-
2
-
-
0035999447
-
Paget's disease in an archeological population
-
Rogers, J., Jeffrey, D.R. and Watt, I. (2002) Paget's disease in an archeological population. J Bone Miner Res 17, 1127-1134
-
(2002)
J Bone Miner Res
, vol.17
, pp. 1127-1134
-
-
Rogers, J.1
Jeffrey, D.R.2
Watt, I.3
-
3
-
-
0032954603
-
The epidemiology of Paget's disease in Britain: Is the prevalence decreasing?
-
Cooper, C. et al. (1999) The epidemiology of Paget's disease in Britain: is the prevalence decreasing? J Bone Miner Res 14, 192-197
-
(1999)
J Bone Miner Res
, vol.14
, pp. 192-197
-
-
Cooper, C.1
-
4
-
-
25144442611
-
Genetics of Paget's disease of bone
-
Daroszewska, A. and Ralston, S.H. (2005) Genetics of Paget's disease of bone. Clin Sci (Lond) 109, 257-263
-
(2005)
Clin Sci (Lond)
, vol.109
, pp. 257-263
-
-
Daroszewska, A.1
Ralston, S.H.2
-
6
-
-
0036177990
-
Incidence and natural history of Paget's disease of bone in England and Wales
-
van Staa, T.P. et al. (2002) Incidence and natural history of Paget's disease of bone in England and Wales. J Bone Miner Res 17, 465-471
-
(2002)
J Bone Miner Res
, vol.17
, pp. 465-471
-
-
van Staa, T.P.1
-
7
-
-
0022634225
-
Osteogenic sarcoma of bones and soft tissues in older persons. A clinicopathologic analysis of 117 patients older than 60 years
-
Huvos, A.G. (1986) Osteogenic sarcoma of bones and soft tissues in older persons. A clinicopathologic analysis of 117 patients older than 60 years. Cancer 57, 1442-1449
-
(1986)
Cancer
, vol.57
, pp. 1442-1449
-
-
Huvos, A.G.1
-
8
-
-
0032868676
-
Cell biology of Paget's disease
-
Reddy, S.V. et al. (1999) Cell biology of Paget's disease. J Bone Miner Res 14, Suppl 2, 3-8
-
(1999)
J Bone Miner Res
, vol.14
, Issue.SUPPL. 2
, pp. 3-8
-
-
Reddy, S.V.1
-
9
-
-
0018275969
-
Radiological prevalence of Paget's disease of bone in British migrants to Australia
-
Gardner, M.J., Guyer, P.B. and Barker, D.J. (1978) Radiological prevalence of Paget's disease of bone in British migrants to Australia. Br Med J 1, 1655-1657
-
(1978)
Br Med J
, vol.1
, pp. 1655-1657
-
-
Gardner, M.J.1
Guyer, P.B.2
Barker, D.J.3
-
10
-
-
0028221605
-
Epidemiological aspects of Paget's disease: Family history and relationship to other medical conditions
-
Siris, E.S. (1994) Epidemiological aspects of Paget's disease: Family history and relationship to other medical conditions. Semin Arthritis Rheum 23, 222-225
-
(1994)
Semin Arthritis Rheum
, vol.23
, pp. 222-225
-
-
Siris, E.S.1
-
11
-
-
0020523615
-
A family study of Paget's disease of bone
-
Sofaer, J.A., Holloway, S.M. and Emery, A.E. (1983) A family study of Paget's disease of bone. J Epidemiol Community Health 37, 226-231
-
(1983)
J Epidemiol Community Health
, vol.37
, pp. 226-231
-
-
Sofaer, J.A.1
Holloway, S.M.2
Emery, A.E.3
-
12
-
-
0028914326
-
Frequency and characteristics of familial aggregation of Paget's disease of bone
-
Morales-Piga, A.A. et al. (1995) Frequency and characteristics of familial aggregation of Paget's disease of bone. J Bone Miner Res 10, 663-670
-
(1995)
J Bone Miner Res
, vol.10
, pp. 663-670
-
-
Morales-Piga, A.A.1
-
13
-
-
0034065196
-
Familial Paget's disease of bone: Patterns of inheritance and frequency of linkage to chromosome 18q
-
Hocking, L. et al. (2000) Familial Paget's disease of bone: Patterns of inheritance and frequency of linkage to chromosome 18q. Bone 26, 577-580
-
(2000)
Bone
, vol.26
, pp. 577-580
-
-
Hocking, L.1
-
14
-
-
0031778038
-
Paget's disease of bone: Evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity
