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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

106 related items for PubMed ID: 7842010

  • 21. A dominant negative mutation in the alpha 1 (X) collagen gene produces spondylometaphyseal defects in mice.
    Jacenko O, LuValle P, Solum K, Olsen BR.
    Prog Clin Biol Res; 1993; 383B():427-36. PubMed ID: 8115362
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  • 26. Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.
    Mundlos S, Olsen BR.
    FASEB J; 1997 Mar; 11(4):227-33. PubMed ID: 9068611
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  • 28. Development dependent collagen gene expression in the rat cranial base growth plate.
    Römer P, Weingärtner J, Roldán JC, Proff P, Reicheneder C.
    Ann Anat; 2010 Aug 20; 192(4):205-9. PubMed ID: 20591638
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  • 29. Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function.
    Kwan KM, Pang MK, Zhou S, Cowan SK, Kong RY, Pfordte T, Olsen BR, Sillence DO, Tam PP, Cheah KS.
    J Cell Biol; 1997 Jan 27; 136(2):459-71. PubMed ID: 9015315
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