Cloning and Characterization of HumanWDR10, a Novel Gene Located at 3q21 Encoding a WD-Repeat Protein That Is Highly Expressed in Pituitary and Testis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cloning and Characterization of HumanWDR10, a Novel Gene Located at 3q21 Encoding a WD-Repeat Protein That Is Highly Expressed in Pituitary and Testis

Published:2001-01 Issue:1 Volume:20 Page:41-52
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Gross Coleman¹,De Baere Elfride²,Lo Annie³,Chang Wenhan¹,Messiaen Ludwine²

Affiliation:

1. Endocrine Section, Department of Veterans Affairs Medical Center, San Francisco, California and Department of Medicine University of California, San Francisco, San Francisco

2. Department of Medical Genetics, Ghent University Hospital, Ghent, Belgium

3. Endocrine Section, Department of Veterans Affairs Medical Center, San Francisco, California

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/10445490150504684

Reference42 articles.

1. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

2. Moebius syndrome, an axonal neuropathy and hypogonadism

3. Characterization of the ligand-dependent transactivation domain of thyroid hormone receptor.

4. Signaling events during male germ cell differentiation bases and perspectives

5. Moebius syndrome in association with hypogonadotropic hypogonadism

Cited by 13 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. A novel variant in IFT122 associated with a severe phenotype of cranioectodermal dysplasia;Congenital Anomalies;2024-04-18

2. A missense variant in IFT122 associated with a canine model of retinitis pigmentosa;Human Genetics;2021-02-19

3. Translocation breakpoints of chromosome 3 in male carriers: a report oftwelve cases and a review of the literature;TURKISH JOURNAL OF MEDICAL SCIENCES;2018

4. New Insights into the Genetic Basis of Monge’s Disease and Adaptation to High-Altitude;Molecular Biology and Evolution;2017-09-19

5. Beemer–Langer syndrome is a ciliopathy due to biallelic mutations in IFT122;American Journal of Medical Genetics Part A;2017-03-28

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