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American Journal of Physiology. Renal Physiology|July 21, 2017
Heterozygous loss-of-function mutation in Odd-skipped related 1 (<i>Osr1</i>) is associated with vesicoureteric reflux, duplex systems, and hydronephrosisMarie-Lyne Fillion, Jasmine El Andalousi, Fatima Tokhmafshan, et al.
Toxicology and Applied Pharmacology|May 1, 2025
Mouse nephron formation is impaired by moderate dose arsenical exposureCarlos Agustin Isidro Alonso, Jenna Haverfield, Gabriela Regalado, et al.
Kidney International|January 8, 2019
Recessive mutation in CD2AP causes focal segmental glomerulosclerosis in humans and miceTomoko Takano, Eric Bareke, Naoki Takeda, et al.
Hormone Research in Paediatrics|July 28, 2021
CYP24A1 and SLC34A1 Pathogenic Variants Are Uncommon in a Canadian Cohort of Children with Hypercalcemia or HypercalciuriaIsabelle Rousseau-Nepton, Glenville Jones, Karlpiet Schlingmann, et al.
Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada|November 9, 2019
Children with vesicoureteric reflux have joint hypermobility and occasional tenascin XB sequence variantsFatima Tokhmafshan, Jasmine El Andalousi, Vasikar Murugapoopathy, et al.
Pediatric Nephrology (Berlin, Germany)|September 27, 2015
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric refluxShan Elahi, Alison Homstad, Himani Vaidya, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2013
TNXB mutations can cause vesicoureteral refluxRasheed A Gbadegesin, Patrick D Brophy, Adebowale Adeyemo, et al.
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