(Q47912961)

6 February 2018

title

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. (English)

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6 February 2018

author name string

Boccaccio I

1

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6 February 2018

Glatt-Deeley H

2

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6 February 2018

Watrin F

3

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6 February 2018

Roëckel N

4

1 reference

6 February 2018

Lalande M

5

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6 February 2018

Muscatelli F

6

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6 February 2018

publication date

1 December 1999

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6 February 2018

published in

Human Molecular Genetics

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6 February 2018

volume

8

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6 February 2018

page(s)

2497-2505

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6 February 2018

issue

13

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6 February 2018

Parental imprinting and human disease

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

21 January 2018

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Imprinting in Angelman and Prader-Willi syndromes.

21 January 2018

1 reference

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Imprinting-mutation mechanisms in Prader-Willi syndrome

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

An imprinted, mammalian bicistronic transcript encodes two independent proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Engineering herpes simplex virus vectors for gene transfer to neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

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/10.1093%2FHMG%2F8.13.2497

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/10.1093%2FHMG%2F8.13.2497

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

AU-rich elements: characterization and importance in mRNA degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Genomic imprinting: a chromatin connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Physical and functional interactions of neuronal growth suppressor necdin with p53

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

A new family of mouse genes homologous to the human MAGE genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2497

21 January 2018

Identifiers

DOI

10.1093/HMG/8.13.2497

1 reference

6 February 2018

PubMed ID

10556298

1 reference

6 February 2018