scispace - formally typeset
F

Fan Yang

Researcher at Shandong University

Publications -  59
Citations -  2484

Fan Yang is an academic researcher from Shandong University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 17, co-authored 43 publications receiving 1682 citations. Previous affiliations of Fan Yang include University of Toronto & Purdue University.

Papers
More filters
Journal ArticleDOI

Widespread Macromolecular Interaction Perturbations in Human Genetic Disorders

TL;DR: This work functionally profile several thousand missense mutations across a spectrum of Mendelian disorders using various interaction assays, suggesting that disease-associated alleles that perturb distinct protein activities rather than grossly affecting folding and stability are relatively widespread.
Journal ArticleDOI

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing

TL;DR: This work cloned full-length open reading frames of alternatively spliced transcripts for a large number of human genes and used protein-protein interaction profiling to functionally compare hundreds of protein isoform pairs, revealing a widespread expansion of protein interaction capabilities through alternative splicing and suggesting that many alternative "isoforms" are functionally divergent (i.e., "functional alloforms").
Journal ArticleDOI

NLRP3 deficiency ameliorates neurovascular damage in experimental ischemic stroke

TL;DR: It is found that NLRP3 deficiency ameliorated cerebral injury in mice after ischemic stroke by reducing infarcts and blood–brain barrier (BBB) damage and that NOX2 deficiency improved outcomes after ischemia stroke by mediatingNLRP3 signaling.
Journal ArticleDOI

Human B cell clonal expansion and convergent antibody responses to SARS-CoV-2

TL;DR: It is shown that patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) who develop coronav virus disease 2019 (COVID-19) display early recruitment of B cells expressing a limited subset of IGHV genes, progressing to a highly polyclonal response of B Cells with broader I GHV gene usage and extensive class switching to IgG and IgA subclasses with limited somatic hypermutation in the initial weeks of infection.