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	1.	G76E substitution in type I collagen is the first nonlethal glutamic acid substitution in the alpha1(I) chain and alters folding of the N-terminal end of the helix. [electronic resource] by Cabral, W A Chernoff, E J Marini, J C Producer: 20010621 In: Molecular genetics and metabolism vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II. [electronic resource] by Bouma, P Cabral, W A Cole, W G Marini, J C Producer: 20010531 In: The Journal of biological chemistry vol. 276 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Biochemical screening of type I collagen in osteogenesis imperfecta: detection of glycine substitutions in the amino end of the alpha chains requires supplementation by molecular analysis. [electronic resource] by Cabral, W A Milgrom, S Letocha, A D Moriarty, E Marini, J C Producer: 20061227 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	High-level expression of the human CB2 cannabinoid receptor using a baculovirus system. [electronic resource] by Nowell, K W Pettit, D A Cabral, W A Zimmerman, H W Abood, M E Cabral, G A Producer: 19980831 In: Biochemical pharmacology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Cortical bone properties in the Brtl/+ mouse model of Osteogenesis imperfecta as evidenced by acoustic transmission microscopy. [electronic resource] by Blouin, S Fratzl-Zelman, N Roschger, A Cabral, W A Klaushofer, K Marini, J C Fratzl, P Roschger, P Producer: 20200210 In: Journal of the mechanical behavior of biomedical materials vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Three novel type I collagen mutations in osteogenesis imperfecta type IV probands are associated with discrepancies between electrophoretic migration of osteoblast and fibroblast collagen. [electronic resource] by Sarafova, A P Choi, H Forlino, A Gajko, A Cabral, W A Tosi, L Reing, C M Marini, J C Producer: 19980709 In: Human mutation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Heterogeneous basis of the type VIB form of Ehlers-Danlos syndrome (EDS VIB) that is unrelated to decreased collagen lysyl hydroxylation. [electronic resource] by Walker, L C Overstreet, M A Willing, M C Marini, J C Cabral, W A Pals, G Bristow, J Atsawasuwan, P Yamauchi, M Yeowell, Heather N Producer: 20050505 In: American journal of medical genetics. Part A vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. [electronic resource] by Valli, M Barnes, A M Gallanti, A Cabral, W A Viglio, S Weis, M A Makareeva, E Eyre, D Leikin, S Antoniazzi, F Marini, J C Mottes, M Producer: 20130321 In: Clinical genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)