Literature DB >> 21573678

Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest.

Toshinobu Miyamoto1, Akira Tsujimura, Yasushi Miyagawa, Eitetsu Koh, Mikio Namiki, Michiharu Horikawa, Yasuaki Saijo, Kazuo Sengoku.   

Abstract

PURPOSE: To investigate the association between the UBR2 gene and the risk of azoospermia caused by meiotic arrest.
METHODS: Mutational analysis of the UBR2 gene was performed using DNA from 30 patients with azoospermia by meiotic arrest to 80 normal controls.
RESULTS: The genotypic and allelic frequencies of c.1,066A>T variant were significantly higher in patient than control groups (p < 0.001).
CONCLUSION: The c.1,066A>T variant in the UBR2 gene is associated with increased susceptibility to azoospermia caused by meiotic arrest.

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Year:  2011        PMID: 21573678      PMCID: PMC3170112          DOI: 10.1007/s10815-011-9576-y

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  26 in total

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  3 in total

1.  Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients.

Authors:  Toshinobu Miyamoto; Akira Tsujimura; Yasushi Miyagawa; Eitetsu Koh; Mikio Namiki; Michiharu Horikawa; Yasuaki Saijo; Kazuo Sengoku
Journal:  Asian J Androl       Date:  2012-03-12       Impact factor: 3.285

2.  Ubiquitin-specific protease (USP26) gene alterations associated with male infertility and recurrent pregnancy loss (RPL) in Iranian infertile patients.

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3.  Male infertility and its causes in human.

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