ResearcherUniversity of PalermoActive in the last 2 years
Patrizia Diana
Matched on ORCID iD 0000-0002-4883-2004; OpenAlex author ID A5052325016. Sources: OpenAlex.
Their work
- Papers
- 22 (first author 0, last author 7)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 31
2012: 1 paper · 2013: none · 2014: none · 2015: none · 2016: none · 2017: none · 2018: none · 2019: 2 papers · 2020: 2 papers · 2021: 5 papers · 2022: 1 paper · 2023: 3 papers · 2024: 4 papers · 2025: 3 papers · 2026: 1 paper
Papers 22
- 3-amino-1,2,4-triazine scaffolds as next-generation PDK inhibitors: Design, mechanistic insights, and efficacy in pancreatic ductal adenocarcinoma. Co-author DOI 10.1016/j.ejmech.2026.119202↗
- Novel Pyrazolo [1,5-a]-1,3,5-Triazine Derivatives as CDK7 Inhibitors: Synthesis and Biological Insights in Pancreatic Ductal Adenocarcinoma Models. Last author DOI 10.1002/cmdc.202500448↗
- Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer activity in pancreatic c… Co-author DOI 10.1016/j.bioorg.2024.107995↗
- New Marine-Inspired Oxadiazole Derivatives for Use Against Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.3390/md23080327↗
- Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer activity in pancreatic cancer models. Co-author DOI 10.1016/j.bioorg.2024.107959↗
- Exploring the therapeutic potential of a novel series of imidazothiadiazoles targeting focal adhesion kinase (FAK) for pancreatic cancer treatment: synthesis, … Co-author DOI 10.1080/1061186x.2024.2385557↗
- Exploring the therapeutic potential of focal adhesion kinase inhibition in overcoming chemoresistance in pancreatic ductal adenocarcinoma. Co-author DOI 10.4155/fmc-2023-0234↗
- Exploring Splicing Modulation as an Innovative Approach to Combat Pancreatic Cancer: SF3B1 Emerges as a Prognostic Indicator and Therapeutic Target. Co-author DOI 10.7150/ijbs.92671↗
- Discovery of the 3-Amino-1,2,4-triazine-Based Library as Selective PDK1 Inhibitors with Therapeutic Potential in Highly Aggressive Pancreatic Ductal Adenocarci… Last author DOI 10.3390/ijms24043679↗
- Structural Manipulations of Marine Natural Products Inspire a New Library of 3-Amino-1,2,4-Triazine PDK Inhibitors Endowed with Antitumor Activity in Pancreati… Last author DOI 10.3390/md21050288↗
- 1,3,4-Oxadiazole and 1,3,4-Thiadiazole Nortopsentin Derivatives against Pancreatic Ductal Adenocarcinoma: Synthesis, Cytotoxic Activity, and Inhibition of CDK1. Co-author DOI 10.3390/md21070412↗
- Interrelationship between miRNA and splicing factors in pancreatic ductal adenocarcinoma. Co-author DOI 10.1080/15592294.2021.1916697↗
- 1,2,4-Oxadiazole Topsentin Analogs with Antiproliferative Activity against Pancreatic Cancer Cells, Targeting GSK3β Kinase. Last author DOI 10.1002/cmdc.202000752↗
- GSK3β as a novel promising target to overcome chemoresistance in pancreatic cancer. Co-author DOI 10.1016/j.drup.2021.100779↗
- SF3B1 modulators affect key genes in metastasis and drug influx: a new approach to fight pancreatic cancer chemoresistance. Co-author DOI 10.20517/cdr.2021.61↗
- Cyclin Dependent Kinase-1 (CDK-1) Inhibition as a Novel Therapeutic Strategy against Pancreatic Ductal Adenocarcinoma (PDAC). Last author DOI 10.3390/cancers13174389↗
- A New Oxadiazole-Based Topsentin Derivative Modulates Cyclin-Dependent Kinase 1 Expression and Exerts Cytotoxic Effects on Pancreatic Cancer Cells. Co-author DOI 10.3390/molecules27010019↗
- Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic cancer cells. Last author DOI 10.1016/j.ejmech.2020.112088↗
