(Q83200069)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Pax3, neural crest and cardiovascular development (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

J A Epstein

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

publication date

1 November 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

Trends in Cardiovascular Medicine

20 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

255-260

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

20 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Essential role for the c-met receptor in the migration of myogenic precursor cells into the limb bud

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Identification of DNA recognition sequences for the Pax3 paired domain

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Pax-3 contains domains for transcription activation and transcription inhibition

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Pax3 inhibits myogenic differentiation of cultured myoblast cells

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Pax3 modulates expression of the c-Met receptor during limb muscle development

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Persistent truncus arteriosus in the Splotch mutant mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Decrease in calcitonin-containing cells in truncus arteriosus

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Mouse small eye results from mutations in a paired-like homeobox-containing gene

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Neural crest cells contribute to normal aorticopulmonary septation

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Endothelin 3 promotes neural crest cell proliferation and mediates a vast increase in melanocyte number in culture

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Pathogenesis of persistent truncus arteriosus induced by nimustine hydrochloride in chick embryos

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Cardiovascular anomalies produced by nimustine hydrochloride in the rat fetus

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Cell origins and tissue boundaries during outflow tract development

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Hereditary defects of the conotruncal septum in Keeshond dogs: pathologic and genetic studies.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

The apical ectodermal ridge regulates Hox-7 and Hox-8 gene expression in developing chick limb buds

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Platelet-derived growth factor receptor alpha subunit deleted Patch mouse exhibits severe cardiovascular dysmorphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Expression of Hox-7.1 in myoblasts inhibits terminal differentiation and induces cell transformation

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

A subclass of bHLH proteins required for cardiac morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Loss of p53 function through PAX-mediated transcriptional repression.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Analysis of the mouse Splotch-delayed mutation indicates that the Pax-3 paired domain can influence homeodomain DNA-binding activity

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Cooperative dimerization of paired class homeo domains on DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2896%2900110-7

7 January 2021

10.1016/S1050-1738(96)00110-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21232305%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference