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COL8A1 encodes one of the two alpha chains of type VIII collagen.
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Lack of collagen VIII (show COX8A Proteins) reduces myofibroblast differentiation and fibrosis and promotes early mortality and left ventricle dilatation in response to pressure overload in mice.
Type VIII (show COX8A Proteins) collagen signals via beta1 integrin and RhoA (show RHOA Proteins) to regulate MMP-2 (show MMP2 Proteins) expression and smooth muscle cell migration.
Type VIII (show COX8A Proteins) collagen mediates vessel wall remodeling after arterial injury and fibrous cap formation in atherosclerosis.
in contrast to diabetic wild-type mice EMT (show ITK Proteins)-like changes were attenuated in diabetic Col8alpha1/alpha2-KO mice, indicating that collagen VIII (show COX8A Proteins) may be 1 of the major inducers of epithelial-to-mesenchymal transition-like changes in kidneys of diabetic wild-type mice
Type VIII (show COX8A Proteins) collagen significantly modulates the effect of TGF-beta1 (show TGFB1 Proteins) on mesangial cells and may therefore play a role in the pathogenesis of diabetic nephropathy.
Crystal structure of mouse alpha1(VIII (show COX8A Proteins))(3) NC1 domain trimer at 1.9 A resolution. Surface of collagen VIII (show COX8A Proteins) NC1 trimer has three strips of partially exposed aromatic residues, likely involved in supramolecular assemblies.
These data indicate that type VIII (show COX8A Proteins) collagen plays an important role in glial scar formation during the repair process by astrocytes.
Smooth muscle cells can modify the matrix microenvironment by producing type VIII (show COX8A Proteins) collagen, using it to overlay type I collagen, and generating a substrate favorable for migration
Downregulation of COL8A1 expression sensitized hepatocarcinoma cells to the action of D-limonene, impeded cell proliferation, and led to decreased invasiveness, indicating that COL8A1 might serve as a target for gene therapy in hepatocarcinoma.
Oxidized phospholipids induce type VIII (show COX8A Proteins) collagen expression and vascular smooth muscle cell migration.
COL8A1 was identified and proved to be correlated with the progression and prognosis of human colon adenocarcinoma, probably through regulating focal adhesion-related pathways.
High COL8A1 level is associated with chronic obstructive pulmonary disease and cancer.
The COL8A1 rs13095226 polymorphism is not associated with nAMD or PCV, which suggesting this gene maybe not a susceptibility gene locus for neovascular age-related macular degeneration (nAMD) or polypoidal choroidal vasculopathy (PCV) in Chinese subjects.
High COL8A1 expression is associated with early loss of kidney function.
Data indicate that complement factor H (CFH (show CFH Proteins)) R1210C and common variants in COL8A1 and RAD51B (show Rad51B Proteins) plus six genes contribute predictive information for advanced macular degeneration (AMD (show AMD1 Proteins)) beyond macular and behavioral phenotypes.
The results are consistent with the proposal that rare CNVs play a role in TS aetiology and suggest a possible role for rearrangements in the COL8A1 and NRXN1 (show NRXN1 Proteins) gene regions.
In addition, eight genes classified as 'second tier' hits in the original study (PAX7 (show PAX7 Proteins), THADA, COL8A1/FILIP1L, DCAF4L2, GADD45G (show GADD45G Proteins), NTN1 (show NTN1 Proteins), RBFOX3 (show RBFOX3 Proteins) and FOXE1 (show FOXE1 Proteins)) showed evidence of linkage and association in this replication sample.
The purpose of this study is to evaluate COL8A1 and COL8A2 (show COL8a2 Proteins) as candidate genes for thin central corneal thickness in human primary open angle glaucoma patients.
The absence of pathogenic mutations identified in the COL8A1 or COL8A2 (show COL8a2 Proteins) genes in affected members of 15 pedigrees with familial FECD (show COL8a2 Proteins) (Fuchs endothelial corneal dystrophy) indicates that other genetic factors are involved.
The absence of pathogenic mutations in COL8A1 and COL8A2 (show COL8a2 Proteins) in patients with keratoconus indicates that other genetic factors are involved in the pathogenesis of this corneal ectatic disorder.
This gene encodes one of the two alpha chains of type VIII collagen. The gene product is a short chain collagen and a major component of the basement membrane of the corneal endothelium. The type VIII collagen fibril can be either a homo- or a heterotrimer. Alternatively spliced transcript variants encoding the same protein have been observed.
collagen, type VIII, alpha 1
, collagen alpha-1(VIII) chain
, procollagen type VIII alpha 1
, procollagen, type VIII, alpha 1
, cell proliferation-inducing protein 41
, collagen VIII, alpha-1 polypeptide
, endothelial collagen
, smooth muscle cell-expressed and macrophage conditioned medium-induced protein smag-64
, alpha 1 type VIII collagen
, collagen VIII
, type VIII collagen alpha 1 chain