- 3-(6-Phenylimidazo [2,1-b][1,3,4]thiadiazol-2-yl)-1H-Indole Derivatives as New Anticancer Agents in the Treatment of Pancreatic Ductal Adenocarcinoma. Last author DOI 10.3390/molecules25020329↗
- Pharmacogenetics of treatments for pancreatic cancer. Co-author DOI 10.1080/17425255.2019.1620731↗
- Biological Evaluation of the Antiproliferative and Anti-migratory Activity of a Series of 3-(6-Phenylimidazo[2,1-b][1,3,4]thiadiazol-2-yl)-1H-indole Derivative… Co-author DOI 10.21873/anticanres.13509↗
- 2-Triazenoazaindoles: α novel class of triazenes inducing transcriptional down-regulation of EGFR and HER-2 in human pancreatic cancer cells. Co-author DOI 10.3892/ijo.2011.1272↗
Closest collaborators
The 25 strongest of 31 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Daniela Carbone · 19 shared papers, 2019–2026 · strength 3.33
- Paper 3-amino-1,2,4-triazine scaffolds as next-generation PDK inhibitors: Design, mechanistic insights, and efficacy in pancr… DOI 10.1016/j.ejmech.2026.119202↗
- Paper New Marine-Inspired Oxadiazole Derivatives for Use Against Pancreatic Ductal Adenocarcinoma. DOI 10.3390/md23080327↗
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Elisa Giovannetti · 18 shared papers, 2019–2025 · strength 2.97
- Paper New Marine-Inspired Oxadiazole Derivatives for Use Against Pancreatic Ductal Adenocarcinoma. DOI 10.3390/md23080327↗
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Paper Novel Pyrazolo [1,5-a]-1,3,5-Triazine Derivatives as CDK7 Inhibitors: Synthesis and Biological Insights in Pancreatic D… DOI 10.1002/cmdc.202500448↗
- Barbara Parrino · 17 shared papers, 2019–2026 · strength 2.97
- Paper 3-amino-1,2,4-triazine scaffolds as next-generation PDK inhibitors: Design, mechanistic insights, and efficacy in pancr… DOI 10.1016/j.ejmech.2026.119202↗
- Paper New Marine-Inspired Oxadiazole Derivatives for Use Against Pancreatic Ductal Adenocarcinoma. DOI 10.3390/md23080327↗
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Camilla Pecoraro · 15 shared papers, 2021–2026 · strength 2.86
- Paper 3-amino-1,2,4-triazine scaffolds as next-generation PDK inhibitors: Design, mechanistic insights, and efficacy in pancr… DOI 10.1016/j.ejmech.2026.119202↗
- Paper New Marine-Inspired Oxadiazole Derivatives for Use Against Pancreatic Ductal Adenocarcinoma. DOI 10.3390/md23080327↗
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Stella Cascioferro · 16 shared papers, 2019–2025 · strength 2.58
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Paper Novel Pyrazolo [1,5-a]-1,3,5-Triazine Derivatives as CDK7 Inhibitors: Synthesis and Biological Insights in Pancreatic D… DOI 10.1002/cmdc.202500448↗
- Paper Exploring the therapeutic potential of focal adhesion kinase inhibition in overcoming chemoresistance in pancreatic duc… DOI 10.4155/fmc-2023-0234↗
- Godefridus J. Peters · 10 shared papers, 2019–2025 · strength 1.40
- Paper Novel Pyrazolo [1,5-a]-1,3,5-Triazine Derivatives as CDK7 Inhibitors: Synthesis and Biological Insights in Pancreatic D… DOI 10.1002/cmdc.202500448↗
- Paper Exploring Splicing Modulation as an Innovative Approach to Combat Pancreatic Cancer: SF3B1 Emerges as a Prognostic Indi… DOI 10.7150/ijbs.92671↗
- Paper Interrelationship between miRNA and splicing factors in pancreatic ductal adenocarcinoma. DOI 10.1080/15592294.2021.1916697↗
- Geng Xu · 5 shared papers, 2023–2025 · strength 1.09
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Paper Novel Pyrazolo [1,5-a]-1,3,5-Triazine Derivatives as CDK7 Inhibitors: Synthesis and Biological Insights in Pancreatic D… DOI 10.1002/cmdc.202500448↗
