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International Heart Journal|January 18, 2021
FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of CardiomyopathyXianyu Qin, Ping Li, Hui-Qi Qu, et al.
Brain, Behavior, and Immunity|April 27, 2024
Shared molecular mechanisms and transdiagnostic potential of neurodevelopmental disorders and immune disordersZhanjie Xiu, Ling Sun, Kunlun Liu, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 28, 2024
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestryHui-Qi Qu, Matthew S Delfiner, Chethan Gangireddy, et al.
Archives of Medical Research|September 11, 2012
Population-based risk factors for elevated alanine aminotransferase in a South Texas Mexican-American populationHui-Qi Qu, Quan Li, Megan L Grove, et al.
Human Molecular Genetics|June 19, 2019
Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic riskJennie G Pouget, , Buhm Han, et al.
FEBS Letters|May 7, 2021
Serum levels of the IgA isotype switch factor TGF-β1 are elevated in patients with COVID-19Er-Yi Wang, Hao Chen, Bao-Qing Sun, et al.
Nature|February 13, 2007
A genome-wide association study identifies novel risk loci for type 2 diabetesRobert Sladek, Ghislain Rocheleau, Johan Rung, et al.
ERJ Open Research|February 10, 2021
Heparin-binding protein levels correlate with aggravation and multiorgan damage in severe COVID-19Mingshan Xue, Yifeng Zeng, Hui-Qi Qu, et al.
Orphanet Journal of Rare Diseases|April 24, 2020
Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndromeYueheng Wu, Yu Xia, Ping Li, et al.
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