(Q51976832)

19 April 2018

title

The imprinted gene Magel2 regulates normal circadian output. (English)

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19 April 2018

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4

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Russell Van Gelder

8

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Erik D. Herzog

9

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19 April 2018

author name string

Serguei V Kozlov

1

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19 April 2018

James W Bogenpohl

2

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19 April 2018

Maureen P Howell

3

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19 April 2018

Satchin Panda

5

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19 April 2018

John B Hogenesch

6

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19 April 2018

Louis J Muglia

7

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19 April 2018

Colin L Stewart

10

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19 April 2018

language of work or name

English

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publication date

23 September 2007

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19 April 2018

published in

Nature Genetics

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19 April 2018

volume

39

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issue

10

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19 April 2018

page(s)

1266-1272

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19 April 2018

https://scigraph.springernature.com/pub.10.1038/ng2114

exact match

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cites work

Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin

1 reference

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

21 January 2018

1 reference

7 January 2021

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

7 January 2021

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

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

1 reference

7 January 2021

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

1 reference

7 January 2021

Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Coordinated transcription of key pathways in the mouse by the circadian clock

1 reference

7 January 2021

Functional morphology of the suprachiasmatic nucleus

1 reference

7 January 2021

The suprachiasmatic nucleus is a functionally heterogeneous timekeeping organ.

1 reference

7 January 2021

PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues

1 reference

7 January 2021

The hypothalamus, hormones, and hunger: alterations in human obesity and illness

1 reference

7 January 2021

Roles of orexin/hypocretin in regulation of sleep/wakefulness and energy homeostasis

1 reference

7 January 2021

Difference in obesity phenotype between orexin-knockout mice and orexin neuron-deficient mice with same genetic background and environmental conditions.

1 reference

7 January 2021

Distinct narcolepsy syndromes in Orexin receptor-2 and Orexin null mice: molecular genetic dissection of Non-REM and REM sleep regulatory processes

1 reference

7 January 2021

Imprinted gene expression in the brain

1 reference

7 January 2021

Genomic imprinting and the differential roles of parental genomes in brain development.

1 reference

7 January 2021

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1 reference

7 January 2021

Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

1 reference

7 January 2021

Targeted disruption of the MHC class II Aa gene in C57BL/6 mice

1 reference

7 January 2021

Temporal precision in the mammalian circadian system: a reliable clock from less reliable neurons.

1 reference

7 January 2021

Neuroanatomical nomenclature

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7 January 2021

Identifiers

DOI

10.1038/NG2114

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19 April 2018

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19 April 2018