-
Haslam, S.I. et al. (1998) Paget's disease of bone: Evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity. J Bone Miner Res 13, 911-917
-
(1998)
J Bone Miner Res
, vol.13
, pp. 911-917
-
-
Haslam, S.I.1
-
15
-
-
11944268320
-
SQSTM1 and Paget's disease of bone
-
Layfield, R. and Hocking, L.J. (2004) SQSTM1 and Paget's disease of bone. Calcif Tissue Int 75, 347-357
-
(2004)
Calcif Tissue Int
, vol.75
, pp. 347-357
-
-
Layfield, R.1
Hocking, L.J.2
-
16
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts, G.D. et al. (2004) Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat Genet 36, 377-381
-
(2004)
Nat Genet
, vol.36
, pp. 377-381
-
-
Watts, G.D.1
-
17
-
-
0442325388
-
The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis
-
Duran, A. et al. (2004) The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis. Dev Cell 6, 303-309
-
(2004)
Dev Cell
, vol.6
, pp. 303-309
-
-
Duran, A.1
-
18
-
-
0043267732
-
Genetic regulation of osteoclast development and function
-
Teitelbaum, S.L. and Ross, F.P. (2003) Genetic regulation of osteoclast development and function. Nat Rev Genet 4, 638-649
-
(2003)
Nat Rev Genet
, vol.4
, pp. 638-649
-
-
Teitelbaum, S.L.1
Ross, F.P.2
-
19
-
-
0036094026
-
Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone
-
Laurin, N. et al. (2002) Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone. Am J Hum Genet 70, 1582-1588
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1582-1588
-
-
Laurin, N.1
-
20
-
-
0037108914
-
Domain specific mutations in Sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease
-
Hocking, L.J. et al. (2002) Domain specific mutations in Sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease. Hum Mol Genet 11, 2735-2739
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2735-2739
-
-
Hocking, L.J.1
-
21
-
-
0142148013
-
Three novel mutations in SQSTM1 identified in familial Paget's disease of bone
-
Johnson-Pais, T.L. et al. (2003) Three novel mutations in SQSTM1 identified in familial Paget's disease of bone. J Bone Miner Res 18, 1748-1753
-
(2003)
J Bone Miner Res
, vol.18
, pp. 1748-1753
-
-
Johnson-Pais, T.L.1
-
22
-
-
2942709744
-
Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees
-
Good, D.A. et al. (2004) Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees. Bone 35, 277-282
-
(2004)
Bone
, vol.35
, pp. 277-282
-
-
Good, D.A.1
-
23
-
-
4444335629
-
Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease
-
Beyens, G. et al. (2004) Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease. Calcif Tissue Int 75, 144-152
-
(2004)
Calcif Tissue Int
, vol.75
, pp. 144-152
-
-
Beyens, G.1
-
24
-
-
2342493320
-
Familial Paget's disease in The Netherlands: Occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations
-
Eekhoff, E.W. et al. (2004) Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations. Arthritis Rheum 50, 1650-1654
-
(2004)
Arthritis Rheum
, vol.50
, pp. 1650-1654
-
-
Eekhoff, E.W.1
-
25
-
-
8644267864
-
Two novel mutations at exon 8 of Sequestosome 1 gene (SQSTM1) in an Italian serie of patients affected by Paget's disease of bone (PDB)
-
Falchetti, A. et al. (2004) Two novel mutations at exon 8 of Sequestosome 1 gene (SQSTM1) in an Italian serie of patients affected by Paget's disease of bone (PDB). J Bone Miner Res 19, 1013-1017
-
(2004)
J Bone Miner Res
, vol.19
, pp. 1013-1017
-
-
Falchetti, A.1
-
26
-
-
4544371010
-
Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: Genotype phenotype correlation, functional analysis and structural consequences
