Gender-sensitive association of CFTR gene mutations and 5T allele emerging from a large survey on infertility-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Gender-sensitive association of CFTR gene mutations and 5T allele emerging from a large survey on infertility

Published:2005-08-01 Issue:8 Volume:11 Page:607-614
ISSN:1460-2407
Container-title:MHR: Basic science of reproductive medicine
language:en
Short-container-title:

Author:

Morea Antonella,Cameran Marilena,Rebuffi Anna Grazia,Marzenta Diana,Marangon Oriana,Picci Luigi,Zacchello Franco,Scarpa Maurizio

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

Link

http://academic.oup.com/molehr/article-pdf/11/8/607/3705325/gah214.pdf

Reference47 articles.

1. Accurso FJ and Sontag MK (2003) Seeking modifier genes in cystic fibrosis. Am J Respir Crit Care Med167,289–290.

2. Acton JD and Wilmott RW (2001) Phenotype of CF and the effects of possible modifier genes. Paediatr Respir Rev2,332–339.

3. Bobadilla JL , Macek M Jr, Fine JP and Farrell PM (2002) Cystic fibrosis: a worldwide analysis of CFTR mutations-correlation with incidence data and application to screening. Hum Mutat19,575–606.

4. Bonizzato A , Bisceglia L, Marigo C, Nicolis E, Bombieri C, Castellani C, Borgo G, Zelante L, Mastella G, Cabrini G et al. (1995) Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from North East Italy: identification of 90% of the mutations. Hum Genet95,397–402.

5. Chehab FF and Wall J (1992) Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening. Hum Genet89,163–168.

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Infertility and the chromosomal abnormalities;Genetics and Epigenetics of Genitourinary Diseases;2025

2. International experience in the primary prevention of cystic fibrosis (part one);Experimental and Clinical Gastroenterology;2023-01-18

3. Systematic review reveals multiple sexually antagonistic polymorphisms affecting human disease and complex traits;Evolution;2021-11-12

4. Systematic review reveals multiple sexually antagonistic polymorphisms affecting human disease and complex traits;2020-12-18

5. Congenital absence of the vas deferens: Cystic fibrosis transmembrane regulatory gene mutations;Best Practice & Research Clinical Endocrinology & Metabolism;2020-12

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3