(Q36577488)

15 August 2017

1 reference

title

Mechanisms of disease: genetics of Paget's disease of bone and related disorders (English)

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15 August 2017

main subject

Paget's disease of bone

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2

Stuart H Ralston

1 reference

15 August 2017

Anna Daroszewska

1

1 reference

15 August 2017

publication date

1 May 2006

1 reference

Nature Clinical Practice Rheumatology

15 August 2017

published in

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15 August 2017

volume

2

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15 August 2017

issue

5

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15 August 2017

page(s)

270-277

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The pro and con of measles virus in Paget's disease: con.

15 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

The epidemiology of Paget's disease in Britain: is the prevalence decreasing?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Incidence and natural history of Paget's disease of bone in England and Wales.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Paget's disease in an archeological population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Paget's disease of bone in New Zealand: continued decline in disease severity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Long-term trends in the incidence of Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Prevalence of Paget's disease of bone in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Frequency and characteristics of familial aggregation of paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Familial aggregation of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

A family study of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

The epidemiology of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Phenotypic characterization of early onset Paget's disease of bone caused by a 27-bp duplication in the TNFRSF11A gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Osteoprotegerin deficiency and juvenile Paget's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Genetic linkage of familial expansile osteolysis to chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Linkage of Paget disease of bone to a novel region on human chromosome 18q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Bone resorption by osteoclasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Identification of a novel tandem duplication in exon 1 of the TNFRSF11A gene in two unrelated patients with familial expansile osteolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Evaluation of the role of RANK and OPG genes in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Evidence for a novel osteosarcoma tumor-suppressor gene in the chromosome 18 region genetically linked with Paget disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Structure of the ubiquitin-associated domain of p62 (SQSTM1) and implications for mutations that cause Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

SQSTM1 and Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Ubiquitin signalling in the NF-kappaB pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Molecular perspectives on p97-VCP: progress in understanding its structure and diverse biological functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Involvement of valosin-containing protein, an ATPase Co-purified with IkappaBalpha and 26 S proteasome, in ubiquitin-proteasome-mediated degradation of IkappaBalpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Management of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Genetic linkage of Paget disease of the bone to chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Familial Paget’s disease of bone: patterns of inheritance and frequency of linkage to chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Loss of Ubiquitin-Binding Associated With Paget's Disease of Bone p62 (SQSTM1) Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

Bone histomorphometry in Paget's disease. Quantitative and dynamic analysis of pagetic and nonpagetic bone tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Prevalence of pelvic Paget's disease of bone in the United States

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Epidemiological aspects of Paget's disease: family history and relationship to other medical conditions

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Billiard-player's fingers: an unusual case of Paget's disease of bone

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Familial expansile osteolysis. A new dysplasia

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

A Probable Linkage Between Familial Paget's Disease and the HLA Loci*

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

A "two-hit" model of cystogenesis in autosomal dominant polycystic kidney disease?

1 reference

https://api.crossref.org/works/10.1038%2FNCPRHEUM0172

7 January 2021

Identifiers

DOI

10.1038/NCPRHEUM0172

1 reference

15 August 2017

1 reference