(Q52178669)

English

Is the genetic basis of DiGeorge syndrome in HAND?

scientific article published in March 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

Is the genetic basis of DiGeorge syndrome in HAND? (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

DiGeorge syndrome

1 reference

based on heuristic

inferred from title

author name string

A Baldini

1

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

language of work or name

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publication date

1 March 1999

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

21

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

3

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

246-247

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

https://scigraph.springernature.com/pub.10.1038/6750

0 references

Dependence of thymus development on derivatives of the neural crest

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

The human homolog of Saccharomyces cerevisiae CDC45

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

A proteolytic pathway that recognizes ubiquitin as a degradation signal

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Ubiquitin-protein conjugates selectively distribute during early chicken embryogenesis.

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

1 reference

https://api.crossref.org/works/10.1038%2F6750

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/10080167

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