These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 25664955)

  • 1. 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]  

  • 2. 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]  

  • 3. Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family.
    Falchetti A; Di Stefano M; Marini F; Del Monte F; Gozzini A; Masi L; Tanini A; Amedei A; Carossino A; Isaia G; Brandi ML
    Arthritis Res Ther; 2005; 7(6):R1289-95. PubMed ID: 16277682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone.
    Gennari L; Gianfrancesco F; Di Stefano M; Rendina D; Merlotti D; Esposito T; Gallone S; Fusco P; Rainero I; Fenoglio P; Mancini M; Martini G; Bergui S; De Filippo G; Isaia G; Strazzullo P; Nuti R; Mossetti G
    J Bone Miner Res; 2010 Jun; 25(6):1375-84. PubMed ID: 20200946
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial Paget disease and SQSTM1 mutations in New Zealand.
    Cundy T; Naot D; Bava U; Musson D; Tong PC; Bolland M
    Calcif Tissue Int; 2011 Sep; 89(3):258-64. PubMed ID: 21735147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences.
    Hocking LJ; Lucas GJ; Daroszewska A; Cundy T; Nicholson GC; Donath J; Walsh JP; Finlayson C; Cavey JR; Ciani B; Sheppard PW; Searle MS; Layfield R; Ralston SH
    J Bone Miner Res; 2004 Jul; 19(7):1122-7. PubMed ID: 15176995
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. The Implications of the Sequestosome 1 Mutation P392L in Patients with Paget's Disease in a United States Cohort.
    Seton M; Hansen M; Solomon DH
    Calcif Tissue Int; 2016 May; 98(5):489-96. PubMed ID: 26713335
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations.
    Eekhoff EW; Karperien M; Houtsma D; Zwinderman AH; Dragoiescu C; Kneppers AL; Papapoulos SE
    Arthritis Rheum; 2004 May; 50(5):1650-4. PubMed ID: 15146436
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.
    Morissette J; Laurin N; Brown JP
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P38-44. PubMed ID: 17229007
    [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. Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations.
    Peeters JJM; De Ridder R; Hamoen EC; Eekhoff EMW; Smit F; Boudin E; Van Hul W; Papapoulos SE; Appelman-Dijkstra NM
    Bone; 2019 Nov; 128():115044. PubMed ID: 31449886
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.