G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome (Q36710142)

15 August 2017

1 reference

title

G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome (English)

1 reference

ORCID Public Data File 2021

15 August 2017

1 reference

author name string

Lee S Weinstein

series ordinal

1

1 reference

15 August 2017

publication date

1 December 2006

1 reference

Journal of Bone and Mineral Research

15 August 2017

published in

1 reference

15 August 2017

volume

21 Suppl 2

1 reference

15 August 2017

page(s)

P120-4

1 reference

Increased IL-6-production by cells isolated from the fibrous bone dysplasia tissues in patients with McCune-Albright syndrome

15 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in Females

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

McCune-Albright syndrome in a male child:A clinical and endocrinologic enigma

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Familial polyostotic fibrous dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Structures of active conformations of Gi alpha 1 and the mechanism of GTP hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

GTPase mechanism of Gproteins from the 1.7-A crystal structure of transducin alpha-GDP-AIF-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Two G protein oncogenes in human endocrine tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Characteristics of gsp-positive growth hormone-secreting pituitary tumors in Korean acromegalic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Gs alpha and Gi2 alpha mutations in clinically non-functioning pituitary tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

G-protein mutations in human pituitary adrenocorticotrophic hormone-secreting adenomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

G protein gene mutations in patients with multiple endocrinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Activating point mutations of the gsp oncogene in human thyroid adenomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

G protein and thyrotropin receptor mutations in thyroid neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Activating GNAS1 gene mutations in patients with premature thelarche.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Activating mutation of GS alpha in McCune-Albright syndrome causes skin pigmentation by tyrosinase gene activation on affected melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

A novel technique based on a PNA hybridization probe and FRET principle for quantification of mutant genotype in fibrous dysplasia/McCune-Albright syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Minireview: GNAS: normal and abnormal functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Diseases of bone and the stromal cell lineage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Forskolin has biphasic effects on osteoprogenitor cell differentiation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha-mutated skeletal progenitor cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Increased expression of the c-fos proto-oncogene in bone from patients with fibrous dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Signaling pathways and c-fos transcriptional response--links to inherited diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Increased interleukin-6 production in mouse osteoblastic MC3T3-E1 cells expressing activating mutant of the stimulatory G protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

Deregulated c-fos expression interferes with normal bone development in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S223

21 January 2018

Identifiers

DOI

10.1359/JBMR.06S223

1 reference

15 August 2017

1 reference