- Paper Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer … DOI 10.1016/j.bioorg.2024.107959↗
- Fabio Scianò · 4 shared papers, 2024–2025 · strength 0.90
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Paper Exploring the therapeutic potential of focal adhesion kinase inhibition in overcoming chemoresistance in pancreatic duc… DOI 10.4155/fmc-2023-0234↗
- Paper Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer … DOI 10.1016/j.bioorg.2024.107959↗
- Juan Deng · 2 shared papers, 2024–2025 · strength 0.47
- Paper Corrigendum to "Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promi… DOI 10.1016/j.bioorg.2024.107995↗
- Paper Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer … DOI 10.1016/j.bioorg.2024.107959↗
- Btissame El Hassouni · 4 shared papers, 2019–2024 · strength 0.47
- Paper Exploring Splicing Modulation as an Innovative Approach to Combat Pancreatic Cancer: SF3B1 Emerges as a Prognostic Indi… DOI 10.7150/ijbs.92671↗
- Paper 3-(6-Phenylimidazo [2,1-b][1,3,4]thiadiazol-2-yl)-1H-Indole Derivatives as New Anticancer Agents in the Treatment of Pa… DOI 10.3390/molecules25020329↗
- Paper Biological Evaluation of the Antiproliferative and Anti-migratory Activity of a Series of 3-(6-Phenylimidazo[2,1-b][1,3… DOI 10.21873/anticanres.13509↗
- Giovanna Li Petri · 4 shared papers, 2019–2020 · strength 0.39
- Paper Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic… DOI 10.1016/j.ejmech.2020.112088↗
- Paper 3-(6-Phenylimidazo [2,1-b][1,3,4]thiadiazol-2-yl)-1H-Indole Derivatives as New Anticancer Agents in the Treatment of Pa… DOI 10.3390/molecules25020329↗
- Paper Biological Evaluation of the Antiproliferative and Anti-migratory Activity of a Series of 3-(6-Phenylimidazo[2,1-b][1,3… DOI 10.21873/anticanres.13509↗
- I Gede Putu Supadmanaba · 2 shared papers, 2022–2024 · strength 0.33
- Cecilia Bergonzini · 2 shared papers, 2020–2024 · strength 0.29
- Paper Exploring the therapeutic potential of a novel series of imidazothiadiazoles targeting focal adhesion kinase (FAK) for … DOI 10.1080/1061186x.2024.2385557↗
- Paper Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic… DOI 10.1016/j.ejmech.2020.112088↗
- Ornella Randazzo · 2 shared papers, 2021–2022 · strength 0.28
- Amir Avan · 2 shared papers, 2021 · strength 0.27
- Paper Cyclin Dependent Kinase-1 (CDK-1) Inhibition as a Novel Therapeutic Strategy against Pancreatic Ductal Adenocarcinoma (… DOI 10.3390/cancers13174389↗
- Paper A New Oxadiazole-Based Topsentin Derivative Modulates Cyclin-Dependent Kinase 1 Expression and Exerts Cytotoxic Effects… DOI 10.3390/molecules27010019↗
- Mahrou Vahabi · 1 shared paper, 2025 · strength 0.27
- Giulia Lencioni · 1 shared paper, 2025 · strength 0.27
- Niccola Funel · 2 shared papers, 2020 · strength 0.20
- Paper Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic… DOI 10.1016/j.ejmech.2020.112088↗
- Paper 3-(6-Phenylimidazo [2,1-b][1,3,4]thiadiazol-2-yl)-1H-Indole Derivatives as New Anticancer Agents in the Treatment of Pa… DOI 10.3390/molecules25020329↗
- Annalisa Comandatore · 1 shared paper, 2024 · strength 0.18
- Amir Avan · 1 shared paper, 2024 · strength 0.18
- Giulia Mantini · 1 shared paper, 2024 · strength 0.18
- Rocco Sciarrillo · 1 shared paper, 2024 · strength 0.18
- Luca Morelli · 1 shared paper, 2024 · strength 0.18
- Mjriam Capula · 1 shared paper, 2022 · strength 0.16
- Rosa Wijnen · 1 shared paper, 2021 · strength 0.14
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.