8 Article(s)Download |
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 |