Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins (Q33591397)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9860993%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins (English)

1 reference

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7 December 2019

4

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7 December 2019

author name string

B E Hayward

series ordinal

1

1 reference

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7 December 2019

V Moran

series ordinal

2

1 reference

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7 December 2019

L Strain

series ordinal

3

1 reference

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7 December 2019

language of work or name

English

0 references

publication date

1 December 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9860993%20AND%20SRC:MED&resulttype=core&format=json

Proceedings of the National Academy of Sciences of the United States of America

7 December 2019

published in

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7 December 2019

volume

95

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7 December 2019

issue

26

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7 December 2019

page(s)

15475-15480

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9860993%20AND%20SRC:MED&resulttype=core&format=json

The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.

7 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Organization of the human glucokinase regulator gene GCKR

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Molecular cloning and characterization of NESP55, a novel chromogranin-like precursor of a peptide with 5-HT1B receptor antagonist activity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Imprinting in Albright's hereditary osteodystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

XL alpha s is a new type of G protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Clonal insulinoma cell line that stably maintains correct glucose responsiveness.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Parental origin of transcription from the human GNAS1 gene.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

A human parthenogenetic chimaera.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Isolation and characterization of the human Gs alpha gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodyst

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Alternative promoter and 5' exon generate a novel Gs alpha mRNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis.

21 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.26.15475

Clinical and biological heterogeneity in pseudohypoparathyroidism syndrome. Results of a multicenter study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.26.15475

Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.26.15475

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.26.15475

Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=28067

Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9860993

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.26.15475

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9860993%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

0 references

1 reference

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7 December 2019

PubMed publication ID

9860993

1 reference