Chaperoning osteogenesis: new protein-folding disease paradigms.
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Endoplasmic Reticulum Stress and Unfolded Protein Response in Cartilage Pathophysiology; Contributing Factors to Apoptosis and Osteoarthritis.Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.Decreasing maternal myostatin programs adult offspring bone strength in a mouse model of osteogenesis imperfectaPulse-chase analysis of procollagen biosynthesis by azidohomoalanine labeling.Osteogenesis imperfecta model peptides: incorporation of residues replacing Gly within a triple helix achieved by renucleation and local flexibilityMolecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta.Mapping the Effect of Gly Mutations in Collagen on α2β1 Integrin Binding.A novel transgenic mouse model of growth plate dysplasia reveals that decreased chondrocyte proliferation due to chronic ER stress is a key factor in reduced bone growth.Recessive osteogenesis imperfecta: clinical, radiological, and molecular findings.Classification of osteogenesis imperfecta.Heat shock protein 47 and 65 KDa FK506 binding protein weakly but synergistically interact during collagen folding in the endoplasmic reticulum.The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta.Pharmacological and biological therapeutic strategies for osteogenesis imperfecta.Osteoblast Malfunction Caused by Cell Stress Response to Procollagen Misfolding in α2(I)-G610C Mouse Model of Osteogenesis Imperfecta.A substrate preference for the rough endoplasmic reticulum resident protein FKBP22 during collagen biosynthesis.A small-molecule compound inhibits a collagen-specific molecular chaperone and could represent a potential remedy for fibrosis.4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion.Cellular and molecular characterization of a novel primary osteoblast culture from the vertebrate model organism Xenopus tropicalis.Osteogenesis imperfecta and therapeutics.Noncanonical autophagy at ER exit sites regulates procollagen turnover
P2860
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P2860
Chaperoning osteogenesis: new protein-folding disease paradigms.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Chaperoning osteogenesis: new protein-folding disease paradigms.
@ast
Chaperoning osteogenesis: new protein-folding disease paradigms.
@en
Chaperoning osteogenesis: new protein-folding disease paradigms.
@nl
type
label
Chaperoning osteogenesis: new protein-folding disease paradigms.
@ast
Chaperoning osteogenesis: new protein-folding disease paradigms.
@en
Chaperoning osteogenesis: new protein-folding disease paradigms.
@nl
prefLabel
Chaperoning osteogenesis: new protein-folding disease paradigms.
@ast
Chaperoning osteogenesis: new protein-folding disease paradigms.
@en
Chaperoning osteogenesis: new protein-folding disease paradigms.
@nl
P2860
P1476
Chaperoning osteogenesis: new protein-folding disease paradigms
@en
P2093
Elena Makareeva
Nydea A Aviles
P2860
P304
P356
10.1016/J.TCB.2010.11.007
P577
2010-12-21T00:00:00Z