525 results on '"Eyre, David R."'
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2. Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta
3. Age-related type I collagen modifications reveal tissue-defining differences between ligament and tendon
4. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay
5. A repeated triple lysine motif anchors complexes containing bone sialoprotein and the type XI collagen A1 chain involved in bone mineralization
6. Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome—osteogenesis imperfecta.
7. New insights on the clinical variability of FKBP10 mutations
8. Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasia
9. Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V
10. COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing
11. Analyses of lysine aldehyde cross-linking in collagen reveal that the mature cross-link histidinohydroxylysinonorleucine is an artifact
12. Growth characteristics in individuals with osteogenesis imperfecta in North America: results from a multicenter study
13. Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies
14. Glycation of type I collagen selectively targets the same helical domain lysine sites as lysyl oxidase–mediated cross-linking
15. P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA
16. Collagen cross-linking and bone pathobiology
17. List of Contributors
18. Collagens of the Disc
19. A Mutation in the Alpha 3 Chain of type IX Collagen Causes Autosomal Dominant Multiple Epiphyseal Dysplasia with Mild Myopathy
20. HIF-1α metabolically controls collagen synthesis and modification in chondrocytes
21. The development of a mature collagen network in cartilage from human bone marrow stem cells in Transwell culture
22. Mmp14 is required for matrisome homeostasis and circadian rhythm in fibroblasts
23. Post-translationally Abnormal Collagens of Prolyl 3-Hydroxylase-2 Null Mice Offer a Pathobiological Mechanism for the High Myopia Linked to Human LEPREL1 Mutations
24. Increased C-telopeptide Cross-linking of Tendon Type I Collagen in Fibromodulin-deficient Mice
25. Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform
26. Biochemical Markers as Surrogate End Points of Joint Disease
27. Collagen Cross-Links
28. Collagen cross-links as markers of bone and cartilage degradation
29. A Role for Prolyl 3-Hydroxylase 2 in Post-translational Modification of Fibril-forming Collagens
30. A Novel 3-Hydroxyproline (3Hyp)-rich Motif Marks the Triple-helical C Terminus of Tendon Type I Collagen
31. Mmp14 is required for matrisome homeostasis and circadian rhythm in fibroblasts
32. Type III Collagen, a Fibril Network Modifier in Articular Cartilage
33. Maturation of Collagen Ketoimine Cross-links by an Alternative Mechanism to Pyridinoline Formation in Cartilage
34. Location of 3-Hydroxyproline Residues in Collagen Types I, II, III, and V/XI Implies a Role in Fibril Supramolecular Assembly
35. Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
36. Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta
37. Molecular alterations due to Col5a1 Haploinsufficiency in a mouse model of classic Ehlers Danlos syndrome
38. Differences in Chain Usage and Cross-linking Specificities of Cartilage Type V/XI Collagen Isoforms with Age and Tissue
39. Collagen: Molecular Diversity in the Body's Protein Scaffold
40. Isolation of a Murine Osteoclast Colony-Stimulating Factor
41. Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta
42. Reducible Crosslinks in Hydroxylysine-Deficient Collagens of a Heritable Disorder of Connective Tissue
43. Advances in collagen cross-link analysis
44. Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13
45. Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene
46. Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding
47. Tendon and motor phenotypes in the Crtap-/- mouse model of recessive osteogenesis imperfecta
48. The post-translational phenotype of collagen synthesized by SAOS-2 osteosarcoma cells
49. Collagen XI chain misassembly in cartilage of the chondrodysplasia ( cho) mouse
50. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta
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