Mouse models of Prader-Willi Syndrome: a systematic review (Q38079927)

28 August 2017

title

Mouse models of Prader-Willi Syndrome: a systematic review (English)

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28 August 2017

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Prader–Willi syndrome

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Sandrina Bervini

1

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28 August 2017

Herbert Herzog

series ordinal

2

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28 August 2017

publication date

4 February 2013

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Frontiers in Neuroendocrinology

28 August 2017

published in

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28 August 2017

volume

34

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28 August 2017

issue

2

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28 August 2017

page(s)

107-119

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snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions

28 August 2017

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

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Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice

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Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain

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

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Imprinted expression of SNRPN in human preimplantation embryos

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The imprinted gene Magel2 regulates normal circadian output.

7 January 2021

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Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival

7 January 2021

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Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter

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7 January 2021

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Imprinting-mutation mechanisms in Prader-Willi syndrome

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7 January 2021

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Chromosome engineering in mice

7 January 2021

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Genomic imprinting: parental influence on the genome

7 January 2021

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

7 January 2021

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Contextual fear conditioning regulates the expression of brain-specific small nucleolar RNAs in hippocampus

7 January 2021

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Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

7 January 2021

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Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

7 January 2021

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A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

7 January 2021

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Human box C/D snoRNA processing conservation across multiple cell types

7 January 2021

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Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

7 January 2021

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Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

7 January 2021

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Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes

7 January 2021

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Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive

7 January 2021

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Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.

7 January 2021

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Necdin is required for terminal differentiation and survival of primary dorsal root ganglion neurons

7 January 2021

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Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.

7 January 2021

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

7 January 2021

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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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2013.01.002

The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2013.01.002

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

7 January 2021

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Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2013.01.002

Hypothalamic expression of snoRNA Snord116 is consistent with a link to the hyperphagia and obesity symptoms of Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2013.01.002

10.1016/J.YFRNE.2013.01.002

7 January 2021

Identifiers

DOI

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28 August 2017

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