Showing results (201-210 of 243) with videos related to

Sort By:
Pageof 25
Frontiers in Cell and Developmental Biology|December 21, 2023
Differential regulation of MYC expression by <i>PKHD1/Pkhd1</i> in human and mouse kidneys: phenotypic implications for recessive polycystic kidney diseaseNaoe Harafuji, Chaozhe Yang, Maoqing Wu, et al.
Cadernos De Saude Publica|January 11, 2002
Perinatal health and mother-child health care in the municipality of São Luís, Maranhão State, BrazilA A de Silva, L C Coimbra, R A da Silva, et al.
American Journal of Physiology. Cell Physiology|October 7, 2005
Heightened epithelial Na+ channel-mediated Na+ absorption in a murine polycystic kidney disease model epithelium lacking apical monociliaDragos Olteanu, Bradley K Yoder, Wen Liu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 8, 2008
CD4+ T cells recognizing a single self-peptide expressed by APCs induce spontaneous autoimmune arthritisAndrew L Rankin, Amy J Reed, Soyoung Oh, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 29, 2005
Sonographic assessment of the severity and progression of autosomal dominant polycystic kidney disease: the Consortium of Renal Imaging Studies in Polycystic Kidney Disease (CRISP)W Charles O'Neill, Michelle L Robbin, Kyongtae T Bae, et al.
American Journal of Physiology. Renal Physiology|March 7, 2002
Autocrine extracellular purinergic signaling in epithelial cells derived from polycystic kidneysErik M Schwiebert, Darren P Wallace, Gavin M Braunstein, et al.
Hepatology (Baltimore, Md.)|March 11, 2011
A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesisPeggy Raynaud, Joshua Tate, Céline Callens, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31M Vollmer, N Jeck, H H Lemmink, et al.
The Journal of Biological Chemistry|April 16, 1998
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchangerP Jarolim, C Shayakul, D Prabakaran, et al.
American Journal of Medical Genetics|March 25, 1998
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphologyK Zerres, G Mücher, J Becker, et al.
Pageof 25