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Items: 1 to 20 of 85

1.

Association analysis identifies ZNF750 regulatory variants in psoriasis.

Birnbaum RY, Hayashi G, Cohen I, Poon A, Chen H, Lam ET, Kwok PY, Birk OS, Liao W.

BMC Med Genet. 2011 Dec 20;12:167. doi: 10.1186/1471-2350-12-167.

2.

A promoter sequence variant of ZNF750 is linked with familial psoriasis.

Yang CF, Hwu WL, Yang LC, Chung WH, Chien YH, Hung CF, Chen HC, Tsai PJ, Fann CS, Liao F, Chen YT.

J Invest Dermatol. 2008 Jul;128(7):1662-8. doi: 10.1038/jid.2008.1. Epub 2008 Feb 7.

3.

Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk.

Dębniak T, Soczawa E, Boer M, Różewicka-Czabańska M, Wiśniewska J, Serrano-Fernandez P, Mirecka A, Paszkowska-Szczur K, Lubinski J, Krysztoforska L, Adamski Z, Maleszka R.

Arch Dermatol Res. 2014 Apr;306(3):231-8. doi: 10.1007/s00403-013-1407-9. Epub 2013 Sep 5.

4.

Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein.

Birnbaum RY, Zvulunov A, Hallel-Halevy D, Cagnano E, Finer G, Ofir R, Geiger D, Silberstein E, Feferman Y, Birk OS.

Nat Genet. 2006 Jul;38(7):749-51. Epub 2006 Jun 4.

PMID:
16751772
5.

Haplotype-oriented genetic analysis and functional assessment of promoter variants in the MDR1 (ABCB1) gene.

Takane H, Kobayashi D, Hirota T, Kigawa J, Terakawa N, Otsubo K, Ieiri I.

J Pharmacol Exp Ther. 2004 Dec;311(3):1179-87. Epub 2004 Jul 27.

6.

Genetic analysis of the promoter region of the GATA4 gene in patients with ventricular septal defects.

Wu G, Shan J, Pang S, Wei X, Zhang H, Yan B.

Transl Res. 2012 May;159(5):376-82. doi: 10.1016/j.trsl.2011.10.012. Epub 2011 Nov 23.

PMID:
22500510
7.

Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53).

Gloyn AL, Hashim Y, Ashcroft SJ, Ashfield R, Wiltshire S, Turner RC; UK Prospective Diabetes Study (UKPDS 53).

Diabet Med. 2001 Mar;18(3):206-12. Erratum in: Diabet Med. 2003 Mar;20(3):252..

PMID:
11318841
8.

Analysis of genetic variants of class II cytokine and their receptor genes in psoriasis patients of two ethnic groups from the Volga-Ural region of Russia.

Galimova E, Akhmetova V, Latipov B, Kingo K, Rätsep R, Traks T, Kõks S, Khusnutdinova E.

J Dermatol Sci. 2012 Oct;68(1):9-18. doi: 10.1016/j.jdermsci.2012.07.002. Epub 2012 Jul 16.

PMID:
22840887
9.

Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis.

Jordan CT, Cao L, Roberson ED, Duan S, Helms CA, Nair RP, Duffin KC, Stuart PE, Goldgar D, Hayashi G, Olfson EH, Feng BJ, Pullinger CR, Kane JP, Wise CA, Goldbach-Mansky R, Lowes MA, Peddle L, Chandran V, Liao W, Rahman P, Krueger GG, Gladman D, Elder JT, Menter A, Bowcock AM.

Am J Hum Genet. 2012 May 4;90(5):796-808. doi: 10.1016/j.ajhg.2012.03.013. Epub 2012 Apr 19.

11.

Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.

Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D.

Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2191-6. doi: 10.1167/iovs.09-3798. Epub 2009 Nov 20.

PMID:
19933195
12.

Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature.

Millar DS, Lewis MD, Horan M, Newsway V, Easter TE, Gregory JW, Fryklund L, Norin M, Crowne EC, Davies SJ, Edwards P, Kirk J, Waldron K, Smith PJ, Phillips JA 3rd, Scanlon MF, Krawczak M, Cooper DN, Procter AM.

Hum Mutat. 2003 Apr;21(4):424-40.

PMID:
12655557
13.

Promoter analysis of RPE65, the gene encoding a 61-kDa retinal pigment epithelium-specific protein.

Nicoletti A, Kawase K, Thompson DA.

Invest Ophthalmol Vis Sci. 1998 Mar;39(3):637-44.

PMID:
9501877
14.

Surfactant protein-C promoter variants associated with neonatal respiratory distress syndrome reduce transcription.

Wambach JA, Yang P, Wegner DJ, An P, Hackett BP, Cole FS, Hamvas A.

Pediatr Res. 2010 Sep;68(3):216-20. doi: 10.1203/00006450-201011001-00421.

15.

Analysis of the HNF4 alpha gene in Caucasian type II diabetic nephropathic patients.

Price JA, Fossey SC, Sale MM, Brewer CS, Freedman BI, Wuerth JP, Bowden DW.

Diabetologia. 2000 Mar;43(3):364-72.

PMID:
10768098
16.

Genomic structure of the human plasma prekallikrein gene, identification of allelic variants, and analysis in end-stage renal disease.

Yu H, Anderson PJ, Freedman BI, Rich SS, Bowden DW.

Genomics. 2000 Oct 15;69(2):225-34.

PMID:
11031105
17.

Insulin Promoter Factor 1 variation is associated with type 2 diabetes in African Americans.

Karim MA, Wang X, Hale TC, Elbein SC.

BMC Med Genet. 2005 Oct 17;6:37.

18.

Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation.

Lira MG, Mazzola S, Tessari G, Malerba G, Ortombina M, Naldi L, Remuzzi G, Boschiero L, Forni A, Rugiu C, Piaserico S, Girolomoni G, Turco A.

Br J Dermatol. 2007 Jul;157(1):49-57.

PMID:
17578436
19.

A comparative search for human FcεRIα gene (FCER1A) 3'-UTR polymorphisms in Japanese and Polish populations.

Potaczek DP, Kamijo M, Hara M, Okumura K, Undas A, Nishiyama C.

Mol Biol Rep. 2012 Apr;39(4):3747-53. doi: 10.1007/s11033-011-1150-2. Epub 2011 Jul 3.

PMID:
21725845
20.

Genetic variants in human sterol regulatory element binding protein-1c in syndromes of severe insulin resistance and type 2 diabetes.

Laudes M, Barroso I, Luan J, Soos MA, Yeo G, Meirhaeghe A, Logie L, Vidal-Puig A, Schafer AJ, Wareham NJ, O'Rahilly S.

Diabetes. 2004 Mar;53(3):842-6.

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