(Q47886958)

English

Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein Treacle

scientific article published in April 2004

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein Treacle (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

1 reference

based on heuristic

inferred from title

author name string

Jill Dixon

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

Michael James Dixon

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

publication date

1 April 2004

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

Developmental Dynamics

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

229

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

907-914

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

Nucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

21 January 2018

Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

21 January 2018

The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

21 January 2018

Tracher Collins syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the complete coding sequence and genomic organization of the Treacher Collins syndrome gene

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Normal mouse strains differ in the site of initiation of closure of the cranial neural tube

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the Treacher Collins syndrome gene lead to mislocalization of the nucleolar protein treacle

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Organogenesis of the liver, thymus and spleen is affected in jumonji mutant mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

The pathogenesis of the Treacher Collins syndrome (mandibulofacial dysostosis).

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening of TCOF1 in patients from different populations: confirmation of mutational hot spots and identification of a novel missense mutation that suggests an important functional domain in the protein treacle

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

jumonji gene is essential for the neurulation and cardiac development of mouse embryos with a C3H/He background

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20004

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/DVDY.20004

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15042714

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47886958&oldid=2174817237"