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Trends in Molecular Medicine|January 22, 2020
Glymphatic System Impairment in Alzheimer's Disease and Idiopathic Normal Pressure HydrocephalusBenjamin C Reeves, Jason K Karimy, Adam J Kundishora, et al.The Journal of Biological Chemistry|September 3, 2009
Deletion of the chloride transporter slc26a7 causes distal renal tubular acidosis and impairs gastric acid secretionJie Xu, Penghong Song, Suguru Nakamura, et al.Plos One|May 2, 2015
Copy Number Variation at the APOL1 LocusRupam Ruchi, Giulio Genovese, Jessica Lee, et al.American Journal of Hematology|July 17, 2015
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)Immacolata Andolfo, Roberta Russo, Francesco Manna, et al.American Journal of Physiology. Cell Physiology|January 26, 2007
Enhanced suicidal death of erythrocytes from gene-targeted mice lacking the Cl-/HCO(3)(-) exchanger AE1Ahmad Akel, Carsten A Wagner, Jana Kovacikova, et al.The Journal of Biological Chemistry|November 16, 2005
Alkaline-shifted pHo sensitivity of AE2c1-mediated anion exchange reveals novel regulatory determinants in the AE2 N-terminal cytoplasmic domainChristine E Kurschat, Boris E Shmukler, Lianwei Jiang, et al.American Journal of Physiology. Cell Physiology|November 13, 2009
The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytesAndrew K Stewart, David H Vandorpe, John F Heneghan, et al.Stroke|June 13, 2015
Inhibition of WNK3 Kinase Signaling Reduces Brain Damage and Accelerates Neurological Recovery After StrokeGulnaz Begum, Hui Yuan, Kristopher T Kahle, et al.Kidney International|August 8, 2014
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1Brendan Nichols, Prachi Jog, Jessica H Lee, et al.Science Translational Medicine|June 4, 2025
Molecular hallmarks of hydrocephalusAndrew T Hale, Blake Zhou, Arjun Rajan, et al.Pageof 27