ResearcherWayne State UniversityActive in the last 2 years
Steve H. Kim
Matched on ORCID iD 0000-0001-9950-1232; OpenAlex author ID A5089628525. Sources: OpenAlex.
Their work
- Papers
- 6 (first author 0, last author 1)
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 24
2020: 2 papers · 2021: none · 2022: 2 papers · 2023: 1 paper · 2024: none · 2025: 1 paper
Papers 6
- Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcinoma Co-author DOI 10.1101/2025.11.21.689857↗
- Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. Co-author DOI 10.1002/ctm2.1513↗
- Potentially curative resection of an abdominal wall metastasis from pancreatic adenocarcinoma: a case report. Last author DOI 10.1093/jscr/rjac138↗
- Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53 fl/+; Pdx1-Cre (KPC) pancreatic cancer … Co-author DOI 10.1101/2022.03.08.481108↗
- Preclinical Assessment with Clinical Validation of Selinexor with Gemcitabine and Nab-Paclitaxel for the Treatment of Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.1158/1078-0432.ccr-19-1728↗
- Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferation and Patient-Derived Tumor Growth. Co-author DOI 10.3390/cancers12030750↗
Closest collaborators
The 24 strongest of 24 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Husain Yar Khan · 5 shared papers, 2020–2025 · strength 0.63
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Amro Aboukameel · 5 shared papers, 2020–2025 · strength 0.63
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Asfar Sohail Azmi · 5 shared papers, 2020–2025 · strength 0.63
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Sahar F. Bannoura · 3 shared papers, 2022–2025 · strength 0.44
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Md. Hafiz Uddin · 3 shared papers, 2022–2025 · strength 0.44
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Anthony Frank Shields · 3 shared papers, 2022–2025 · strength 0.44
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Ramzi M. Mohammad · 3 shared papers, 2020–2025 · strength 0.36
- Paper Co-targeting KRAS and Exportin1 as an effective therapeutic strategy for KRASG12D mutant pancreatic ductal adenocarcino… DOI 10.1101/2025.11.21.689857↗
- Paper Preclinical Assessment with Clinical Validation of Selinexor with Gemcitabine and Nab-Paclitaxel for the Treatment of P… DOI 10.1158/1078-0432.ccr-19-1728↗
- Paper Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferat… DOI 10.3390/cancers12030750↗
- Philip A. Philip · 3 shared papers, 2020–2023 · strength 0.33
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Preclinical Assessment with Clinical Validation of Selinexor with Gemcitabine and Nab-Paclitaxel for the Treatment of P… DOI 10.1158/1078-0432.ccr-19-1728↗
- Paper Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferat… DOI 10.3390/cancers12030750↗
- Tanya Odisho · 2 shared papers, 2022–2023 · strength 0.33
- Yiwei Li · 2 shared papers, 2022–2023 · strength 0.27
- Paper Molecular analysis of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in KPC pancreatic cancer mouse model. DOI 10.1002/ctm2.1513↗
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Rachel E. Sexton · 2 shared papers, 2020–2022 · strength 0.22
- Paper Molecular profiling of XPO1 inhibitor and gemcitabine-nab-paclitaxel combination in cellular and LSL-Kras G12D/+; Trp53… DOI 10.1101/2022.03.08.481108↗
- Paper Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferat… DOI 10.3390/cancers12030750↗
- Anteneh A. Tesfaye · 2 shared papers, 2020 · strength 0.19
- Paper Preclinical Assessment with Clinical Validation of Selinexor with Gemcitabine and Nab-Paclitaxel for the Treatment of P… DOI 10.1158/1078-0432.ccr-19-1728↗
- Paper Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferat… DOI 10.3390/cancers12030750↗
- Mandana Kamgar · 2 shared papers, 2020 · strength 0.19
- Paper Preclinical Assessment with Clinical Validation of Selinexor with Gemcitabine and Nab-Paclitaxel for the Treatment of P… DOI 10.1158/1078-0432.ccr-19-1728↗
- Paper Calcium Release-Activated Calcium (CRAC) Channel Inhibition Suppresses Pancreatic Ductal Adenocarcinoma Cell Proliferat… DOI 10.3390/cancers12030750↗
- P. A. Philip · 1 shared paper, 2025 · strength 0.17
- Bin Bao · 1 shared paper, 2025 · strength 0.17
- Boris Pasche · 1 shared paper, 2025 · strength 0.17
- Eliza Wright Beal · 1 shared paper, 2025 · strength 0.17
- Muhammad Wasif Saif · 1 shared paper, 2025 · strength 0.17
- Azeddine Atfi · 1 shared paper, 2025 · strength 0.17
- Bassel F. El‐Rayes · 1 shared paper, 2025 · strength 0.17
- Ibrahim Hanna Azar · 1 shared paper, 2023 · strength 0.14
- Irfana Muqbil · 1 shared paper, 2020 · strength 0.09
- Maria Diab · 1 shared paper, 2020 · strength 0.09
- Amit Mahipal · 1 shared paper, 2020 · strength 0.09
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.