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Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region (Q28208127)

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scientific article (publication date: December 1992)

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English	Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region	scientific article (publication date: December 1992)

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scholarly article

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

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ribonucleoprotein complex

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Prader–Willi syndrome

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author name string

T Ozçelik

1

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S Leff

2

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W Robinson

3

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T Donlon

4

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M Lalande

5

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E Sanjines

6

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A Schinzel

7

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U Francke

8

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publication date

December 1992

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language of work or name

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Nature Genetics

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2

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4

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265-9

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Monoallelic expression of the human H19 gene

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https://api.crossref.org/works/10.1038/NG1292-265

21 April 2017

Parental imprinting of the mouse H19 gene

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https://api.crossref.org/works/10.1038/NG1292-265

21 April 2017

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

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https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

Uniparental paternal disomy in Angelman's syndrome

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https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

Regulated expression of the small nuclear ribonucleoprotein particle protein SmN in embryonic stem cell differentiation

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene

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https://api.crossref.org/works/10.1038%2FNG1292-265

21 January 2018

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

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https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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Prader-Willi syndrome: current understanding of cause and diagnosis

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https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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Is Angelman syndrome an alternate result of del(15)(q11q13)?

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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Messenger RNA Splicing in Yeast: Clues to Why the Spliceosome Is a Ribonucleoprotein

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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Isolation of cDNA clones encoding small nuclear ribonucleoparticle-associated proteins with different tissue specificities

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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A comparison of snRNP-associated Sm-autoantigens: human N, rat N and human B/B'

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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Genes for beta 2-adrenergic receptor and platelet-derived growth factor receptor map to mouse chromosome 18

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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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/10.1038%2FNG1292-265

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

inferred from DOI database lookup

Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and beta 2-microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrier.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

based on heuristic

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Identifiers

10.1038/NG1292-265

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release_b634ej4o5bbw7mtpv6nhnjzope

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https://api.fatcat.wiki/v0/release/b634ej4o5bbw7mtpv6nhnjzope

24 November 2022

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PubMed publication ID

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