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Kidney International|August 18, 2019
From podocyte biology to novel cures for glomerular diseaseElena Torban, Fabian Braun, Nicola Wanner, et al.
European Journal of Human Genetics : EJHG|July 10, 2024
Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisisZachary T Sentell, Zachary W Nurcombe, Lina Mougharbel, et al.
Kidney International|March 11, 2011
T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney diseaseMichelle M Miller, Diana M Iglesias, Zhao Zhang, et al.
American Journal of Physiology. Renal Physiology|May 12, 2007
Canonical WNT signaling during kidney developmentDiana M Iglesias, Pierre-Alain Hueber, LeeLee Chu, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 1, 2008
PAX3 is expressed in the stromal compartment of the developing kidney and in Wilms tumors with myogenic phenotypePierre-Alain Hueber, Ryuji Fukuzawa, Reyhan Elkares, et al.
Human Molecular Genetics|December 18, 2024
Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisisZachary T Sentell, Lina Mougharbel, Zachary W Nurcombe, et al.
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