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The EMBO Journal|August 23, 2012
AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosisKatja Höpker, Henning Hagmann, Safiya Khurshid, et al.Cell Death & Disease|September 20, 2022
Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumorsLena Blümel, Nan Qin, Johannes Berlandi, et al.Kidney International|January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summaryVicente E Torres, Curie Ahn, Thijs R M Barten, et al.Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.Kidney International Reports|August 19, 2024
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 MicrodeletionsBénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, et al.Kidney International|March 23, 2025
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countriesCharlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.Cell|August 7, 2012
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingMoumita Chaki, Rannar Airik, Amiya K Ghosh, et al.Pageof 9