ResearcherShanghai UniversityActive in the last 2 years
Yanyi Xiao
Matched on OpenAlex author ID A5103950557. Sources: OpenAlex.
Their work
- Papers
- 13 (first author 7, last author 2)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 14
2020: 1 paper · 2021: 5 papers · 2022: 3 papers · 2023: none · 2024: 3 papers · 2025: 1 paper
Papers 13
- Correction: Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR signaling pathway. First author DOI 10.1007/s12094-025-03997-9↗
- Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR signaling pathway. First author DOI 10.1007/s12094-023-03328-w↗
- Lymphocyte antigen 6 family member E suppresses apoptosis and promotes pancreatic cancer growth and migration via Wnt/β-catenin pathway activation. Last author DOI 10.1038/s41598-024-70764-1↗
- Author Correction: Lymphocyte antigen 6 family member E suppresses apoptosis and promotes pancreatic cancer growth and migration via Wnt/β-catenin pathway acti… Last author DOI 10.1038/s41598-024-73144-x↗
- The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, reduce immune evasion ability and suppress p… Co-author DOI 10.1038/s41419-022-04573-7↗
- Correction: The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, reduce immune evasion ability an… Co-author DOI 10.1038/s41419-022-04705-z↗
- Inhibition of STAT3Y705 phosphorylation by Stattic suppresses proliferation and induces mitochondrial-dependent apoptosis in pancreatic cancer cells. First author DOI 10.1038/s41420-022-00922-9↗
- Quercetin suppresses pancreatic ductal adenocarcinoma progression via inhibition of SHH and TGF-β/Smad signaling pathways. Co-author DOI 10.1007/s10565-020-09562-0↗
- The anti-dysenteric drug fraxetin enhances anti-tumor efficacy of gemcitabine and suppresses pancreatic cancer development by antagonizing STAT3 activation. First author DOI 10.18632/aging.203301↗
- Fisetin inhibits the proliferation, migration and invasion of pancreatic cancer by targeting PI3K/AKT/mTOR signaling. Co-author DOI 10.18632/aging.203713↗
- The isoflavone puerarin exerts anti-tumor activity in pancreatic ductal adenocarcinoma by suppressing mTOR-mediated glucose metabolism. First author DOI 10.18632/aging.203725↗
- Pharmacological Inhibition of STAT3 Attenuates Pancreatic Cancer Cell Invasion and Migration By Interacting with TGF-Β/Smad Signaling First author DOI 10.21203/rs.3.rs-1055773/v1↗
- The Anti-Dysenteric Drug Fraxetin Enhances Anti-Tumor Efficacy of Gemcitabine and Suppresses Pancreatic Cancer Development by Antagonizing STAT3 Activation First author DOI 10.21203/rs.3.rs-125318/v1↗
Closest collaborators
The 14 strongest of 14 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Qiyu Zhang · 8 shared papers, 2020–2025 · strength 1.31
- Paper Correction: Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR sign… DOI 10.1007/s12094-025-03997-9↗
- Paper Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR signaling pathwa… DOI 10.1007/s12094-023-03328-w↗
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Hangcheng Guo · 8 shared papers, 2020–2022 · strength 1.05
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Paper Correction: The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine ac… DOI 10.1038/s41419-022-04705-z↗
- Paper Inhibition of STAT3Y705 phosphorylation by Stattic suppresses proliferation and induces mitochondrial-dependent apoptos… DOI 10.1038/s41420-022-00922-9↗
- Yongheng Bai · 8 shared papers, 2020–2022 · strength 1.05
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Paper Correction: The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine ac… DOI 10.1038/s41419-022-04705-z↗
- Paper Inhibition of STAT3Y705 phosphorylation by Stattic suppresses proliferation and induces mitochondrial-dependent apoptos… DOI 10.1038/s41420-022-00922-9↗
- Miaomiao Lin · 4 shared papers, 2022–2025 · strength 0.83
- Paper Correction: Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR sign… DOI 10.1007/s12094-025-03997-9↗
- Paper Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR signaling pathwa… DOI 10.1007/s12094-023-03328-w↗
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Hengyue Zhu · 6 shared papers, 2020–2022 · strength 0.79
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Paper Correction: The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine ac… DOI 10.1038/s41419-022-04705-z↗
- Paper The isoflavone puerarin exerts anti-tumor activity in pancreatic ductal adenocarcinoma by suppressing mTOR-mediated glu… DOI 10.18632/aging.203725↗
- Yangyang Guo · 6 shared papers, 2020–2022 · strength 0.79
- Paper The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine activity, redu… DOI 10.1038/s41419-022-04573-7↗
- Paper Correction: The anthelmintic drug niclosamide induces GSK-β-mediated β-catenin degradation to potentiate gemcitabine ac… DOI 10.1038/s41419-022-04705-z↗
- Paper The isoflavone puerarin exerts anti-tumor activity in pancreatic ductal adenocarcinoma by suppressing mTOR-mediated glu… DOI 10.18632/aging.203725↗
- Kenan Cen · 2 shared papers, 2024 · strength 0.56
- Paper Lymphocyte antigen 6 family member E suppresses apoptosis and promotes pancreatic cancer growth and migration via Wnt/β… DOI 10.1038/s41598-024-70764-1↗
- Paper Author Correction: Lymphocyte antigen 6 family member E suppresses apoptosis and promotes pancreatic cancer growth and … DOI 10.1038/s41598-024-73144-x↗
- Zhe Chen · 2 shared papers, 2024–2025 · strength 0.52
- Paper Correction: Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR sign… DOI 10.1007/s12094-025-03997-9↗
- Paper Chloroxine inhibits pancreatic cancer progression through targeted antagonization of the PI3K/AKT/mTOR signaling pathwa… DOI 10.1007/s12094-023-03328-w↗
- Jiawei Chen · 2 shared papers, 2021–2022 · strength 0.26
- Paper Inhibition of STAT3Y705 phosphorylation by Stattic suppresses proliferation and induces mitochondrial-dependent apoptos… DOI 10.1038/s41420-022-00922-9↗
- Paper Pharmacological Inhibition of STAT3 Attenuates Pancreatic Cancer Cell Invasion and Migration By Interacting with TGF-Β/… DOI 10.21203/rs.3.rs-1055773/v1↗
- Qinbo Chen · 2 shared papers, 2021–2022 · strength 0.26
- Paper Inhibition of STAT3Y705 phosphorylation by Stattic suppresses proliferation and induces mitochondrial-dependent apoptos… DOI 10.1038/s41420-022-00922-9↗
- Paper Pharmacological Inhibition of STAT3 Attenuates Pancreatic Cancer Cell Invasion and Migration By Interacting with TGF-Β/… DOI 10.21203/rs.3.rs-1055773/v1↗
- Junjie Deng · 2 shared papers, 2020–2021 · strength 0.23
- Paper The anti-dysenteric drug fraxetin enhances anti-tumor efficacy of gemcitabine and suppresses pancreatic cancer developm… DOI 10.18632/aging.203301↗
- Paper The Anti-Dysenteric Drug Fraxetin Enhances Anti-Tumor Efficacy of Gemcitabine and Suppresses Pancreatic Cancer Developm… DOI 10.21203/rs.3.rs-125318/v1↗
- Linxiao Sun · 1 shared paper, 2021 · strength 0.14
- Xiangyang Lin · 1 shared paper, 2021 · strength 0.13
- Yunfeng Shan · 1 shared paper, 2021 · strength 0.13
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.