Recurrent Mutation of the Gene Encoding sequestosome 1 (SQSTM1/p62) in Paget Disease of Bone
Top Cited Papers
- 1 June 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 70 (6), 1582-1588
- https://doi.org/10.1086/340731
Abstract
No abstract availableKeywords
Funding Information
- Fonds pour la Formation de Chercheurs et l'Aide à la Recherche
- Canadian Institutes of Health Research (MOP-3804)
- Fonds de Recherche du Québec - Santé
- Canada Foundation for Innovation (548)
This publication has 40 references indexed in Scilit:
- The Tumor-Necrosis-Factor Receptor–Associated Periodic Syndrome: New Mutations in TNFRSF1A, Ancestral Origins, Genotype-Phenotype Studies, and Evidence for Further Genetic Heterogeneity of Periodic FeversAmerican Journal of Human Genetics, 2001
- Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldEuropean Journal of Human Genetics, 2001
- Familial Paget's Disease of Bone: Nonlinkage to the PDB1 and PDB2 Loci on Chromosomes 6p and 18q in a Large PedigreeJournal of Bone and Mineral Research, 2001
- Heterogeneity in Paget disease of the boneAmerican Journal of Medical Genetics, 2000
- Activation of NF-κB by RANK Requires Tumor Necrosis Factor Receptor-associated Factor (TRAF) 6 and NF-κB-inducing KinasePublished by Elsevier ,1999
- Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic HeterogeneityJournal of Bone and Mineral Research, 1998
- Genetic linkage of familial expansile osteolysis to chromosome 18qHuman Molecular Genetics, 1994
- Absence of HLA linkage in a family with osteitis deformans (Paget's disease of bone)Tissue Antigens, 1988
- A Probable Linkage Between Familial Paget's Disease and the HLA Loci*Australian and New Zealand Journal of Medicine, 1982
- Microfilaments Associated with Paget’s Disease of Bone: Comparison with Nucleocapsids of Measles Virus and Respiratory Syncytial VirusIntervirology, 1982