-
Hocking, L.J. et al. (2004) Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: Genotype phenotype correlation, functional analysis and structural consequences. J Bone Miner Res 19, 1122-1127
-
(2004)
J Bone Miner Res
, vol.19
, pp. 1122-1127
-
-
Hocking, L.J.1
-
27
-
-
33845435884
-
Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American family
-
Beyens, G. et al. (2006) Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American family. Calcif Tissue Int 79, 281-288
-
(2006)
Calcif Tissue Int
, vol.79
, pp. 281-288
-
-
Beyens, G.1
-
28
-
-
33745510646
-
A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signalling and Paget's disease of bone with a severe phenotype
-
Rea, S.L. et al. (2006) A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signalling and Paget's disease of bone with a severe phenotype. J Bone Miner Res 21, 1136-1145
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1136-1145
-
-
Rea, S.L.1
-
29
-
-
33846479861
-
Paget's disease of bone in the French population: Novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations
-
Collet, C. et al. (2007) Paget's disease of bone in the French population: Novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations. J Bone Miner Res 22, 310-317
-
(2007)
J Bone Miner Res
, vol.22
, pp. 310-317
-
-
Collet, C.1
-
30
-
-
0033987358
-
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis
-
Hughes, A.E. et al. (2000) Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis. Nat Genet 24, 45-48
-
(2000)
Nat Genet
, vol.24
, pp. 45-48
-
-
Hughes, A.E.1
-
31
-
-
0036133351
-
Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis
-
Whyte, M.P. and Hughes, A.E. (2002) Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis. J Bone Miner Res 17, 26-29
-
(2002)
J Bone Miner Res
, vol.17
, pp. 26-29
-
-
Whyte, M.P.1
Hughes, A.E.2
-
32
-
-
0038643034
-
Phenotypic characterisation of early onset Paget's disease of bone caused by a 27 bp duplication in the TNFRSF11A gene
-
Nakatsuka, K., Nishizawa, K. and Ralston, S.H. (2003) Phenotypic characterisation of early onset Paget's disease of bone caused by a 27 bp duplication in the TNFRSF11A gene. J Bone Miner Res 18, 1381-1385
-
(2003)
J Bone Miner Res
, vol.18
, pp. 1381-1385
-
-
Nakatsuka, K.1
Nishizawa, K.2
Ralston, S.H.3
-
33
-
-
0037130183
-
Osteoprotegerin deficiency and juvenile Paget's disease
-
Whyte, M.P. et al. (2002) Osteoprotegerin deficiency and juvenile Paget's disease. N Engl J Med 347, 175-184
-
(2002)
N Engl J Med
, vol.347
, pp. 175-184
-
-
Whyte, M.P.1
-
34
-
-
18544371504
-
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
-
Cundy, T. et al. (2002) A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype. Hum Mol Genet 11, 2119-2127
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2119-2127
-
-
Cundy, T.1
-
35
-
-
0036240410
-
VCP (p97) regulates NFkappaB signaling pathway, which is important for metastasis of osteosarcoma cell line
-
Asai, T. et al. (2002) VCP (p97) regulates NFkappaB signaling pathway, which is important for metastasis of osteosarcoma cell line. Jpn J Cancer Res 93, 296-304
-
(2002)
Jpn J Cancer Res
, vol.93
, pp. 296-304
-
-
Asai, T.1
-
36
-
-
13044316551
-
Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand
-
Hsu, H. et al. (1999) Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand. Proc Natl Acad Sci U S A 96, 3540-3545
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 3540-3545
-
-
Hsu, H.1
-
37
-
-
0032545465
-
