نتایج جستجو برای: methylenetetrahydrofolate reductase gene

تعداد نتایج: 1173819  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Amin Khaleghparast, Hossein Khaleghparast Sharif Khaleghparast

Introduction: One factor known to cause thrombophilia in women with unexplained recurrent spontaneous abortion (RSA) is C677T polymorphism of methylenetetrahydrofolate reductase gene. This study aimed to determine the association between RSA and MTHFR C677T polymorphism in Iranian patients. Methods: In this case-control study, 30 patients with previous history of two or more consecutive unexpla...

Fariba Nanbakhsh Isa Abdi Rad Mir Davood Omrani Morteza Bagheri,

Background To assess whether the C677T and A1298C mutations in the methylenetetrahydrofolate reductase (MTHER) gene are associated with recurrent abortion (RA), we determined the frequencies of the T677 and C1298 mutations in patients and controls. MaterialsAndMethods Mutations were determined by a RFLP-PCR method in 53 patients and 61 matched controls. Results The frequencies of T alleles were...

2010

A. 510(k) Number: k093974 B. Purpose for Submission: New Device C. Measurand: Factor II (FII) (Prothrombin) Factor V (FV) Leiden 5, 10 methylenetetrahydrofolate reductase (MTHFR) D. Type of Test: Qualitative genotyping test for single nucleotide polymorphism detection E. Applicant: Osmetech Molecular Diagnostics F. Proprietary and Established Names: eSensor® Thrombophilia Risk Test eSensor® FII...

Journal: :International journal of reproduction, contraception, obstetrics and gynecology 2022

Recurrent pregnancy loss (RPL) defined as of two or more pregnancies is one the reasons why couples visit an ART clinic. 2-5% RPL cases show abnormal parental karyotype. Folic acid essential B vitamin involved in processes fundamental importance for cell division and embryo development. deficiency can have effect on many oocyte development, acquisition endometrial receptivity, implantation also...

2012
Hongli Wang Dongsheng Fan Tianpei Hong

The present study enrolled 251 diabetic patients, including 101 with neuropathy and 150 without neuropathy. Of the 150 patients, 100 had no complications, such as retinopathy, nephropathy, or neuropathy. Polymerase chain reaction-restriction fragment length polymorphism analysis was used to identify methylenetetrahydrofolate reductase gene variants. Plasma homocysteine levels were also measured...

Journal: :Jurnal farmasi sains dan komunitas 2023

Methylenetetrahydrofolate reductase (MTHFR) is an essential enzyme for the homeostasis and metabolism of intracellular folate. However, it known that one commonly found MTHFR gene SNPs (A222V) causes a decrease in activity which decreases folate levels increases accumulation homocysteine blood. The purpose this study was to investigate molecular dynamics wild-type protein A222V mutant silico. A...

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