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

216 related items for PubMed ID: 12116252

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

  • 2. A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene.
    Balemans W, Cleiren E, Siebers U, Horst J, Van Hul W.
    Bone; 2005 Jun; 36(6):943-7. PubMed ID: 15869924
    [Abstract] [Full Text] [Related]

  • 3. Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.
    Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W.
    J Med Genet; 2002 Feb; 39(2):91-7. PubMed ID: 11836356
    [Abstract] [Full Text] [Related]

  • 4. SOST/sclerostin, an osteocyte-derived negative regulator of bone formation.
    van Bezooijen RL, ten Dijke P, Papapoulos SE, Löwik CW.
    Cytokine Growth Factor Rev; 2005 Jun; 16(3):319-27. PubMed ID: 15869900
    [Abstract] [Full Text] [Related]

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

  • 6. Identification of the disease-causing gene in sclerosteosis--discovery of a novel bone anabolic target?
    Balemans W, Van Hul W.
    J Musculoskelet Neuronal Interact; 2004 Jun; 4(2):139-42. PubMed ID: 15615113
    [Abstract] [Full Text] [Related]

  • 7.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Appelman-Dijkstra N, Van Lierop A, Papapoulos S.
    ; 1993 Jun. PubMed ID: 36508511
    [Abstract] [Full Text] [Related]

  • 8. Bone morphogenetic proteins and their antagonists: the sclerostin paradigm.
    van Bezooijen RL, Papapoulos SE, Löwik CW.
    J Endocrinol Invest; 2005 Jun; 28(8 Suppl):15-7. PubMed ID: 16323824
    [Abstract] [Full Text] [Related]

  • 9. Genetics of Sost/SOST in sclerosteosis and van Buchem disease animal models.
    Sebastian A, Loots GG.
    Metabolism; 2018 Mar; 80():38-47. PubMed ID: 29080811
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.
    Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ.
    Am J Hum Genet; 1998 Feb; 62(2):391-9. PubMed ID: 9463328
    [Abstract] [Full Text] [Related]

  • 12. Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites.
    Uitterlinden AG, Arp PP, Paeper BW, Charmley P, Proll S, Rivadeneira F, Fang Y, van Meurs JB, Britschgi TB, Latham JA, Schatzman RC, Pols HA, Brunkow ME.
    Am J Hum Genet; 2004 Dec; 75(6):1032-45. PubMed ID: 15514891
    [Abstract] [Full Text] [Related]

  • 13. Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genes.
    Borra VM, Waterval JJ, Stokroos RJ, Manni JJ, Van Hul W.
    Calcif Tissue Int; 2013 Jul; 93(1):93-100. PubMed ID: 23640157
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease.
    Loots GG, Kneissel M, Keller H, Baptist M, Chang J, Collette NM, Ovcharenko D, Plajzer-Frick I, Rubin EM.
    Genome Res; 2005 Jul; 15(7):928-35. PubMed ID: 15965026
    [Abstract] [Full Text] [Related]

  • 16. SOST is a target gene for PTH in bone.
    Keller H, Kneissel M.
    Bone; 2005 Aug; 37(2):148-58. PubMed ID: 15946907
    [Abstract] [Full Text] [Related]

  • 17. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
    Masmoudi S, Charfedine I, Rebeh IB, Rebai A, Tlili A, Ghorbel AM, Belguith H, Petit C, Drira M, Ayadi H.
    Clin Genet; 2004 Oct; 66(4):358-64. PubMed ID: 15355440
    [Abstract] [Full Text] [Related]

  • 18. A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin.
    Kim CA, Honjo R, Bertola D, Albano L, Oliveira L, Jales S, Siqueira J, Castilho A, Balemans W, Piters E, Jennes K, Van Hul W.
    Genet Test; 2008 Dec; 12(4):475-9. PubMed ID: 19072561
    [Abstract] [Full Text] [Related]

  • 19. Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility.
    Speckman RA, Wright Daw JA, Helms C, Duan S, Cao L, Taillon-Miller P, Kwok PY, Menter A, Bowcock AM.
    Hum Genet; 2003 Jan; 112(1):34-41. PubMed ID: 12483297
    [Abstract] [Full Text] [Related]

  • 20. First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin function.
    Piters E, Culha C, Moester M, Van Bezooijen R, Adriaensen D, Mueller T, Weidauer S, Jennes K, de Freitas F, Löwik C, Timmermans JP, Van Hul W, Papapoulos S.
    Hum Mutat; 2010 Jul; 31(7):E1526-43. PubMed ID: 20583295
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.