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PUBMED FOR HANDHELDS

Journal Abstract Search

86 related items for PubMed ID: 3070812

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  • 2. Disrupted expression of matrix genes in the growth plate of the mouse cartilage matrix deficiency (cmd) mutant.
    Wai AW, Ng LJ, Watanabe H, Yamada Y, Tam PP, Cheah KS.
    Dev Genet; 1998; 22(4):349-58. PubMed ID: 9664687
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  • 3. Disproportionate micromelia (Dmm): an incomplete dominant mouse dwarfism with abnormal cartilage matrix.
    Brown KS, Cranley RE, Greene R, Kleinman HK, Pennypacker JP.
    J Embryol Exp Morphol; 1981 Apr; 62():165-82. PubMed ID: 7276808
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  • 5. Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1.
    Pace JM, Li Y, Seegmiller RE, Teuscher C, Taylor BA, Olsen BR.
    Dev Dyn; 1997 Jan; 208(1):25-33. PubMed ID: 8989518
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  • 6. Chondrodystrophic mice with coincidental agnathia: evidence for the tongue obstruction hypothesis in cleft palate.
    Clarke L, Hepworth WB, Carey JC, Seegmiller RE.
    Teratology; 1988 Dec; 38(6):565-70. PubMed ID: 3266374
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  • 7. Osteoarthritis-like changes and decreased mechanical function of articular cartilage in the joints of mice with the chondrodysplasia gene (cho).
    Xu L, Flahiff CM, Waldman BA, Wu D, Olsen BR, Setton LA, Li Y.
    Arthritis Rheum; 2003 Sep; 48(9):2509-18. PubMed ID: 13130470
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  • 8. Scanning electron microscopy of cartilage in mice with hereditary chondrodysplasia.
    Seegmiller RE, Monson CB.
    Scan Electron Microsc; 1982 Sep; (Pt 3):1259-67. PubMed ID: 6820573
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  • 11. Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence.
    Ricks JE, Ryder VM, Bridgewater LC, Schaalje B, Seegmiller RE.
    Teratology; 2002 Mar; 65(3):116-20. PubMed ID: 11877774
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  • 12. New genetic approaches to craniofacial growth and malformation in the mouse.
    Brown KS, Yamada Y, Abramczuk J, Kimata K.
    J Craniofac Genet Dev Biol; 1991 Mar; 11(4):357-65. PubMed ID: 1812135
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  • 15. Reduced chondrocyte proliferation and chondrodysplasia in mice lacking the integrin-linked kinase in chondrocytes.
    Terpstra L, Prud'homme J, Arabian A, Takeda S, Karsenty G, Dedhar S, St-Arnaud R.
    J Cell Biol; 2003 Jul 07; 162(1):139-48. PubMed ID: 12835312
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  • 16. Ultrastructural studies of cartilage matrix in mice homozygous for chondrodysplasia.
    Monson CB, Seegmiller RE.
    J Bone Joint Surg Am; 1981 Apr 07; 63(4):637-44. PubMed ID: 6163783
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  • 18. Transgenic mice expressing D469Delta mutated cartilage oligomeric matrix protein (COMP) show growth plate abnormalities and sternal malformations.
    Schmitz M, Niehoff A, Miosge N, Smyth N, Paulsson M, Zaucke F.
    Matrix Biol; 2008 Mar 07; 27(2):67-85. PubMed ID: 17889519
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