Somatic and germline mutations of the TSH receptor and thyroid diseases-Reference-Cited by-同舟云学术

Somatic and germline mutations of the TSH receptor and thyroid diseases

Published:2001-08 Issue:2 Volume:55 Page:143-158
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Corvilain B.,Van Sande J.,Dumont J. E.,Vassart G.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2001.01365.x-i2/fullpdf

Reference109 articles.

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2. The spectrum of thyroid disorders in an iodine-deficient community: the Pescopagano survey;Aghini-Lombardi;Journal of Clinical Endocrinology and Metabolism,1999

3. Genomic DNA analysis of thyrotropin receptor in a family with hereditary hyperthyroidism;Aoshima;Endocrine Journal,2000

4. Substitutions of tyrosine 601 in the human thyrotropin receptor result in increase or loss of basal activation of the cyclic adenosine monophosphate pathway and disrupt coupling to Gq/11;Arseven;Thyroid,2000

5. Interrelationships between age, thyroid volume, thyroid nodularity, and thyroid function in patients with sporadic nontoxic goitre;Berghout;American Journal of Medicine,1990

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