The involvement of multiple tumor necrosis factor receptor (TNFR)-associated factors in the signaling mechanisms of receptor activator of NF-kappaB, a member of the TNFR superfamily
-
Galibert, L. et al. (1998) The involvement of multiple tumor necrosis factor receptor (TNFR)-associated factors in the signaling mechanisms of receptor activator of NF-kappaB, a member of the TNFR superfamily. J Biol Chem 273, 34120-341277
-
(1998)
J Biol Chem
, vol.273
, pp. 34120-341277
-
-
Galibert, L.1
-
38
-
-
18444390259
-
Distinct molecular mechanism for initiating TRAF6 signalling
-
Ye, H. et al. (2002) Distinct molecular mechanism for initiating TRAF6 signalling. Nature 418, 443-447
-
(2002)
Nature
, vol.418
, pp. 443-447
-
-
Ye, H.1
-
39
-
-
0034644474
-
Activation of the IkappaB kinase complex by TRAF6 requires a dimeric ubiquitin-conjugating enzyme complex and a unique polyubiquitin chain
-
Deng, L. et al. (2000) Activation of the IkappaB kinase complex by TRAF6 requires a dimeric ubiquitin-conjugating enzyme complex and a unique polyubiquitin chain. Cell 103, 351-361
-
(2000)
Cell
, vol.103
, pp. 351-361
-
-
Deng, L.1
-
40
-
-
23144449789
-
Ubiquitin signalling in the NF-kappaB pathway
-
Chen, Z.J. (2005) Ubiquitin signalling in the NF-kappaB pathway Nat Cell Biol 7, 758-765
-
(2005)
Nat Cell Biol
, vol.7
, pp. 758-765
-
-
Chen, Z.J.1
-
41
-
-
27144503391
-
Ubiquitin-binding proteins: Similar, but different
-
Andersen, K.M., Hofmann, K. and Hartmann-Petersen, R. (2005) Ubiquitin-binding proteins: Similar, but different. Essays Biochem 41, 49-67
-
(2005)
Essays Biochem
, vol.41
, pp. 49-67
-
-
Andersen, K.M.1
Hofmann, K.2
Hartmann-Petersen, R.3
-
42
-
-
4344712350
-
TAB2 and TAB3 activate the NF-kappaB pathway through binding to polyubiquitin chains
-
Kanayama, A. et al. (2004) TAB2 and TAB3 activate the NF-kappaB pathway through binding to polyubiquitin chains. Mol Cell 15, 535-548
-
(2004)
Mol Cell
, vol.15
, pp. 535-548
-
-
Kanayama, A.1
-
43
-
-
2942703810
-
Selective inhibition of NF-kappa B blocks osteoclastogenesis and prevents inflammatory bone destruction in vivo
-
Jimi, E. et al. (2004) Selective inhibition of NF-kappa B blocks osteoclastogenesis and prevents inflammatory bone destruction in vivo. Nat Med 10, 617-624
-
(2004)
Nat Med
, vol.10
, pp. 617-624
-
-
Jimi, E.1
-
44
-
-
33746644136
-
p62 ubiquitin binding-associated domain mediated the receptor activator of nuclear factor-kappaB ligand-induced osteoclast formation: A new insight into the pathogenesis of Paget's disease of bone
-
Yip, K.H. et al. (2006) p62 ubiquitin binding-associated domain mediated the receptor activator of nuclear factor-kappaB ligand-induced osteoclast formation: A new insight into the pathogenesis of Paget's disease of bone. Am J Pathol 169, 503-514
-
(2006)
Am J Pathol
, vol.169
, pp. 503-514
-
-
Yip, K.H.1
-
45
-
-
26944465404
-
Diverse polyubiquitin interaction properties of ubiquitin-associated domains
-
Raasi, S. et al. (2005) Diverse polyubiquitin interaction properties of ubiquitin-associated domains. Nat Struct Mol Biol 12, 708-714
-
(2005)
Nat Struct Mol Biol
, vol.12
, pp. 708-714
-
-
Raasi, S.1
-
46
-
-
0029809134
-
p62, a phosphotyrosine-independent ligand of the SH2 domain of p561ck, belongs to a new class of ubiquitin-binding proteins
-
Vadlamudi, R.K. et al. (1996) p62, a phosphotyrosine-independent ligand of the SH2 domain of p561ck, belongs to a new class of ubiquitin-binding proteins. J Biol Chem 271, 20235-20237
-
(1996)
J Biol Chem
