(Q28594321)

31 January 2017

title

Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 (English)

1 reference

Transcription factor AP-2, alpha

31 January 2017

main subject

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GOA release 2020-03-11

2

S. Hagopian-Donaldson

1 reference

31 January 2017

J. Zhang

1

1 reference

31 January 2017

G. Serbedzija

3

1 reference

31 January 2017

J. Elsemore

4

1 reference

31 January 2017

D. Plehn-Dujowich

5

1 reference

31 January 2017

A. P. McMahon

6

1 reference

31 January 2017

R. A. Flavell

7

1 reference

31 January 2017

T. Williams

8

1 reference

31 January 2017

language of work or name

English

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publication date

16 May 1996

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31 January 2017

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31 January 2017

volume

381

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31 January 2017

issue

6579

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31 January 2017

page(s)

238–241

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Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis

31 January 2017

cites work

1 reference

7 January 2021

Alternative mRNAs encode multiple isoforms of transcription factor AP-2 during murine embryogenesis.

1 reference

7 January 2021

Regulation of transcription factor AP-2 by the morphogen retinoic acid and by second messengers.

1 reference

7 January 2021

Cloning and expression of AP-2, a cell-type-specific transcription factor that activates inducible enhancer elements

1 reference

7 January 2021

The developmentally regulated transcription factor AP-2 is involved in c-erbB-2 overexpression in human mammary carcinoma

1 reference

7 January 2021

Absence of radius and ulna in mice lacking hoxa-11 andhoxd-11

1 reference

7 January 2021

Patterning of neural crest derivatives in the avian embryo: in vivo and in vitro studies

1 reference

7 January 2021

The embryonic development of mammalian neural tube defects.

1 reference

7 January 2021

Neural crest cell formation and migration in the developing embryo

1 reference

7 January 2021

twist is required in head mesenchyme for cranial neural tube morphogenesis

1 reference

7 January 2021

MARCKS deficiency in mice leads to abnormal brain development and perinatal death

1 reference

7 January 2021

Retinoic acid and craniofacial development: molecules and morphogenesis

1 reference

7 January 2021

Experimental fetal alcohol syndrome: proposed pathogenic basis for a variety of associated facial and brain anomalies

1 reference

7 January 2021

Pathogenesis of craniofacial and body wall malformations induced by ochratoxin A in mice

1 reference

7 January 2021

Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region

1 reference

7 January 2021

Physical and genetic localization of the gene encoding the AP-2 transcription factor to mouse chromosome 13.

1 reference

7 January 2021

Analysis of the DNA-binding and activation properties of the human transcription factor AP-2

1 reference

7 January 2021

Characterization of a dimerization motif in AP-2 and its function in heterologous DNA-binding proteins

1 reference

7 January 2021

Altered cytokine export and apoptosis in mice deficient in interleukin-1 beta converting enzyme

1 reference

7 January 2021

The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages

1 reference

7 January 2021

Mouse Otx2 functions in the formation and patterning of rostral head.

1 reference

7 January 2021