Found: 6
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ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
- Published in:
- 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
Tissue Distribution of Kir7.1 Inwardly Rectifying K<sup>+</sup> Channel Probed in a Knock-in Mouse Expressing a Haemagglutinin-Tagged Protein.
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- Frontiers in Physiology, 2018, p. 1, doi. 10.3389/fphys.2018.00428
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- Article
Complicaciones derivadas del uso de fijadores externos. Revisión de la literatura.
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- Revista Salud Bosque, 2020, v. 10, n. 2, p. 1, doi. 10.18270/rsb.v10i2.3073
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- Article
K<sub>2P</sub> TASK‐2 and KCNQ1–KCNE3 K<sup>+</sup> channels are major players contributing to intestinal anion and fluid secretion.
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- Journal of Physiology, 2018, v. 596, n. 3, p. 393, doi. 10.1113/JP275178
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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
Cleft Palate, Moderate Lung Developmental Retardation and Early Postnatal Lethality in Mice Deficient in the Kir7.1 Inwardly Rectifying K<sup>+</sup> Channel.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0139284
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- Article