(Q55159900)

23 June 2018

title

Whole genome microarray analysis of gene expression in Prader-Willi syndrome. (English)

1 reference

23 June 2018

main subject

whole genome sequencing

1 reference

Douglas C Bittel

1

1 reference

23 June 2018

Nataliya Kibiryeva

2

1 reference

23 June 2018

Susan M Sell

3

1 reference

23 June 2018

Theresa V Strong

4

1 reference

23 June 2018

Merlin G Butler

5

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23 June 2018

language of work or name

English

0 references

publication date

1 March 2007

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23 June 2018

American Journal of Medical Genetics

published in

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23 June 2018

volume

143A

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23 June 2018

issue

5

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23 June 2018

page(s)

430-442

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23 June 2018

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

cites work

1 reference

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

24 June 2018

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Neurosteroids: endogenous regulators of the GABA(A) receptor

24 June 2018

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Transduction of receptor signals by beta-arrestins

24 June 2018

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

Neurosteroid modulation of GABAA receptors

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

An imprinted, mammalian bicistronic transcript encodes two independent proteins

24 June 2018

1 reference

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Targeted disruption of the mouse gene encoding steroidogenic acute regulatory protein provides insights into congenital lipoid adrenal hyperplasia

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome

24 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

Hypocretin deficiency in 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=5467864

Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream 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=5467864

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=5467864

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

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

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5467864

Elevated plasma gamma-aminobutyric acid (GABA) levels in individuals with either Prader-Willi syndrome or Angelman 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=5467864

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

13 August 2018

1 reference

12 December 2020

Incriminating gene suspects, Prader-Willi style

1 reference

12 December 2020

Steroid metabolic disturbances in Prader-Willi syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.31606

1 reference

23 June 2018

PMC publication ID

5467864

1 reference

23 June 2018

PubMed publication ID

17236194

1 reference

23 June 2018