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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 17229006

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.
    Lucas GJ, Mehta SG, Hocking LJ, Stewart TL, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Watts GD, Ralston SH, Kimonis VE.
    Bone; 2006 Feb; 38(2):280-5. PubMed ID: 16199218
    [Abstract] [Full Text] [Related]

  • 7. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
    Whyte MP.
    Ann N Y Acad Sci; 2006 Apr; 1068():143-64. PubMed ID: 16831914
    [Abstract] [Full Text] [Related]

  • 8. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
    Lucas GJ, Riches PL, Hocking LJ, Cundy T, Nicholson GC, Walsh JP, Ralston SH.
    J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
    [Abstract] [Full Text] [Related]

  • 9. SQSTM1 and Paget's disease of bone.
    Layfield R, Hocking LJ.
    Calcif Tissue Int; 2004 Nov; 75(5):347-57. PubMed ID: 15365659
    [Abstract] [Full Text] [Related]

  • 10. Rare Inherited forms of Paget's Disease and Related Syndromes.
    Ralston SH, Taylor JP.
    Calcif Tissue Int; 2019 May; 104(5):501-516. PubMed ID: 30756140
    [Abstract] [Full Text] [Related]

  • 11. Valosin-containing protein gene mutations: clinical and neuropathologic features.
    Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D.
    Neurology; 2006 Aug 22; 67(4):644-51. PubMed ID: 16790606
    [Abstract] [Full Text] [Related]

  • 12. 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 22; 19(7):1122-7. PubMed ID: 15176995
    [Abstract] [Full Text] [Related]

  • 13. 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 22; 20(2):227-31. PubMed ID: 15647816
    [Abstract] [Full Text] [Related]

  • 14. Genetics and aetiology of Pagetic disorders of bone.
    Helfrich MH, Hocking LJ.
    Arch Biochem Biophys; 2008 May 15; 473(2):172-82. PubMed ID: 18359282
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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 15; 24(7):1216-23. PubMed ID: 19257822
    [Abstract] [Full Text] [Related]

  • 17. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
    Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ, Zhang ZL.
    Bone; 2013 Jan 15; 52(1):9-16. PubMed ID: 23000505
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 18(10):1748-53. PubMed ID: 14584883
    [Abstract] [Full Text] [Related]

  • 19. Mutation screening of the TNFRSF11A gene encoding receptor activator of NF kappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma.
    Sparks AB, Peterson SN, Bell C, Loftus BJ, Hocking L, Cahill DP, Frassica FJ, Streeten EA, Levine MA, Fraser CM, Adams MD, Broder S, Venter JC, Kinzler KW, Vogelstein B, Ralston SH.
    Calcif Tissue Int; 2001 Mar 15; 68(3):151-5. PubMed ID: 11351498
    [Abstract] [Full Text] [Related]

  • 20. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.
    Guinto JB, Ritson GP, Taylor JP, Forman MS.
    Acta Neuropathol; 2007 Jul 15; 114(1):55-61. PubMed ID: 17457594
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.