2023RUB01 Allegato 7 - SSD: MAT/08 - SC: 01/A5

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2023RUB01 Allegato 7 - SSD: MAT/08 - SC: 01/A5

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2023RUB01 Allegato 6 - SSD: ING-IND/32 - SC: 09/E2

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How cancer cells interact with the immune system

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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

A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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

A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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

A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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

A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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

A study, conducted by researchers from the Institute of Oncology Research (IOR) and the Veneto Institute of Molecular Medicine (VIMM) in collaboration with the University of Padua, reveals an alternative mechanism of resistance to therapy involving neutrophils.

Neutrophils represent 50-70% of white blood cells found in human blood and act as the first line of defense against pathogens.

Thanks to the production of specific substances, tumors attract a particular type of neutrophil that block our defense system, promoting tumor growth and resistance to drug treatments.

Knowing that immunosuppressive neutrophils possess a short circulating half-life, the studypublished in Cancer Cell, entitled Apolipoprotein E induces pathogenic senescent-like myeloid cells in prostate cancer, has identified a subgroup of neutrophils that can persist for a long time.  While in the tumor microenvironment, this subgroup of neutrophils blocks our natural system of antitumor defense compared to the rest of the immunosuppressive neutrophils.

This subgroup of neutrophils can enhance tumor development and increase resistance to therapies.

This opens the possibility of identifying an alternative mechanism of tumor immune evasion and supports the development of immune senolytics pharmaceuticals targeting senescent-like neutrophils for cancer therapy.

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2023RUB01 Allegato 8 - SSD: MED/04 - SC: 06/A2

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2023RUB01 Allegato 5 - SSD: ING-IND/16 - SC: 09/B1

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2023RUB01 Allegato 6 - SSD: ING-IND/32 - SC: 09/E2

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[num_revisions] => 1 [current_revision_id] => 427889 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) [5] => Array ( [nid] => 100986 [access] => 1 [node] => stdClass Object ( [vid] => 428779 [uid] => 8831 [title] => 2023RUB01 Allegato 6 - Verbale 4 - Giudizi, punteggi e vincitore [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 100986 [type] => allegato [language] => it [created] => 1687766259 [changed] => 1707376920 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1707376920 [revision_uid] => 102 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => Verbale 4 - Giudizi, punteggi e vincitore [format] => [safe_value] => Verbale 4 - Giudizi, punteggi e vincitore ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 120144 [uid] => 8831 [filename] => Verbale_4_INGIND32.pdf.pdf [uri] => public://2023/Verbale_4_INGIND32.pdf.pdf [filemime] => application/pdf [filesize] => 177234 [status] => 1 [timestamp] => 1687766302 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 428779 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) [6] => Array ( [nid] => 100987 [access] => 1 [node] => stdClass Object ( [vid] => 428780 [uid] => 8831 [title] => 2023RUB01 Allegato 6 DR approvazione atti [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 100987 [type] => allegato [language] => it [created] => 1687766385 [changed] => 1687766385 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1687766385 [revision_uid] => 8831 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => DR approvazione atti [format] => [safe_value] => DR approvazione atti ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 120145 [uid] => 8831 [filename] => DR_approvazione_atti_ING-IND32.pdf.pdf [uri] => public://2023/DR_approvazione_atti_ING-IND32.pdf.pdf [filemime] => application/pdf [filesize] => 116000 [status] => 1 [timestamp] => 1687766379 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 428780 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) ) ) [field_outline_level] => Array ( [und] => Array ( [0] => Array ( [value] => h3 ) ) ) [field_titolo_frontend] => Array ( [und] => Array ( [0] => Array ( [value] => Allegato 6 - SSD: ING-IND/32 - SC: 09/E2 [format] => [safe_value] => Allegato 6 - SSD: ING-IND/32 - SC: 09/E2 ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 418290 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [value] => h3 ) ) [#formatter] => text_default [0] => Array ( [#markup] => h3 ) ) )

2023RUB01 Allegato 5 - SSD: ING-IND/16 - SC: 09/B1

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2023RUB01 Allegato 4 - SSD: ING-IND/10 - SC: 09/C2

