Reactome | Eyre, DR

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Eyre, DR Show undefined attributes

created	[InstanceEdit:1458406] Jupe, S, 2011-07-21
dbId	1458416
displayName	Eyre, DR
initial	DR
modified	[InstanceEdit:1458439] Jupe, S, 2011-07-21
publications	[LiteratureReference:2127621] Cross-linking in collagen and elastin [LiteratureReference:2566493] Collagen Cross-Links [LiteratureReference:2210330] Covalent cross-linking of the NC1 domain of collagen type IX to collagen type II in cartilage [LiteratureReference:1564182] The cartilage collagens: structural and metabolic studies [LiteratureReference:2161313] Collagen type IX: evidence for covalent linkages to type II collagen in cartilage [LiteratureReference:1564123] All three chains of 1 alpha 2 alpha 3 alpha collagen from hyaline cartilage resist human collagenase [LiteratureReference:2168034] Structural analysis of cross-linking domains in cartilage type XI collagen. Insights on polymeric assembly [LiteratureReference:2210336] Identification of cross-linking sites in bovine cartilage type IX collagen reveals an antiparallel type II-type IX molecular relationship and type IX to type IX bonding [LiteratureReference:1458402] Sites of stromelysin cleavage in collagen types II, IX, X, and XI of cartilage [LiteratureReference:1980259] Location of 3-hydroxyproline residues in collagen types I, II, III, and V/XI implies a role in fibril supramolecular assembly [LiteratureReference:1980176] Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta [LiteratureReference:2002463] Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis [LiteratureReference:1980181] Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta [LiteratureReference:1980173] CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta
schemaClass	Person
surname	Eyre

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