نتایج جستجو برای: mtrr

تعداد نتایج: 307  

Journal: :Nevrologiâ, nejropsihiatriâ, psihosomatika 2022

Genetic polymorphisms associated with impaired one-carbon metabolism (1-CM) can be a risk factor not only for somatic and neurological diseases, but also affective disorders (AD). Objective : to compare the frequency of genetic MTHFR, MTR, MTRR 1-CM among patients AD, their blood relatives healthy individuals. Patients methods . This cross-sectional study ( ) included AD (n=24), (n=40), as well...

Journal: :The Journal of biological chemistry 2004
Nicole A Leal Horatiu Olteanu Ruma Banerjee Thomas A Bobik

The final step in the conversion of vitamin B(12) into coenzyme B(12) (adenosylcobalamin, AdoCbl) is catalyzed by ATP:cob(I)alamin adenosyltransferase (ATR). Prior studies identified the human ATR and showed that defects in its encoding gene underlie cblB methylmalonic aciduria. Here two common polymorphic variants of the ATR that are found in normal individuals are expressed in Escherichia col...

2015
Wen-Xing Li Shao-Xing Dai Jun-Juan Zheng Jia-Qian Liu Jing-Fei Huang

Folate deficiency is strongly associated with cardiovascular disease. We aimed to explore the joint effect of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C, methionine synthase (MTR) A2756G, and methionine synthase reductase (MTRR) A66G polymorphisms on folate deficiency in a Chinese hypertensive population. A total of 480 subjects aged 28-75 were enrolled in this study from ...

2017
Mirna Gisel González-Mercado Fernando Rivas M. Patricia Gallegos-Arreola M. Cristina Morán-Moguel Mario Salazar-Páramo Laura González-López J. Iván Gámez-Nava J. Francisco Muñoz-Valle Ricardo Medina-Coss y León Anahí González-Mercado Mario A. Aceves Nory O. Dávalos Agustín Macías-Chumacera Ingrid P. Dávalos

AIM To investigate the relationships of polymorphisms in genes whose protein products are related in the metabolic pathway of folic acid, particularly MTRR A66G, RFC1 G80A, and MTHFR C677T and A1298C, and disease activity in Mexican patients with rheumatoid arthritis (RA) treated with methotrexate (MTX). MATERIALS AND METHODS Sixty-eight patients with RA were included in the study who were be...

2012
Ahmad Aleyasin Mojgan Mirakhorli

Background & Objective: Fragile X syndrome is one of the most common causes of inherited mental retardation in males after Down syndrome. To date less attention was to study secondary genetic factor that may play role in fragile X neuropathology. In central nervous system, folic acid derivatives participate in different process such as neural development and function, synthesis of neurotransmit...

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