نتایج جستجو برای: ژن mtr a2756g

تعداد نتایج: 16808  

Journal: :Journal of nutrigenetics and nutrigenomics 2008
Susan E Steck Temitope Keku Lesley M Butler Joseph Galanko Beri Massa Robert C Millikan Robert S Sandler

BACKGROUND/AIMS We examined associations among folate and alcohol intake, single nucleotide polymorphisms (SNPs) in genes involved in one-carbon metabolism, and colon cancer risk. METHODS Colon cancer cases (294 African-Americans and 349 whites) were frequency matched to population controls (437 African-Americans and 611 whites) by age, race and sex from 33 North Carolina counties from 1996 t...

Journal: :Seizure 2011
Aleksandra Sniezawska Jolanta Dorszewska Agata Rozycka Elzbieta Przedpelska-Ober Margarita Lianeri Pawel P. Jagodzinski Wojciech Kozubski

PURPOSE The purpose of the study was to determine the frequency of occurrence of polymorphisms of genes MTHFR (C677T), MTR (A2756G), and MTHFD1 (G1958A), as well as to analyze the concentration of homocysteine (Hcy), methionine (Met), asymmetric dimethylarginine (ADMA), and arginine (Arg) in epileptics treatment with antiepileptic drugs (AEDs), and controls. METHOD The study included 65 epile...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006
Richard A Hubner Kenneth R Muir Jo-Fen Liu Gabrielle S Sellick Richard F A Logan Matthew Grainge Nicholas Armitage Ian Chau Richard S Houlston

Folate intake is inversely related to risk of developing colorectal neoplasia. Associations between risk of colorectal neoplasia and polymorphisms in genes coding for enzymes involved in folate metabolism have also been reported, suggesting a relationship between genotype and development of colorectal neoplasia. To further investigate the effects of folate metabolism genotypes on colorectal neo...

Journal: :Medical History 2006
GAYLE DAVIS ROGER DAVIDSON

Background. Hyperhomocysteinemia has been suggested to play a role in the NonValvular Atrial Fibrillation (NVAF) pathogenesis. Polymorphisms in genes coding for homocysteine (Hcy) metabolism enzymes may be associated with hyperhomocysteinemia and NVAF. Methodologies. 456 NVAF patients and 912 matched controls were genotyped by an electronic microchip technology for C677T and A1298C MTHFR, A2756...

Journal: :PLoS ONE 2007
Betti Giusti Anna Maria Gori Rossella Marcucci Ilaria Sestini Claudia Saracini Elena Sticchi Francesca Gensini Cinzia Fatini Rosanna Abbate Gian Franco Gensini

BACKGROUND Hyperhomocysteinemia has been suggested to play a role in the NonValvular Atrial Fibrillation (NVAF) pathogenesis. Polymorphisms in genes coding for homocysteine (Hcy) metabolism enzymes may be associated with hyperhomocysteinemia and NVAF. METHODOLOGIES 456 NVAF patients and 912 matched controls were genotyped by an electronic microchip technology for C677T and A1298C MTHFR, A2756...

2016
Lisiane Lopes da Conceição Milene Cristine Pessoa

Breast cancer (BC) is the second most common cancer, and mortality rates remain high among Brazilian women. However, the role of single nucleotide polymorphisms (SNPs) in one-carbon metabolism genes in breast cancer in Brazilian women is less clear. We aimed examine the association between the SNPs, in two genes in one-carbon metabolism alone and in cumulation, and the risk of breast cancer in ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008
Lasse S Kristensen Alexander Dobrovic

High-resolution melting (HRM) shows great promise for high-throughput, rapid genotyping of individual polymorphic loci. We have developed HRM assays for genotyping single nucleotide polymorphisms (SNP) in several key genes that are involved in methyl metabolism and may directly or indirectly affect the methylation status of the DNA. The SNPs are in the 5,10-methylenetetrahydrofolate reductase (...

Journal: :Mutagenesis 2011
Varinderpal S Dhillon Philip Thomas G Iarmarcovai Micheline Kirsch-Volders Stefano Bonassi Michael Fenech

The cytokinesis-block micronucleus cytome (CBMNCyt) assay is a widely used technique for measuring DNA damage in human populations. The formation of micronuclei (MN) in dividing cells can result from chromosome breakage due to unrepaired or mis-repaired DNA lesions or chromosome malsegregation due to mitotic malfunction. The sensitivity of the MN assay to polymorphisms in various genes involved...

Journal: :Indian journal of biochemistry & biophysics 2011
Shaik Mohammad Naushad Addepalli Pavani Yedluri Rupasree Deepti Sripurna Suryanarayana Raju Gottumukkala Raghunadha Rao Digumarti Vijay Kumar Kutala

The present study was aimed to investigate the modulatory role of plasma folate and eight putatively functional polymorphisms of one-carbon metabolism on catecholamine methyltransferase (COMT)-mediated oxidative DNA damage and breast cancer risk. Plasma folate and 8-oxo-2'-deoxyguanosine (8-oxodG) were estimated by commercially available kits, while polymorphisms were screened by PCR-RFLP and P...

2013
Agata Rozycka Pawel P. Jagodzinski Wojciech Kozubski Margarita Lianeri Jolanta Dorszewska

An elevated concentration of total homocysteine (tHcy) in plasma and cerebrospinal fluid is considered to be a risk factor for Alzheimer's disease (AD) and Parkinson's disease (PD). Homocysteine (Hcy) levels are influenced by folate concentrations and numerous genetic factors through the folate cycle, however, their role in the pathogenesis of PD remains controversial. Hcy exerts a neurotoxic a...

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