, vol.271
, pp. 20235-20237
-
-
Vadlamudi, R.K.1
-
47
-
-
33751259129
-
p62 mutations, ubiquitin recognition and Paget's disease of bone
-
Layfield, R. et al. (2006) p62 mutations, ubiquitin recognition and Paget's disease of bone. Biochem Soc Trans 34, 735-737
-
(2006)
Biochem Soc Trans
, vol.34
, pp. 735-737
-
-
Layfield, R.1
-
48
-
-
15344339092
-
Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations
-
Cavey, J.R. et al. (2005) Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations. J Bone Miner Res 20, 619-624
-
(2005)
J Bone Miner Res
, vol.20
, pp. 619-624
-
-
Cavey, J.R.1
-
49
-
-
33646597289
-
Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of bone
-
Cavey, J.R. et al. (2006) Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of bone. Calcif Tissue Int 78, 271-277
-
(2006)
Calcif Tissue Int
, vol.78
, pp. 271-277
-
-
Cavey, J.R.1
-
50
-
-
27444433045
-
The p62 scaffold regulates nerve growth factor-induced NF-kappaB activation by influencing TRAF6 polyubiquitination
-
Wooten, M.W. et al. (2005) The p62 scaffold regulates nerve growth factor-induced NF-kappaB activation by influencing TRAF6 polyubiquitination. J Biol Chem 280, 35625-35629
-
(2005)
J Biol Chem
, vol.280
, pp. 35625-35629
-
-
Wooten, M.W.1
-
51
-
-
0034735773
-
T-cell-mediated regulation of osteoclastogenesis by signalling cross-talk between RANKL and IFN-gamma
-
Takayanagi, H. et al. (2000) T-cell-mediated regulation of osteoclastogenesis by signalling cross-talk between RANKL and IFN-gamma. Nature 408, 600-605
-
(2000)
Nature
, vol.408
, pp. 600-605
-
-
Takayanagi, H.1
-
52
-
-
0033932526
-
Enhanced RANK ligand expression and responsivity of bone marrow cells in Paget's disease of bone
-
Menaa, C. et al. (2000) Enhanced RANK ligand expression and responsivity of bone marrow cells in Paget's disease of bone. J Clin Invest 105, 1833-1938
-
(2000)
J Clin Invest
, vol.105
, pp. 1833-1938
-
-
Menaa, C.1
-
53
-
-
0034937704
-
Role of receptor activator of nuclear factor-kappaB ligand and osteoprotegerin in bone cell biology
-
Hofbauer, L.C. and Heufelder, A.E. (2001) Role of receptor activator of nuclear factor-kappaB ligand and osteoprotegerin in bone cell biology J Mol Med 79, 243-253
-
(2001)
J Mol Med
, vol.79
, pp. 243-253
-
-
Hofbauer, L.C.1
Heufelder, A.E.2
-
54
-
-
33845967453
-
Serum OPG and RANKL levels before and after intravenous bisphosphonate treatment in Paget's disease of bone
-
Martini, G. et al. (2007) Serum OPG and RANKL levels before and after intravenous bisphosphonate treatment in Paget's disease of bone. Bone 40, 457-463
-
(2007)
Bone
, vol.40
, pp. 457-463
-
-
Martini, G.1
-
56
-
-
31144470450
-
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
-
Weihl, C.C. et al. (2006) Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Hum Mol Genet 15, 189-199
-
(2006)
Hum Mol Genet
, vol.15
, pp. 189-199
-
-
Weihl, C.C.1
-
57
-
-
15444361471
-
Involvement of valosin-containing protein, an ATPase Co-purified with IkappaBalpha and 26S proteasome, in ubiquitin-proteasome-mediated degradation of IkappaBalpha
-
Dai, R.M. et al. (1998) Involvement of valosin-containing protein, an ATPase Co-purified with IkappaBalpha and 26S proteasome, in ubiquitin-proteasome-mediated degradation of IkappaBalpha. J Biol Chem 273, 3562-3573
-
(1998)
J Biol Chem
, vol.273
, pp. 3562-3573
-
-
Dai, R.M.1
-
58
-
-
0034918873
-
The ubiquitin protein catabolic disorders
-
Layfield, R. et al. (2001) The ubiquitin protein catabolic disorders. Neuropathol Appl Neurobiol 27, 171-179
