نتایج جستجو برای: methylenetetrahydrofolate reductase gene

تعداد نتایج: 1173819  

Journal: :journal of research in medical sciences 0
asghar ebadifar nazila ameli hamid reza khorramkhorshid koorosh kamali mehdi salehizeinabadi

background: we studied the role of maternal folic acid supplementation in modifying the effects of  methylenetetrahydrofolate reductase (mthfr c677t and a1298c) gene polymorphisms in iranian children with oral clefts. materials and methods: forty?seven newborn infants with orofacial cleft and their mothers were selected randomly. mothers were matched regarding dietary folate intake.the genotypi...

Journal: :iranian red crescent medical journal 0
elham yousefian department of midwifery, islamic azad university falavarjan branch, isfahan, ir iran; department of midwifery, islamic azad university falavarjan branch, isfahan, ir iran. tel: +98-3123120136 mohammad taghi kardi department of biology, university of isfahan, isfahan, ir iran azra allahveisi department of anatomy, faculty of medicine, kurdistan university of medical sciences, sannandaj, ir iran

background recurrent pregnancy loss (rpl) is a serious problem for pregnancy. there is evidence that vascular complications play a principal role in rpl. methylenetetrahydrofolate reductase (mthfr) is a key enzyme in folate metabolism. polymorphisms (c677t, a1298c) of mthfr gene are associated with decreased mthfr activity. objectives the aim of this study was to determine the association betwe...

Journal: :Clinics 2007
Suely Kazue Nagahashi Marie Samuel Katsuyuki Shinjo Sueli Mieko Oba-Shinjo Roseli da Silva Keila Cardoso Barbosa Fabio Yamamoto Milberto Scaff

PURPOSE Data are conflicting concerning the risk for ischemic stroke associated with a common polymorphism in the gene encoding 5,10-methylenetetrahydrofolate reductase C677T, which predisposes carriers to hyperhomocysteinemia. A meta-analysis study suggested that the 5,10-methylenetetrahydrofolate reductase 677TT genotype might have a small influence in determining susceptibility to ischemic s...

Journal: :The Eurasian journal of medicine 2016
Nurinnisa Ozturk Ebubekir Bakan Mehmet Ali Gul Nuri Bakan Engin Sebin Ahmet Kiziltunc

OBJECTIVE Factor V / Factor II / Methylenetetrahydrofolate reductase, gene polymorphisms are closely associated with thrombophilia. Regional frequencies of these mutations may show a characteristic state. The aim of our study was to evaluate the frequency of commonly seen Factor V / Factor II / Methylenetetrahydrofolate reductase gene polymorphisms in Eastern Turkey. MATERIALS AND METHODS In ...

Journal: :research in molecular medicine 0
mahboobeh nasiri department of natural sciences, arsanjan branch, islamic azad university, arsanjan, iran. ali roostaei department of microbiology, science and research branch, islamic azad university, fars, iran zeinab ehsanian department of microbiology, science and research branch, islamic azad university, fars, iran

background: the association between methylene tetrahydrofolate reductase polymorphism and coronary artery diseases risk has been both confirmed and refuted in a number of published studies. the aim of this study was to investigate whether genetic polymorphisms of mthfr (c677t, a1298c) contributed to the development of myocardial infarction (mi). materials and methods: the present case-control s...

Journal: :Journal of the Korean neurological association 2022

Decrease in the activity of methylenetetrahydrofolate reductase (MTHFR) increases level homocysteine. MTHFR C677T gene polymorphism has been reported as a well-known cause elevated homocysteine associated with cerebral venous sinus thrombosis (CVST). A 34-year-old male was admitted severe headache after generalized seizure. Brain magnetic resonance venography showed thrombus superior sagittal s...

Journal: :iranian journal of psychiatry 0
seyed masoud arzaghi psychosomatic research group, endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran arash hossein-nezhad endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran seyed vahid shariat mental health research center, tehran university of medical sciences, tehran, iran alireza ghodsipour endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran jamal shams neuroscience research center, national neuroscience research network, shaheed beheshti university of medical sciences, tehran, iran bagher larijani endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran

objective: the methylenetetrahydrofolate reductase (mthfr) gene polymorphism c677t is suspected to be a risk factor for psychiatric disorders, but it remains inconclusive whether the mthfr polymorphism c677t is imputed to vulnerability to schizophrenia and bipolar disorder. method: we prompted impetus to appraise this polymorphism in an iranian population. therefore, 90 patients with bipolar di...

Journal: :Genetic testing and molecular biomarkers 2010
Mohamed A Mohamed Mahasen A El Moaty Adel F El Kholy Shuzan A Mohamed Amal I Ali

AIM One of the main problems concerning repeated spontaneous miscarriage (RSM) is the etiological diagnosis. The relation of thrombophilia to RSM is a matter of debate. In this case-control study, we determined the percentages of three thrombophilic mutations (factor V leiden, prothrombin, and methylenetetrahydrofolate reductase) amongst 20 cases with RSM and 20 control normal parous women. R...

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