Literature DB >> 32111150

The Thyrotropin Receptor Mutation Database Update.

Alexandra Stephenson1,2, Lorraine Lau3, Markus Eszlinger1,2,4,5, Ralf Paschke1,2,3,4,5,6.   

Abstract

The thyrotropin receptor (TSHR) mutation database, consisting of all known TSHR mutations and their clinical characterizations, was established in 1999. The database contents are updated here with the same website (tsh-receptor-mutation-database.org). The new database contains 638 cases of TSHR mutations: 448 cases of gain of function mutations (7 novel mutations and 41 new cases for previously described mutations since its last update in 2012) and 190 cases of loss of function mutations (28 novel mutations and 31 new cases for previously described mutations since its last update in 2012). This database is continuously updated and allows for rapid validation of patient TSHR mutations causing hyper- or hypothyroidism or insensitivity to TSH.

Entities:  

Keywords:  FNAH; SNAH; TSH insensitivity; TSHR; congenital hypothyroidism; hot thyroid nodule

Mesh:

Substances:

Year:  2020        PMID: 32111150     DOI: 10.1089/thy.2019.0807

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  9 in total

1.  Macro-TSH: A Diagnostic Challenge.

Authors:  Camilla Bøgelund Larsen; Eva Rabing Brix Petersen; Martin Overgaard; Steen Joop Bonnema
Journal:  Eur Thyroid J       Date:  2020-08-21

2.  Familial Non-autoimmune Hyperthyroidism in Family Members Across Four Generations Due To a Novel Disease-causing Variant in The Thyrotropin Receptor Gene.

Authors:  A Malej; M Avbelj Stefanija; N Bratanič; K Trebušak Podkrajšek
Journal:  Balkan J Med Genet       Date:  2021-03-23       Impact factor: 0.519

3.  Report of a family with three generations of undiagnosed familial nonautoimmune hyperthyroidism.

Authors:  Alexandra Stephenson; Zoya Punjwani; Markus Eszlinger; Beata Sawicka; Artur Bossowski; Ralf Paschke
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2021-12-01

4.  Locally invasive classical papillary thyroid carcinoma with TSH receptor I568T mutation: case report.

Authors:  Jay Nguyen; Dennis Joseph
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2022-03-01

Review 5.  The Mysterious Universe of the TSH Receptor.

Authors:  Inês Henriques Vieira; Dírcea Rodrigues; Isabel Paiva
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-12       Impact factor: 6.055

6.  Hyperfunctioning Papillary Thyroid Carcinoma with a BRAF Mutation: The First Case Report and a Literature Review.

Authors:  Shinsuke Shinkai; Kenji Ohba; Kennichi Kakudo; Takayuki Iwaki; Yoshihiro Mimura; Akio Matsushita; Go Kuroda; Yuki Sakai; Nobuhiko Nishino; Kazuo Umemura; Takafumi Suda; Shigekazu Sasaki
Journal:  Eur Thyroid J       Date:  2021-03-05

Review 7.  Novel presentation of the c.1856A > G (p.Asp619Gly) TSHR gene-activating variant: relapsing hyperthyroidism in three subsequent generations manifesting in early childhood and an in vitro functional study.

Authors:  Martin Bezdicka; Petra Kleiblova; Jiri Soucek; Marianna Borecka; Eva El-Lababidi; Daniel Smrz; Michal Rataj; Zdenek Sumnik; Jana Malikova; Ondrej Soucek
Journal:  Hormones (Athens)       Date:  2021-06-18       Impact factor: 2.885

8.  Next-Generation Sequencing Enhances the Diagnosis Efficiency in Thyroid Nodules.

Authors:  Li-Cheng Tan; Wan-Lin Liu; Xiao-Li Zhu; Peng-Cheng Yu; Xiao Shi; Pei-Zhen Han; Ling Zhang; Liang-Yu Lin; Arseny Semenov; Yu Wang; Qing-Hai Ji; Dong-Mei Ji; Yu-Long Wang; Ning Qu
Journal:  Front Oncol       Date:  2021-07-12       Impact factor: 6.244

9.  Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.

Authors:  Miao Huang; Xiyan Lu; Guoqing Dong; Jianxu Li; Chengcong Chen; Qiuxia Yu; Mingzhu Li; Yueyue Su
Journal:  Front Endocrinol (Lausanne)       Date:  2021-07-02       Impact factor: 5.555

  9 in total

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