Folate: metabolism, genes, polymorphisms and the associated diseases

FH Nazki, AS Sameer, BA Ganaie - Gene, 2014 - Elsevier
Folate being an important vitamin of B Complex group in our diet plays an important role not
only in the synthesis of DNA but also in the maintenance of methylation reactions in the …

Homocysteine and age-associated disorders

EA Ostrakhovitch, S Tabibzadeh - Ageing research reviews, 2019 - Elsevier
There are numerous theories of aging, a process which still seems inevitable. Aging leads to
cancer and multi-systemic disorders as well as chronic diseases. Decline in age-associated …

Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: a HuGE review

L Sharp, J Little - American journal of epidemiology, 2004 - academic.oup.com
Epidemiologic and mechanistic evidence suggests that folate is involved in colorectal
neoplasia. Some polymorphic genes involved in folate metabolism …

[图书][B] Folate in health and disease

LB Bailey - 2009 - taylorfrancis.com
During the fifteen years since the bestselling first edition of Folate in Health and Disease
was published, there have been thousands of new research studies related to folate and its …

Gene-nutrient interactions in one-carbon metabolism

S Friso, SW Choi - Current drug metabolism, 2005 - ingentaconnect.com
Advances in molecular biology greatly contributed, in the past decades, to a deeper
understanding of the role of gene function in disease development. Environmental as well …

[HTML][HTML] A mathematical model gives insights into nutritional and genetic aspects of folate-mediated one-carbon metabolism

MC Reed, HF Nijhout, ML Neuhouser… - The Journal of …, 2006 - Elsevier
Impaired folate-mediated 1-carbon metabolism has been linked to multiple disease
outcomes. A better understanding of the nutritional and genetic influences on this complex …

Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L

D Watkins, M Ru, HY Hwang, CD Kim, A Murray… - The American Journal of …, 2002 - cell.com
Mutations in the MTR gene, which encodes methionine synthase on human chromosome
1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by …

Chromosome 9p21. 3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men

PJ Talmud, JA Cooper, J Palmen, R Lovering… - Clinical …, 2008 - academic.oup.com
Background: We investigated whether chromosome 9p21. 3 single-nucleotide
polymorphisms (SNPs), identified in coronary heart disease (CHD) genome-wide …

Family history is a coronary heart disease risk factor in the Second Northwick Park Heart Study

E Hawe, PJ Talmud, GJ Miller… - Annals of human …, 2003 - Wiley Online Library
We have estimated the risk of coronary heart disease (CHD) from family history of CHD
(FHCHD) in 2827 healthy European middle‐aged men, and explored the extent to which this …

Potential links between impaired one-carbon metabolism due to polymorphisms, inadequate B-vitamin status, and the development of Alzheimer's disease

B Troesch, P Weber, MH Mohajeri - Nutrients, 2016 - mdpi.com
Alzheimer's disease (AD) is the major cause of dementia and no preventive or effective
treatment has been established to date. The etiology of AD is poorly understood, but genetic …