:type] => Array ( [value] => ) [video:actor] => Array ( [value] => ) [video:actor:role] => Array ( [value] => ) [video:director] => Array ( [value] => ) [video:writer] => Array ( [value] => ) [video:duration] => Array ( [value] => ) [video:release_date] => Array ( [value] => ) [video:tag] => Array ( [value] => ) [video:series] => Array ( [value] => ) ) ) [alt] => Immagine decorativa [metadata] => Array ( [height] => 1363 [width] => 550 ) [height] => 1363 [width] => 550 [title] => ) ) ) [field_link_in_evidenza] => Array ( ) [field_usa_layout_pagina_link] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_etichetta_link_in_evidenza] => Array ( ) [field_tabs] => Array ( ) [field_condividi_social] => Array ( [und] => Array ( [0] => Array ( [value] => 1 ) ) ) [field_formato_immagine] => Array ( ) [field_video_link] => Array ( ) [field_nosidebar] => Array ( [und] => Array ( [0] => Array ( [value] => 1 ) ) ) [field_chatbot] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_chatbot_codice_chat] => Array ( ) [field_header_custom] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_header_custom_ref] => Array ( ) [field_accessiway] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_footer_custom] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_footer_custom_ref] => Array ( ) [field_usa_layout_hero] => Array ( [und] => Array ( [0] => Array ( [value] => 0 ) ) ) [field_note_interne] => Array ( ) [field_url_en_page] => Array ( ) [field_crawler_ai] => Array ( ) [path] => Array ( [pathauto] => 0 ) [name] => stefano.zampieri [picture] => 0 [data] => a:2:{s:13:"form_build_id";s:48:"form-WsCySmos4vAVlyFhG6gU5T7knfAyqco8LxlocSU_yIA";s:14:"wysiwyg_status";a:1:{i:1;i:1;}} [num_revisions] => 5 [current_revision_id] => 447050 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[summary] => [format] => 2 [safe_value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[safe_summary] => ) ) [#formatter] => text_summary_or_trimmed [0] => Array ( [#markup] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

) ) [field_foglia_complessa_accordion] => Array ( [#theme] => field [#weight] => -1 [#title] => accordion [#access] => 1 [#label_display] => above [#view_mode] => teaser [#language] => und [#field_name] => field_foglia_complessa_accordion [#field_type] => node_reference [#field_translatable] => 0 [#entity_type] => node [#bundle] => foglia_complessa [#object] => stdClass Object ( [vid] => 447050 [uid] => 32 [title] => Procedure valutative per professori di seconda fascia [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105847 [type] => foglia_complessa [language] => it [created] => 1701262387 [changed] => 1705917962 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917962 [revision_uid] => 32 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_3] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[summary] => [format] => 2 [safe_value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[safe_summary] => ) ) ) [field_foglia_complessa_accordion] => Array ( [und] => Array ( [0] => Array ( [nid] => 105846 [access] => 1 [node] => stdClass Object ( [vid] => 447049 [uid] => 8831 [title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105846 [type] => accordion [language] => it [created] => 1701262371 [changed] => 1705917950 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917950 [revision_uid] => 32 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 105844 [access] => 1 ) [1] => Array ( [nid] => 105845 [access] => 1 ) [2] => Array ( [nid] => 106602 [access] => 1 ) [3] => Array ( [nid] => 106837 [access] => 1 ) [4] => Array ( [nid] => 106959 [access] => 1 ) [5] => Array ( [nid] => 106960 [access] => 1 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 5 [current_revision_id] => 447049 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) [1] => Array ( [nid] => 58783 [access] => 1 [node] => stdClass Object ( [vid] => 438805 [uid] => 8831 [title] => Concorsi docenti altre informazioni [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 58783 [type] => accordion [language] => it [created] => 1559112888 [changed] => 1697443786 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697443786 [revision_uid] => 4 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[summary] => [format] => 2 [safe_value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[safe_summary] => ) ) ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( [und] => Array ( [0] => Array ( [value] =>

Altre informazioni

[format] => 1 [safe_value] =>

Altre informazioni

) ) ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 58782 ) [1] => Array ( [nid] => 82541 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 18 [current_revision_id] => 438805 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_foglia_complessa_allegato] => Array ( ) [field_image_fc] => Array ( ) [field_testo_opzionale_fc] => Array ( [und] => Array ( [0] => Array ( [nid] => 8456 [access] => 1 [node] => stdClass Object ( [vid] => 443433 [uid] => 4 [title] => Ufficio Personale docente - Settore Reclutamento [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 8456 [type] => testo_opzionale [language] => und [created] => 1341050862 [changed] => 1701255566 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1701255566 [revision_uid] => 4 [field_testo_opz] => Array ( [und] => Array ( [0] => Array ( [value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