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[num_revisions] => 1 [current_revision_id] => 418284 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) ) [1] => Array ( [nid] => 100211 [access] => 1 [node] => stdClass Object ( [vid] => 426205 [uid] => 8831 [title] => 2023RUB01 Allegato 4 - DR nomina Commissione [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 100211 [type] => allegato [language] => it [created] => 1685092355 [changed] => 1686742316 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1686742316 [revision_uid] => 102 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => DR nomina Commissione [format] => [safe_value] => DR nomina Commissione ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 119255 [uid] => 32 [filename] => DR nomina commissione ING-IND 10.pdf [uri] => public://2023/DR nomina commissione ING-IND 10_0.pdf [filemime] => application/pdf [filesize] => 152882 [status] => 1 [timestamp] => 1685092371 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 426205 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) [2] => Array ( [nid] => 100699 [access] => 1 [node] => stdClass Object ( [vid] => 427874 [uid] => 8831 [title] => 2023RUB01 Allegato 4 Verbale 1 - Criteri [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 100699 [type] => allegato [language] => it [created] => 1687160932 [changed] => 1697709810 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1697709810 [revision_uid] => 102 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => Verbale 1 - Criteri [format] => [safe_value] => Verbale 1 - Criteri ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 119806 [uid] => 4 [filename] => 2023RUB01 ING-IND 10_Verbale 1 signed.pdf [uri] => public://2023/2023RUB01 ING-IND 10_Verbale 1 signed.pdf [filemime] => application/pdf [filesize] => 288348 [status] => 1 [timestamp] => 1687160925 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 427874 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) [3] => Array ( [nid] => 101135 [access] => 1 [node] => stdClass Object ( [vid] => 429222 [uid] => 8831 [title] => 2023RUB01 Allegato 4 Verbale 2 - Elenco candidati e convocazione [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 101135 [type] => allegato [language] => it [created] => 1688030020 [changed] => 1689324185 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1689324185 [revision_uid] => 102 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => Verbale 2 - Elenco candidati e convocazione [format] => [safe_value] => Verbale 2 - Elenco candidati e convocazione ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 120328 [uid] => 4 [filename] => 2023RUB01 ING-IND 10_Verbale 2 signed.pdf [uri] => public://2023/2023RUB01 ING-IND 10_Verbale 2 signed.pdf [filemime] => application/pdf [filesize] => 253877 [status] => 1 [timestamp] => 1688030015 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; [num_revisions] => 1 [current_revision_id] => 429222 [is_current] => 1 [is_pending] => [revision_moderation] => ) ) [4] => Array ( [nid] => 101941 [access] => 1 [node] => stdClass Object ( [vid] => 431890 [uid] => 8831 [title] => 2023RUB01 Allegato 4 - Verbale 3 - Giudizi analitici [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 101941 [type] => allegato [language] => it [created] => 1690441328 [changed] => 1690957888 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1690957888 [revision_uid] => 102 [taxonomy_vocabulary_2] => Array ( ) [taxonomy_vocabulary_8] => Array ( ) [body] => Array ( ) [field_titolo_frontend_all] => Array ( [und] => Array ( [0] => Array ( [value] => Verbale 3 - Giudizi analitici [format] => [safe_value] => Verbale 3 - Giudizi analitici ) ) ) [field_allegato_file] => Array ( [und] => Array ( [0] => Array ( [fid] => 121343 [uid] => 32 [filename] => 2023RUB01 ING-IND 10_Verbale 3 signed.pdf [uri] => public://2023/2023RUB01 ING-IND 10_Verbale 3 signed.pdf [filemime] => application/pdf [filesize] => 200928 [status] => 1 [timestamp] => 1690441238 [type] => document [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2529 ) ) ) [metadata] => Array ( ) [display] => 1 [description] => ) ) ) [name] => carriere.docenti [picture] => 0 [data] => b:0; 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2023RUB01 Allegato 4 - SSD: ING-IND/10 - SC: 09/C2

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Pagine