(Q34390727)

1 August 2017

1 reference

title

Developing models of DiGeorge syndrome (English)

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1 August 2017

Epstein JA

1

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1 August 2017

publication date

1 October 2001

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1 August 2017

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1 August 2017

volume

17

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1 August 2017

issue

10

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1 August 2017

page(s)

S13-7

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Neural crest cells contribute to normal aorticopulmonary septation

1 August 2017

cites work

1 reference

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7 January 2021

Generalized lacZ expression with the ROSA26 Cre reporter strain

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7 January 2021

A novel transgenic technique that allows specific marking of the neural crest cell lineage in mice

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7 January 2021

Neural crest expression of Cre recombinase directed by the proximal Pax3 promoter in transgenic mice

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7 January 2021

Persistent truncus arteriosus in the Splotch mutant mouse

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7 January 2021

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

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7 January 2021

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

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7 January 2021

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

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7 January 2021

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

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7 January 2021

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

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7 January 2021

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

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

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Role of Endothelin-1/Endothelin-A receptor-mediated signaling pathway in the aortic arch patterning in mice

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Disruption of ECE-1 and ECE-2 reveals a role for endothelin-converting enzyme-2 in murine cardiac development

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7 January 2021

Genetic basis of DiGeorge and velocardiofacial syndromes.

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7 January 2021

Transcriptional regulation of cardiac development: implications for congenital heart disease and DiGeorge syndrome

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7 January 2021

Frequency of 22q11 deletions in patients with conotruncal defects

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7 January 2021

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

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7 January 2021

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region

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7 January 2021

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes

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7 January 2021

Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development

1 reference

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7 January 2021

Congenital heart disease in mice deficient for the DiGeorge syndrome region

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7 January 2021

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region

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7 January 2021

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

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7 January 2021

HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3

1 reference

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7 January 2021

HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.

1 reference

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7 January 2021

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

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7 January 2021

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

1 reference

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7 January 2021

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

1 reference

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7 January 2021

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

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7 January 2021

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2801%2902450-7

7 January 2021

10.1016/S0168-9525(01)02450-7

Identifiers

DOI

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release_cut5wnzrejadtougufzi5srnyu

1 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/cut5wnzrejadtougufzi5srnyu

24 November 2022

mapped directly with Wikidata item

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