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Human Genetics|June 24, 2019
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humansThomas M Kitzler, Ronen Schneider, Stefan Kohl, et al.The New England Journal of Medicine|April 18, 2019
Effect of Anti-CD4 Antibody UB-421 on HIV-1 Rebound after Treatment InterruptionChang-Yi Wang, Wing-Wai Wong, Hung-Chin Tsai, et al.Journal of the American Heart Association|September 14, 2022
Sex Differences and Utility of Treadmill Testing in Long-QT SyndromeLauren A Yee, Hui-Chen Han, Brianna Davies, et al.The American Journal of Cardiology|April 8, 2022
Meta-Analysis of Percutaneous Coronary Intervention Versus Coronary Artery Bypass Grafting for Left Main NarrowingNicholas W S Chew, Chen-Han Ng, Gwyneth Kong, et al.American Journal of Medical Genetics. Part A|January 18, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse modelsChunyan Wang, Steve Seltzsam, Bixia Zheng, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 26, 2022
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasisAmar J Majmundar, Eugen Widmeier, John F Heneghan, et al.Journal of the American Society of Nephrology : JASN|November 22, 2022
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and FrogsVerena Klämbt, Florian Buerger, Chunyan Wang, et al.The Journal of Clinical Investigation|August 1, 2022
IgE-neutralizing UB-221 mAb, distinct from omalizumab and ligelizumab, exhibits CD23-mediated IgE downregulation and relieves urticaria symptomsBe-Sheng Kuo, Chao-Hung Li, Jiun-Bo Chen, et al.JAMA Cardiology|April 5, 2023
Association of the Timing and Extent of Cardiac Implantable Electronic Device Infections With MortalityHui-Chen Han, Jia Wang, David H Birnie, et al.American Journal of Human Genetics|November 12, 2019
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor MutationsNina Mann, Franziska Kause, Erik K Henze, et al.Pageof 55