Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex.
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Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaLack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingProlyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bonesProlyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complexA novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfectaExome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfectaNull mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfectaProlyl 4-hydroxylaseProtein folding and quality control in the EROsteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formationDifferential effects of collagen prolyl 3-hydroxylation on skeletal tissuesStructural and functional analysis of Nro1/Ett1: a protein involved in translation termination in S. cerevisiae and in O2-mediated gene control in S. pombeCrystal structures of wild-type and mutated cyclophilin B that causes hyperelastosis cutis in the American quarter horseSevere osteogenesis imperfecta in cyclophilin B-deficient miceProlyl 3-hydroxylase-1 null mice exhibit hearing impairment and abnormal morphology of the middle ear bone joints.Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.Generalized connective tissue disease in Crtap-/- mouse.Location of 3-hydroxyproline residues in collagen types I, II, III, and V/XI implies a role in fibril supramolecular assembly.Identification of Conus peptidylprolyl cis-trans isomerases (PPIases) and assessment of their role in the oxidative folding of conotoxins.Insights on the evolution of prolyl 3-hydroxylation sites from comparative analysis of chicken and Xenopus fibrillar collagens.Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta.An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1·cartilage-associated protein·cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.Mechano-regulation of collagen biosynthesis in periodontal ligament.A novel 3-hydroxyproline (3Hyp)-rich motif marks the triple-helical C terminus of tendon type I collagen.Chaperoning osteogenesis: new protein-folding disease paradigms.Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes.Osteogenesis Imperfecta: A Review with Clinical Examples.Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap(-/-) Mice, a Model of Recessive Osteogenesis Imperfecta.Posttranslational modifications in type I collagen from different tissues extracted from wild type and prolyl 3-hydroxylase 1 null mice.PPIB mutations cause severe osteogenesis imperfecta.Proteomic analysis of cellular soluble proteins from human bronchial smooth muscle cells by combining nondenaturing micro 2DE and quantitative LC-MS/MS. 2. Similarity search between protein maps for the analysis of protein complexes.Collagen prolyl 3-hydroxylation: a major role for a minor post-translational modification?An overview of cyclophilins in human cancers.New perspectives on osteogenesis imperfectaRecessive osteogenesis imperfecta: clinical, radiological, and molecular findings.The many functions of the endoplasmic reticulum chaperones and folding enzymes.Pharmacological and biological therapeutic strategies for osteogenesis imperfecta.EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta.
P2860
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P2860
Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Biochemical characterization o ...... protein.cyclophilin B complex.
@en
type
label
Biochemical characterization o ...... protein.cyclophilin B complex.
@en
prefLabel
Biochemical characterization o ...... protein.cyclophilin B complex.
@en
P2093
P2860
P356
P1476
Biochemical characterization o ...... protein.cyclophilin B complex
@en
P2093
Hans Peter Bächinger
Janice A Vranka
Kazuhiro Nagata
Yoshihiro Ishikawa
P2860
P304
17641-17647
P356
10.1074/JBC.M109.007070
P407
P577
2009-05-06T00:00:00Z