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Items: 1 to 20 of 56

1.

Evidence for a mitochondrial ATP-regulated potassium channel in human dermal fibroblasts.

Bednarczyk P, Kicinska A, Laskowski M, Kulawiak B, Kampa R, Walewska A, Krajewska M, Jarmuszkiewicz W, Szewczyk A.

Biochim Biophys Acta Bioenerg. 2018 May;1859(5):309-318. doi: 10.1016/j.bbabio.2018.02.005. Epub 2018 Feb 16.

PMID:
29458000
2.

KCNJ1 inhibits tumor proliferation and metastasis and is a prognostic factor in clear cell renal cell carcinoma.

Guo Z, Liu J, Zhang L, Su B, Xing Y, He Q, Ci W, Li X, Zhou L.

Tumour Biol. 2015 Feb;36(2):1251-9. doi: 10.1007/s13277-014-2746-7. Epub 2014 Oct 26.

PMID:
25344677
3.

Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II.

Fretzayas A, Gole E, Attilakos A, Daskalaki A, Nicolaidou P, Papadopoulou A.

Pediatr Int. 2013 Jun;55(3):371-3. doi: 10.1111/j.1442-200X.2012.03716.x.

PMID:
23782368
4.

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions.

Amin N, Hottenga JJ, Hansell NK, Janssens AC, de Moor MH, Madden PA, Zorkoltseva IV, Penninx BW, Terracciano A, Uda M, Tanaka T, Esko T, Realo A, Ferrucci L, Luciano M, Davies G, Metspalu A, Abecasis GR, Deary IJ, Raikkonen K, Bierut LJ, Costa PT, Saviouk V, Zhu G, Kirichenko AV, Isaacs A, Aulchenko YS, Willemsen G, Heath AC, Pergadia ML, Medland SE, Axenovich TI, de Geus E, Montgomery GW, Wright MJ, Oostra BA, Martin NG, Boomsma DI, van Duijn CM.

Eur J Hum Genet. 2013 Aug;21(8):876-82. doi: 10.1038/ejhg.2012.263. Epub 2012 Dec 5.

5.

Association of KCNJ1 variation with change in fasting glucose and new onset diabetes during HCTZ treatment.

Karnes JH, McDonough CW, Gong Y, Vo TT, Langaee TY, Chapman AB, Gums JG, Beitelshees AL, Bailey KR, Del-Aguila JL, Boerwinkle EA, Pepine CJ, Turner ST, Johnson JA, Cooper-DeHoff RM.

Pharmacogenomics J. 2013 Oct;13(5):430-6. doi: 10.1038/tpj.2012.34. Epub 2012 Aug 21.

6.

Structural changes in the cytoplasmic pore of the Kir1.1 channel during pHi-gating probed by FRET.

Lee JR, Shieh RC.

J Biomed Sci. 2009 Mar 6;16:29. doi: 10.1186/1423-0127-16-29.

7.

A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.

Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M.

Pediatr Nephrol. 2007 Aug;22(8):1219-23. Epub 2007 Mar 31.

PMID:
17401586
8.

Phosphorylation-regulated endoplasmic reticulum retention signal in the renal outer-medullary K+ channel (ROMK).

O'Connell AD, Leng Q, Dong K, MacGregor GG, Giebisch G, Hebert SC.

Proc Natl Acad Sci U S A. 2005 Jul 12;102(28):9954-9. Epub 2005 Jun 29.

9.

Expression of the potassium channel ROMK in adult and fetal human kidney.

Nüsing RM, Pantalone F, Gröne HJ, Seyberth HW, Wegmann M.

Histochem Cell Biol. 2005 Jun;123(6):553-9. Epub 2005 May 14.

PMID:
15895241
10.

Molecular mechanism of a COOH-terminal gating determinant in the ROMK channel revealed by a Bartter's disease mutation.

Flagg TP, Yoo D, Sciortino CM, Tate M, Romero MF, Welling PA.

J Physiol. 2002 Oct 15;544(Pt 2):351-62.

11.

Protein kinase C (PKC)-induced phosphorylation of ROMK1 is essential for the surface expression of ROMK1 channels.

Lin D, Sterling H, Lerea KM, Giebisch G, Wang WH.

J Biol Chem. 2002 Nov 15;277(46):44278-84. Epub 2002 Sep 6.

12.

Nucleotide sequence analysis of the human KCNJ1 potassium channel locus.

Bock JH, Shuck ME, Benjamin CW, Chee M, Bienkowski MJ, Slightom JL.

Gene. 1997 Mar 25;188(1):9-16.

PMID:
9099852
13.

Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function.

Derst C, Konrad M, Köckerling A, Károlyi L, Deschenes G, Daut J, Karschin A, Seyberth HW.

Biochem Biophys Res Commun. 1997 Jan 23;230(3):641-5.

PMID:
9015377
15.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP.

Nat Genet. 1996 Oct;14(2):152-6.

PMID:
8841184
16.

Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.

Yano H, Philipson LH, Kugler JL, Tokuyama Y, Davis EM, Le Beau MM, Nelson DJ, Bell GI, Takeda J.

Mol Pharmacol. 1994 May;45(5):854-60.

PMID:
8190102
17.

Cloning and characterization of multiple forms of the human kidney ROM-K potassium channel.

Shuck ME, Bock JH, Benjamin CW, Tsai TD, Lee KS, Slightom JL, Bienkowski MJ.

J Biol Chem. 1994 Sep 30;269(39):24261-70.

18.

Isolation and chromosomal localization of a human ATP-regulated potassium channel.

Krishnan SN, Desai T, Ward DC, Haddad GG.

Hum Genet. 1995 Aug;96(2):155-60.

PMID:
7635463
19.

Endoplasmic reticulum-associated degradation of the renal potassium channel, ROMK, leads to type II Bartter syndrome.

O'Donnell BM, Mackie TD, Subramanya AR, Brodsky JL.

J Biol Chem. 2017 Aug 4;292(31):12813-12827. doi: 10.1074/jbc.M117.786376. Epub 2017 Jun 19.

20.

Calcium intake and ion transporter genetic polymorphisms interact in human colorectal neoplasia risk in a 2-phase study.

Zhu X, Liang J, Shrubsole MJ, Ness RM, Cai Q, Long J, Chen Z, Li G, Wiese D, Zhang B, Smalley WE, Edwards TL, Giovannucci E, Zheng W, Dai Q.

J Nutr. 2014 Nov;144(11):1734-41. doi: 10.3945/jn.114.196709. Epub 2014 Aug 27.

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