(Q24301402)

GOA release 2020-03-11

NK2 homeobox 5

1 reference

GOA release 2020-03-11

1 reference

2

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Marco Tartaglia

19

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Paolo Emidio Macchia

20

Alfonso Massimiliano Ferrara

Paolo Emidio Macchia

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Alfonso Massimiliano Ferrara

4

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Domenico Salvatore

Domenico Salvatore

6

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Libero Santarpia

Libero Santarpia

5

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Antonella Olivieri

Antonella Olivieri

11

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Luca Chiovato

Luca Chiovato

7

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author name string

Monica Dentice

1

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Annamaria Rosica

3

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Anna Perri

8

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Lidia Moschini

9

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Cristina Fazzini

10

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Pietro Costa

12

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Vera Stoppioni

13

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Mariangiola Baserga

14

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Mario De Felice

15

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Mariella Sorcini

16

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Gianfranco Fenzi

17

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Roberto Di Lauro

The Journal of Clinical Endocrinology and Metabolism

18

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language of work or name

English

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publication date

April 2006

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published in

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volume

91

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issue

4

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page(s)

1428-33

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cites work

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Distribution of the titf2/foxe1 gene product is consistent with an important role in the development of foregut endoderm, palate, and hair.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Chicken Nkx-2.8: a novel homeobox gene expressed in early heart progenitor cells and pharyngeal pouch-2 and -3 endoderm.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

NKX2.5mutations in patients with congenital heart disease

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

An integrated regulatory network controlling survival and migration in thyroid organogenesis

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Csx: a murine homeobox-containing gene specifically expressed in the developing heart

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

The tissue-specific expression of the thyroglobulin gene requires interaction between thyroid-specific and ubiquitous factors

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Nkx2.5 and Nkx2.6, homologs of Drosophila tinman, are required for development of the pharynx

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Transcription factor Nkx-2.5 induces sodium/iodide symporter gene expression and participates in retinoic acid- and lactation-induced transcription in mammary cells

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

A mouse model demonstrates a multigenic origin of congenital hypothyroidism

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Thyroid dysgenesis: multigenic or epigenetic ... or both?

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

Thyroid Development and Its Disorders: Genetics and Molecular Mechanisms

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021

The different cardiac expression of the type 2 iodothyronine deiodinase gene between human and rat is related to the differential response of the Dio2 genes to Nkx-2.5 and GATA-4 transcription factors

1 reference

https://api.crossref.org/works/10.1210%2FJC.2005-1350

7 January 2021