(Q37563887)

English

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

scientific article published on 28 July 2009

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

author name string

J Lueblinghoff

1

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

S Mueller

2

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

J Sontheimer

3

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

R Paschke

4

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

publication date

28 July 2009

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Journal of Endocrinological Investigation

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

33

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

228-233

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Congenital neonatal hyperthyroidism caused by germline mutations in the TSH receptor gene

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Long-term carbimazole treatment of neonatal nonautoimmune hyperthyroidism due to a new activating TSH receptor gene mutation (Ala428Val).

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patient.

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Persistent neonatal thyrotoxicosis in a neonate secondary to a rare thyroid-stimulating hormone receptor activating mutation: case report and literature review

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Multiple relapses of hyperthyroidism after thyroid surgeries in a patient with long term follow-up of sporadic non-autoimmune hyperthyroidism

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Functional characterization of five constitutively activating thyrotrophin receptor mutations

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

A conserved Asn in TM7 of the thyrotropin receptor is a common requirement for activation by both mutations and its natural agonist.

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Cases of borderline in vitro constitutive thyrotropin receptor activity: how to decide whether a thyrotropin receptor mutation is constitutively active or not?

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Preferences of transmembrane helices for cooperative amplification of G(alpha)s and G (alpha)q signaling of the thyrotropin receptor

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Iodine deficiency in Europe and its consequences: an update

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

An aromatic environment in the vicinity of serine 281 is a structural requirement for thyrotropin receptor function

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Evidence for cooperative signal triggering at the extracellular loops of the TSH receptor

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Activation of the beta 2-adrenergic receptor involves disruption of an ionic lock between the cytoplasmic ends of transmembrane segments 3 and 6.

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

A family with a novel TSH receptor activating germline mutation (p.Ala485Val).

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

A novel TSHR gene mutation (Ile691Phe) in a Chinese family causing autosomal dominant non-autoimmune hyperthyroidism

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

A novel activating mutation in transmembrane helix 6 of the thyrotropin receptor as cause of hereditary nonautoimmune hyperthyroidism.

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

The TSH receptor and its role in thyroid disease

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Similarities and differences in the phenotype of members of an Italian family with hereditary non-autoimmune hyperthyroidism associated with an activating TSH receptor germline mutation

1 reference

https://api.crossref.org/works/10.1007%2FBF03345784

21 January 2018

Constitutive activity of the melanocortin-4 receptor is maintained by its N-terminal domain and plays a role in energy homeostasis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term follow-Up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of thyroid-stimulating hormone receptor and Gsalpha mutations: in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Similar prevalence of somatic TSH receptor and Gsalpha mutations in toxic thyroid nodules in geographical regions with different iodine supply in Turkey

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

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/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of the cAMP pathway by the TSH receptor involves switching of the ectodomain from a tethered inverse agonist to an agonist

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diversity and prevalence of somatic mutations in the thyrotropin receptor and Gs alpha genes as a cause of toxic thyroid adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thyroid volumes and urinary iodine in Swiss school children, 17 years after improved prophylaxis of iodine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutive activation of the TSH receptor by spontaneous mutations affecting the N-terminal extracellular domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iodine nutrition in the United States. Trends and public health implications: iodine excretion data from National Health and Nutrition Examination Surveys I and III (1971-1974 and 1988-1994)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel thyrotropin receptor mutation in an infant with severe thyrotoxicosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of iodine deficiency in Western and Central Europe.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutive activity of glucagon receptor mutants

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of mutations involving the highly conserved S281HCC motif in the extracellular domain of the thyrotropin (TSH) receptor on TSH binding and constitutive activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/19636218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03345784

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37563887&oldid=2200541270"