Showing results (41-50 of 57) with videos related to
Sort By:
Pageof 6
Proceedings of the National Academy of Sciences of the United States of America|November 3, 2006
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channelsTobias B Huber, Bernhard Schermer, Roman Ulrich Müller, et al.Nature Methods|December 19, 2018
U-Net: deep learning for cell counting, detection, and morphometryThorsten Falk, Dominic Mai, Robert Bensch, et al.Nature Methods|February 27, 2019
Author Correction: U-Net: deep learning for cell counting, detection, and morphometryThorsten Falk, Dominic Mai, Robert Bensch, et al.Journal of the American Society of Nephrology : JASN|March 9, 2017
Targeting mTOR Signaling Can Prevent the Progression of FSGSStefan Zschiedrich, Tillmann Bork, Wei Liang, et al.Frontiers in Endocrinology|March 17, 2023
Four missense genetic variants in <i>CUBN</i> are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in EuropeansNicoline Uglebjerg, Fariba Ahmadizar, Dina M Aly, et al.Science Advances|November 28, 2025
Arp2/3-dependent regulation of ciliogenesis governs adaptive distal tubular epithelial cell states in kidney diseaseManuel Rogg, Lisa Weißer, Jasmin I Maier, et al.Plos Genetics|May 17, 2018
A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and fliesSara Gonçalves, Julie Patat, Maria Clara Guida, et al.Plos Genetics|October 27, 2018
Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and fliesSara Gonçalves, Julie Patat, Maria Clara Guida, et al.The Journal of Experimental Medicine|November 12, 2017
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defectsMaria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.Diabetologia|December 15, 2018
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuriaTarunveer S Ahluwalia, Christina-Alexandra Schulz, Johannes Waage, et al.Pageof 6