(Q48275476)

10 February 2018

title

Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X-linked cleft palate gene. (English)

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10 February 2018

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Jeffrey O Bush

1

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10 February 2018

Yu Lan

series ordinal

2

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10 February 2018

Kathleen M Maltby

series ordinal

3

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10 February 2018

Rulang Jiang

series ordinal

4

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10 February 2018

publication date

1 November 2002

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10 February 2018

published in

Developmental Dynamics

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10 February 2018

volume

225

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10 February 2018

issue

3

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10 February 2018

page(s)

322-326

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10 February 2018

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Osr2, a new mouse gene related to Drosophila odd-skipped, exhibits dynamic expression patterns during craniofacial, limb, and kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Molecular characterization of a new human T-box gene (TBX22) located in xq21.1 encoding a protein containing a truncated T-domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

T-box genes in development: from hydra to humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

21 January 2018

The T-box gene family

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10154

21 January 2018

Identifiers

DOI

10.1002/DVDY.10154

1 reference

10 February 2018

PubMed ID

12412015

1 reference

10 February 2018