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Kidney International|December 14, 2012
Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complementSanjeev Sethi, Fernando C Fervenza, Yuzhou Zhang, et al.Human Genetics|January 17, 2022
AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing lossRyan K Thorpe, W Daniel Walls, Rae Corrigan, et al.Journal of the American Society of Nephrology : JASN|July 26, 2011
Allelic variants of complement genes associated with dense deposit diseaseMaria Asuncion Abrera-Abeleda, Carla Nishimura, Kathy Frees, et al.American Journal of Medical Genetics. Part A|February 27, 2010
miRNA mutations are not a common cause of deafnessMichael S Hildebrand, P Dane Witmer, Shunbin Xu, et al.Journal of Human Genetics|December 13, 2019
A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated familiesLeigh A M Demain, Erica H Gerkes, Richard J H Smith, et al.The Pharmacogenomics Journal|June 20, 2003
Generation and analysis of mice with a targeted disruption of the arylamine N-acetyltransferase type 2 geneV A Cornish, K Pinter, S Boukouvala, et al.Nucleic Acids Research|July 4, 2012
Transposon-mediated BAC transgenesis in human ES cellsMaria Rostovskaya, Jun Fu, Mandy Obst, et al.Human Mutation|May 18, 2004
Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequencesEugene H Chang, Maithilee Menezes, Nicole C Meyer, et al.Hearing Research|April 24, 2008
Gene expression analysis of human otosclerotic stapedial footplatesMegan Ealy, Wenjie Chen, Gi-Yung Ryu, et al.Stem Cells (Dayton, Ohio)|May 8, 2013
Hes1 desynchronizes differentiation of pluripotent cells by modulating STAT3 activityXinzhi Zhou, Andrew J H Smith, Anna Waterhouse, et al.Pageof 71