(Q24655671)

1

0 references

Tom A Maher

2

0 references

Geping Zhao

3

0 references

Amy E Roberts

4

0 references

Heather J Stalker

5

0 references

Roberto T Zori

6

0 references

Michelle N Burch

7

0 references

Michele Clemens

8

0 references

John B Mulliken

9

0 references

Rosemarie Smith

10

0 references

Angela E Lin

American Journal of Human Genetics

11

0 references

language of work or name

English

0 references

publication date

May 2008

0 references

published in

0 references

volume

82

0 references

issue

5

0 references

page(s)

1171-7

0 references

cites work

The AP-2 family of transcription factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Transcriptional activation by Myc is under negative control by the transcription factor AP-2

7 April 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

7 April 2017

https://api.crossref.org/works/10.1016%2FJ.AJHG.2008.03.005

7 January 2021

inferred from DOI database lookup

Transcription factor AP-2 essential for cranial closure and craniofacial development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

AP-2alpha transcription factor is required for early morphogenesis of the lens vesicle

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Mouse genetic models of cleft lip with or without cleft palate

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

The AP-2alpha transcription factor regulates tumor cell migration and apoptosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Transcription factor AP-2 and monoaminergic functions in the central nervous system

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Loss of the AP-2alpha transcription factor is associated with the grade of human gliomas.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Frontonasal process-specific disruption of AP-2alpha results in postnatal midfacial hypoplasia, vascular anomalies, and nasal cavity defects

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Tumor suppressor activity of AP2alpha mediated through a direct interaction with p53.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Further delineation of the branchio-oculo-facial syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

The branchio-oculo-facial syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Craniofacial defects in AP-2 null mutant mice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Branchio-oculo-facial and branchio-oto-renal syndromes are distinct entities

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Loss of AP-2 results in up-regulation of MCAM/MUC18 and an increase in tumor growth and metastasis of human melanoma cells

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2427243

Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome

28 November 2018

1 reference

12 December 2020

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

12 December 2020

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

1 reference

12 December 2020

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

1 reference

12 December 2020

AP2alpha alters the transcriptional activity and stability of p53

1 reference

12 December 2020

Exclusion of genes from the EYA-DACH-SIX-PAX pathway as candidates for Branchio-Oculo-Facial syndrome (BOFS)

1 reference

12 December 2020

10.1016/J.AJHG.2008.03.005

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

18423521

1 reference