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American Journal of Physiology. Renal Physiology|July 10, 2015
The cpk model of recessive PKD shows glutamine dependence associated with the production of the oncometabolite 2-hydroxyglutarateVicki J Hwang, Jeffrey Kim, Amy Rand, et al.
Kidney International|June 18, 2010
Renal CD14 expression correlates with the progression of cystic kidney diseaseJuling Zhou, Xiaosen Ouyang, Xiangqin Cui, et al.
BMC Nephrology|February 14, 2023
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney diseaseDjalila Mekahli, Max C Liebau, Melissa A Cadnapaphornchai, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 15, 2023
Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells: A mechanistic connection between the kidney defects in cpk mice and human ARPKDYiming J Zhang, Chaozhe Yang, Wei Wang, et al.
Kidney International|October 26, 2007
Determinants of renal volume in autosomal-dominant polycystic kidney diseaseJ J Grantham, L T Cook, V E Torres, et al.
Molecular Endocrinology (Baltimore, Md.)|February 1, 1994
Identification of a point mutation in the thyrotropin receptor of the hyt/hyt hypothyroid mouseS A Stein, E L Oates, C R Hall, et al.
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