ResearcherWenzhou Medical UniversityActive in the last 2 years
Hongchun Guo
Matched on OpenAlex author ID A5108083191. Sources: OpenAlex.
Their work
- Papers
- 6
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 9
2012: 4 papers · 2013: none · 2014: none · 2015: none · 2016: none · 2017: none · 2018: none · 2019: none · 2020: 1 paper · 2021: none · 2022: none · 2023: none · 2024: 1 paper
Papers 6
- [Retracted] Emodin alleviates gemcitabine resistance in pancreatic cancer by inhibiting MDR1/P‑glycoprotein and MRPs expression. Co-author DOI 10.3892/ol.2024.14568↗
- Emodin alleviates gemcitabine resistance in pancreatic cancer by inhibiting MDR1/P-glycoprotein and MRPs expression. Co-author DOI 10.3892/ol.2020.12030↗
- Antitumor activity of emodin against pancreatic cancer depends on its dual role: promotion of apoptosis and suppression of angiogenesis. Co-author DOI 10.1371/journal.pone.0042146↗
- Emodin reverses gemcitabine resistance in pancreatic cancer cells via the mitochondrial apoptosis pathway in vitro. Co-author DOI 10.3892/ijo.2011.1285↗
- Oridonin enhances antitumor activity of gemcitabine in pancreatic cancer through MAPK-p38 signaling pathway. Co-author DOI 10.3892/ijo.2012.1519↗
- Enhanced antitumor efficacy of gemcitabine by evodiamine on pancreatic cancer via regulating PI3K/Akt pathway. Co-author DOI 10.7150/ijbs.8.1↗
Closest collaborators
The 9 strongest of 9 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Tao Xue · 2 shared papers, 2020–2024 · strength 0.47
- Paper [Retracted] Emodin alleviates gemcitabine resistance in pancreatic cancer by inhibiting MDR1/P‑glycoprotein and MRPs ex… DOI 10.3892/ol.2024.14568↗
- Paper Emodin alleviates gemcitabine resistance in pancreatic cancer by inhibiting MDR1/P-glycoprotein and MRPs expression. DOI 10.3892/ol.2020.12030↗
- Zhaohong Wang · 3 shared papers, 2012 · strength 0.09
- Paper Oridonin enhances antitumor activity of gemcitabine in pancreatic cancer through MAPK-p38 signaling pathway. DOI 10.3892/ijo.2012.1519↗
- Paper Enhanced antitumor efficacy of gemcitabine by evodiamine on pancreatic cancer via regulating PI3K/Akt pathway. DOI 10.7150/ijbs.8.1↗
- Paper Antitumor activity of emodin against pancreatic cancer depends on its dual role: promotion of apoptosis and suppression… DOI 10.1371/journal.pone.0042146↗
- Sheng‐Zhang Lin · 3 shared papers, 2012 · strength 0.09
- Paper Oridonin enhances antitumor activity of gemcitabine in pancreatic cancer through MAPK-p38 signaling pathway. DOI 10.3892/ijo.2012.1519↗
- Paper Antitumor activity of emodin against pancreatic cancer depends on its dual role: promotion of apoptosis and suppression… DOI 10.1371/journal.pone.0042146↗
- Paper Emodin reverses gemcitabine resistance in pancreatic cancer cells via the mitochondrial apoptosis pathway in vitro. DOI 10.3892/ijo.2011.1285↗
- Hongfei Tong · 3 shared papers, 2012 · strength 0.09
- Paper Enhanced antitumor efficacy of gemcitabine by evodiamine on pancreatic cancer via regulating PI3K/Akt pathway. DOI 10.7150/ijbs.8.1↗
- Paper Antitumor activity of emodin against pancreatic cancer depends on its dual role: promotion of apoptosis and suppression… DOI 10.1371/journal.pone.0042146↗
- Paper Emodin reverses gemcitabine resistance in pancreatic cancer cells via the mitochondrial apoptosis pathway in vitro. DOI 10.3892/ijo.2011.1285↗
- Dian-Lei Liu · 3 shared papers, 2012 · strength 0.09
- Paper Enhanced antitumor efficacy of gemcitabine by evodiamine on pancreatic cancer via regulating PI3K/Akt pathway. DOI 10.7150/ijbs.8.1↗
- Paper Antitumor activity of emodin against pancreatic cancer depends on its dual role: promotion of apoptosis and suppression… DOI 10.1371/journal.pone.0042146↗
- Paper Emodin reverses gemcitabine resistance in pancreatic cancer cells via the mitochondrial apoptosis pathway in vitro. DOI 10.3892/ijo.2011.1285↗
- Heqi Bu · 2 shared papers, 2012 · strength 0.06
- Weitian Wei · 2 shared papers, 2012 · strength 0.06
- Jian-Hong Zhang · 1 shared paper, 2012 · strength 0.03
- Shengzhang Lin · 1 shared paper, 2012 · strength 0.03
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.