ResearcherCedars-Sinai Medical CenterActive in the last 2 years
Qiang Wang
Matched on ORCID iD 0000-0001-9409-0251; OpenAlex author ID A5100686126. Sources: OpenAlex.
Their work
- Papers
- 7 (first author 0, last author 3)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 26
2014: 1 paper · 2015: 1 paper · 2016: none · 2017: 1 paper · 2018: 1 paper · 2019: 1 paper · 2020: none · 2021: 1 paper · 2022: none · 2023: none · 2024: 1 paper
Papers 7
- Verteporfin induces lipid peroxidation and ferroptosis in pancreatic cancer cells. Co-author DOI 10.1016/j.freeradbiomed.2024.01.003↗
- Epithelial cell transforming 2 is regulated by Yes-associated protein 1 and mediates pancreatic cancer progression and metastasis. Last author DOI 10.1152/ajpgi.00185.2020↗
- MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal Adenocarcinoma (PDAC). Last author DOI 10.3389/fphys.2019.00147↗
- An Inhibitor of GSK3B and HDACs Kills Pancreatic Cancer Cells and Slows Pancreatic Tumor Growth and Metastasis in Mice. Co-author DOI 10.1053/j.gastro.2018.08.028↗
- Cadherin-11 Is a Cell Surface Marker Up-Regulated in Activated Pancreatic Stellate Cells and Is Involved in Pancreatic Cancer Cell Migration. Co-author DOI 10.1016/j.ajpath.2016.09.012↗
- Role of YAP and TAZ in pancreatic ductal adenocarcinoma and in stellate cells associated with cancer and chronic pancreatitis. Last author DOI 10.1038/srep16759↗
- Establishment of an orthotopic pancreatic cancer mouse model: cells suspended and injected in Matrigel. Co-author DOI 10.3748/wjg.v20.i28.9476↗
Closest collaborators
The 25 strongest of 26 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Stephen Jacob Pandol · 6 shared papers, 2015–2024 · strength 0.61
- Paper Verteporfin induces lipid peroxidation and ferroptosis in pancreatic cancer cells. DOI 10.1016/j.freeradbiomed.2024.01.003↗
- Paper Epithelial cell transforming 2 is regulated by Yes-associated protein 1 and mediates pancreatic cancer progression and … DOI 10.1152/ajpgi.00185.2020↗
- Paper MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal… DOI 10.3389/fphys.2019.00147↗
- Mouad Edderkaoui · 4 shared papers, 2017–2024 · strength 0.42
- Paper Verteporfin induces lipid peroxidation and ferroptosis in pancreatic cancer cells. DOI 10.1016/j.freeradbiomed.2024.01.003↗
- Paper MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal… DOI 10.3389/fphys.2019.00147↗
- Paper An Inhibitor of GSK3B and HDACs Kills Pancreatic Cancer Cells and Slows Pancreatic Tumor Growth and Metastasis in Mice. DOI 10.1053/j.gastro.2018.08.028↗
- Susan Morvaridi · 3 shared papers, 2015–2019 · strength 0.21
- Paper MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal… DOI 10.3389/fphys.2019.00147↗
- Paper Role of YAP and TAZ in pancreatic ductal adenocarcinoma and in stellate cells associated with cancer and chronic pancre… DOI 10.1038/srep16759↗
- Paper Cadherin-11 Is a Cell Surface Marker Up-Regulated in Activated Pancreatic Stellate Cells and Is Involved in Pancreatic … DOI 10.1016/j.ajpath.2016.09.012↗
- Ce Li · 2 shared papers, 2019–2021 · strength 0.21
- Paper Epithelial cell transforming 2 is regulated by Yes-associated protein 1 and mediates pancreatic cancer progression and … DOI 10.1152/ajpgi.00185.2020↗
- Paper MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal… DOI 10.3389/fphys.2019.00147↗
- Nicholas N. Nissen · 2 shared papers, 2019–2021 · strength 0.21
- Paper Epithelial cell transforming 2 is regulated by Yes-associated protein 1 and mediates pancreatic cancer progression and … DOI 10.1152/ajpgi.00185.2020↗
- Paper MSP-RON Signaling Is Activated in the Transition From Pancreatic Intraepithelial Neoplasia (PanIN) to Pancreatic Ductal… DOI 10.3389/fphys.2019.00147↗
- Tao Liu · 1 shared paper, 2024 · strength 0.21
- Omer Hany Miligy Elmadbouh · 1 shared paper, 2024 · strength 0.21
- Wei Jie Zhou · 1 shared paper, 2024 · strength 0.21
- Raul A. Urrutia · 1 shared paper, 2024 · strength 0.21
- Arsen Osipov · 1 shared paper, 2024 · strength 0.21
- Neil A. Bhowmick · 1 shared paper, 2018 · strength 0.07
- Aida Habtezion · 1 shared paper, 2018 · strength 0.07
- László G. Boros · 1 shared paper, 2018 · strength 0.07
- Jian Tajbakhsh · 1 shared paper, 2018 · strength 0.07
- Richard Tuli · 1 shared paper, 2018 · strength 0.07
- Ramachandran Murali · 1 shared paper, 2018 · strength 0.07
- Deepti Dhall · 1 shared paper, 2015 · strength 0.06
- Chiara Birtolo · 1 shared paper, 2017 · strength 0.06
- Hung Pham · 1 shared paper, 2017 · strength 0.06
- Brent K. Larson · 1 shared paper, 2017 · strength 0.06
- Vay Liang W. Go · 1 shared paper, 2017 · strength 0.06
- Chong-Lek Lee · 1 shared paper, 2014 · strength 0.05
- Feng Yang · 1 shared paper, 2014 · strength 0.05
- Chen Jin · 1 shared paper, 2014 · strength 0.05
- Yongjian Jiang · 1 shared paper, 2014 · strength 0.05
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.