-
(2001)
Neuropathol Appl Neurobiol
, vol.27
, pp. 171-179
-
-
Layfield, R.1
-
59
-
-
33645046107
-
Etiologic factors in Paget's disease of bone
-
Reddy, S.V. (2006) Etiologic factors in Paget's disease of bone. Cell Mol Life Sci 63, 391-398
-
(2006)
Cell Mol Life Sci
, vol.63
, pp. 391-398
-
-
Reddy, S.V.1
-
60
-
-
0019996989
-
Ultrastructural features of the osteoclasts from Paget's disease of bone in relation to a viral etiology
-
Harvey, L. et al. (1982) Ultrastructural features of the osteoclasts from Paget's disease of bone in relation to a viral etiology. J Clin Pathol 35, 771-779
-
(1982)
J Clin Pathol
, vol.35
, pp. 771-779
-
-
Harvey, L.1
-
61
-
-
0017114175
-
Nuclear inclusions in Paget's disease of bone
-
Mills, B.G. and Singer, F.R. (1976) Nuclear inclusions in Paget's disease of bone. Science 194, 201-202
-
(1976)
Science
, vol.194
, pp. 201-202
-
-
Mills, B.G.1
Singer, F.R.2
-
62
-
-
0021337486
-
Evidence for both respiratory synctial virus and measles virus antigens in the osteoclasts of patients with Paget's disease of bone
-
Mills, B.G. et al. (1984) Evidence for both respiratory synctial virus and measles virus antigens in the osteoclasts of patients with Paget's disease of bone. Clin Orthop Relat Res 183, 303-311
-
(1984)
Clin Orthop Relat Res
, vol.183
, pp. 303-311
-
-
Mills, B.G.1
-
63
-
-
0018930834
-
Bone tissue in Paget's disease of bone. Ultrastructure and immunocytology
-
Rebel, A. et al. (1980) Bone tissue in Paget's disease of bone. Ultrastructure and immunocytology. Arthritis Rheum 23, 1104-1144
-
(1980)
Arthritis Rheum
, vol.23
, pp. 1104-1144
-
-
Rebel, A.1
-
64
-
-
0032883330
-
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone
-
Reddy, S.V. et al. (1999) Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone. Exp Hematol 27, 1528-1532
-
(1999)
Exp Hematol
, vol.27
, pp. 1528-1532
-
-
Reddy, S.V.1
-
65
-
-
0036133370
-
Sequence analysis of measles virus nucleocapsid transcripts in patients with Paget's disease
-
Friedrichs, W.E. et al. (2002) Sequence analysis of measles virus nucleocapsid transcripts in patients with Paget's disease. J Bone Miner Res 17, 145-151
-
(2002)
J Bone Miner Res
, vol.17
, pp. 145-151
-
-
Friedrichs, W.E.1
-
66
-
-
0033713488
-
A negative search for a paramyxoviral etiology of Paget's disease of bone: Molecular, immunological, and ultrastructural studies in UK patients
-
Helfrich, M.H. et al. (2000) A negative search for a paramyxoviral etiology of Paget's disease of bone: Molecular, immunological, and ultrastructural studies in UK patients. J Bone Miner Res 15, 2315-2329
-
(2000)
J Bone Miner Res
, vol.15
, pp. 2315-2329
-
-
Helfrich, M.H.1
-
67
-
-
34249704670
-
Multicenter blinded analysis of RT-PCR detection methods for paramyoviruses in relation to Paget's disease of bone
-
Ralston, S.H. et al. (2007) Multicenter blinded analysis of RT-PCR detection methods for paramyoviruses in relation to Paget's disease of bone. J Bone Miner Res 22, 569-577
-
(2007)
J Bone Miner Res
, vol.22
, pp. 569-577
-
-
Ralston, S.H.1
-
68
-
-
0034104393
-
Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype
-
Kurihara, N. et al. (2000) Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype. J Clin Invest 105, 607-614
-
(2000)
J Clin Invest
, vol.105
, pp. 607-614
-
-
Kurihara, N.1
-
69
-
-
0033963129
-
1,25-Dihydroxyvitamin D3 hypersensitivity of osteoclast precursors from patients with Paget's disease
-
