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Journal Abstract Search

142 related items for PubMed ID: 22058000

  • 1. Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population.
    Bulut H, Pehlivan M, Alper S, Tomatir AG, Onay H, Yüksel SE, Ozkinay F, Pehlivan S.
    Genet Mol Res; 2011 Oct 31; 10(4):4126-32. PubMed ID: 22058000
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  • 3. Analysis of allelic variants in the catalase gene in patients with the skin depigmenting disorder vitiligo.
    Gavalas NG, Akhtar S, Gawkrodger DJ, Watson PF, Weetman AP, Kemp EH.
    Biochem Biophys Res Commun; 2006 Jul 14; 345(4):1586-91. PubMed ID: 16729966
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  • 4. The polymorphism of catalase T/C codon 389 in exon 9 and vitiligo susceptibility: a meta-analysis.
    Lv YJ, Liao WJ, Luan Q, Wang H, Wang L, Li Q.
    J Eur Acad Dermatol Venereol; 2011 Aug 14; 25(8):955-8. PubMed ID: 21054578
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  • 6. The association between endothelin-1 gene polymorphisms and susceptibility to vitiligo in a Korean population.
    Kim HJ, Choi CP, Uhm YK, Kim YI, Lee JW, Yoon SH, Chung JH, Lee MH.
    Exp Dermatol; 2007 Jul 14; 16(7):561-6. PubMed ID: 17576235
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  • 7. Association of catalase T/C exon 9 and glutathione peroxidase codon 200 polymorphisms in relation to their activities and oxidative stress with vitiligo susceptibility in Gujarat population.
    Em S, Laddha NC, Chatterjee S, Gani AR, Malek RA, Shah BJ, Begum R.
    Pigment Cell Res; 2007 Oct 14; 20(5):405-7. PubMed ID: 17850515
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  • 8. Interleukin-4 genetic variants correlate with its transcript and protein levels in patients with vitiligo.
    Imran M, Laddha NC, Dwivedi M, Mansuri MS, Singh J, Rani R, Gokhale RS, Sharma VK, Marfatia YS, Begum R.
    Br J Dermatol; 2012 Aug 14; 167(2):314-23. PubMed ID: 22512783
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  • 9. The catalase gene promoter and 5'-untranslated region variants lead to altered gene expression and enzyme activity in vitiligo.
    Mansuri MS, Jadeja SD, Singh M, Laddha NC, Dwivedi M, Begum R.
    Br J Dermatol; 2017 Dec 14; 177(6):1590-1600. PubMed ID: 28542879
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  • 10. Computer simulation of heterogeneous single nucleotide polymorphisms in the catalase gene indicates structural changes in the enzyme active site, NADPH-binding and tetramerization domains: a genetic predisposition for an altered catalase in patients with vitiligo?
    Wood JM, Gibbons NC, Chavan B, Schallreuter KU.
    Exp Dermatol; 2008 Apr 14; 17(4):366-71. PubMed ID: 18315617
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  • 11. Genetic association of the catalase gene (CAT) with vitiligo susceptibility.
    Casp CB, She JX, McCormack WT.
    Pigment Cell Res; 2002 Feb 14; 15(1):62-6. PubMed ID: 11837458
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  • 12. Vitiligo susceptibility and catalase gene polymorphisms in Sicilian population.
    Caputo V, Niceta M, Fiorella S, La Vecchia M, Bastonini E, Bongiorno MR, Pistone G.
    G Ital Dermatol Venereol; 2018 Oct 14; 153(5):619-623. PubMed ID: 28206724
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  • 16. Catalase -262C>T polymorphisms in Hungarian vitiligo patients and in controls: further acatalasemia mutations in Hungary.
    Kósa Z, Fejes Z, Nagy T, Csordás M, Simics E, Remenyik E, Góth L.
    Mol Biol Rep; 2012 Apr 14; 39(4):4787-95. PubMed ID: 21947853
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  • 17. Association of estrogen receptor 1 intron 1 C/T polymorphism in Korean vitiligo patients.
    Jin SY, Park HH, Li GZ, Lee HJ, Hong MS, Park HJ, Park HK, Seo JC, Yim SV, Chung JH, Lee MH.
    J Dermatol Sci; 2004 Sep 14; 35(3):181-6. PubMed ID: 15381239
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  • 18. Association of FOXP3 (rs3761548) promoter polymorphism with nondermatomal vitiligo: A study from India.
    Jahan P, Cheruvu R, Tippisetty S, Komaravalli PL, Valluri V, Ishaq M.
    J Am Acad Dermatol; 2013 Aug 14; 69(2):262-6. PubMed ID: 23498308
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  • 19. Tobacco smoking, fruit and vegetable intake modify association between -21A>T polymorphism of catalase gene and risk of bronchial asthma.
    Polonikov AV, Ivanov VP, Solodilova MA, Kozhuhov MA, Panfilov VI.
    J Asthma; 2009 Apr 14; 46(3):217-24. PubMed ID: 19373626
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  • 20. The association of FOXO3A gene polymorphisms with serum FOXO3A levels and oxidative stress markers in vitiligo patients.
    Ozel Turkcu U, Solak Tekin N, Gokdogan Edgunlu T, Karakas Celik S, Oner S.
    Gene; 2014 Feb 15; 536(1):129-34. PubMed ID: 24333267
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