Showing results (181-190 of 261) with videos related to

Sort By:
Pageof 27
Journal of the American Society of Nephrology : JASN|March 2, 2022
DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk VariantsJustin Chun, Cristian V Riella, Hyunjae Chung, et al.
World Journal of Otorhinolaryngology|May 12, 2015
SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Human Mutation|April 29, 2026
De Novo TRIO Missense Variants Disrupt Ras-GEF Domains and Cause Congenital Ventriculomegaly and HydrocephalusNeel H Mehta, Evan Dennis, Garrett Allington, et al.
American Journal of Physiology. Cell Physiology|May 16, 2019
Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cellsAlicia Rivera, David H Vandorpe, Boris E Shmukler, et al.
Frontiers in Physiology|July 10, 2015
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393WFabian R Reimold, Savithri Balasubramanian, David B Doroquez, et al.
Plos One|February 19, 2013
Transcriptional patterns in peritoneal tissue of encapsulating peritoneal sclerosis, a complication of chronic peritoneal dialysisFabian R Reimold, Niko Braun, Zsuzsanna K Zsengellér, et al.
JCI Insight|February 23, 2018
Inducible podocyte-specific deletion of CTCF drives progressive kidney disease and bone abnormalitiesMarta Christov, Abbe R Clark, Braden Corbin, et al.
Journal of the American Society of Nephrology : JASN|May 8, 2026
Purine Metabolism Regulates the Severity of APOL1 NephropathyHuihui Huang, Calum Tattersfield, Sonako Jacas, et al.
Pageof 27