(Q21092847)

positive regulation of thyroid hormone generation

GOA release 2020-03-11

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GOA release 2020-03-11

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1 reference

1 reference

Katherine U. Gaynor

1

Katherine U

Gaynor

1 reference

15 August 2022

Irina V. Grigorieva

2

Irina V

Grigorieva

1 reference

15 August 2022

M. Andrew Nesbit

3

M Andrew

Nesbit

1 reference

15 August 2022

Treena Cranston

4

Treena

Cranston

1 reference

15 August 2022

Thushari Gomes

5

Thushari

Gomes

1 reference

15 August 2022

Ludwig Gortner

6

Ludwig

Gortner

1 reference

15 August 2022

Rajesh V. Thakker

7

Rajesh V

Thakker

1 reference

The Journal of Clinical Endocrinology and Metabolism

15 August 2022

language of work or name

English

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publication date

October 2009

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published in

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volume

94

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issue

10

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page(s)

3897-3904

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cites work

Novel mutation in the gene encoding the GATA3 transcription factor in a Spanish familial case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with female genital tract malformations

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13).

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Studies on the transformation of intact yeast cells by the LiAc/SS-DNA/PEG procedure

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Transcription factor GATA3 and the human HDR syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Hearing loss following Gata3 haploinsufficiency is caused by cochlear disorder

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Dosage-dependent rescue of definitive nephrogenesis by a distant Gata3 enhancer

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

FOG, a multitype zinc finger protein, acts as a cofactor for transcription factor GATA-1 in erythroid and megakaryocytic differentiation

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

The solution structure of the N-terminal zinc finger of GATA-1 reveals a specific binding face for the transcriptional co-factor FOG

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

GATA3 haplo-insufficiency causes human HDR syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

An early haematopoietic defect in mice lacking the transcription factor GATA-2

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

FOG-2: A novel GATA-family cofactor related to multitype zinc-finger proteins Friend of GATA-1 and U-shaped

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Molecular cloning of FOG-2: a modulator of transcription factor GATA-4 in cardiomyocytes

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Hepatic erythropoietin gene regulation by GATA-4.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Human GATA-3 trans-activation, DNA-binding, and nuclear localization activities are organized into distinct structural domains

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome

1 reference

https://api.crossref.org/works/10.1210%2FJC.2009-0717

7 January 2021

Identifiers

DOI

10.1210/JC.2009-0717

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