Sodium Chloride

potassium inwardly rectifying channel subfamily J member 1 ; Homo sapiens







8 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 31795491 The Molecular Genetics of Gordon Syndrome. 2019 Nov 29 1
2 26069764 Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology. 2012 Jun 1
3 14604981 Assembly and trafficking of a multiprotein ROMK (Kir 1.1) channel complex by PDZ interactions. 2004 Feb 20 3
4 15283766 The role of cyclooxygenases and prostanoid receptorsin furosemide-like salt losing tubulopathy: the hyperprostaglandin E syndrome. 2004 Aug 1
5 12130653 Absence of small conductance K+ channel (SK) activity in apical membranes of thick ascending limb and cortical collecting duct in ROMK (Bartter's) knockout mice. 2002 Oct 4 1
6 12381810 Molecular mechanism of a COOH-terminal gating determinant in the ROMK channel revealed by a Bartter's disease mutation. 2002 Oct 15 1
7 11734858 Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion. 2001 Nov 29 1
8 10611379 pH gating of ROMK (K(ir)1.1) channels: control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome. 1999 Dec 21 1