Menaa, C. et al. (2000) 1,25-Dihydroxyvitamin D3 hypersensitivity of osteoclast precursors from patients with Paget's disease. J Bone Miner Res 15, 228-236
-
(2000)
J Bone Miner Res
, vol.15
, pp. 228-236
-
-
Menaa, C.1
-
70
-
-
15244347056
-
Role of TAFII-17, a VDR binding protein, in the increased osteoclast formation in Paget's disease
-
Kurihara, N. et al. (2004) Role of TAFII-17, a VDR binding protein, in the increased osteoclast formation in Paget's disease. J. Bone Miner Res 19, 1154-1164
-
(2004)
J. Bone Miner Res
, vol.19
, pp. 1154-1164
-
-
Kurihara, N.1
-
71
-
-
34247848056
-
Experimental models of Paget's disease
-
Kurihara, N. et al. (2006) Experimental models of Paget's disease. J Bone Miner Res 21, Suppl 2, 55-57
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
, pp. 55-57
-
-
Kurihara, N.1
-
72
-
-
33644529415
-
Expression of the measles virus nucleocapsid protein in osteoclasts in vivo induces Paget's disease like bone lesions in mice
-
Kurihara, N. et al. (2006) Expression of the measles virus nucleocapsid protein in osteoclasts in vivo induces Paget's disease like bone lesions in mice. J Bone Miner Res 21, 446-455
-
(2006)
J Bone Miner Res
, vol.21
, pp. 446-455
-
-
Kurihara, N.1
-
73
-
-
0032146198
-
Detection of canine distemper virus in 100% of Paget's disease samples by in situ reverse transcriptase polymerase chain reaction
-
Mee, A.P. et al. (1998) Detection of canine distemper virus in 100% of Paget's disease samples by in situ reverse transcriptase polymerase chain reaction. Bone 23, 171-175
-
(1998)
Bone
, vol.23
, pp. 171-175
-
-
Mee, A.P.1
-
74
-
-
33846433786
-
Canine distemper virus induces human osteoclastogenesis through NF-kappB and sequestosome1/p62 activation
-
Selby, P.L., Davies, M. and. Mee, A.P. (2006) Canine distemper virus induces human osteoclastogenesis through NF-kappB and sequestosome1/p62 activation. J Bone Miner Res 21, 1750-1756
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1750-1756
-
-
Selby, P.L.1
Davies, M.2
Mee, A.P.3
-
75
-
-
33846516300
-
Is the prevalence of Paget's disease of bone decreasing?
-
Cundy, T. (2006) Is the prevalence of Paget's disease of bone decreasing? J Bone Miner Res 21, Suppl 2, 9-13
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
, pp. 9-13
-
-
Cundy, T.1
-
76
-
-
34247188567
-
Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations
-
Bolland, M.J. et al. (2007) Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations. J Bone Miner Res 22, 411-415
-
(2007)
J Bone Miner Res
, vol.22
, pp. 411-415
-
-
Bolland, M.J.1
-
77
-
-
0028221605
-
Epidemiological aspects of Paget's disease: Family history and relationship to other medical conditions
-
Siris, E.S. (1994) Epidemiological aspects of Paget's disease: Family history and relationship to other medical conditions. Semin Arthritis Rheum 23, 222-225
-
(1994)
Semin Arthritis Rheum
, vol.23
, pp. 222-225
-
-
Siris, E.S.1
-
78
-
-
0036755763
-
Paget's disease of bone in Lancashire and arsenic pesticide in cotton mill wastewater: A speculative hypothesis
-
Lever, J.H. (2002) Paget's disease of bone in Lancashire and arsenic pesticide in cotton mill wastewater: A speculative hypothesis. Bone 31, 434-436
-
(2002)
Bone
, vol.31
, pp. 434-436
-
-
Lever, J.H.1
-
79
-
-
0038367669
-
Activation of Nrf2 and accumulation of ubiquitinated A170 by arsenic in osteoblasts
-
Aono, J. et al. (2003) Activation of Nrf2 and accumulation of ubiquitinated A170 by arsenic in osteoblasts. Biochem Biophys Res Commun 305, 271-277
-
(2003)
Biochem Biophys Res Commun
, vol.305
, pp. 271-277
