Author

Jie Yan

First Affiliated Hospital of GuangXi Medical UniversityORCID 0000-0003-2040-5964Unclaimed ORCID profile · follow to get notified of new preprints

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2019-2020 · peak 1/yr

10 top collaborators · 20 mutual co-author links

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1 shared paperMolecular Biology

Ailin TaoORCID

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2 papers

Molecular BiologybioRxivPreprintJan 29, 2020

This study identifies a novel γAla327Val mutation in the FGG gene causing congenital dysfibrinogenemia by altering fibrinogen structure and function.

DOI 10.1101/2020.01.29.925172

Molecular BiologyCell Death and DiseasePeer-reviewedApr 24, 2019

This study shows that inhibiting HtrA2 reduces colitis by preventing necroptosis in intestinal epithelial cells in DSS-induced colitis models.

52 citations