Distribution of genetic polymorphisms of genes encoding drug metabolizing enzymes & drug transporters-a review with Indian perspective
G Umamaheswaran, DK Kumar… - Indian Journal of Medical …, 2014 - journals.lww.com
Phase I and II drug metabolizing enzymes (DME) and drug transporters are involved in the
absorption, distribution, metabolism as well as elimination of many therapeutic agents …
absorption, distribution, metabolism as well as elimination of many therapeutic agents …
Distribution of methionine synthase reductase (MTRR) gene A66G polymorphism in Indian population
U Yadav, P Kumar, V Rai - Indian Journal of Clinical Biochemistry, 2021 - Springer
Methionine synthase reductase (MTRR) is an important enzyme of the folate/homocysteine
pathway. It is responsible for regulation of methionine enzyme by reductive methylation. A …
pathway. It is responsible for regulation of methionine enzyme by reductive methylation. A …
[PDF][PDF] The association between the 844ins68 polymorphism in the CBS gene and breast cancer
M Gallegos-Arreola, LE Figuera-Villanueva… - Archives of Medical …, 2014 - termedia.pl
Results: The observed genotype frequencies for controls and BC patients were 1% and 2%
for Ins/Ins, 13% and 26% for W/Ins, and 86% and 72% for W/W, respectively. We found that …
for Ins/Ins, 13% and 26% for W/Ins, and 86% and 72% for W/W, respectively. We found that …
Association of MTR and MTRR genes and oral health-related quality of life in children with dental caries
LAA Antunes, W Fialho, TO Fernandes… - Brazilian Oral …, 2023 - SciELO Brasil
This study aimed to assess whether genetic polymorphisms in MTR and MTRR are potential
biomarkers of oral health-related quality of life (OHRQoL) in children with caries. A cross …
biomarkers of oral health-related quality of life (OHRQoL) in children with caries. A cross …
Global DNA Methylation Levels Viz-a-Viz Genetic and Biochemical Variations in One Carbon Metabolic Pathway: An Exploratory Study from North India
V Chaudhary, D Bhattacharjee, NK Devi… - Biochemical …, 2024 - Springer
Despite the importance of one carbon metabolic pathway (OCMP) in modulating the DNA
methylation process, only a few population-based studies have explored their relationship …
methylation process, only a few population-based studies have explored their relationship …
Effect of thymidylate synthase (TYMS) gene polymorphisms with methotrexate treatment outcome in south Indian Tamil patients with rheumatoid arthritis
Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease causing joint damage
and significant functional impairment. Methotrexate (MTX) remains the mainstay for the …
and significant functional impairment. Methotrexate (MTX) remains the mainstay for the …
[HTML][HTML] Association of Single Nucleotide Polymorphisms (SNPs) in genes encoding for folate metabolising enzymes with glioma and meningioma in Indian population
R Kumawat, SH Gowda, E Debnath… - Asian Pacific journal …, 2018 - ncbi.nlm.nih.gov
Background: The association of primary brain tumors with Single Nucleotide polymorphisms
(SNPs) in genes of folate metabolising enzymes have been reported to vary among different …
(SNPs) in genes of folate metabolising enzymes have been reported to vary among different …
MTRR 66A>G Polymorphism as Maternal Risk Factor for Down Syndrome: A Meta-Analysis
Down syndrome (DS) is the most common cause of mental retardation. Recent reports have
investigated possible genetic factors that may increase maternal risk for DS. Methionine …
investigated possible genetic factors that may increase maternal risk for DS. Methionine …
Paternal transmission of MTHFD1 G1958A variant predisposes to neural tube defects in the offspring
KR Prasoona, T Sunitha, B Srinadh… - … Medicine & Child …, 2016 - Wiley Online Library
Aim This study aimed to evaluate the role of methylenetetrahydrofolate dehydrogenase
(MTHFD 1) G1958A variant (rs2236225) as a 'maternal, paternal, or embryonic'genetic risk …
(MTHFD 1) G1958A variant (rs2236225) as a 'maternal, paternal, or embryonic'genetic risk …
[HTML][HTML] Significant association of MTHFD1 1958G> A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population
J Murthy, VB Gurramkonda… - Medicina oral, patologia …, 2014 - ncbi.nlm.nih.gov
Objectives: Nonsyndromic cleft lip and palate (NSCLP) is genetically distinct from those with
syndromic clefts, and accounts for~ 70% of cases with Oral clefts. Folate, or vitamin B9, is an …
syndromic clefts, and accounts for~ 70% of cases with Oral clefts. Folate, or vitamin B9, is an …