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1.
Genet Mol Res ; 14(2): 3257-63, 2015 Apr 13.
Artículo en Inglés | MEDLINE | ID: mdl-25966091

RESUMEN

Inheritance of polymorphisms in the interleukin (IL)-10 promoter and IL-12B genes, which influence cytokine production and activities, may define the balance in T helper response in infection and autoimmune diseases. In the present study, we investigated the distribution of the IL-10 promoter and IL-12B gene polymorphisms in a multiethnic Malaysian population. Overall, our findings suggest that the IL-12B and IL-10 -592 genotypes were distributed homogenously across all major ethnic groups, including Malays, Chinese, and Indians, except for polymorphisms at IL-10 -1082. At this gene locus, the ethnic Chinese showed a significantly lower allele frequency of -1082G (2.1%) compared to the Malay (12.2%) and Indian (15.3%) populations. Results for the IL-12B and IL-10 gene polymorphisms were consistent with those reported for the Asian population, but markedly different from those of the African and Caucasian populations. Our findings suggest that there are specific genetic variations between different ethnic groups, which should be examined in all gene population-based association studies.


Asunto(s)
Interleucina-10/genética , Subunidad p40 de la Interleucina-12/genética , Polimorfismo de Nucleótido Simple , China/etnología , Frecuencia de los Genes , Genotipo , Humanos , India/etnología , Malasia , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción
2.
Genet Mol Res ; 13(1): 980-5, 2014 Feb 19.
Artículo en Inglés | MEDLINE | ID: mdl-24634119

RESUMEN

Copy number variation (CNV) is a form of genetic variation in addition to single nucleotide polymorphisms. The significance of CNV in the manifestation of a number of diseases is only recently receiving considerable attention. We genotyped 163 dengue patients from Peninsular Malaysia for genes possibly linked to dengue infection using quantitative real-time PCR. Here, we report a serendipitous discovery of a novel rare CNV of the ABCF1 gene among the dengue patients. Among these patients, two had a gain of 1 copy (CN = 3) and one had lost 1 copy (CN = 1), indicating that a rare CNV of the ABCF1 gene was detected among dengue patients from Peninsular Malaysia. Although the gene is suspected to regulate inflammatory responses and pathogen-induced cytokine storm, its relevance to dengue requires further investigation.


Asunto(s)
Transportadoras de Casetes de Unión a ATP/genética , Variaciones en el Número de Copia de ADN , Dengue/genética , Dengue/patología , Predisposición Genética a la Enfermedad , Variación Genética , Genotipo , Humanos , Malasia
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