(Q31456359)

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Selective resistance to parathyroid hormone caused by a novel uncoupling mutation in the carboxyl terminus of G alpha(s). A cause of pseudohypoparathyroidism type Ib.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Selective resistance to parathyroid hormone caused by a novel uncoupling mutation in the carboxyl terminus of G alpha(s). A cause of pseudohypoparathyroidism type Ib (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

pseudohypoparathyroidism type IB

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Michael A. Levine

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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Wu WI

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Schwindinger WF

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Aparicio LF

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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1 January 2001

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1 November 2019

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7

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Journal of Biological Chemistry

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1 November 2019

276

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1 November 2019

1

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1 November 2019

165-171

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Europe PubMed Central

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1 November 2019

Pseudohypoparathyroidism: from bedside to bench and back

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Cloning and Characterization of the Promoter Regions of the Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene: Analysis of Deoxyribonucleic Acid from Normal Subjects and Patients with Pseudohypoparathyroidism Type 1b

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Probing the bimolecular interactions of parathyroid hormone and the human parathyroid hormone/parathyroid hormone-related protein receptor. 2. Cloning, characterization, and photoaffinity labeling of the recombinant human receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Antisera against a guanine nucleotide binding protein from retina cross-react with the beta subunit of the adenylyl cyclase-associated guanine nucleotide binding proteins, Ns and Ni.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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/10.1074%2FJBC.M006032200

21 January 2018

Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Reproductive dysfunction in women with Albright's hereditary osteodystrophy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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/10.1074%2FJBC.M006032200

21 January 2018

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/10.1074%2FJBC.M006032200

21 January 2018

Inhibitory and stimulatory G proteins of adenylate cyclase: cDNA and amino acid sequences of the alpha chains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Identical complementary deoxyribonucleic acids encode a human renal and bone parathyroid hormone (PTH)/PTH-related peptide receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

How receptors talk to trimeric G proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Crystal structure of the adenylyl cyclase activator Gsalpha

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Evolutionarily conserved Galphabetagamma binding surfaces support a model of the G protein-receptor complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Receptor and effector interactions of Gs. Functional studies with antibodies to the alpha s carboxyl-terminal decapeptide

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Functional domains of the Gs alpha subunit: role of the C-terminus in the receptor-dependent and receptor-independent activation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Identification of receptor contact site involved in receptor-G protein coupling

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Identification of the lesion in the stimulatory GTP-binding protein of the uncoupled S49 lymphoma

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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/10.1074%2FJBC.M006032200

21 January 2018

Imprinting in Albright's hereditary osteodystrophy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Differential expression of novel Gs alpha signal transduction protein cDNA species

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Identification of a methylation imprint mark within the mouse Gnas locus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Metabolic bone disease in pseudohypoparathyroidism: radiologic features.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

Parental origin of transcription from the human GNAS1 gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006032200

21 January 2018

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/10.1074%2FJBC.M006032200

21 January 2018

Identifiers

10.1074/JBC.M006032200

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11029463%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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