(Q24322560)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

title

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

1 reference

GOA release 2020-03-11

positive regulation of transcription, DNA-templated

1 reference

GOA release 2020-03-11

1 reference

1 reference

Roderick J Clifton-Bligh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

John Lazarus

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

Marian Ludgate

7

1 reference

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2 December 2019

author name string

Wentworth JM

2

1 reference

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2 December 2019

Heinz P

3

1 reference

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2 December 2019

Crisp MS

4

1 reference

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2 December 2019

John R

5

1 reference

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2 December 2019

Chatterjee VK

8

1 reference

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2 December 2019

language of work or name

English

0 references

publication date

1 August 1998

1 reference

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2 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

volume

19

1 reference

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2 December 2019

page(s)

399-401

1 reference

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2 December 2019

issue

4

1 reference

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Survey of neonatal screening for primary hypothyroidism in England, Wales, and Northern Ireland 1982-4.

2 December 2019

cites work

1 reference

7 January 2021

Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene

1 reference

7 January 2021

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland

1 reference

7 January 2021

Thyroid nuclear factor 1 (TTF-1) contains a homeodomain and displays a novel DNA binding specificity

1 reference

7 January 2021

Thyroid-specific enhancer-binding protein (T/EBP): cDNA cloning, functional characterization, and structural identity with thyroid transcription factor TTF-1.

1 reference

7 January 2021

Cell-type-specific expression of the rat thyroperoxidase promoter indicates common mechanisms for thyroid-specific gene expression

1 reference

7 January 2021

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

1 reference

7 January 2021

Pax-8, a paired domain-containing protein, binds to a sequence overlapping the recognition site of a homeodomain and activates transcription from two thyroid-specific promoters

1 reference

7 January 2021

Five years on the wings of fork head

1 reference

7 January 2021

FKHL15, a new human member of the forkhead gene family located on chromosome 9q22

1 reference

7 January 2021

Congenital hypothyroidism, spiky hair, and cleft palate

1 reference

7 January 2021

Congenital hypothyroidism detected by neonatal screening: relationship between biochemical severity and early clinical features

1 reference

7 January 2021

Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor gene

1 reference

7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

1 reference

7 January 2021

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

1 reference

7 January 2021

The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

1 reference

7 January 2021

Absence of mutations in the gene encoding thyroid transcription factor-1 (TTF-1) in patients with thyroid dysgenesis.

1 reference

7 January 2021

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis.

1 reference

7 January 2021

Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure

1 reference

7 January 2021

Congenital abnormalities and congenital hypothyroidism

1 reference

7 January 2021

Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992.

1 reference

7 January 2021

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

7 January 2021

Thyroid hormone action: in vitro characterization of solubilized nuclear receptors from rat liver and cultured GH1 cells.

1 reference

7 January 2021

Genetic analysis of 29 kindreds with generalized and pituitary resistance to thyroid hormone. Identification of thirteen novel mutations in the thyroid hormone receptor beta gene

1 reference

7 January 2021

Identifiers

DOI

10.1038/1294

2 references

Consolidated OpenCitations Corpus – April 2017

2213836

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 December 2019

1029730098

0 references

2213836

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2213836

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9697705%20AND%20SRC:MED&resulttype=core&format=json