The Role of Genomic Imprinting of Galpha in the Pathogenesis of Albright Hereditary Osteodystrophy (Q77735585)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10322399 AND SRC:MED&resulttype=core&format=json

7 December 2019

title

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

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7 December 2019

1

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7 December 2019

author name string

Yu S

series ordinal

2

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7 December 2019

publication date

1 April 1999

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Trends in Endocrinology and Metabolism

7 December 2019

published in

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7 December 2019

volume

10

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7 December 2019

issue

3

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7 December 2019

page(s)

81-85

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Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone

7 December 2019

cites work

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https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Defect of Receptor–Cyclase Coupling Protein in Pseudohypoparathyroidism

1 reference

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7 January 2021

Deficient activity of receptor-cyclase coupling protein in platelets of patients with pseudohypoparathyroidism

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Fibroblast Defect in Pseudohypoparathyroidism, Type I: Reduced Activity of Receptor-Cyclase Coupling Protein*

1 reference

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7 January 2021

Deficient Activity of Receptor-Cyclase Coupling Protein in Transformed Lymphoblasts of Patients with Pseudohypoparathyroidism, Type I*

1 reference

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7 January 2021

Deficient guanine nucleotide regulatory unit activity in cultured fibroblast membranes from patients with pseudohypoparathyroidism type I. A cause of impaired synthesis of 3',5'-cyclic AMP by intact and broken cells

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Reduced expression of multiple forms of the alpha subunit of the stimulatory GTP-binding protein in pseudohypoparathyroidism type Ia

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Immunochemical analysis of the alpha-subunit of the stimulatory G-protein of adenylyl cyclase in patients with Albright's hereditary osteodystrophy.

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Albright's hereditary osteodystrophy and defective G proteins

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Isolation and characterization of the human Gs alpha gene

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https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Mapping studies of the distal imprinting region of mouse chromosome 2

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https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

XL alpha s is a new type of G protein

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Differential expression of novel Gs alpha signal transduction protein cDNA species

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Imprinting in Albright's hereditary osteodystrophy

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

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https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Genomic imprinting in mammals.

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https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Responses to glucagon infusion in pseudohypoparathyroidism.

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Blunted Plasma Cyclic Adenosine Monophosphate Response to Isoproterenol in Pseudohypoparathyroidism*

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Parental origin of transcription from the human GNAS1 gene.

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

The renal response to exogenous parathyroid hormone in treated pseudohypoparathyroidism

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Competition- a common motif for the imprinting mechanism?

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1016/S1043-2760(98)00124-6

7 January 2021

10.1016/S1043-2760(98)00124-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10322399 AND SRC:MED&resulttype=core&format=json

7 December 2019

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