(Q48678528)

14 February 2018

title

A candidate model for Angelman syndrome in the mouse (English)

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14 February 2018

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J Noebels

5

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author name string

B M Cattanach

1

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14 February 2018

J A Barr

2

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14 February 2018

C V Beechey

3

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14 February 2018

J Martin

4

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14 February 2018

J Jones

6

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14 February 2018

publication date

1 July 1997

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14 February 2018

number of pages

7

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inferred from page(s)

published in

Mammalian Genome

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14 February 2018

volume

8

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14 February 2018

issue

7

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14 February 2018

page(s)

472-478

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14 February 2018

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

DNA deletion and its parental origin in Angelman syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Puppet-like syndrome of Angelman: a pathologic and neurochemical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Uniparental paternal disomy in Angelman's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Epilepsy in Angelman syndrome associated with chromosome 15q deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Angelman syndrome in three siblings: characteristic epileptic seizures and EEG abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900479

The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5

21 January 2018

1 reference

12 December 2020

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

1 reference

12 December 2020

Prader-Willi syndrome: consensus diagnostic criteria.

1 reference

12 December 2020

A chemically-induced variegated-type position effect in the mouse

1 reference

12 December 2020

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

1 reference

12 December 2020

Meiotic disjunction in mouse translocations and the determination of centromere position

1 reference

12 December 2020

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

12 December 2020

The association of Angelman's syndrome with deletions within 15q11-13

1 reference

12 December 2020

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele

1 reference

12 December 2020

1 reference

12 December 2020

An Analysis of Translocations in the Mouse

1 reference

12 December 2020

The Open-Field Test: a critical review.

1 reference

12 December 2020

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

1 reference

12 December 2020

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

1 reference

12 December 2020

Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene

1 reference

12 December 2020

Genome imprinting phenomena on mouse chromosome 7

1 reference

12 December 2020

Identifiers

DOI

10.1007/S003359900479

1 reference

14 February 2018

release_tvzj3onuunelpk7rfim5ps4wpi

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tvzj3onuunelpk7rfim5ps4wpi

24 November 2022

mapped directly with Wikidata item

1 reference

14 February 2018