• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人类BOULE基因突变并非精子发生受损的主要原因。

Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis.

作者信息

Westerveld G Henrike, Repping Sjoerd, Leschot Nico J, van der Veen Fulco, Lombardi M Paola

机构信息

Center for Reproductive Medicine, Department of Obstetrics and Gynaecology, Academic Medical Center, Meibergdreef 9, H4-205, 1105 AZ Amsterdam, The Netherlands.

出版信息

Fertil Steril. 2005 Feb;83(2):513-5. doi: 10.1016/j.fertnstert.2004.10.013.

DOI:10.1016/j.fertnstert.2004.10.013
PMID:15705409
Abstract

Mutation screening of the BOULE gene in 156 men with azoospermia or severe oligozoospermia revealed no relevant mutations; thus, mutations in BOULE can be eliminated as a major cause of impaired spermatogenesis.

摘要

对156名无精子症或严重少精子症男性的BOULE基因进行突变筛查,未发现相关突变;因此,可排除BOULE基因突变是精子发生受损的主要原因。

相似文献

1
Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis.人类BOULE基因突变并非精子发生受损的主要原因。
Fertil Steril. 2005 Feb;83(2):513-5. doi: 10.1016/j.fertnstert.2004.10.013.
2
Mutations of the cyclin A1 gene are not a common cause of male infertility.cyclin A1 基因突变不是男性不育症的常见原因。
Syst Biol Reprod Med. 2009 Aug;55(4):125-8. doi: 10.3109/19396360902839828.
3
Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment.促性腺激素调节的睾丸解旋酶(GRTH)基因的单核苷酸多态性可能与人精子发生受损有关。
Hum Reprod. 2006 Mar;21(3):755-9. doi: 10.1093/humrep/dei388. Epub 2005 Nov 17.
4
Sequence alterations in the YBX2 gene are associated with male factor infertility.YBX2基因的序列改变与男性因素不育有关。
Fertil Steril. 2009 Apr;91(4):1090-5. doi: 10.1016/j.fertnstert.2008.01.009. Epub 2008 Mar 12.
5
Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesis.精子发生受损男性中的异质性核糖核蛋白G-T(HNRNP G-T)突变
Mol Hum Reprod. 2004 Apr;10(4):265-9. doi: 10.1093/molehr/gah042. Epub 2004 Mar 2.
6
Expression profiles of the DAZ gene family in human testis with and without spermatogenic failure.DAZ基因家族在有或无生精功能障碍的人类睾丸中的表达谱。
Fertil Steril. 2004 Apr;81(4):1034-40. doi: 10.1016/j.fertnstert.2003.08.047.
7
Association of three isoforms of the meiotic BOULE gene with spermatogenic failure in infertile men.减数分裂BOULE基因的三种亚型与不育男性生精功能障碍的关联。
Mol Hum Reprod. 2007 Feb;13(2):85-93. doi: 10.1093/molehr/gal101. Epub 2006 Nov 17.
8
Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.MSY2基因的某些单核苷酸多态性可能会导致特发性不育男性发生生精障碍的易感性增加。
Urology. 2008 May;71(5):878-82. doi: 10.1016/j.urology.2007.12.055. Epub 2008 Apr 18.
9
Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.特发性不育男性中FKBP6基因的突变筛查及其与生精障碍的关联研究。
Reproduction. 2007 Feb;133(2):511-6. doi: 10.1530/REP-06-0125.
10
Association of partial AZFc region deletions with spermatogenic impairment and male infertility.部分AZFc区域缺失与生精功能障碍及男性不育的关联
J Med Genet. 2005 Mar;42(3):209-13. doi: 10.1136/jmg.2004.025833.

引用本文的文献

1
Novel Genome-Wide Interactions Mediated via BOLL and EDNRA Polymorphisms in Intracranial Aneurysm.通过BOLL和EDNRA多态性介导的颅内动脉瘤新型全基因组相互作用。
J Korean Neurosurg Soc. 2023 Jul;66(4):409-417. doi: 10.3340/jkns.2022.0026. Epub 2022 Oct 24.
2
Polymorphisms within the Gene Detected by Tetra-Primer Amplification Refractory Mutation System PCR (T-ARMS-PCR) are Significantly Associated with Goat Litter Size.通过四引物扩增不应性突变系统PCR(T-ARMS-PCR)检测到的基因内多态性与山羊产仔数显著相关。
Animals (Basel). 2019 Nov 1;9(11):910. doi: 10.3390/ani9110910.
3
RNA-binding proteins in human oogenesis: Balancing differentiation and self-renewal in the female fetal germline.
人类卵子发生过程中的RNA结合蛋白:平衡雌性胎儿生殖系中的分化与自我更新
Stem Cell Res. 2017 May;21:193-201. doi: 10.1016/j.scr.2017.04.008. Epub 2017 Apr 18.
4
Evolutionary comparison of the reproductive genes, DAZL and BOULE, in primates with and without DAZ.有DAZ和无DAZ灵长类动物中生殖基因DAZL和BOULE的进化比较
Dev Genes Evol. 2006 Mar;216(3):158-68. doi: 10.1007/s00427-005-0039-2. Epub 2006 Jan 20.