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cartilage oligomeric matrix protein


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'cartilage oligomeric matrix protein' can also refer to...

cartilage oligomeric matrix protein

cartilage oligomeric matrix protein

Cartilage oligomeric matrix protein in systemic sclerosis

Trinucleotide Expansion Mutations in the Cartilage Oligomeric Matrix Protein (Comp) Gene

Associations between cartilage oligomeric matrix protein and several articular tissues in early knee joint osteoarthritis

Increased serum levels of cartilage oligomeric matrix protein and bone sialoprotein in rats with collagen arthritis.

Analysis of cartilage oligomeric matrix protein (COMP) in synovial fibroblasts and synovial fluids.

Response of Cartilage Oligomeric Matrix Protein to Monoclonal Antibody Drugs in Patients with Rheumatoid Arthritis Impact of Biological Variability

Serum concentrations of cartilage oligomeric matrix protein, fibrinogen and hyaluronan distinguish inflammation and cartilage destruction in experimental arthritis in rats

Small fragments of cartilage oligomeric matrix protein in synovial fluid and serum as markers for cartilage degradation.

Serum cartilage oligomeric matrix protein and other biomarker profiles in tibiofemoral and patellofemoral osteoarthritis of the knee

HLA DRB1* typing and cartilage oligomeric matrix protein (COMP) as predictors of joint destruction in recent-onset rheumatoid arthritis.

Cytokines, metalloproteinases, their inhibitors and cartilage oligomeric matrix protein: relationship to radiological progression and inflammation in early rheumatoid arthritis. A prospective 5‐year study

Value of serum cartilage oligomeric matrix protein as a prognostic marker of large-joint damage in rheumatoid arthritis—data from the RAPIT study

Up-regulation of Cartilage Oligomeric Matrix Protein Gene Expression by Insulin-like Growth Factor-I Revealed by Real Time Reverse Transcription-Polymerase Chain Reaction

 

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One of the thrombospondin family of proteins (757 aa), present at high levels in the matrix surrounding chondrocytes. There are five identical glycoprotein subunits, each with EGF-like and calcium-binding domains. Mutations cause pseudoachondroplasia or a milder allelic disorder, epiphyseal dysplasia.

Subjects: Chemistry.


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