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3. An inbred line of transgenic mice expressing an internally deleted gene for type II procollagen (COL2A1). Young mice have a variable phenotype of a chondrodysplasia and older mice have osteoarthritic changes in joints. Helminen HJ, Kiraly K, Pelttari A, Tammi MI, Vandenberg P, Pereira R, Dhulipala R, Khillan JS, Ala-Kokko L, Hume EL. J Clin Invest; 1993 Aug; 92(2):582-95. PubMed ID: 8349798 [Abstract] [Full Text] [Related]
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9. Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytes. Freisinger P, Ala-Kokko L, LeGuellec D, Franc S, Bouvier R, Ritvaniemi P, Prockop DJ, Bonaventure J. J Biol Chem; 1994 May 06; 269(18):13663-9. PubMed ID: 8175802 [Abstract] [Full Text] [Related]
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13. Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia. Vandenberg P, Khillan JS, Prockop DJ, Helminen H, Kontusaari S, Ala-Kokko L. Proc Natl Acad Sci U S A; 1991 Sep 01; 88(17):7640-4. PubMed ID: 1881905 [Abstract] [Full Text] [Related]
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18. Ultrastructural localization of collagen types II, IX, and XI in the growth plate of human rib and fetal bovine epiphyseal cartilage: type XI collagen is restricted to thin fibrils. Keene DR, Oxford JT, Morris NP. J Histochem Cytochem; 1995 Oct 01; 43(10):967-79. PubMed ID: 7560887 [Abstract] [Full Text] [Related]