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Respiratory Physiology & Neurobiology|November 14, 2016
Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouseStefan Jungbauer, Philipp Karl Buehler, Jacqueline Neubauer, et al.
The Journal of Clinical Endocrinology and Metabolism|September 17, 2013
a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type IIISilvia Monticone, Namita G Hattangady, David Penton, et al.
The Journal of Physiology|December 8, 2004
Heteromeric KCNE2/KCNQ1 potassium channels in the luminal membrane of gastric parietal cellsDirk Heitzmann, Florian Grahammer, Thomas von Hahn, et al.
Journal of the American Society of Nephrology : JASN|March 9, 2007
Early aldosterone-induced gene product regulates the epithelial sodium channel by deubiquitylationPanagiotis Fakitsas, Gabriele Adam, Dorothée Daidié, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2014
A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassiumManiselvan Kuppusamy, Brasilina Caroccia, Julia Stindl, et al.
Frontiers in Cell and Developmental Biology|October 30, 2023
A missense mutation in <i>Ehd1</i> associated with defective spermatogenesis and male infertilityKatrin Meindl, Naomi Issler, Sara Afonso, et al.
Neurogenetics|February 17, 2020
Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotypeMatias Morin, Anna-Lena Forst, Paula Pérez-Torre, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transportRichard Warth, Hervé Barrière, Pierre Meneton, et al.
Endocrinology|August 11, 2012
Task3 potassium channel gene invalidation causes low renin and salt-sensitive arterial hypertensionDavid Penton, Sascha Bandulik, Frank Schweda, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
Somatic Mutations in <i>MCOLN3</i> in Aldosterone-Producing Adenomas cause Primary AldosteronismDesmaré van Rooyen, Sascha Bandulik, Grace Coon, et al.
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