Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin, and recruit alphavbeta3 Instead of alpha5beta1 integrin
about
Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenanceExtracellular Matrix and Dermal Fibroblast Function in the Healing WoundIntegrin-mediated signaling induced by simian virus 40 leads to transient uncoupling of cortical actin and the plasma membraneExpression microarray meta-analysis identifies genes associated with Ras/MAPK and related pathways in progression of muscle-invasive bladder transition cell carcinoma.Genes involved in TGF beta1-driven epithelial-mesenchymal transition of renal epithelial cells are topologically related in the human interactome mapHydrolyzed eggshell membrane immobilized on phosphorylcholine polymer supplies extracellular matrix environment for human dermal fibroblasts.Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing lossCoordinate regulation of fibronectin matrix assembly by the plasminogen activator system and vitronectin in human osteosarcoma cells.Diminished type III collagen promotes myofibroblast differentiation and increases scar deposition in cutaneous wound healing.Type III collagen regulates osteoblastogenesis and the quantity of trabecular boneTranscriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility TypeGLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblastsBruch's membrane abnormalities in PRDM5-related brittle cornea syndrome.Minor fibrillar collagens, variable regions alternative splicing, intrinsic disorder, and tyrosine sulfationClinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutationsJoint hypermobility and headache: understanding the glue that binds the two together--part 1.Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations.COL6A5 variants in familial neuropathic chronic itch.Current Therapeutic Approach to Hypertrophic Scars.Fibronectin-dependent collagen I deposition modulates the cell response to fibronectin.Myofibroblast expression in skin wounds is enhanced by collagen III suppression.The shed ectodomain of type XIII collagen associates with the fibrillar fibronectin matrix and may interfere with its assembly in vitro.Extracellular Matrix Reorganization During Wound Healing and Its Impact on Abnormal Scarring.No association between COL3A1, COL6A1 or COL12A1 gene variants and range of motion.Identification of binding partners interacting with the α1-N-propeptide of type V collagen.Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome.Multifaced Roles of the αvβ3 Integrin in Ehlers-Danlos and Arterial Tortuosity Syndromes' Dermal Fibroblasts.The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations.Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene
P2860
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P2860
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin, and recruit alphavbeta3 Instead of alpha5beta1 integrin
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@ast
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en-gb
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@nl
type
label
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@ast
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en-gb
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@nl
prefLabel
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@ast
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en-gb
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@nl
P2093
P921
P3181
P356
P1476
Human fibroblasts with mutatio ...... nstead of alpha5beta1 integrin
@en
P2093
Nicoletta Zoppi
Rita Gardella
Sergio Barlati
P304
P3181
P356
10.1074/JBC.M312609200
P407
P577
2004-04-30T00:00:00Z