(Q37352572)

19 August 2017

A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene (English)

1 reference

19 August 2017

G Medeiros-Neto

1

1 reference

19 August 2017

D T Herodotou

2

1 reference

19 August 2017

S Rajan

3

1 reference

19 August 2017

S Kommareddi

4

1 reference

19 August 2017

L de Lacerda

5

1 reference

19 August 2017

R Sandrini

6

1 reference

19 August 2017

M C Boguszewski

7

1 reference

19 August 2017

A N Hollenberg

8

1 reference

19 August 2017

S Radovick

9

1 reference

19 August 2017

F E Wondisford

10

1 reference

19 August 2017

language of work or name

English

0 references

publication date

1 March 1996

1 reference

Journal of Clinical Investigation

19 August 2017

1 reference

19 August 2017

97

1 reference

19 August 2017

5

1 reference

19 August 2017

1250-1256

1 reference

Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Crystal structure of human chorionic gonadotropin

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Glycoprotein Hormones: Structure and Function

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Cloning of the Human Thyrotropin β-Subunit Gene and Transient Expression of Biologically Active Human Thyrotropin after Gene Transfection

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the beta-subunit

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Isolation and characterization of the human thyrotropin beta-subunit gene. Differences in gene structure and promoter function from murine species

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone beta-subunit gene.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Hypogonadism Caused by a Single Amino Acid Substitution in the β Subunit of Luteinizing Hormone

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

DNA sequencing with chain-terminating inhibitors

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Human growth hormone as a reporter gene in regulation studies employing transient gene expression

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Isolation of high-molecular-weight DNA from mammalian cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

Serum free thyrotropin subunit in congenital isolated thyrotropin deficiency

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507178

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

26 June 2018

1 reference

12 December 2020

Familial isolated thyrotropin deficiency with cretinism

1 reference

12 December 2020

Pituitary Secretion of Free Alpha and Beta Subunit of Human Thyrotropin in Patients with Thyroid Disorders1

1 reference

12 December 2020

Inappropriate secretion of thyroid-stimulating hormone

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI118540

1 reference

release_ktbr3k37fjbihi3h6pe7fxoi5u

19 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ktbr3k37fjbihi3h6pe7fxoi5u

24 November 2022

mapped directly with Wikidata item

1 reference

19 August 2017

PubMed publication ID

8636437

1 reference