Collagen Type IX

"Collagen Type IX" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A fibril-associated collagen usually found crosslinked to the surface of COLLAGEN TYPE II fibrils. It is a heterotrimer containing alpha1(IX), alpha2(IX) and alpha3(IX) subunits.

Descriptor ID

D024081

MeSH Number(s)

D12.776.860.300.250.400.550.200

Concept/Terms

Collagen Type IX

Procollagen Type IX

Collagen Type IX, alpha3 Subunit

Collagen Type IX, alpha1 Subunit

Collagen Type IX, alpha2 Subunit

Below are MeSH descriptors whose meaning is more general than "Collagen Type IX".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Scleroproteins [D12.776.860]
Extracellular Matrix Proteins [D12.776.860.300]
Collagen [D12.776.860.300.250]
Non-Fibrillar Collagens [D12.776.860.300.250.400]
Fibril-Associated Collagens [D12.776.860.300.250.400.550]
Collagen Type IX [D12.776.860.300.250.400.550.200]

Below are MeSH descriptors whose meaning is related to "Collagen Type IX".

Below are MeSH descriptors whose meaning is more specific than "Collagen Type IX".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Collagen Type IX" by people in Harvard Catalyst Profiles by year, and whether "Collagen Type IX" was a major or minor topic of these publication.

Below are the most recent publications written about "Collagen Type IX" by people in Profiles.

Genetic testing results of children suspected to have Stickler syndrome type collagenopathy after ocular examination. Mol Genet Genomic Med. 2021 05; 9(5):e1628.

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MRI Phenotyping of COL9A2/Trp2 and COL9A3/Trp3 Alleles in Lumbar Disc Disease: A Case-control Study in South-Western Iranian Population Reveals a Significant Trp3-Disease Association in Males. Spine (Phila Pa 1976). 2016 Nov 01; 41(21):1661-1667.

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CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. PLoS One. 2013; 8(3):e59061.

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Skeletal abnormalities in mice lacking extracellular matrix proteins, thrombospondin-1, thrombospondin-3, thrombospondin-5, and type IX collagen. Am J Pathol. 2008 Jun; 172(6):1664-74.

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Early-onset degeneration of the intervertebral disc and vertebral end plate in mice deficient in type IX collagen. Arthritis Rheum. 2008 Jan; 58(1):164-71.

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Structural and functional characterization of recombinant matrilin-3 A-domain and implications for human genetic bone diseases. J Biol Chem. 2007 Nov 30; 282(48):34634-43.

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Regulation of skeletogenic differentiation in cranial dermal bone. Development. 2007 Sep; 134(17):3133-44.

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Expression of cartilage-related genes in bovine synovial tissue. J Orthop Res. 2007 Jun; 25(6):813-9.

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Age-dependent increase of discoidin domain receptor 2 and matrix metalloproteinase 13 expression in temporomandibular joint cartilage of type IX and type XI collagen-deficient mice. Arch Oral Biol. 2007 Jun; 52(6):579-84.

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Pathogenesis of osteoarthritis-like changes in the joints of mice deficient in type IX collagen. Arthritis Rheum. 2006 Sep; 54(9):2891-900.

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