(Q59062255)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10517636%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Congenital heart disease in mice deficient for the DiGeorge syndrome region (English)

1 reference

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1 November 2019

1 reference

congenital heart disease

1 reference

2

1 reference

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1 November 2019

author name string

Lindsay EA

1

1 reference

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1 November 2019

Jurecic V

3

1 reference

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1 November 2019

Carattini-Rivera S

4

1 reference

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1 November 2019

Cheah YC

5

1 reference

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1 November 2019

Rosenblatt HM

6

1 reference

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1 November 2019

Bradley A

7

1 reference

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1 November 2019

Baldini A

8

1 reference

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1 November 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

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1 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10517636%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

401

1 reference

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1 November 2019

page(s)

379-383

1 reference

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1 November 2019

issue

6751

1 reference

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https://scigraph.springernature.com/pub.10.1038/43900

1 November 2019

exact match

0 references

cites work

Congenital heart defects and 22q11 deletions: which genes count?

1 reference

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

21 January 2018

1 reference

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.

21 January 2018

1 reference

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

21 January 2018

1 reference

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

21 January 2018

1 reference

Chromosome engineering in mice

21 January 2018

1 reference

ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene

21 January 2018

1 reference

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

21 January 2018

1 reference

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Alpha-inhibin is a tumour-suppressor gene with gonadal specificity in mice

21 January 2018

1 reference

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

21 January 2018

1 reference

Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/43900

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10517636%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 November 2019

0 references

1 reference