(Q37372779)

English

Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor

scientific article published on September 1997

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

congenital disorder

0 references

congenital hyperthyroidism

1 reference

based on heuristic

inferred from title

author name string

P Kopp

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

S Muirhead

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

N Jourdain

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

W X Gu

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

J L Jameson

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

C Rodd

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 September 1997

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

100

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1634-1639

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Specific activation of the thyrotropin receptor by trypsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

The thyrotropin (TSH) receptor transmembrane domain mutation (Pro556-Leu) in the hypothyroid hyt/hyt mouse results in plasma membrane targeting but defective TSH binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Rarity of oncogenic mutations in the thyrotropin receptor of autonomously functioning thyroid nodules in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Two G protein oncogenes in human endocrine tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Clonal composition of benign and malignant human thyroid tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

The Thyrotropin Receptor and the Regulation of Thyrocyte Function and Growth*

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

6 September 2017

Somatic and germline mutations of the TSH receptor gene in thyroid diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

14 September 2017

G protein-coupled receptor structure and function: the impact of disease-causing mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

14 September 2017

Iodide-induced thyrotoxicosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

14 September 2017

Mutations in G proteins and G protein-coupled receptors in endocrine disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

Constitutive activity of receptors coupled to guanine nucleotide regulatory proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosph

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

Identification and functional characterization of two new somatic mutations causing constitutive activation of the thyrotropin receptor in hyperfunctioning autonomous adenomas of the thyroid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

Constitutive activation of the thyrotropin receptor by deletion of a portion of the extracellular domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

28 September 2017

Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

26 June 2018

Genetic alterations in thyroid hyperfunctioning adenomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

26 June 2018

Solitary polyclonal autonomous thyroid nodule: a rare cause of childhood hyperthyroidism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

26 June 2018

Suppression of pituitary TSH in a child with a hyperfunctioning thyroid nodule

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508345

26 June 2018

Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas. Rapid identification by fine needle aspiration biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thyrotropin receptor gene alterations in thyroid hyperfunctioning adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TSH receptor and Gs-alpha gene mutations in the pathogenesis of toxic thyroid adenomas--a note of caution

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oncogenic mutations in thyroid adenoma: methodological criteria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thyroid nodule producing T3 toxicosis in a child

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of thyroid-stimulating antibody-specific interaction sites in the N-terminal region of the thyrotropin receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pregnancy-Associated Changes in the Thyroid-Stimulating Antibody of Graves’ Disease and the Relationship to Neonatal Hyperthyroidism*

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the mechanism of desensitization of the cyclic AMP response to TSH stimulation in a cloned rat thyroid cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction and therapy of intrauterine and late-onset neonatal hyperthyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal thyroid disease: differential expression in three successive offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polyclonal and monoclonal thyroid nodules coexist within human multinodular goiters

1 reference

https://pubmed.ncbi.nlm.nih.gov/9294132

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI119687

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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