[format] => 1 [safe_value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

) ) ) [name] => simonetta.capparotto [picture] => 0 [data] => a:2:{s:13:"form_build_id";s:37:"form-fe5ebd9e5e240c4294455b6b42fa6a76";s:14:"wysiwyg_status";a:1:{i:1;i:1;}} [num_revisions] => 21 [current_revision_id] => 443433 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_immagine_top] => Array ( ) [field_immagine_bottom] => Array ( ) [field_immagine_decorativa_latera] => Array ( [und] => Array ( [0] => Array ( [fid] => 72106 [uid] => 4 [filename] => selezioni.png [uri] => public://selezioni.png [filemime] => image/png [filesize] => 67347 [status] => 1 [timestamp] => 1634297584 [type] => image [field_file_image_alt_text] => Array ( [und] => Array ( [0] => Array ( [value] => Immagine decorativa [format] => [safe_value] => Immagine decorativa ) ) ) [field_file_image_title_text] => Array ( ) [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2048 ) ) ) [metatags] => Array ( [und] => Array ( [title] => Array ( [value] => [current-page:title] | 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Array ( [value] => ) [og:latitude] => Array ( [value] => ) [og:longitude] => Array ( [value] => ) [og:street_address] => Array ( [value] => ) [og:locality] => Array ( [value] => ) [og:region] => Array ( [value] => ) [og:postal_code] => Array ( [value] => ) [og:country_name] => Array ( [value] => ) [og:email] => Array ( [value] => ) [og:phone_number] => Array ( [value] => ) [og:fax_number] => Array ( [value] => ) [og:locale] => Array ( [value] => ) [og:locale:alternate] => Array ( [value] => ) [article:author] => Array ( [value] => ) [article:publisher] => Array ( [value] => ) [article:section] => Array ( [value] => ) [article:tag] => Array ( [value] => ) [article:published_time] => Array ( [value] => ) [article:modified_time] => Array ( [value] => ) [article:expiration_time] => Array ( [value] => ) [profile:first_name] => Array ( [value] => ) [profile:last_name] => Array ( [value] => ) [profile:username] => Array ( [value] => ) [profile:gender] => Array ( [value] => ) [og:audio] => 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[path] => Array ( [pathauto] => 0 ) [name] => stefano.zampieri [picture] => 0 [data] => a:2:{s:13:"form_build_id";s:48:"form-WsCySmos4vAVlyFhG6gU5T7knfAyqco8LxlocSU_yIA";s:14:"wysiwyg_status";a:1:{i:1;i:1;}} [num_revisions] => 5 [current_revision_id] => 447050 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [nid] => 105846 [access] => 1 [node] => stdClass Object ( [vid] => 447049 [uid] => 8831 [title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105846 [type] => accordion [language] => it [created] => 1701262371 [changed] => 1705917950 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917950 [revision_uid] => 32 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 105844 [access] => 1 ) [1] => Array ( [nid] => 105845 [access] => 1 ) [2] => Array ( [nid] => 106602 [access] => 1 ) [3] => Array ( [nid] => 106837 [access] => 1 ) [4] => Array ( [nid] => 106959 [access] => 1 ) [5] => Array ( [nid] => 106960 [access] => 1 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 5 [current_revision_id] => 447049 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) [1] => Array ( [nid] => 58783 [access] => 1 [node] => stdClass Object ( [vid] => 438805 [uid] => 8831 [title] => Concorsi docenti altre informazioni [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 58783 [type] => accordion [language] => it [created] => 1559112888 [changed] => 1697443786 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697443786 [revision_uid] => 4 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[summary] => [format] => 2 [safe_value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[safe_summary] => ) ) ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( [und] => Array ( [0] => Array ( [value] =>

