A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism-Reference-Cited by-同舟云学术

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A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

Published:2016-03 Issue:3 Volume:101 Page:847-851
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Koulouri O.,Nicholas A. K.,Schoenmakers E.,Mokrosinski J.,Lane F.,Cole T.,Kirk J.,Farooqi I. S.,Chatterjee V. K.,Gurnell M.,Schoenmakers N.

Publisher

The Endocrine Society

Subject

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

Cited by 24 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. Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disorders;Genetics in Medicine;2023-09

2. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency;European Journal of Endocrinology;2022-11-03

3. Biochemical and physiological insights into TRH receptor-mediated signaling;Frontiers in Cell and Developmental Biology;2022-09-06

4. Structural insights into ligand binding and activation of the human thyrotropin-releasing hormone receptor;Cell Research;2022-04-01

5. The Molecular Basis of Congenital Hypopituitarism and Related Disorders;The Journal of Clinical Endocrinology & Metabolism;2019-11-08

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