Found: 13
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An inward rectifier K<sup>+</sup> channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.
- Published in:
- Journal of Physiology, 2002, v. 538, n. 2, p. 391, doi. 10.1113/jphysiol.2001.012961
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- Article
Régulation de la pression artérielle: Un rôle majeur de l'apport en potassium.
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- Médecine Sciences, 2022, v. 38, n. 8/9, p. 743, doi. 10.1051/medsci/2022115
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- Article
Novel CLCN5 mutations in patients with Dent’s disease result in altered ion currents or impaired exchanger processing.
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- Kidney International, 2009, v. 76, n. 9, p. 999, doi. 10.1038/ki.2009.305
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- Article
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca dependence of ClC-Kb channels.
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- Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 9, p. 1713, doi. 10.1007/s00424-013-1401-2
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- Article
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
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- Pflügers Archiv: European Journal of Physiology, 2012, v. 463, n. 2, p. 247, doi. 10.1007/s00424-011-1052-0
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- Article
Study of the Involvement of Mitochondria in Dent's Disease Using a Mice Model.
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- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.0R573
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- Article
Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins.
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- Nature, 2005, v. 436, n. 7049, p. 424, doi. 10.1038/nature03860
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- Article
Diversity of functional alterations of the ClC‐5 exchanger in the region of the proton glutamate in patients with Dent disease 1.
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- Human Mutation, 2021, v. 42, n. 5, p. 537, doi. 10.1002/humu.24184
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- Article
A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification.
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- Human Mutation, 2018, v. 39, n. 8, p. 1139, doi. 10.1002/humu.23556
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- Article
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.
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- Human Mutation, 2015, v. 36, n. 8, p. 743, doi. 10.1002/humu.22804
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- Article
Novel CLCNKB Mutations Causing Bartter Syndrome Affect Channel Surface Expression.
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- Human Mutation, 2013, v. 34, n. 9, p. 1269, doi. 10.1002/humu.22361
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- Article
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
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- Human Mutation, 2011, v. 32, n. 4, p. 476, doi. 10.1002/humu.21467
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- Article
A Focus on the Proximal Tubule Dysfunction in Dent Disease Type 1.
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- Genes, 2024, v. 15, n. 9, p. 1175, doi. 10.3390/genes15091175
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- Article