Altre informazioni

[format] => 1 [safe_value] =>

Altre informazioni

) ) ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 58782 ) [1] => Array ( [nid] => 82541 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 18 [current_revision_id] => 438805 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) [#formatter] => node_reference_default [0] => Array ( [#type] => link [#title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [#href] => node/105846 [#options] => Array ( [entity_type] => node [entity] => stdClass Object ( [vid] => 447049 [uid] => 8831 [title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105846 [type] => accordion [language] => it [created] => 1701262371 [changed] => 1705917950 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917950 [revision_uid] => 32 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 105844 [access] => 1 ) [1] => Array ( [nid] => 105845 [access] => 1 ) [2] => Array ( [nid] => 106602 [access] => 1 ) [3] => Array ( [nid] => 106837 [access] => 1 ) [4] => Array ( [nid] => 106959 [access] => 1 ) [5] => Array ( [nid] => 106960 [access] => 1 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 5 [current_revision_id] => 447049 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) ) [1] => Array ( [#type] => link [#title] => Concorsi docenti altre informazioni [#href] => node/58783 [#options] => Array ( [entity_type] => node [entity] => stdClass Object ( [vid] => 438805 [uid] => 8831 [title] => Concorsi docenti altre informazioni [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 58783 [type] => accordion [language] => it [created] => 1559112888 [changed] => 1697443786 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697443786 [revision_uid] => 4 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[summary] => [format] => 2 [safe_value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[safe_summary] => ) ) ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( [und] => Array ( [0] => Array ( [value] =>

Altre informazioni

[format] => 1 [safe_value] =>

Altre informazioni

) ) ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 58782 ) [1] => Array ( [nid] => 82541 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 18 [current_revision_id] => 438805 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [links] => Array ( [#theme] => links__node [#pre_render] => Array ( [0] => drupal_pre_render_links ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) [node] => Array ( [#theme] => links__node__node [#links] => Array ( [node-readmore] => Array ( [title] => Read more about Procedure valutative per professori di seconda fascia [href] => node/105847 [html] => 1 [attributes] => Array ( [rel] => tag [title] => Procedure valutative per professori di seconda fascia ) ) ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) ) ) [field_testo_opzionale_fc] => Array ( [#theme] => field [#weight] => 1 [#title] => Testo Opzionale [#access] => 1 [#label_display] => above [#view_mode] => teaser [#language] => und [#field_name] => field_testo_opzionale_fc [#field_type] => node_reference [#field_translatable] => 0 [#entity_type] => node [#bundle] => foglia_complessa [#object] => stdClass Object ( [vid] => 447050 [uid] => 32 [title] => Procedure valutative per professori di seconda fascia [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105847 [type] => foglia_complessa [language] => it [created] => 1701262387 [changed] => 1705917962 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917962 [revision_uid] => 32 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_3] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[summary] => [format] => 2 [safe_value] =>

Il documento ufficiale è reperibile all’Albo on line di Ateneo

Procedura valutativa per la chiamata di un Professore di seconda fascia, ai sensi dell’art. 24, comma 5, Legge 30 dicembre 2010, n. 240, riservata a ricercatori a tempo determinato di cui all’art. 24 comma 3 lett. b) della Legge 30 dicembre 2010, n. 240 nel terzo anno del contratto triennale di lavoro subordinato, a tempo determinato, stipulato con la medesima Università ed in possesso dell’Abilitazione Scientifica Nazionale ai sensi dell’art. 16 della Legge 30 dicembre 2010, n. 240 – 2023PA558 - Dipartimento di Scienze chimiche - DiSC – settore concorsuale 03/B1 - FONDAMENTI DELLE SCIENZE CHIMICHE E SISTEMI INORGANICI – settore scientifico-disciplinare CHIM/03 - CHIMICA GENERALE ED INORGANICA

Scadenza: 21 dicembre 2023, ore 13

Domanda telematica

[safe_summary] => ) ) ) [field_foglia_complessa_accordion] => Array ( [und] => Array ( [0] => Array ( [nid] => 105846 [access] => 1 [node] => stdClass Object ( [vid] => 447049 [uid] => 8831 [title] => 2023PA558 - Lettera di pubblicazione avviso e allegati [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 105846 [type] => accordion [language] => it [created] => 1701262371 [changed] => 1705917950 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1705917950 [revision_uid] => 32 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 105844 [access] => 1 ) [1] => Array ( [nid] => 105845 [access] => 1 ) [2] => Array ( [nid] => 106602 [access] => 1 ) [3] => Array ( [nid] => 106837 [access] => 1 ) [4] => Array ( [nid] => 106959 [access] => 1 ) [5] => Array ( [nid] => 106960 [access] => 1 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 5 [current_revision_id] => 447049 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) [1] => Array ( [nid] => 58783 [access] => 1 [node] => stdClass Object ( [vid] => 438805 [uid] => 8831 [title] => Concorsi docenti altre informazioni [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 58783 [type] => accordion [language] => it [created] => 1559112888 [changed] => 1697443786 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697443786 [revision_uid] => 4 [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[summary] => [format] => 2 [safe_value] =>

