(Q42605402)

English

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

scientific article published on August 1999

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scholarly article

1 reference

Europe PubMed Central

3 November 2017

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome (English)

1 reference

Europe PubMed Central

3 November 2017

1 reference

based on heuristic

inferred from title

author name string

T F Tsai

1

1 reference

Europe PubMed Central

3 November 2017

Y H Jiang

2

1 reference

Europe PubMed Central

3 November 2017

J Bressler

3

1 reference

Europe PubMed Central

3 November 2017

D Armstrong

4

1 reference

Europe PubMed Central

3 November 2017

A L Beaudet

5

1 reference

Europe PubMed Central

3 November 2017

publication date

1 August 1999

1 reference

Europe PubMed Central

3 November 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

3 November 2017

8

1 reference

Europe PubMed Central

3 November 2017

1357-1364

1 reference

Europe PubMed Central

3 November 2017

8

1 reference

Europe PubMed Central

3 November 2017

Parental imprinting and human disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Imprinting in Prader-Willi and Angelman syndromes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Mutation analysis of UBE3A in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

The spectrum of mutations in UBE3A causing Angelman syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

A mouse model for Prader-Willi syndrome imprinting-centre mutations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Prader-Willi syndrome is caused by disruption of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Structure and function correlations at the imprinted mouse Snrpn locus.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Chromosome engineering in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1357

21 January 2018

Identifiers

10.1093/HMG/8.8.1357

1 reference

Europe PubMed Central

3 November 2017

1 reference

Europe PubMed Central

3 November 2017

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