Associated Papers
Evaluation of CAT Variants A-89T, C389T, and C419T in Patients with Vitiligo in the Saudi Population.
Saif GAB et al.
Medicina (kaunas, Lithuania), 2023
Predicting the functional consequences of genetic variants in co-stimulatory ligand B7-1 using in-silico approaches.
Mathur R et al.
Human Immunology, 2021
Catalase but not vitamin D receptor gene polymorphisms are associated with nonsegmental vitiligo in Northwestern Mexicans.
Ochoa-Ramírez LA et al.
International Journal of Dermatology, 2019
Vitiligo susceptibility and catalase gene polymorphisms in Sicilian population.
Caputo V et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia, 2018
The catalase gene promoter and 5'-untranslated region variants lead to altered gene expression and enzyme activity in vitiligo.
Mansuri MS et al.
The British Journal of Dermatology, 2017
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.
Nava C et al.
Amino Acids, 2015
26215737 (PubMed )
Supplement: 726_2015_2057_MOESM2_ESM.xlsx › Sup_Table_3
Lack of association between the 389C>T polymorphism (rs769217) in the catalase (CAT) gene and the risk of vitiligo: an update by meta-analysis.
He J et al.
The Australasian Journal of Dermatology, 2015
Human catalase, its polymorphisms, regulation and changes of its activity in different diseases.
Kodydková J et al.
Folia Biologica, 2014
Promoter variant in the catalase gene is associated with vitiligo in Chinese people.
Liu L et al.
The Journal of Investigative Dermatology, 2010
Analysis of allelic variants in the catalase gene in patients with the skin depigmenting disorder vitiligo.
Gavalas NG et al.
Biochemical and Biophysical Research Communications, 2006
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