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REFERENCES

  • 1
    van Staa TP, Selby P, Leufkens HG, Lyles K, Sprafka JM, Cooper C 2002 Incidence and natural history of Paget's disease of bone in England and Wales. J Bone Miner Res 17: 465471.
  • 2
    Siris ES, Ottman R, Flaster E, Kelsey JL 1991 Familial aggregation of Paget's disease of bone. J Bone Miner Res 6: 495500.
  • 3
    Sofaer JA, Holloway SM, Emery AE 1983 A family study of Paget's disease of bone. J Epidemiol Community Health 37: 226231.
  • 4
    Hughes AE, Shearman AM, Weber JL, Barr RJ, Wallace RG, Osterberg PH, Nevin NC, Mollan RA 1994 Genetic linkage of familial expansile osteolysis to chromosome 18q. Hum Mol Genet 3: 359361.
  • 5
    Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH 1998 Paget's disease of bone: Evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity. J Bone Miner Res 13: 911917.
  • 6
    Cody JD, Singer FR, Roodman GD, Otterund B, Lewis TB, Leppert M, Leach RJ 1997 Genetic linkage of Paget disease of the bone to chromosome 18q. Am J Hum Genet 61: 11171122.
  • 7
    Laurin N, Brown JP, Lemainque A, Duchesne A, Huot D, Lacourciere Y, Drapeau G, Verreault J, Raymond V, Morissette J 2001 Paget disease of bone: Mapping of two loci at 5q35-qter and 5q31. Am J Hum Genet 69: 528543.
  • 8
    Hocking LJ, Herbert CA, Nicholls RK, Williams F, Bennett ST, Cundy T, Nicholson GC, Wuyts W, Van Hul W, Ralston SH 2001 Genomewide search in familial paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35. Am J Hum Genet 69: 10551061.
  • 9
    Good DA, Busfield F, Fletcher BH, Duffy DL, Kesting JB, Andersen J, Shaw JT 2001 Linkage of Paget disease of bone to a novel region on human chromosome 18q23. Am J Hum Genet 70: 517525.
  • 10
    Laurin N, Brown JP, Morissette J, Raymond V 2002 Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone. Am J Hum Genet 70: 15821588.
  • 11
    Hocking LJ, Lucas GJA, Daroszewska A, Mangion J, Olavesen M, Nicholson GC, Ward L, Bennett ST, Wuyts W, Van Hul W, Ralston BH 2002 Domain specific mutations in Sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease. Hum Mol Genet 11: 27352739.
  • 12
    Johnson-Pais TL, Wisdom JH, Weldon KS, Cody JD, Hansen MF, Singer FR, Leach RJ 2003 Three novel mutations in SQSTM1 identified in familial Paget's disease of bone. J Bone Miner Res 18: 17481753.
  • 13
    Hocking L, Slee F, Cundy T, Nicholson G, Van Hul W, Ralston SH 2000 Familial Paget's disease of bone: Patterns of inheritance and frequency of linkage to chromosome 18q. Bone 26: 577580.
  • 14
    Ciani B, Layfield R, Cavey JR, Sheppard PW, Searle MS 2003 Structure of the UBA domain of p62 (SQSTM1) and implications for mutations which cause Paget's disease of bone. J Biol Chem 278: 3740937412.
  • 15
    Mueller TD, Feigon J 2002 Solution structures of UBA domains reveal a conserved hydrophobic surface for protein-protein interactions. J Mol Biol 319: 12431255.
  • 16
    Good D, Busfield F, Duffy D, Lovelock PK, Kesting JB, Cameron DP, Shaw JT 2001 Familial Paget's disease of bone: Nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigree. J Bone Miner Res 16: 3338.
  • 17
    Friedrichs WE, Reddy SV, Singer FR, Roodman GD 2002 The pro and con of measles virus in Paget's disease: Pro. J Bone Miner Res 17: 2293.
  • 18
    Rima BK, Gassen U, Helfrich MH, Ralston SH 2002 The pro and con of measles virus in Paget's disease: Con. J Bone Miner Res 17: 22902292.