Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33697249)
Watch
English
Gender influences monoallelic expression of ATP10A in human brain
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
title
Gender influences monoallelic expression of ATP10A in human brain
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
author
Janine M. LaSalle
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
author name string
Amber Hogart
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
Katherine A Patzel
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
publication date
23 August 2008
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
published in
Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
volume
124
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
page(s)
235-242
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
exact match
https://scigraph.springernature.com/pub.10.1007/s00439-008-0546-0
0 references
cites work
MeCP2, a key contributor to neurological disease, activates and represses transcription
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Widespread monoallelic expression on human autosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Mice heterozygous for Atp10c, a putative amphipath, represent a novel model of obesity and type 2 diabetes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Characterization of a putative type IV aminophospholipid transporter P-type ATPase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Distinct phenotypes distinguish the molecular classes of Angelman syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Prader-Willi and Angelman syndromes: sister imprinted disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
21 June 2018
Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1007%2FS00439-008-0546-0
retrieved
21 January 2018
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
30 October 2018
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
30 October 2018
Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2830741
retrieved
30 October 2018
Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18726118
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A novel ATPase on mouse chromosome 7 is a candidate gene for increased body fat
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18726118
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18726118
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): an interdisciplinary study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18726118
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00439-008-0546-0
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
Dimensions Publication ID
1017797098
0 references
PMC publication ID
2830741
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
PubMed publication ID
18726118
1 reference
stated in
Europe PubMed Central
PMC publication ID
2830741
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18726118%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
ResearchGate publication ID
23192857
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
