(Q48162186)

9 February 2018

title

A MAGE/NDN-like gene in zebrafish (English)

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9 February 2018

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3

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9 February 2018

author name string

Jocelyn M Bischof

series ordinal

1

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9 February 2018

Marc Ekker

series ordinal

2

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9 February 2018

publication date

1 November 2003

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9 February 2018

published in

Developmental Dynamics

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9 February 2018

volume

228

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9 February 2018

issue

3

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9 February 2018

page(s)

475-479

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9 February 2018

The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Prader-Willi and Angelman syndromes: sister imprinted disorders

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

An efficient algorithm for large-scale detection of protein families

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Disruption of the mouse necdin gene results in early post-natal lethality

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

The LN54 radiation hybrid map of zebrafish expressed sequences

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Expression analysis of a novel p75(NTR) signaling protein, which regulates cell cycle progression and apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin receptor and facilitates nerve growth factor-dependent apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Cell cycle regulators in neural stem cells and postmitotic neurons

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10398

7 January 2021

Identifiers

DOI

10.1002/DVDY.10398

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9 February 2018

1 reference

9 February 2018