Showing results (91-100 of 161) with videos related to
Sort By:
Pageof 17
Elife|December 18, 2015
The serine protease hepsin mediates urinary secretion and polymerisation of Zona Pellucida domain protein uromodulinMartina Brunati, Simone Perucca, Ling Han, et al.Journal of the American Society of Nephrology : JASN|July 28, 2018
Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease RecognitionKarl X Knaup, Thomas Hackenbeck, Bernt Popp, et al.Kidney International Reports|August 15, 2025
Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney DiseaseChristin Findeisen, Maria Papazian, Linda Pöschla, et al.ACS Sensors|June 25, 2026
CRISPR-Based Assay for Point-of-Care Pharmacogenetic CYP2C19 GenotypingAlexander J Schubert, Qiyao Meng, Joshua Hoffmann, et al.Human Genetics|February 20, 2019
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasisAli Amar, Amar J Majmundar, Ihsan Ullah, et al.Brain Communications|August 23, 2021
Identification of LAMA1 mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndromeLaura Powell, Eric Olinger, Sarah Wedderburn, et al.American Journal of Human Genetics|January 5, 2019
Mutations of ADAMTS9 Cause Nephronophthisis-Related CiliopathyYo Jun Choi, Jan Halbritter, Daniela A Braun, et al.Journal of Lipid Research|September 12, 2013
THOC5: a novel gene involved in HDL-cholesterol metabolismMaria Keller, Dorit Schleinitz, Julia Förster, et al.Clinical Kidney Journal|July 3, 2026
Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group surveyMalte P Bartram, Giovambattista Capasso, Emilie Cornec-Le Gall, et al.Kidney International Reports|August 19, 2024
Pathogenic PHIP Variants are Variably Associated With CAKUTJonathan de Fallois, Tobias Sieckmann, Ria Schönauer, et al.Pageof 17