Literature DB >> 7800007

Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.

P Kopp1, J van Sande, J Parma, L Duprez, H Gerber, E Joss, J L Jameson, J E Dumont, G Vassart.   

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Year:  1995        PMID： 7800007     DOI： 10.1056/NEJM199501193320304

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  38 in total

1.  Pregnant rat uterus expresses high levels of the type 3 iodothyronine deiodinase.

Authors:  V A Galton; E Martinez; A Hernandez; E A St Germain; J M Bates; D L St Germain
Journal:  J Clin Invest       Date:  1999-04       Impact factor: 14.808

Review 2.  Thyrotropin receptor mutations in thyroid diseases.

Authors:  P M Yen
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

Review 3.  The PTH/PTHrP receptor in Jansen's metaphyseal chondrodysplasia.

Authors:  L M Calvi; E Schipani
Journal:  J Endocrinol Invest       Date:  2000-09       Impact factor: 4.256

4.  Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene.

Authors:  Zehra Aycan; Sebahat Yılmaz Ağladıoğlu; Serdar Ceylaner; Semra Cetinkaya; Veysel Nijat Baş; Havva Nur Peltek Kendirici
Journal:  J Clin Res Pediatr Endocrinol       Date:  2010-11-07

5.  Free thyroxine levels after very preterm birth and neurodevelopmental outcomes at age 7 years.

Authors:  Shannon E Scratch; Rodney W Hunt; Deanne K Thompson; Zohra M Ahmadzai; Lex W Doyle; Terrie E Inder; Peter J Anderson
Journal:  Pediatrics       Date:  2014-03-31       Impact factor: 7.124

6.  Ras homolog enriched in striatum inhibits the functional activity of wild type thyrotropin, follicle-stimulating hormone, luteinizing hormone receptors and activating thyrotropin receptor mutations by altering their expression in COS-7 cells.

Authors:  P Agretti; G De Marco; A Pinchera; P Vitti; J Bernal; M Tonacchera
Journal:  J Endocrinol Invest       Date:  2007-04       Impact factor: 4.256

7.  Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidism.

Authors:  Stephanie A Roberts; Jennifer E Moon; Andrew Dauber; Jessica R Smith
Journal:  J Pediatr Endocrinol Metab       Date:  2017-03-01       Impact factor: 1.634

Review 8.  Constitutive activation of G protein-coupled receptors and diseases: insights into mechanisms of activation and therapeutics.

Authors:  Ya-Xiong Tao
Journal:  Pharmacol Ther       Date:  2008-08-09       Impact factor: 12.310

Review 9.  Advances in endocrinology.

Authors:  P E Clayton; V Tillmann
Journal:  Arch Dis Child       Date:  1998-03       Impact factor: 3.791

Review 10.  Thyrotropin receptor-associated diseases: from adenomata to Graves disease.

Authors:  Terry F Davies; Takao Ando; Reigh-Yi Lin; Yaron Tomer; Rauf Latif
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808
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