Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome (Q24305283)

https://scigraph.springernature.com/pub.10.1038/ng0294-163

GOA release 2020-03-11

Prader–Willi syndrome

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M L Reed

1

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S E Leff

series ordinal

2

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language of work or name

English

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publication date

February 1994

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published in

Nature Genetics

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volume

6

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issue

2

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page(s)

163-7

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exact match

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cites work

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

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Parental imprinting of the mouse H19 gene

20 April 2017

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Monoallelic expression of the human H19 gene

20 April 2017

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Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism

20 April 2017

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Expression of the SmN splicing protein is developmentally regulated in the rodent brain but not in the rodent heart

20 April 2017

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

20 April 2017

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0294-163

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

21 January 2018

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Relaxation of imprinted genes in human cancer.

21 January 2018

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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

21 January 2018

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A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0294-163

Allele-specific replication timing of imprinted gene regions

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0294-163

The trimethylguanosine cap structure of U1 snRNA is a component of a bipartite nuclear targeting signal

21 January 2018

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Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0294-163

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

21 January 2018

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

21 January 2018

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

21 January 2018

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7 January 2021

Cell biology of the snRNP particles

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https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA

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https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG0294-163

7 January 2021

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

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7 January 2021