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10. Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfecta. Cabral WA; Perdivara I; Weis M; Terajima M; Blissett AR; Chang W; Perosky JE; Makareeva EN; Mertz EL; Leikin S; Tomer KB; Kozloff KM; Eyre DR; Yamauchi M; Marini JC PLoS Genet; 2014 Jun; 10(6):e1004465. PubMed ID: 24968150 [TBL] [Abstract][Full Text] [Related]
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14. Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development. Marini JC; Cabral WA; Barnes AM; Chang W Cell Cycle; 2007 Jul; 6(14):1675-81. PubMed ID: 17630507 [TBL] [Abstract][Full Text] [Related]
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16. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta. Morello R; Bertin TK; Chen Y; Hicks J; Tonachini L; Monticone M; Castagnola P; Rauch F; Glorieux FH; Vranka J; Bächinger HP; Pace JM; Schwarze U; Byers PH; Weis M; Fernandes RJ; Eyre DR; Yao Z; Boyce BF; Lee B Cell; 2006 Oct; 127(2):291-304. PubMed ID: 17055431 [TBL] [Abstract][Full Text] [Related]
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