-
-
Aono, J.1
-
80
-
-
33646383590
-
Recent advances in understanding the mechanism of action of bisphosphonates
-
Coxon, F.P., Thompson, K. and. Rogers, M.J. (2006) Recent advances in understanding the mechanism of action of bisphosphonates. Curr Opin Pharmacol 6, 307-312
-
(2006)
Curr Opin Pharmacol
, vol.6
, pp. 307-312
-
-
Coxon, F.P.1
Thompson, K.2
Rogers, M.J.3
-
81
-
-
33846932080
-
Extra-skeletal effects of bisphosponates
-
Corrado, A., Santoro, N. and Cantatore, F.P. (2007) Extra-skeletal effects of bisphosponates. Joint Bone Spine 74, 32-38
-
(2007)
Joint Bone Spine
, vol.74
, pp. 32-38
-
-
Corrado, A.1
Santoro, N.2
Cantatore, F.P.3
-
82
-
-
31744441494
-
Pharmacological therapy of Paget's and other metabolic bone diseases
-
Hoskins, D. (2006) Pharmacological therapy of Paget's and other metabolic bone diseases. Bone 38, Suppl 2, 3-7
-
(2006)
Bone
, vol.38
, Issue.SUPPL. 2
, pp. 3-7
-
-
Hoskins, D.1
-
83
-
-
33846219426
-
Clinical determinants of quality of life in Paget's disease of bone
-
Langston, A.L. et al. (2007) Clinical determinants of quality of life in Paget's disease of bone. Calcif Tissue Int 80, 1-9
-
(2007)
Calcif Tissue Int
, vol.80
, pp. 1-9
-
-
Langston, A.L.1
-
84
-
-
18844386517
-
Mechanism of osteoclast mediated bone resorption-rationale for the design of new therapeutics
-
Vaananen, K. (2005) Mechanism of osteoclast mediated bone resorption-rationale for the design of new therapeutics. Adv Drug Deliv Rev 57, 959-971
-
(2005)
Adv Drug Deliv Rev
, vol.57
, pp. 959-971
-
-
Vaananen, K.1
-
85
-
-
33748199511
-
OPG/membranous-RANKL complex is internalized via the clathrin pathway before a lysosomal and a proteasomal degradation
-
Tat, S.K. et al. (2006) OPG/membranous-RANKL complex is internalized via the clathrin pathway before a lysosomal and a proteasomal degradation. Bone 39, 706-715
-
(2006)
Bone
, vol.39
, pp. 706-715
-
-
Tat, S.K.1
-
86
-
-
33344469853
-
Denosumab in postmenopausal women with low bone mineral density
-
McClung, M.R. et al. (2006) Denosumab in postmenopausal women with low bone mineral density. N Engl J Med 354, 821-831
-
(2006)
N Engl J Med
, vol.354
, pp. 821-831
-
-
McClung, M.R.1
-
87
-
-
24044504089
-
Recombinant osteoprotegerin for juvenile Paget's disease
-
Cundy, T. et al. (2005) Recombinant osteoprotegerin for juvenile Paget's disease. N Engl J Med 353, 918-923
-
(2005)
N Engl J Med
, vol.353
, pp. 918-923
-
-
Cundy, T.1
-
88
-
-
34247848058
-
Clinical and cellular phenotypes associated with Sequestosome 1 (SQSTM1) mutations
-
Leach, R.J. et al. (2006) Clinical and cellular phenotypes associated with Sequestosome 1 (SQSTM1) mutations. J Bone Miner Res 21, Suppl 2, 45-50
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
, pp. 45-50
-
-
Leach, R.J.1
-
89
-
-
34247861003
-
Sequestosome 1: Mutation frequencies, haplotypes and phenotypes in familial Paget's disease of bone
-
Morisette, J., Laurin, N. and. Brown, J.P. (2006) Sequestosome 1: mutation frequencies, haplotypes and phenotypes in familial Paget's disease of bone. J Bone Miner Res 21, Suppl 2, 38-44
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
, pp. 38-44
-
-
Morisette, J.1
Laurin, N.2
Brown, J.P.3
-
90
-
-
33846009075
-
Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease
-
Kurihara, N. et al. (2007) Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease. J Clin Invest 117, 133-142
-
(2007)
J Clin Invest
, vol.117
, pp. 133-142
-
-
Kurihara, N.1
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