• 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

The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis.

作者信息

Oates R D, Amos J A

机构信息

Department of Urology, New England Male Reproductive Center, Boston University School of Medicine, Massachusetts.

出版信息

J Androl. 1994 Jan-Feb;15(1):1-8.

PMID:8188533
Abstract
摘要

相似文献

1
The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis.先天性双侧输精管缺如与囊性纤维化的遗传基础。
J Androl. 1994 Jan-Feb;15(1):1-8.
2
Congenital absence of vas deferens and cystic fibrosis.先天性输精管缺如与囊性纤维化。
Minerva Pediatr. 2003 Feb;55(1):43-7, 47-50.
3
[Agenesis of vas deferens and cystic fibrosis].[输精管缺如与囊性纤维化]
Actas Urol Esp. 1997 Sep;21(8):773-6.
4
[Congenital bilateral agenesis of the vas deferens associated with cystic fibrosis. A molecular genetic study].[先天性双侧输精管缺如与囊性纤维化。一项分子遗传学研究]
Arch Esp Urol. 1998 Jun;51(5):451-5.
5
High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferens.先天性输精管缺如患者中R117H囊性纤维化突变的高频率。
N Engl J Med. 1993 Feb 11;328(6):446-7. doi: 10.1056/NEJM199302113280619.
6
Normal vas deferens in fetuses with cystic fibrosis.患有囊性纤维化胎儿的正常输精管。
J Urol. 1997 Oct;158(4):1549-52.
7
[Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].[囊性纤维化和先天性双侧输精管缺如的分子基础]
Contracept Fertil Sex. 1996 Jun;24(6):495-500.
8
Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).先天性双侧输精管缺如（CBAVD）患者CFTR基因中两个突变（S50Y和4173delC）的鉴定。
Hum Mutat. 1997;9(2):183-4. doi: 10.1002/(SICI)1098-1004(1997)9:2<183::AID-HUMU13>3.0.CO;2-Z.
9
Congenital bilateral absence of the vas deferens.先天性双侧输精管缺如
J Pediatr Surg. 2008 Jun;43(6):1222-3. doi: 10.1016/j.jpedsurg.2008.01.059.
10
Molecular screening of CFTR gene in Brazilian men with bilateral agenesis of the vas deferens.对巴西双侧输精管缺如男性进行囊性纤维化跨膜传导调节因子（CFTR）基因的分子筛查。
Hum Fertil (Camb). 2006 Mar;9(1):53-6. doi: 10.1080/14647270500440598.

引用本文的文献

1
Genetic and epigenetic landscape of male infertility.男性不育的遗传和表观遗传格局
Trends Genet. 2025 Aug 21. doi: 10.1016/j.tig.2025.07.007.
2
Differentiation between nonobstructive azoospermia and obstructive azoospermia: then and now.非梗阻性无精子症与梗阻性无精子症的鉴别诊断：过去与现在
Asian J Androl. 2025 May 1;27(3):298-306. doi: 10.4103/aja202475. Epub 2024 Sep 13.
3
Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens.先天性双侧输精管缺如患者的遗传学分析及卵胞浆内单精子注射结局。
J Assist Reprod Genet. 2022 Mar;39(3):719-728. doi: 10.1007/s10815-022-02417-z. Epub 2022 Feb 4.
4
Cystic fibrosis transmembrane conductance regulator-related male infertility: Relevance of genetic testing & counselling in Indian population.囊性纤维化跨膜电导调节因子相关男性不育症：印度人群中遗传检测和咨询的相关性。
Indian J Med Res. 2020 Dec;152(6):575-583. doi: 10.4103/ijmr.IJMR_906_18.
5
Congenital unilateral absence of the vas deferens with ipsilateral renal agenesis encountered during laparoscopic totally extraperitoneal inguinal hernia repair in an adult patient: A case report.成年患者腹腔镜完全腹膜外腹股沟疝修补术中发现先天性单侧输精管缺如伴同侧肾缺如：一例报告
Ann Med Surg (Lond). 2021 May 27;66:102449. doi: 10.1016/j.amsu.2021.102449. eCollection 2021 Jun.
6
How do we counsel men with obstructive azoospermia due to CF mutations?-a review of treatment options and outcomes.我们如何为因囊性纤维化（CF）基因突变导致梗阻性无精子症的男性提供咨询？——治疗选择与结果综述
Transl Androl Urol. 2021 Mar;10(3):1467-1478. doi: 10.21037/tau-19-681.
7
Genetics of Azoospermia.无精子症的遗传学。
Int J Mol Sci. 2021 Mar 23;22(6):3264. doi: 10.3390/ijms22063264.
8
CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.CFTR 变体与先天性单侧输精管缺如（CUAVD）男性的肾脏异常：观察性研究的系统评价和荟萃分析。
Genet Med. 2019 Apr;21(4):826-836. doi: 10.1038/s41436-018-0262-7. Epub 2018 Sep 14.
9
Recent advances in the genetics of testicular failure.睾丸功能衰竭遗传学的最新进展。
Asian J Androl. 2016 May-Jun;18(3):350-5. doi: 10.4103/1008-682X.178857.
10
The spectrum of renal involvement in male patients with infertility related to excretory-system abnormalities: phenotypes, genotypes, and genetic counseling.与排泄系统异常相关的男性不育患者的肾脏受累谱：表型、基因型及遗传咨询
J Nephrol. 2017 Apr;30(2):211-218. doi: 10.1007/s40620-016-0286-5. Epub 2016 Mar 5.