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124 related items for PubMed ID: 12369779

  • 1. Localization of the mutation responsible for osteopetrosis in the op rat to a 1.5-cM genetic interval on rat chromosome 10: identification of positional candidate genes by radiation hybrid mapping.
    Dobbins DE, Joe B, Hashiramoto A, Salstrom JL, Dracheva S, Ge L, Wilder RL, Remmers EF.
    J Bone Miner Res; 2002 Oct; 17(10):1761-7. PubMed ID: 12369779
    [Abstract] [Full Text] [Related]

  • 2. Localization of the gene responsible for the op (osteopetrotic) defect in rats on chromosome 10.
    Remmers EF, Du Y, Ding YP, Kotake S, Ge L, Zha H, Goldmuntz EA, Hansen C, Wilder RL.
    J Bone Miner Res; 1996 Dec; 11(12):1856-61. PubMed ID: 8970886
    [Abstract] [Full Text] [Related]

  • 3. Localization of the gene causing the osteopetrotic phenotype in the incisors absent (ia) rat on chromosome 10q32.1.
    van Wesenbeeck L, Odgren PR, Mackay CA, Van Hul W.
    J Bone Miner Res; 2004 Feb; 19(2):183-9. PubMed ID: 14969387
    [Abstract] [Full Text] [Related]

  • 4. Mutation of macrophage colony stimulating factor (Csf1) causes osteopetrosis in the tl rat.
    Dobbins DE, Sood R, Hashiramoto A, Hansen CT, Wilder RL, Remmers EF.
    Biochem Biophys Res Commun; 2002 Jun 28; 294(5):1114-20. PubMed ID: 12074592
    [Abstract] [Full Text] [Related]

  • 5. Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) gene.
    Odgren PR, Kim N, van Wesenbeeck L, MacKay C, Mason-Savas A, Safadi FF, Popoff SN, Lengner C, van-Hul W, Choi Y, Marks SC.
    Int J Dev Biol; 2001 Dec 28; 45(8):853-9. PubMed ID: 11804028
    [Abstract] [Full Text] [Related]

  • 6. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
    Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D.
    Genomics; 1998 Nov 15; 54(1):19-30. PubMed ID: 9806826
    [Abstract] [Full Text] [Related]

  • 7. A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps.
    Bihoreau MT, Sebag-Montefiore L, Godfrey RF, Wallis RH, Brown JH, Danoy PA, Collins SC, Rouard M, Kaisaki PJ, Lathrop M, Gauguier D.
    Genomics; 2001 Jul 15; 75(1-3):57-69. PubMed ID: 11472068
    [Abstract] [Full Text] [Related]

  • 8. Osteoclast biology in the osteopetrotic (op) rat.
    Marks SC, Popoff SN.
    Am J Anat; 1989 Dec 15; 186(4):325-34. PubMed ID: 2589217
    [Abstract] [Full Text] [Related]

  • 9. Refined genomic localization of the genetic lesion in the osteopetrosis (op) rat and exclusion of three positional and functional candidate genes, Clcn7, Atp6v0c, and Slc9a3r2.
    Perdu B, Odgren PR, Van Wesenbeeck L, Jennes K, Mackay CC, Van Hul W.
    Calcif Tissue Int; 2009 May 15; 84(5):355-60. PubMed ID: 19259722
    [Abstract] [Full Text] [Related]

  • 10. Human osteopetrosis and other sclerosing disorders: recent genetic developments.
    de Vernejoul MC, Bénichou O.
    Calcif Tissue Int; 2001 Jul 15; 69(1):1-6. PubMed ID: 11685426
    [Abstract] [Full Text] [Related]

  • 11. A gene-based high-resolution comparative radiation hybrid map as a framework for genome sequence assembly of a bovine chromosome 6 region associated with QTL for growth, body composition, and milk performance traits.
    Weikard R, Goldammer T, Laurent P, Womack JE, Kuehn C.
    BMC Genomics; 2006 Mar 16; 7():53. PubMed ID: 16542434
    [Abstract] [Full Text] [Related]

  • 12. [Bones and bone marrow of the newborn " op " osteopetrotic rat, and the early diagnosis of the disease].
    Thillard MJ.
    Ann Anat Pathol (Paris); 1979 Mar 16; 24(2):149-60. PubMed ID: 525845
    [Abstract] [Full Text] [Related]

  • 13. An integrated genetic linkage map with 1,137 markers constructed from five F2 crosses of autoimmune disease-prone and -resistant inbred rat strains.
    Dracheva SV, Remmers EF, Chen S, Chang L, Gulko PS, Kawahito Y, Longman RE, Wang J, Du Y, Shepard J, Ge L, Joe B, Kotake S, Salstrom JL, Furuya T, Hoffman J, Cannon GW, Griffiths MM, Wilder RL.
    Genomics; 2000 Jan 15; 63(2):202-26. PubMed ID: 10673333
    [Abstract] [Full Text] [Related]

  • 14. [Genetic basis for skeletal disease. Molecular advances in sclerosing bone disorders].
    Michigami T.
    Clin Calcium; 2010 Aug 15; 20(8):1196-202. PubMed ID: 20675930
    [Abstract] [Full Text] [Related]

  • 15. Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human.
    Chalhoub N, Benachenhou N, Rajapurohitam V, Pata M, Ferron M, Frattini A, Villa A, Vacher J.
    Nat Med; 2003 Apr 15; 9(4):399-406. PubMed ID: 12627228
    [Abstract] [Full Text] [Related]

  • 16. Osteoclast biology: lessons from mammalian mutations.
    Marks SC.
    Am J Med Genet; 1989 Sep 15; 34(1):43-54. PubMed ID: 2683780
    [Abstract] [Full Text] [Related]

  • 17. [Morphological study of congenital osteopetrosis in op rats].
    Graf B.
    Pathol Biol (Paris); 1985 Feb 15; 33(2):82-9. PubMed ID: 3889786
    [Abstract] [Full Text] [Related]

  • 18. Study of the nonresorptive phenotype of osteoclast-like cells from patients with malignant osteopetrosis: a new approach to investigating pathogenesis.
    Flanagan AM, Sarma U, Steward CG, Vellodi A, Horton MA.
    J Bone Miner Res; 2000 Feb 15; 15(2):352-60. PubMed ID: 10703938
    [Abstract] [Full Text] [Related]

  • 19. Detailed comparative gene map of rat chromosome 1 with mouse and human genomes and physical mapping of an evolutionary chromosomal breakpoint.
    Kaisaki PJ, Rouard M, Danoy PA, Wallis RH, Collins SC, Rice M, Levy ER, Lathrop M, Bihoreau MT, Gauguier D.
    Genomics; 2000 Feb 15; 64(1):32-43. PubMed ID: 10708516
    [Abstract] [Full Text] [Related]

  • 20. A clinical and molecular overview of the human osteopetroses.
    Balemans W, Van Wesenbeeck L, Van Hul W.
    Calcif Tissue Int; 2005 Nov 15; 77(5):263-74. PubMed ID: 16307387
    [Abstract] [Full Text] [Related]

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