Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex
about
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaA 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 imperfectaOsteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formationNew genes in bone development: what's new in osteogenesis imperfectaDifferential effects of collagen prolyl 3-hydroxylation on skeletal tissuesGeneralized connective tissue disease in Crtap-/- mouse.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.New perspectives on osteogenesis imperfectaRecessive osteogenesis imperfecta: clinical, radiological, and molecular findings.Heat shock protein 47 and 65 KDa FK506 binding protein weakly but synergistically interact during collagen folding in the endoplasmic reticulum.Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization.Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective.Mathematical model for bone mineralization.The ciliary Evc/Evc2 complex interacts with Smo and controls Hedgehog pathway activity in chondrocytes by regulating Sufu/Gli3 dissociation and Gli3 trafficking in primary cilia.Osteogenesis imperfecta and therapeutics.Severe osteogenesis imperfecta caused by a small in-frame deletion in CRTAP.Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype-phenotype correlations
P2860
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P2860
Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին 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
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@ast
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en-gb
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@nl
type
label
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@ast
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en-gb
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@nl
prefLabel
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@ast
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en-gb
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@nl
P2093
P2860
P921
P356
P1476
Prolyl 3-hydroxylase 1 and CRT ...... prolyl 3-hydroxylation complex
@en
P2093
Joan C Marini
Joann N Bodurtha
Wayne A Cabral
Weizhong Chang
P2860
P304
P356
10.1093/HMG/DDP481
P407
P577
2009-10-21T00:00:00Z