Polymorphism in genes
Web1 day ago · Glycogen storage disease type II (Pompe disease: PD) is an autosomal recessively inherited fatal genetic disorder that results from the deficiency of a glycogen hydrolyzing enzyme, acid α-glucosidase encoded by the GAA gene. Here, we describe the molecular basis of genetic defects in an 8-month-old domestic short-haired cat with … WebT (NC_000020.10:g.57478807C. >. T), a silent polymorphism situated in the exon 5, were significantly (p<. 0.05) associated with susceptibility to malaria in the South Indians participants. Our results demonstrate that population specific polymorphisms that exist in GNAS gene may alter the risk of occurrence of malaria.
Polymorphism in genes
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WebGenetic polymorphisms of the genes coding for enzymes involved in the metabolism of genotoxins result in different phenotypes with respect to their ability to detoxify these … WebApr 13, 2024 · Polymorphism COL3A1 /rs1800255 has been also linked with strokes in Chinese populations. The A allele of this gene appeared to be significantly associated …
WebThe TP53 gene, codon 72 polymorphism (Arg72Pro), has been found to be associated with cancer susceptibility but has not been investigated in kangri cancer risk. A case control study was conducted to find the genotype distribution of TP53 Arg72Pro SNP and to elucidate the possible role of this SNP as risk factor in kangri can ... WebApr 12, 2024 · GST gene family. Polymorphism in the GST gene family has been reported in three independent studies [19,20,21]. Mlakar, in 2011, reported a borderline significant …
WebMay 13, 2024 · The purpose of this study is to assess the SNP (rs2279115; - 938 C>A) polymorphism in the BCL-2 gene of Iraqi leukemic patients. The B-cell lymphoma 2 (BCL … WebNov 30, 2024 · Abstract Genes carrying high-penetrance germline mutations may also be associated with cancer susceptibility through common low-penetrance genetic variants. ... The T allele of the rs1412832 polymorphism, that is situated in the CDKN2B-AS1/ANRIL, showed a genome-wide significant association with increased risk of developing PDAC ...
WebThis review summarized the molecular characteristics of the CYP3A5 gene, and discusses the association of the CYP3A5*3 polymorphism with disease risks such as cancer and hypertension, along with its role in the pharmacokinetics of CYP3A substrates. KW - CYP3A53. KW - Cancer. KW - Cytochrome. KW - P450. KW - Pharmacogenetics. KW - …
WebJun 29, 2012 · Background & objectives: Genetic polymorphisms in glutathione-S-transferase genes (GSTM1 and GSTT1) have been studied intensively for their potential … lits trainingWebCONCLUSION: The CAG polymorphism is not associated with development of breast cancer, but patients with more CAG repeats of the AR gene are prone to poor prognoses. AB - BACKGROUND: The polymorphic CAG repeats of the androgen receptor (AR) gene have been suggested to affect the risk of breast cancer, but the results are controversial. lit strawana hybrid cartridgeWebMar 9, 2024 · This research topic will serve to collate many ideas of the varied roles played by polymorphisms especially single nucleotide polymorphisms (SNPs) in genes involved … litsupport sydneyWebPolymorphism in these genes may be responsible for the high prevalence and increased severity of hypertension in black persons. 16, 26 – 28 The enhanced effects of diuretics in … lits wescoWebBackground: Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme regulating the intracellular folate metabolism which plays an important role in carcinogenesis through DNA methylation. Objectives: The current study aimed to determine the association between MTHFR C677T polymorphisms and the risks of chronic myeloid leukemia (CML). lit supply \\u0026 sourcingWebFeb 13, 2024 · Polymorphic traits are traits that are associated with two or more genes. Polymorphic traits, such as the difference in skin and eye color and height, result from … lits trinity collegeWebThe objective of this study is to investigate the relationship between the polymorphisms of two DNA repair genes, the nucleotide excision repair xeroderma pigmentosum group D (XPD) gene (codons 312 and 751) and the base excision repair X-ray repair cross-complementing group 1 (XRCC1) gene (codon 399), and p53 mutations among lung … lits united