Fibrous dysplasia as a stem cell disease (Q36710147)

15 August 2017

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title

Fibrous dysplasia as a stem cell disease (English)

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15 August 2017

Isabella Saggio

2

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Pamela Robey

object named as

Pamela Gehron Robey

series ordinal

3

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author name string

Mara Riminucci

series ordinal

1

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PubMed ID

17229001

15 August 2017

Paolo Bianco

series ordinal

4

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15 August 2017

1 December 2006

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Journal of Bone and Mineral Research

15 August 2017

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15 August 2017

21 Suppl 2

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15 August 2017

P125-31

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

15 August 2017

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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.06S224

Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Hydrolysis of GTP by the alpha-chain of Gs and other GTP binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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.06S224

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.06S224

Mutations in G proteins and G protein-coupled receptors in endocrine disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

CpG mutation rates in the human genome are highly dependent on local GC content

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Genomic imprinting in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Epigenetic reprogramming during early development in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Identification of a methylation imprint mark within the mouse Gnas locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Dynamic interrelationships between DNA replication, methylation, and repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Embryo-derived stem cells: of mice and men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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.06S224

Diseases of bone and the stromal cell lineage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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.06S224

Fracture incidence in polyostotic fibrous dysplasia and the McCune-Albright syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

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.06S224

Osteoclastogenesis in fibrous dysplasia of bone: in situ and in vitro analysis of IL-6 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Human fetal mesenchymal stem cells as vehicles for gene delivery

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Bone marrow mesenchymal cells for haemophilia A gene therapy using retroviral vectors with modified long-terminal repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Stem cells in tissue engineering.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Effective expression of small interfering RNA in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Lentiviral transduction of human postnatal skeletal (stromal, mesenchymal) stem cells: in vivo transplantation and gene silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

Gene targeting in stem cells from individuals with osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S224

21 January 2018

Identifiers

DOI

10.1359/JBMR.06S224

1 reference

15 August 2017

1 reference

PubMed ID

17229001