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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.
Nature Communications|November 23, 2023
The extrafollicular B cell response is a hallmark of childhood idiopathic nephrotic syndromeTho-Alfakar Al-Aubodah, Lamine Aoudjit, Giuseppe Pascale, 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.
American Journal of Physiology. Renal Physiology|January 1, 2016
Novel unbiased assay for circulating podocyte-toxic factors associated with recurrent focal segmental glomerulosclerosisNadezda Kachurina, Chen-Fang Chung, Erin Benderoff, et al.
Canadian Journal of Kidney Health and Disease|May 17, 2021
Making the Correct Diagnosis in Thrombotic Microangiopathy: A Narrative ReviewPhilip A McFarlane, Martin Bitzan, Catherine Broome, et al.
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