Shared Sporadic and Somatic Thyrotropin Receptor Mutations Display More ActiveIn VitroActivities than Familial Thyrotropin Receptor Mutations-Reference-Cited by-同舟云学术

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Shared Sporadic and Somatic Thyrotropin Receptor Mutations Display More ActiveIn VitroActivities than Familial Thyrotropin Receptor Mutations

Published:2011-03 Issue:3 Volume:21 Page:221-229
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Lueblinghoff Julia¹,Eszlinger Markus¹,Jaeschke Holger¹,Mueller Sandra¹,Bircan Rifat²,Gozu Hulya³,Sancak Seda⁴,Akalin Sema⁴,Paschke Ralf¹

Affiliation:

1. Division for Endocrinology and Nephrology, Department of Medicine, University of Leipzig, Leipzig, Germany.

2. Department of Molecular Biology, Faculty of Arts and Sciences, Namik Kemal University, Tekirdag, Turkey.

3. Section of Endocrinology and Metabolism, Dr. Lufti Kirdal Kartal Education and Research Hospital, Istanbul, Turkey.

4. Section of Endocrinology and Metabolism, Department of Internal Medicine, Marmara University Medical School, Istanbul, Turkey.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2010.0312

Reference89 articles.

1. Early Malignant Progression of Hereditary Medullary Thyroid Cancer

2. Prophylactic Thyroidectomy in RET Carriers at Risk for Hereditary Medullary Thyroid Cancer

3. Difference in development of medullary thyroid carcinoma among carriers of RET mutations in codons 790 and 791*

4. Characterization of the RET protooncogene transmembrane domain mutation S649L associated with nonaggressive medullary thyroid carcinoma.

5. Lack of consistent association of thyrotropin receptor mutations in vitro activity with the clinical course of patients with sporadic non-autoimmune hyperthyroidism

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1. G protein-coupled receptor (GPCR) gene variants and human genetic disease;Critical Reviews in Clinical Laboratory Sciences;2024-03-18

2. Mechanisms of thyrotropin receptor–mediated phenotype variability deciphered by gene mutations and M453T-knockin model;JCI Insight;2024-01-09

3. Diagnostica del nodulo tiroideo autonomo: è sufficiente misurare il TSH?;L'Endocrinologo;2021-10-25

4. Central TSH Dysregulation in a Patient with Familial Non-Autoimmune Autosomal Dominant Hyperthyroidism Due to a Novel Thyroid-Stimulating Hormone Receptor Disease-Causing Variant;Medicina;2021-02-25

5. An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial nonautoimmune hyperthyroidism;Annals of Pediatric Endocrinology & Metabolism;2020-12-31

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