(Q44803556)

6 December 2017

title

Recommendations for the investigation of animal models of Prader-Willi syndrome (English)

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6 December 2017

James L Resnick

1

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6 December 2017

Robert D Nicholls

series ordinal

2

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6 December 2017

Rachel Wevrick

series ordinal

3

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6 December 2017

Prader-Willi Syndrome Animal Models Working Group

series ordinal

4

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6 December 2017

publication date

23 April 2013

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6 December 2017

number of pages

14

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inferred from page(s)

published in

Mammalian Genome

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6 December 2017

volume

24

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6 December 2017

issue

5-6

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6 December 2017

page(s)

165-178

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https://scigraph.springernature.com/pub.10.1007/s00335-013-9454-2

6 December 2017

exact match

0 references

cites work

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Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

21 January 2018

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De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

21 January 2018

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Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome

21 January 2018

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Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.

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Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice

21 January 2018

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

21 January 2018

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The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs

21 January 2018

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

21 January 2018

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The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito.

21 January 2018

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Prader-Willi syndrome and Angelman syndrome

21 January 2018

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Loss of Necdin impairs myosin activation and delays cell polarization

21 January 2018

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Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis.

21 January 2018

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21 January 2018

Prader-Willi syndrome.

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Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

21 January 2018

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

21 January 2018

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The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.

21 January 2018

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Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes

21 January 2018

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Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13.

21 January 2018

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Impact of induced pluripotent stem cells on the study of central nervous system disease

21 January 2018

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Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation

21 January 2018

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Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice

21 January 2018

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SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models

21 January 2018

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Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

21 January 2018

1 reference

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Temporal and developmental requirements for the Prader-Willi imprinting center

21 January 2018

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A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center

21 January 2018

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Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

21 January 2018

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Necdin controls proliferation of white adipocyte progenitor cells

21 January 2018

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

21 January 2018

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Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome.

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Recommendations for the diagnosis and management of Prader-Willi syndrome

21 January 2018

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An imprinted, mammalian bicistronic transcript encodes two independent proteins

21 January 2018

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Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons

21 January 2018

1 reference

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A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

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Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

The imprinted gene Magel2 regulates normal circadian output.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin restricts proliferation of hematopoietic stem cells during hematopoietic regeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin promotes tangential migration of neocortical interneurons from basal forebrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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/10.1007%2FS00335-013-9454-2

Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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/10.1007%2FS00335-013-9454-2

A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Nutritional phases in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin is expressed in cachectic skeletal muscle to protect fibers from tumor-induced wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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/10.1007%2FS00335-013-9454-2

Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

A guide to analysis of mouse energy metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Frat is dispensable for canonical Wnt signaling in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Neurobehavioral phenotype in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Long noncoding RNAs with snoRNA ends

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Necdin gene, respiratory disturbances and Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9454-2

Breathing deficits of the Prader-Willi syndrome

21 January 2018

1 reference

12 December 2020

Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse

1 reference

12 December 2020

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

1 reference

12 December 2020

A targeted deletion upstream of Snrpn does not result in an imprinting defect

1 reference

12 December 2020

Energy homeostasis in Prader-Willi Syndrome: How clinical research informs studies of animal models of genetic obesity

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00335-013-9454-2

Identifiers

DOI

1 reference

6 December 2017

1 reference