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Journal of the American Society of Nephrology : JASN|March 3, 2012
Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencingSandro Rossetti, Katharina Hopp, Robert A Sikkink, et al.Journal of the American Society of Nephrology : JASN|October 11, 2015
Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney DiseaseYoung-Hwan Hwang, John Conklin, Winnie Chan, et al.Human Molecular Genetics|April 16, 2011
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysisKatharina Hopp, Christina M Heyer, Cynthia J Hommerding, et al.Kidney International|June 14, 2013
Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 familiesBinu M Paul, Mark B Consugar, Moonnoh Ryan Lee, et al.Pituitary|July 12, 2011
Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutationLuis V Syro, Jamie L Sundsbak, Bernd W Scheithauer, et al.Journal of the American Society of Nephrology : JASN|December 6, 2014
Identification of Biomarkers for PKD1 Using Urinary ExosomesMarie C Hogan, Jason L Bakeberg, Vladimir G Gainullin, et al.Journal of the American Society of Nephrology : JASN|June 7, 2014
Imaging classification of autosomal dominant polycystic kidney disease: a simple model for selecting patients for clinical trialsMaría V Irazabal, Laureano J Rangel, Eric J Bergstralh, et al.BMC Nephrology|November 19, 2015
Strategy and rationale for urine collection protocols employed in the NEPTUNE studyMarie C Hogan, John C Lieske, Chrysta C Lienczewski, et al.Journal of the American Society of Nephrology : JASN|January 30, 2016
Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney DiseaseChristina M Heyer, Jamie L Sundsbak, Kaleab Z Abebe, et al.Pageof 2