نتایج جستجو برای: methylenetetrahydrofolate

تعداد نتایج: 3961  

Journal: :The Biochemical journal 1983
P Sur M T Doig D G Priest

Levels of methylenetetrahydrofolate in Krebs ascites cells subsequent to transplantation and the effects of methotrexate on these levels have been measured. To directly measure methylenetetrahydrofolate in tissue extracts, the cofactor was incorporated into a covalent ternary complex with thymidylate synthase and 3H-labelled fluorodeoxyuridine monophosphate. A 3-4-day lag preceded rapid growth ...

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...

2005
Soo-Sang Kang

Background. To determine whether or not a moderate genetic defect of homocysteine metabolism is associated with the development of coronary artery disease, we studied the prevalence of thermolabile methylenetetrahydrofolate reductase, which is probably the most common genetic defect of homocysteine metabolism. Methods and Results. Three hundred thirty-nine subjects who underwent coronary angiog...

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: :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: :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...

2016
Muzeyyen Izmirli Bilge Bulbul Sen Eminenur Rifaioglu Bulent Gogebakan Ozgur Aldemir Tuba Sen Ozlem Ekiz Davut Alptekin

Background: Psoriasis is a multigenic and multifactorial dermatological disease linked to cardiovascular diseases. Increased levels of homocysteine in patients with psoriasis have been demonstrated in many studies. The most frequently investigated genetic defect that plays a role in homocysteine metabolism is single point substitution (C to T) located on the 677th nucleotide of the methylenetet...

Journal: :journal of dental research, dental clinics, dental prospects 0
asghar ebadifar shahid beheshti university of medical sciences nazila ameli postgraduate student of orthodontics, dental school, shahid beheshti university of medical sciences, tehran, iran hamid reza khorramkhorshid professor, genetic research centre, university of social welfare and rehabilitation sciences, tehran, iran mehdi salehi zeinabadi postgraduate student of pediatric dentistry, shahed dental school, tehran, iran 5reproductive biotechnology research center, avicenna research institute, acecr, tehran, iran kourosh kamali reproductive biotechnology research center, avicenna research institute, acecr, tehran, iran tayyebeh khoshbakht msc, genetic research centre, university of social welfare and rehabilitation sciences, tehran, iran

background and aims. the aim of the present study is to determine the incidence of mthfr c677 t and a1298c mutations in iranian patients with cleft lip and/or cleft palate. materials and methods. we screened 61 iranian patients with cleft lip and/or cleft palate for mutations in the two alleles of mthfr gene associated with cleft lip and/or palate: a1298c and c677t, using polymerase chain react...

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