A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation
about
A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth diseaseBiochemistry and molecular biology of gelatinase B or matrix metalloproteinase-9 (MMP-9): the next decadePeriventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneA novel catechol-O-methyltransferase variant associated with human disc degeneration.Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomesPharmacogenetic associations of MMP9 and MMP12 variants with cardiovascular disease in patients with hypertension.Genetic susceptibility of intervertebral disc degeneration among young Finnish adults.Role of functional single nucleotide polymorphisms of MMP1, MMP2, and MMP9 in open angle glaucomasGenetic association studies in lumbar disc degeneration: a systematic reviewEvidence for an inherited predisposition to lumbar disc disease.Genetic polymorphisms of interleukin-1 alpha and the vitamin d receptor in mexican mestizo patients with intervertebral disc degenerationDisc degeneration of cervical spine on MRI in patients with lumbar disc herniation: comparison study with asymptomatic volunteers.Matrix metalloproteinase-9 genetic variation and primary angle closure glaucoma in a Caucasian population.The thrombospondins.Thrombospondin-2 deficiency in growing mice alters bone collagen ultrastructure and leads to a brittle bone phenotype.Expression levels of IL-17 and TNF-α in degenerated lumbar intervertebral discs and their correlation.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.Association of the tag SNPs in the human SKT gene (KIAA1217) with lumbar disc herniation.Current evidence for a modulation of low back pain by human genetic variants.Progression of lumbar spinal stenosis is influenced by polymorphism of thrombospondin 2 gene in the Korean populationGenetics of disc-related disorders: current findings and lessons from other complex diseases.Invoking the power of thrombospondins: regulation of thrombospondins expressionTranslational research of herniated discs: current status of diagnosis and treatmentGenetic aspects of intervertebral disc degeneration.2,2',4,4'-Tetrabromodiphenyl ether promotes human neuroblastoma SH-SY5Y cells migration via the GPER/PI3K/Akt signal pathway.MiR-1246 promotes SiHa cervical cancer cell proliferation, invasion, and migration through suppression of its target gene thrombospondin 2.Biological functions of fucose in mammals.Hemostatic and Wound Healing Properties of Chromolaena odorata Leaf ExtractIdentification of critical genes in nucleus pulposus cells isolated from degenerated intervertebral discs using bioinformatics analysis.Variants within the COMP and THBS2 genes are not associated with Achilles tendinopathy in a case-control study of South African and Australian populations.Contributions of aryl hydrocarbon receptor genetic variants to the risk of glioma and PAH-DNA adducts.Meta-analysis of the effects of genetic polymorphisms on intervertebral disc degeneration.Assessment of interaction between maternal polycyclic aromatic hydrocarbons exposure and genetic polymorphisms on the risk of congenital heart diseases.A genetic variant in COL11A1 is functionally associated with lumbar disc herniation in Chinese population.Polymorphisms in aryl hydrocarbon receptor gene are associated with idiopathic male factor infertility.Transcriptome and alternative splicing analysis of nucleus pulposus cells in response to high oxygen tension: Involvement of high oxygen tension in the pathogenesis of intervertebral disc degeneration.MMP2, MMP9 and TIMP2 polymorphisms affect sperm parameters but not fertility in Polish males.Association analysis between thrombospondin-2 gene polymorphisms and intervertebral disc degeneration in a Chinese Han population.A common polymorphism of COMT was associated with symptomatic lumbar disc herniation based on a large sample with Chinese Han ancestry
P2860
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P2860
A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A functional polymorphism in T ...... ed with lumbar-disc herniation
@ast
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en-gb
A functional polymorphism in T ...... ed with lumbar-disc herniation
@nl
type
label
A functional polymorphism in T ...... ed with lumbar-disc herniation
@ast
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en-gb
A functional polymorphism in T ...... ed with lumbar-disc herniation
@nl
prefLabel
A functional polymorphism in T ...... ed with lumbar-disc herniation
@ast
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en-gb
A functional polymorphism in T ...... ed with lumbar-disc herniation
@nl
P2093
P2860
P1476
A functional polymorphism in T ...... ed with lumbar-disc herniation
@en
P2093
Atsushi Miyake
Atsushi Takahashi
Futoshi Mio
Hiroshi Mizuta
Kazuhiro Chiba
Masahiro Nakajima
Shiro Ikegawa
Takeshi Miyamoto
Tatsuki Karasugi
Tatsuya Furuichi
P2860
P304
P356
10.1016/J.AJHG.2008.03.013
P407
P577
2008-05-01T00:00:00Z