A GNAS1 imprinting defect in pseudohypoparathyroidism type IB (Q34457845)

2 August 2017

title

A GNAS1 imprinting defect in pseudohypoparathyroidism type IB (English)

1 reference

pseudohypoparathyroidism type IB

2 August 2017

main subject

1 reference

Liu J

1

1 reference

2 August 2017

Litman D

2

1 reference

2 August 2017

Rosenberg MJ

3

1 reference

2 August 2017

Yu S

4

1 reference

2 August 2017

Biesecker LG

5

1 reference

2 August 2017

Weinstein LS

6

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2 August 2017

language of work or name

English

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publication date

1 November 2000

1 reference

Journal of Clinical Investigation

2 August 2017

published in

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2 August 2017

volume

106

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2 August 2017

issue

9

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2 August 2017

page(s)

1167-1174

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Identification of a methylation imprint mark within the mouse Gnas locus

2 August 2017

cites work

1 reference

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CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

6 July 2018

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Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

6 July 2018

1 reference

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An imprinted antisense transcript at the human GNAS1 locus

6 July 2018

1 reference

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An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus

6 July 2018

1 reference

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Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism

6 July 2018

1 reference

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The impact of genomic imprinting for neurobehavioral and developmental disorders

6 July 2018

1 reference

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Enhancer competition between H19 and Igf2 does not mediate their imprinting

6 July 2018

1 reference

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A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

6 July 2018

1 reference

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

6 July 2018

1 reference

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

6 July 2018

1 reference

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6 July 2018

Imprinting mechanisms.

1 reference

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

6 July 2018

1 reference

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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

6 July 2018

1 reference

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Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia

6 July 2018

1 reference

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Genomic imprinting in mammals.

6 July 2018

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A novel mutation adjacent to the switch III domain of G(S alpha) in a patient with pseudohypoparathyroidism

6 July 2018

1 reference

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Imprinting in Albright's hereditary osteodystrophy

6 July 2018

1 reference

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Parental origin of transcription from the human GNAS1 gene.

6 July 2018

1 reference

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Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene

6 July 2018

1 reference

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Defect of Receptor–Cyclase Coupling Protein in Pseudohypoparathyroidism

6 July 2018

1 reference

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Nucleotide sequence of a full-length cDNA for mouse cytoskeletal beta-actin mRNA.

6 July 2018

1 reference

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Isolation and characterization of the human Gs alpha gene

6 July 2018

1 reference

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Selective resistance to parathyroid hormone in cultured skin fibroblasts from patients with pseudohypoparathyroidism type Ib.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

Differential expression of novel Gs alpha signal transduction protein cDNA species

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

The sins of the fathers and mothers: genomic imprinting in mammalian development.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=301417

27 October 2018

HYPO-HYPERPARATHYROIDISM

1 reference

12 December 2020

The Role of Genomic Imprinting of Galpha in the Pathogenesis of Albright Hereditary Osteodystrophy

1 reference

12 December 2020

Pseudohypoparathyroidism with osteitis fibrosa cystica: direct demonstration of skeletal responsiveness to parathyroid hormone in cells cultured from bone

1 reference

12 December 2020

Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein

1 reference

12 December 2020

Pseudohypoparathyroidism with Secondary Hyperparathyroidism and Osteitis Fibrosa*

1 reference

12 December 2020

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI10431

1 reference

2 August 2017

1 reference

2 August 2017

1 reference