Studies on the Thyroidal Defect in an Atypical Form of Pendred's Syndrome*
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/41/3/590/10522527/jcem0590.pdf
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. Role of Megalin (gp330) in Transcytosis of Thyroglobulin by Thyroid Cells;Journal of Biological Chemistry;2000-03
2. The importance of thyroglobulin structure for thyroid hormone biosynthesis**We shared with our friend and colleague, the late Gaetano Salvatore, a long–standing interest in thyroglobulin structure, as well as a broader interest in the optimal production of thyroid hormone and its dependence on adequate iodine supply. Over the years, we frequently discussed progress in this field with him and his many co–workers. We now welcome the opportunity to review some of our investigative work in one of his favorite fields, in his honor.;Biochimie;1999-05
3. The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q;Genomics;1997-02
4. Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification;Nature Genetics;1996-04
5. Thyroids from siblings with Pendred's syndrome contain thyroglobulin messenger ribonucleic acid variants;Journal of Clinical Endocrinology & Metabolism;1995-02-01
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