Expression of Pendrin and the Pendred Syndrome (PDS) Gene in Human Thyroid Tissues*-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Expression of Pendrin and the Pendred Syndrome (PDS) Gene in Human Thyroid Tissues*

Published:2000-05-01 Issue:5 Volume:85 Page:2028-2033
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Bidart Jean-Michel¹,Mian Caterina²,Lazar Vladimir¹,Russo Diego³,Filetti Sebastiano³,Caillou Bernard⁴,Schlumberger Martin²

Affiliation:

1. Departments of Clinical Biology (J.M.B., V.L.), 94805 Villejuif, France

2. Nuclear Medicine (C.M., M.S.), Institut Gustave-Roussy, 94805 Villejuif, France

3. Dipartimento di Medicina Sperimentale e Clinica, Policlinico Mater Domini (D.R., S.F.), 88100 Catanzaro, Italy

4. Pathology (B.C.), 94805 Villejuif, France

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/85/5/2028/9061530/jcem2028.pdf

Reference27 articles.

1. Clinical and molecular genetics studies in Pendred’s syndrome.;Billerbeck;Thyroid,1994

2. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).;Everett;Nat Genet,1997

3. Molecular analysis of the PDS gene in Pendred syndrome.;Coyle;Hum Mol Genet,1998

4. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.;Hastbacka;Cell,1994

5. Identification of a colon mucosa gene that is down-regulated in colon adenomas and adenocarcinomas.;Schweinfest;Proc Natl Acad Sci,1993

Cited by 6 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. Radio-Iodide Treatment: From Molecular Aspects to the Clinical View;Cancers;2021-02-27

2. Regulation of solute carrier family 26 member 7 (Slc26a7) by thyroid stimulating hormone in thyrocytes;Endocrine Journal;2021

3. Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes;BMC Medical Genetics;2020-04-15

4. Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features;Frontiers in Genetics;2018-11-30

5. Novel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway Diseases;Mediators of Inflammation;2015

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