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Clinical Nephrology|September 22, 2017
Renal histology and MRI findings in a 37-year-old Japanese patient with autosomal recessive polycystic kidney disease
Yusuke Ito, Akinari Sekine, Daisuke Takada, et al.Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
<i>CFAP47</i> is a novel causative gene implicated in X-linked polycystic kidney diseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.Kidney International Reports|December 19, 2024
CFAP47 is Implicated in X-Linked Polycystic Kidney DiseaseTakayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.Proceedings of the National Academy of Sciences of the United States of America|April 28, 2026
LRBA organizes distinct vesicular trafficking systems in distal nephron segments for water and sodium conservationKanako Nagaoka, Fumiaki Ando, Tamami Fujiki, et al.Kidney International|October 20, 2024
ULK1-regulated AMP sensing by AMPK and its application for the treatment of chronic kidney diseaseTomoki Yanagi, Hiroaki Kikuchi, Koh Takeuchi, et al.Kidney International Reports|May 20, 2021
Genetic Background and Clinicopathologic Features of Adult-onset NephronophthisisTakuya Fujimaru, Kunio Kawanishi, Takayasu Mori, et al.Pageof 8