BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 21986510)

  • 1. Paget's disease of bone: an update.
    Naot D
    Curr Opin Endocrinol Diabetes Obes; 2011 Dec; 18(6):352-8. PubMed ID: 21986510
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathogenesis of Paget's disease of bone.
    Ralston SH
    Bone; 2008 Nov; 43(5):819-25. PubMed ID: 18672105
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Paget's disease of bone: evidence for complex pathogenetic interactions.
    Chung PY; Van Hul W
    Semin Arthritis Rheum; 2012 Apr; 41(5):619-41. PubMed ID: 21959292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.
    Lucas GJ; Hocking LJ; Daroszewska A; Cundy T; Nicholson GC; Walsh JP; Fraser WD; Meier C; Hooper MJ; Ralston SH
    J Bone Miner Res; 2005 Feb; 20(2):227-31. PubMed ID: 15647816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic epidemiology of Paget's disease of bone in italy: sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone.
    Falchetti A; Di Stefano M; Marini F; Ortolani S; Ulivieri MF; Bergui S; Masi L; Cepollaro C; Benucci M; Di Munno O; Rossini M; Adami S; Del Puente A; Isaia G; Torricelli F; Brandi ML;
    Calcif Tissue Int; 2009 Jan; 84(1):20-37. PubMed ID: 19067022
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evolution of Paget's disease of bone in adults inheriting SQSTM1 mutations.
    Cundy T; Rutland MD; Naot D; Bolland M
    Clin Endocrinol (Oxf); 2015 Sep; 83(3):315-9. PubMed ID: 25664955
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Development of a molecular test of Paget's disease of bone.
    Guay-Bélanger S; Simonyan D; Bureau A; Gagnon E; Albert C; Morissette J; Siris ES; Orcel P; Brown JP; Michou L
    Bone; 2016 Mar; 84():213-221. PubMed ID: 26772620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Paget's disease of bone: clinical review and update.
    Bolland MJ; Cundy T
    J Clin Pathol; 2013 Nov; 66(11):924-7. PubMed ID: 24043712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone.
    Merchant A; Smielewska M; Patel N; Akunowicz JD; Saria EA; Delaney JD; Leach RJ; Seton M; Hansen MF
    J Bone Miner Res; 2009 Mar; 24(3):484-94. PubMed ID: 19016598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations.
    Collet C; Michou L; Audran M; Chasseigneaux S; Hilliquin P; Bardin T; Lemaire I; Cornélis F; Launay JM; Orcel P; Laplanche JL
    J Bone Miner Res; 2007 Feb; 22(2):310-7. PubMed ID: 17129171
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mechanisms of disease: genetics of Paget's disease of bone and related disorders.
    Daroszewska A; Ralston SH
    Nat Clin Pract Rheumatol; 2006 May; 2(5):270-7. PubMed ID: 16932700
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetics of Paget's disease of bone.
    Daroszewska A; Ralston SH
    Clin Sci (Lond); 2005 Sep; 109(3):257-63. PubMed ID: 16104845
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Three novel mutations in SQSTM1 identified in familial Paget's disease of bone.
    Johnson-Pais TL; Wisdom JH; Weldon KS; Cody JD; Hansen MF; Singer FR; Leach RJ
    J Bone Miner Res; 2003 Oct; 18(10):1748-53. PubMed ID: 14584883
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States.
    Rhodes EC; Johnson-Pais TL; Singer FR; Ankerst DP; Bruder JM; Wisdom J; Hoon DS; Lin E; Bone HG; Simcic KJ; Leach RJ
    Calcif Tissue Int; 2008 Apr; 82(4):271-7. PubMed ID: 18379713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Epidemiogenetic study of French families with Paget's disease of bone.
    Michou L; Collet C; Morissette J; Audran M; Thomas T; Gagnon E; Launay JM; Laplanche JL; Brown JP; Orcel P
    Joint Bone Spine; 2012 Jul; 79(4):393-8. PubMed ID: 21962384
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel SQSTM1 mutations in patients with Paget's disease of bone in an unrelated multiethnic American population.
    Michou L; Morissette J; Gagnon ER; Marquis A; Dellabadia M; Brown JP; Siris ES
    Bone; 2011 Mar; 48(3):456-60. PubMed ID: 21073987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Paget's disease: epidemiology and pathophysiology.
    Seton M
    Curr Osteoporos Rep; 2008 Dec; 6(4):125-9. PubMed ID: 19032921
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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).
    Falchetti A; Di Stefano M; Marini F; Del Monte F; Mavilia C; Strigoli D; De Feo ML; Isaia G; Masi L; Amedei A; Cioppi F; Ghinoi V; Bongi SM; Di Fede G; Sferrazza C; Rini GB; Melchiorre D; Matucci-Cerinic M; Brandi ML
    J Bone Miner Res; 2004 Jun; 19(6):1013-7. PubMed ID: 15125799
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding.
    Rea SL; Walsh JP; Ward L; Magno AL; Ward BK; Shaw B; Layfield R; Kent GN; Xu J; Ratajczak T
    J Bone Miner Res; 2009 Jul; 24(7):1216-23. PubMed ID: 19257822
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations.
    Bolland MJ; Tong PC; Naot D; Callon KE; Wattie DJ; Gamble GD; Cundy T
    J Bone Miner Res; 2007 Mar; 22(3):411-5. PubMed ID: 17181397
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.