Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. (Q54566126)

1 June 2018

title

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

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1 June 2018

main subject

whole genome sequencing

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Steven G McNulty

3

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author name string

Douglas C Bittel

1

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1 June 2018

Nataliya Kibiryeva

2

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1 June 2018

Daniel J Driscoll

4

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1 June 2018

Merlin G Butler

5

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1 June 2018

Robert A White

6

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1 June 2018

language of work or name

English

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publication date

1 March 2007

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1 June 2018

American Journal of Medical Genetics

published in

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1 June 2018

volume

143A

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1 June 2018

issue

5

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1 June 2018

page(s)

422-429

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1 June 2018

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

cites work

1 reference

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

4 June 2018

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Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD

4 June 2018

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Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

4 June 2018

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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

4 June 2018

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Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome

4 June 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

4 June 2018

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

4 June 2018

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

4 June 2018

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Necdin acts as a transcriptional repressor that interacts with multiple guanosine clusters

4 June 2018

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A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

4 June 2018

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

4 June 2018

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

4 June 2018

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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

4 June 2018

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Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci

4 June 2018

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

4 June 2018

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Mechanisms of genomic imprinting

4 June 2018

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An imprinted, mammalian bicistronic transcript encodes two independent proteins

4 June 2018

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Agouti antagonism of melanocortin-4 receptor: greater effect with desacetyl-alpha-melanocyte-stimulating hormone (MSH) than with alpha-MSH.

4 June 2018

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

4 June 2018

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Exocrine gland dysfunction in MC5-R-deficient mice: evidence for coordinated regulation of exocrine gland function by melanocortin peptides

4 June 2018

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4 June 2018

Prader-Willi syndrome

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Investigation of thermoregulatory characteristics in patients with Prader-Willi syndrome

4 June 2018

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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.

4 June 2018

1 reference

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Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjects.

13 August 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.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5453790

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5453790

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5453790

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

13 August 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5453790

A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis

13 August 2018

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12 December 2020

Incriminating gene suspects, Prader-Willi style

1 reference

12 December 2020

Positional cloning of the Ttc7 gene required for normal iron homeostasis and mutated in hea and fsn anemia mice

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12 December 2020

Characteristics of hyperthermia and its complications in patients with Prader Willi syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

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12 December 2020

Identifiers

DOI

10.1002/AJMG.A.31504

1 reference

1 June 2018

PMC publication ID

5453790

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1 June 2018

PubMed publication ID

17036336

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1 June 2018