(Q42609192)

3 November 2017

Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone (English)

1 reference

3 November 2017

Jean Morissette

1

1 reference

PubMed ID

17229007

3 November 2017

Nancy Laurin

series ordinal

2

1 reference

PubMed ID

17229007

3 November 2017

Jacques P Brown

series ordinal

3

1 reference

3 November 2017

1 December 2006

1 reference

Journal of Bone and Mineral Research

3 November 2017

1 reference

3 November 2017

21 Suppl 2

1 reference

3 November 2017

P38-44

1 reference

Paget's disease of bone in early adult life.

3 November 2017

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Familial aggregation of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Prevalence of Paget's disease of bone in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Epidemiological study of Paget's disease of bone in a zone of the Province of Salamanca (Spain). The Paget's disease of the bone study group of Salamanca.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Epidemiology of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Prevalence and clinical features of Paget's disease of bone in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

A family study of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB).

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

21 January 2018

Paget disease of bone

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

Expression of measles virus nucleocapsid protein in osteoclasts induces Paget's disease-like bone lesions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.06S207

21 January 2018

Identifiers

DOI

10.1359/JBMR.06S207

1 reference

3 November 2017

1 reference

PubMed ID

17229007