Functional expression of a vertebrate inwardly rectifying K+ channel in yeast.

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Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channel.

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Mutations that disrupt function of the human inwardly rectifying potassium channel KIR2.1 are associated with the craniofacial and digital defects of Andersen-Tawil Syndrome, but the contribution of Kir channels to development is undefined. Deletion of mouse Kir2.1 also causes cleft palate and digital defects. These defects are strikingly similar to phenotypes that result from disrupted TGFβ/BM...

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ژورنال

عنوان ژورنال: Molecular Biology of the Cell

سال: 1995

ISSN: 1059-1524,1939-4586

DOI: 10.1091/mbc.6.9.1231