Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36283882)
Watch
English
The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
title
The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
author
David T. Bonthron
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
author name string
B E Hayward
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
M Kamiya
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
L Strain
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
V Moran
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
R Campbell
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
Y Hayashizaki
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
language of work or name
English
0 references
publication date
1 August 1998
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
volume
95
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
issue
17
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
page(s)
10038-10043
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
cites work
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann 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=21457
retrieved
30 September 2017
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene
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=21457
retrieved
30 September 2017
Neural expression of a novel alternatively spliced and polyadenylated Gs alpha transcript.
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=21457
retrieved
30 September 2017
Imprinting in Albright's hereditary osteodystrophy
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=21457
retrieved
30 September 2017
XL alpha s is a new type of G protein
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=21457
retrieved
30 September 2017
Parental origin of transcription from the human GNAS1 gene.
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=21457
retrieved
30 September 2017
Direct detection and isolation of restriction landmark genomic scanning (RLGS) spot DNA markers tightly linked to a specific trait by using the RLGS spot-bombing method
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=21457
retrieved
30 September 2017
p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
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=21457
retrieved
30 September 2017
Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
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=21457
retrieved
30 September 2017
Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast
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=21457
retrieved
30 September 2017
Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse
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=21457
retrieved
30 September 2017
Isolation and characterization of the human Gs alpha gene
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=21457
retrieved
30 September 2017
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.
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=21457
retrieved
30 September 2017
Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis
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=21457
retrieved
30 September 2017
Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy
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=21457
retrieved
30 September 2017
A genomic scanning method for higher organisms using restriction sites as landmarks
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=21457
retrieved
30 September 2017
Differential expression of novel Gs alpha signal transduction protein cDNA species
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=21457
retrieved
30 September 2017
Conservation of a maternal-specific methylation signal at the human IGF2R locus
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=21457
retrieved
30 September 2017
Quantitative and qualitative genetic variation in two-dimensional DNA gels of human lymphocytoid 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=21457
retrieved
30 September 2017
A human parthenogenetic chimaera.
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=21457
retrieved
29 June 2018
Clinical and biological heterogeneity in pseudohypoparathyroidism syndrome. Results of a multicenter study.
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=21457
retrieved
22 September 2018
Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M.
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=21457
retrieved
22 September 2018
Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method
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=21457
retrieved
22 September 2018
Genetic mapping and systematic screening of mouse endogenously imprinted loci detected with restriction landmark genome scanning method (RLGS)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9707596
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Characteristics of imprinted genes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9707596
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9707596
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.95.17.10038
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
ADS bibcode
1998PNAS...9510038H
0 references
PMC publication ID
21457
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
PubMed publication ID
9707596
1 reference
stated in
Europe PubMed Central
PMC publication ID
21457
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9707596%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
ResearchGate publication ID
235615712
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