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Mol Genet Genomic Med. 2019 Sep;7(9):e891. doi: 10.1002/mgg3.891. Epub 2019 Jul 30.
2
HSPA1L and HSPA1B gene polymorphisms and haplotypes are associated with idiopathic male infertility in Iranian population.HSPA1L 和 HSPA1B 基因多态性和单倍型与伊朗人群特发性男性不育有关。
Eur J Obstet Gynecol Reprod Biol. 2019 Sep;240:57-61. doi: 10.1016/j.ejogrb.2019.06.014. Epub 2019 Jun 13.
3
Expression Analysis of the CRISP2, CATSPER1, PATE1 and SEMG1 in the Sperm of Men with Idiopathic Asthenozoospermia.特发性弱精子症男性精子中CRISP2、CATSPER1、PATE1和SEMG1的表达分析
J Reprod Infertil. 2019 Apr-Jun;20(2):70-75.
4
Evaluation of the NOX5 protein expression and oxidative stress in sperm from asthenozoospermic men compared to normozoospermic men.评估弱精症男性与正常精子男性的 NOX5 蛋白表达和精子氧化应激。
J Endocrinol Invest. 2019 Oct;42(10):1181-1189. doi: 10.1007/s40618-019-01035-4. Epub 2019 Apr 8.
5
Analysis of PRM1 and PRM2 Polymorphisms in Iranian Infertile Men with Idiopathic Teratozoospermia.伊朗特发性畸形精子症不育男性中PRM1和PRM2基因多态性分析
Int J Fertil Steril. 2019 Apr;13(1):77-82. doi: 10.22074/ijfs.2019.5650. Epub 2019 Jan 6.
6
BMP4 circulating levels and promoter (rs17563) polymorphism in risk prediction of idiopathic male infertility.骨形态发生蛋白4循环水平及启动子(rs17563)多态性在特发性男性不育风险预测中的作用
Br J Biomed Sci. 2019 Apr;76(2):98-100. doi: 10.1080/09674845.2018.1564419. Epub 2019 Mar 26.
7
Expressions of miR-525-3p and its target gene SEMG1 in the spermatozoa of patients with asthenozoospermia.miR-525-3p 及其靶基因 SEMG1 在弱精子症患者精子中的表达。
Andrology. 2019 Mar;7(2):220-227. doi: 10.1111/andr.12573. Epub 2018 Dec 21.
8
Synergistic effects of TIMP2-418G/C and MMP9-1562C/T variants on the male infertility risk.TIMP2 - 418G/C和MMP9 - 1562C/T变异对男性不育风险的协同作用。
Mol Biol Rep. 2019 Feb;46(1):861-866. doi: 10.1007/s11033-018-4541-9. Epub 2018 Dec 4.
9
Association between expression of TNF-α, P53 and HIF1α with asthenozoospermia.肿瘤坏死因子-α、P53和低氧诱导因子1α的表达与弱精子症之间的关联。
Hum Fertil (Camb). 2019 Jun;22(2):145-151. doi: 10.1080/14647273.2018.1493750. Epub 2018 Sep 17.
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The Effect of Heroin Addiction on Human Sperm Parameters, Histone-to-Protamine Transition, and Serum Sexual Hormones Levels.海洛因成瘾对人类精子参数、组蛋白向鱼精蛋白转变及血清性激素水平的影响。
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伊朗人群男性不育的遗传学与分子生物学:最新进展

Genetics and molecular biology of male infertility among Iranian population: an update.

作者信息

Mojarrad Majid, Saburi Ehsan, Golshan Alireza, Moghbeli Meysam

机构信息

Department of Medical Genetics and Molecular Medicine, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran.

Department of Urology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran.

出版信息

Am J Transl Res. 2021 Jun 15;13(6):5767-5785. eCollection 2021.

PMID:34306325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8290737/
Abstract

Infertility is one of the main social and health problems among young couples. Although a noticeable ratio of infertilities are asymptomatic, about half of the cases are observed among males. Various environmental factors such as life style, dietary patterns, and pathogens are associated with male infertility. Mutations and chromosomal abnormalities are also the most important genetic risk factors of male infertility. Similar to other populations, there is a dramatically rising trend of male infertility among Iranian. Regarding the high ratio of asymptomatic cases, it is required to clarify the molecular biology and cellular processes involved in male infertility in this population to suggest an efficient panel of diagnostic markers. In this review, we have summarized all of the cellular and molecular processes which have been reported among Iranian infertile males to clarify the molecular biology of male infertility in this population. It was observed that the stress response, cellular detoxification, and DNA repair processes were the most common aberrant cellular mechanisms among Iranian infertile males. This review paves the way of introducing a population-based diagnostic panel of genetic markers among Iranian infertile males.

摘要

不孕不育是年轻夫妇面临的主要社会和健康问题之一。尽管相当比例的不孕不育症没有症状,但约一半的病例出现在男性身上。各种环境因素,如生活方式、饮食模式和病原体,都与男性不育有关。突变和染色体异常也是男性不育最重要的遗传风险因素。与其他人群类似,伊朗男性不育的趋势也在急剧上升。鉴于无症状病例的比例很高,有必要阐明该人群中男性不育所涉及的分子生物学和细胞过程,以提出一套有效的诊断标志物。在这篇综述中,我们总结了伊朗不育男性中已报道的所有细胞和分子过程,以阐明该人群中男性不育的分子生物学。据观察,应激反应、细胞解毒和DNA修复过程是伊朗不育男性中最常见的异常细胞机制。这篇综述为在伊朗不育男性中引入基于人群的遗传标志物诊断面板铺平了道路。