A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease - Wikidata - awgldk - TriplyDB

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

http://www.wikidata.org/entity/Q24301216

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A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation Phenotypic and population differences in the association between CILP and lumbar disc disease Regeneration of intervertebral disc by mesenchymal stem cells: potentials, limitations, and future direction Genetic Alterations in Intervertebral Disc Disease Hypoxia-inducible factor regulation of ANK expression in nucleus pulposus cells: possible implications in controlling dystrophic mineralization in the intervertebral disc Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2 Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern Chinese Molecular profiling of the developing mouse axial skeleton: a role for Tgfbr2 in the development of the intervertebral disc.IL-1β increases asporin expression via the NF-κB p65 pathway in nucleus pulposus cells during intervertebral disc degeneration.EMG analysis of lumbar paraspinal muscles as a predictor of the risk of low-back pain.Identification and validation of novel adipokines released from primary human adipocytes Genetic susceptibility of intervertebral disc degeneration among young Finnish adults.Genetic association studies in lumbar disc degeneration: a systematic review Single-nucleotide gene polymorphisms involving cell death pathways: a study of Chinese patients with lumbar disc herniation.Genetic polymorphisms of interleukin-1 alpha and the vitamin d receptor in mexican mestizo patients with intervertebral disc degeneration An ancient autoproteolytic domain found in GAIN, ZU5 and Nucleoporin98 Disc degeneration of cervical spine on MRI in patients with lumbar disc herniation: comparison study with asymptomatic volunteers.Cartilage Intermediate Layer Protein and Asporin Polymorphisms Are Independent Risk Factors of Lumbar Disc Degeneration in Male Collegiate Athletes.Tissue engineering of articular cartilage with biomimetic zones A novel, non-functional, COL1A1 polymorphism is not associated with lumbar disk disease in young male Greek subjects unlike that of the Sp1 site.Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation.Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis.An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration.The postnatal role of Sox9 in cartilage.Association between the -1306C/T polymorphism of matrix metalloproteinase-2 gene and lumbar disc disease in Chinese young adults.Biological treatment strategies for disc degeneration: potentials and shortcomings.Absence of the mutated Trp2 allele but a common polymorphism of the COL9A2 collagen gene is associated with early recurrence after lumbar discectomy in a German population.Mesenchymal stem cells: potential application in intervertebral disc regeneration.A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation.Genetics of disc degeneration.Prevention of disc degeneration with growth factors.Association of the asporin D14 allele with lumbar-disc degeneration in Asians Genetic polymorphisms associated with intervertebral disc degeneration.Advances in susceptibility genetics of intervertebral degenerative disc disease.Genetic Factors in Intervertebral Disc Degeneration.Association of the tag SNPs in the human SKT gene (KIAA1217) with lumbar disc herniation.Evidence update-association between CILP and degeneration of the intervertebral disc: a meta-analysis DNA variations in human and medical genetics: 25 years of my experience.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 population

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P2860

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

http://www.wikidata.org/entity/Q24301216

description

2005 nî lūn-bûn

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2005 թուականի Յունիսին հրատարակուած գիտական յօդուած

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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Nature Genetics

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A functional SNP in CILP, enco ...... ibility to lumbar disc disease

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Futoshi Mio

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Hideki Kizawa

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Ikuko Masuda

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Kazuhiro Chiba

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Masaki Mori

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Michihiro Kamata

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Shiro Ikegawa

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Shoji Seki

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Takeshi Oya

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Tatsuhiko Tsunoda

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P2860

Assessing the impact of population stratification on genetic association studies

One of two chondrocyte-expressed isoforms of cartilage intermediate-layer protein functions as an insulin-like growth factor 1 antagonist

Cloning and deduced amino acid sequence of a novel cartilage protein (CILP) identifies a proform including a nucleotide pyrophosphohydrolase

An allele of COL9A2 associated with intervertebral disc disease

Nonoperative treatment of herniated lumbar intervertebral disc with radiculopathy. An outcome study

An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis

Transforming growth factor beta receptor induction in herniated intervertebral disc tissue: an immunohistochemical study

Conditional deletion of the TGF-beta type II receptor in Col2a expressing cells results in defects in the axial skeleton without alterations in chondrocyte differentiation or embryonic development of long bones

Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome

Epidemiological features of chronic low-back pain.

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10.1038/NG1557

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6

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37

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