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Paper
Title

An in-depth study of specific pathway associated to abnormal reproductive system: A meta-analysis in a specific Caucasian ethnicity

مجله نوآوری علوم پزشکی و داروسازی آسیای مرکزی، دوره: 1، شماره: 1
Year: 1400
COI: JR_CAJMPSI-1-1_001
Language: EnglishView: 126
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Authors

Mohsen Mohammadi - Department of Educational Medicine, Tehran University of Medical Sciences, Tehran, Iran

Abstract:

Human methylenetetrahydrofolate reductase (MTHFR) gene plays a vital role in folate metabolism. This gene is located on chromosome ۱ and has ۱۲ exons. Many single nucleotide polymorphisms are found in MTHFR gene, in which the C۶۷۷T variation is one of the key polymorphism. In this literature review, four experimental studies investigating the correlation of the abovementioned polymorphism with male infertility in Iranian population were enrolled (a specific Caucasian ethnicity). To obtain more comprehensive outcomes, a meta-analysis was made by data extraction from four published papers. Eligible studies were found through a comprehensive search using appropriate electronic databases and were analyzed by Metagenyo online software. Finally, significant associations between C۶۷۷T gene polymorphism and male infertility in TT vs. CC, CT vs. CC, TT+TC vs. CC, and TT vs. TC+CC genetic models were found in Iranian population with no publication bias. MTHFR gene polymorphisms could be associated with infertility in men. Thus, determination of a polymorphism genotype in this gene could be useful for infertile individuals screening.

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This Paper COI Code is JR_CAJMPSI-1-1_001. Also You can use the following address to link to this article. This link is permanent and is used as an article registration confirmation in the Civilica reference:

https://civilica.com/doc/1220577/

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Mohammadi, Mohsen,1400,An in-depth study of specific pathway associated to abnormal reproductive system: A meta-analysis in a specific Caucasian ethnicity,https://civilica.com/doc/1220577

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Type of center: علوم پزشکی
Paper count: 9,613
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