Per il rimborso spese di missione consultare la pagina dedicata

[safe_summary] => ) ) ) [field_accordion_element] => Array ( ) [field_accordion_sottotitolo] => Array ( ) [field_accordion_titolo_fro] => Array ( [und] => Array ( [0] => Array ( [value] =>

Altre informazioni

[format] => 1 [safe_value] =>

Altre informazioni

) ) ) [field_allegato_element] => Array ( [und] => Array ( [0] => Array ( [nid] => 58782 ) [1] => Array ( [nid] => 82541 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 18 [current_revision_id] => 438805 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_foglia_complessa_allegato] => Array ( ) [field_image_fc] => Array ( ) [field_testo_opzionale_fc] => Array ( [und] => Array ( [0] => Array ( [nid] => 8456 [access] => 1 [node] => stdClass Object ( [vid] => 443433 [uid] => 4 [title] => Ufficio Personale docente - Settore Reclutamento [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 8456 [type] => testo_opzionale [language] => und [created] => 1341050862 [changed] => 1701255566 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1701255566 [revision_uid] => 4 [field_testo_opz] => Array ( [und] => Array ( [0] => Array ( [value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

[format] => 1 [safe_value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

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Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

[format] => 1 [safe_value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

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Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

[format] => 1 [safe_value] =>

Ufficio Personale docente - Settore Reclutamento

Palazzo Storione
Riviera Tito Livio 6, 35123 Padova
tel. 049 827 3936/ 3170/ 3172/ 3173/ 3176/ 3162/ 3178/ 1934/ 3035/ 1937/ 1929/ 3994/ 3288
email: reclutamento.docenti@unipd.it

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2023PA558 - Lettera di pubblicazione avviso e allegati

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2023PA558 - Lettera di pubblicazione avviso

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2023RUB07 - Allegato 1 - Verbale 2- Elenco candidati e convocazioneAllegato 1 -

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Unipd research. New possibilities identified for chemotherapy-resistant medulloblastoma

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

[summary] => [format] => 2 [safe_value] =>

Resistance to chemotherapy is one of the most demanding challenges faced while treating cancer patients. Researchers must try to resolve this with experimental studies. The onset of tumor cells resistant to therapy is one of the major obstacles to the complete elimination of tumors. This is particularly relevant for medulloblastoma, a pediatric brain tumor that is still difficult to treat and often refractory to chemotherapy. Current therapeutic options involve the use of drugs that are only partially effective, as they cause numerous side effects and toxicity for young patients. This leaves room for potential relapses, along with the sometimes long-lasting consequences of not entirely tolerable medications.

In order to identify the molecular mechanisms that allow some tumor cells to resist chemotherapy, researchers from the Department of Women's and Children's Health at the University of Padua and the Pediatric Research Institute - Città della Speranza have cyclically exposed patient-derived medulloblastoma cells to the same drug combination commonly used in the clinic. They thus tried to reproduce in the laboratory what happens when a tumor shows its resistance to chemotherapy.

The results were published in the international journal Acta Neuropathologica Communications in an article entitled “Molecular and functional profiling of chemotolerant cells unveils nucleoside metabolism-dependent vulnerabilities in medulloblastoma”. The study was coordinated by Giampietro Viola and Luca Persano of the Department of Women's and Children's Health at the University of Padua and was conducted with equal contributions by Elena Mariotto, Elena Rampazzo, and Roberta Bortolozzi. The research was supported by the AIRC Foundation for Cancer Research, the Just Italia Foundation, the Cassa di Risparmio di Padova e Rovigo Foundation (CARIPARO), and the US charity Rally Foundation for Childhood Cancer Research.

Thanks to these experiments, the research team showed that chemotherapy-resistant medulloblastoma cells are capable of completely disrupting multiple intracellular processes. Tumor cells thus counteract the damage caused by drugs, adapt to pharmacological treatments, and satisfy the growing needs for nutrients. However, this metabolic reconfiguration can become the Achilles' heel of these cells.

Researchers were able to identify vulnerabilities thanks to a screening of more than 2000 drugs, demonstrating that drugs that act on the metabolism of tumor cells, commonly called antimetabolites, are particularly active in the treatment of resistant cells. This result is particularly relevant since many of the drugs identified are already approved and currently used in the treatment of other tumors, including pediatric ones, thus facilitating their potential future use in the context of medulloblastoma.

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