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Items: 1 to 20 of 67

1.

Functional analysis of a potassium-chloride co-transporter 3 (SLC12A6) promoter polymorphism leading to an additional DNA methylation site.

Moser D, Ekawardhani S, Kumsta R, Palmason H, Bock C, Athanassiadou Z, Lesch KP, Meyer J.

Neuropsychopharmacology. 2009 Jan;34(2):458-67. doi: 10.1038/npp.2008.77. Epub 2008 Jun 4.

2.

Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.

Meyer J, Johannssen K, Freitag CM, Schraut K, Teuber I, Hahner A, Mainhardt C, Mössner R, Volz HP, Wienker TF, McKeane D, Stephan DA, Rouleau G, Reif A, Lesch KP.

Int J Neuropsychopharmacol. 2005 Dec;8(4):495-504. Epub 2005 Aug 5.

PMID:
16098236
3.

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, Zhan FQ, Mercado A, Siesser WB, George AL Jr, McDonald MP, Bouchard JP, Mathieu J, Delpire E, Rouleau GA.

Nat Genet. 2002 Nov;32(3):384-92. Epub 2002 Oct 7. Erratum in: Nat Genet 2002 Dec;32(4):681.

PMID:
12368912
4.

Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy.

Steinlein OK, Neubauer BA, Sander T, Song L, Stoodt J, Mount DB.

Epilepsy Res. 2001 May;44(2-3):191-5.

PMID:
11325574
5.

Hypomethylation of the serotonin receptor type-2A Gene (HTR2A) at T102C polymorphic site in DNA derived from the saliva of patients with schizophrenia and bipolar disorder.

Ghadirivasfi M, Nohesara S, Ahmadkhaniha HR, Eskandari MR, Mostafavi S, Thiagalingam S, Abdolmaleky HM.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):536-45. doi: 10.1002/ajmg.b.31192. Epub 2011 May 19.

PMID:
21598376
6.
7.

DNA hypomethylation of MB-COMT promoter in the DNA derived from saliva in schizophrenia and bipolar disorder.

Nohesara S, Ghadirivasfi M, Mostafavi S, Eskandari MR, Ahmadkhaniha H, Thiagalingam S, Abdolmaleky HM.

J Psychiatr Res. 2011 Nov;45(11):1432-8. doi: 10.1016/j.jpsychires.2011.06.013. Epub 2011 Aug 5.

PMID:
21820670
8.

Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder.

Dagdan E, Morris DW, Campbell M, Hill M, Rothermundt M, Kästner F, Hohoff C, von Eiff C, Krakowitzky P, Gill M, McKeon P, Roche S.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):691-9. doi: 10.1002/ajmg.b.31211. Epub 2011 Jun 28.

PMID:
21714070
9.

Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report.

Abdolmaleky HM, Cheng KH, Russo A, Smith CL, Faraone SV, Wilcox M, Shafa R, Glatt SJ, Nguyen G, Ponte JF, Thiagalingam S, Tsuang MT.

Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):60-6.

PMID:
15717292
10.

Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum.

Shekarabi M, Moldrich RX, Rasheed S, Salin-Cantegrel A, Laganière J, Rochefort D, Hince P, Huot K, Gaudet R, Kurniawan N, Sotocinal SG, Ritchie J, Dion PA, Mogil JS, Richards LJ, Rouleau GA.

J Neurosci. 2012 Mar 14;32(11):3865-76. doi: 10.1523/JNEUROSCI.3679-11.2012.

12.

Identification of a DNA methylation-dependent activator sequence in the pseudoxanthoma elasticum gene, ABCC6.

Arányi T, Ratajewski M, Bardóczy V, Pulaski L, Bors A, Tordai A, Váradi A.

J Biol Chem. 2005 May 13;280(19):18643-50. Epub 2005 Mar 9.

13.

Human Vav1 expression in hematopoietic and cancer cell lines is regulated by c-Myb and by CpG methylation.

Ilan L, Katzav S.

PLoS One. 2012;7(1):e29939. doi: 10.1371/journal.pone.0029939. Epub 2012 Jan 11.

14.

Analysis of the GAD1 promoter: trans-acting factors and DNA methylation converge on the 5' untranslated region.

Chen Y, Dong E, Grayson DR.

Neuropharmacology. 2011 Jun;60(7-8):1075-87. doi: 10.1016/j.neuropharm.2010.09.017. Epub 2010 Sep 28.

PMID:
20869372
15.

Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder.

Carrard A, Salzmann A, Malafosse A, Karege F.

J Affect Disord. 2011 Aug;132(3):450-3. doi: 10.1016/j.jad.2011.03.018. Epub 2011 Mar 30.

PMID:
21453976
16.

Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome.

Uyanik G, Elcioglu N, Penzien J, Gross C, Yilmaz Y, Olmez A, Demir E, Wahl D, Scheglmann K, Winner B, Bogdahn U, Topaloglu H, Hehr U, Winkler J.

Neurology. 2006 Apr 11;66(7):1044-8. Erratum in: Neurology. 2006 Oct 24;67(8):1528.

PMID:
16606917
19.

Identification and functional characterization of the human EXT1 promoter region.

Jennes I, Zuntini M, Mees K, Palagani A, Pedrini E, De Cock G, Fransen E, Vanden Berghe W, Sangiorgi L, Wuyts W.

Gene. 2012 Jan 15;492(1):148-59. doi: 10.1016/j.gene.2011.10.034. Epub 2011 Oct 19.

PMID:
22037484

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