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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 10, 2020
Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney diseaseMiranda Durkie, Jiehan Chong, Manoj K Valluru, et al.
Journal of the American Society of Nephrology : JASN|January 5, 2007
Endothelin B receptor blockade accelerates disease progression in a murine model of autosomal dominant polycystic kidney diseaseMing-Yang Chang, Emma Parker, Meguid El Nahas, et al.
Journal of Cell Science|April 9, 2009
Homophilic and heterophilic polycystin 1 interactions regulate E-cadherin recruitment and junction assembly in MDCK cellsAndrew J Streets, Bart E Wagner, Peter C Harris, et al.
Clinical Kidney Journal|June 27, 2022
Individualized everolimus treatment for tuberous sclerosis-related angiomyolipoma promotes treatment adherence and responseNoelle K X Chung, Peter Metherall, Janet A McCormick, et al.
Transplantation|October 24, 2014
Genetic testing in the assessment of living related kidney donors at risk of autosomal dominant polycystic kidney diseaseRoslyn J Simms, Debbie L Travis, Miranda Durkie, et al.
Clinical Kidney Journal|June 3, 2026
Health-related quality of life in people with autosomal dominant polycystic kidney disease: a systematic reviewMatt Gittus, Yanan Zhang, Sue Harnan, et al.
Small (Weinheim an Der Bergstrasse, Germany)|July 11, 2013
Fabrication and luminescence of monolayered boron nitride quantum dotsLiangxu Lin, Yaoxian Xu, Shaowei Zhang, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 19, 2025
Monoallelic IFT140 Variants Causing Childhood-Onset Autosomal Dominant Polycystic Kidney DiseaseJoshua D Griffiths, Grace Ehidiamhen, Sergio Camilo Lopez-Garcia, et al.
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