Mamld1 Deficiency Significantly Reduces mRNA Expression Levels of Multiple Genes Expressed in Mouse Fetal Leydig Cells but Permits Normal Genital and Reproductive Development

Author:

Miyado Mami1,Nakamura Michiko1,Miyado Kenji2,Morohashi Ken-ichirou3,Sano Shinichiro4,Nagata Eiko4,Fukami Maki1,Ogata Tsutomu14

Affiliation:

1. Departments of Molecular Endocrinology (M.M., M.N., M.F., T.O.), National Research Institute of Child Health and Development, Tokyo 157-8535, Japan

2. Reproductive Biology (K.Mi.), National Research Institute of Child Health and Development, Tokyo 157-8535, Japan

3. Department of Molecular Biology (K.Mo.), Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan

4. Department of Pediatrics (S.S., E.N., T.O.), Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan

Publisher

The Endocrine Society

Subject

Endocrinology

Reference33 articles.

1. CXorf6 is a causative gene for hypospadias.;Fukami;Nat Genet,2006

2. Mutations of CXorf6 are associated with a range of severities of hypospadias.;Kalfa;Eur J Endocrinol,2008

3. MAMLD1 (CXorf6): a new gene involved in hypospadias.;Ogata;Horm Res,2009

4. Mutational study of the MAMLD1-gene in hypospadias.;Chen;Eur J Med Genet,2010

5. Aetiology of hypospadias: a systematic review of genes and environment.;van der Zanden;Hum Reprod Update,2012

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