(Q44924708)

7 December 2017

title

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

1 reference

7 December 2017

1

1 reference

7 December 2017

Martin Hrabě de Angelis

7

object named as

Martin Hrabe de Angelis

0 references

Karen Avraham

object named as

Karen B Avraham

8

0 references

Ruth Asehry-Padan

5

object named as

Ruth Ashery-Padan

1 reference

7 December 2017

9

Karen P Steel

1 reference

7 December 2017

Alexandra Erven

2

1 reference

7 December 2017

Helmut Fuchs

3

1 reference

7 December 2017

Keren Guy

4

1 reference

7 December 2017

Trevor Williams

6

1 reference

7 December 2017

publication date

1 June 2004

1 reference

7 December 2017

number of pages

9

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

7 December 2017

volume

15

1 reference

7 December 2017

issue

6

1 reference

7 December 2017

page(s)

424-432

1 reference

https://scigraph.springernature.com/pub.10.1007/s00335-004-2334-z

7 December 2017

exact match

0 references

cites work

Hearing in chronic suppurative otitis media.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-004-2334-Z

Coactivator PC4 mediates AP-2 transcriptional activity and suppresses ras-induced transformation dependent on AP-2 transcriptional interference

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-004-2334-Z

A family of AP-2 proteins regulates c-erbB-2 expression in mammary carcinoma

21 January 2018

1 reference

12 December 2020

Identification of novel human WW domain-containing proteins by cloning of ligand targets

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of the activation domains of AP-2 family transcription factors.

1 reference

12 December 2020

The Sharpening of cochlear frequency selectivity in the normal and abnormal cochlea

1 reference

12 December 2020

Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control

1 reference

12 December 2020

The WW domain of Yes-associated protein binds a proline-rich ligand that differs from the consensus established for Src homology 3-binding modules

1 reference

12 December 2020

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

1 reference

12 December 2020

Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports

1 reference

12 December 2020

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

1 reference

12 December 2020

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

1 reference

12 December 2020

The WW domain: linking cell signalling to the membrane cytoskeleton

1 reference

12 December 2020

lockjaw encodes a zebrafish tfap2a required for early neural crest development.

1 reference

12 December 2020

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

1 reference

12 December 2020

Transcriptional dysregulation in skeletal malformation syndromes

1 reference

12 December 2020

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation

1 reference

12 December 2020

The coactivator p15 (PC4) initiates transcriptional activation during TFIIA-TFIID-promoter complex formation

1 reference

12 December 2020

Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation properties

1 reference

12 December 2020

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

12 December 2020

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

1 reference

12 December 2020

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

1 reference

12 December 2020

A WW domain-containing yes-associated protein (YAP) is a novel transcriptional co-activator

1 reference

12 December 2020

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

1 reference

12 December 2020

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

1 reference

12 December 2020

Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2

1 reference

12 December 2020

Embryological and genetic aspects of middle ear development.

1 reference

12 December 2020

Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye

1 reference

12 December 2020

10.1007/S00335-004-2334-Z

Identifiers

DOI

1 reference

7 December 2017

1 reference