Collagen Type XI

"Collagen Type XI" 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 fibrillar collagen found primarily in interstitial CARTILAGE. Collagen type XI is heterotrimer containing alpha1(XI), alpha2(XI) and alpha3(XI) subunits.

Descriptor ID

D024161

MeSH Number(s)

D05.750.078.280.300.500

D12.776.860.300.250.300.500

Concept/Terms

Collagen Type XI

Procollagen Type XI

Collagen Type XI, alpha3 Subunit

Collagen Type XI, alpha1 Subunit

Collagen Type XI, alpha2 Subunit

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

Chemicals and Drugs [D]
Macromolecular Substances [D05]
Polymers [D05.750]
Biopolymers [D05.750.078]
Collagen [D05.750.078.280]
Fibrillar Collagens [D05.750.078.280.300]
Collagen Type XI [D05.750.078.280.300.500]
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]
Fibrillar Collagens [D12.776.860.300.250.300]
Collagen Type XI [D12.776.860.300.250.300.500]

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

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

publications

Timeline | Most Recent

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

Below are the most recent publications written about "Collagen Type XI" 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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Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus. Hum Mutat. 2021 01; 42(1):25-30.

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Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37. Genet Med. 2019 04; 21(4):948-954.

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Cephalometrics in Stickler syndrome: Objectification of the typical facial appearance. J Craniomaxillofac Surg. 2016 Jul; 44(7):848-53.

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Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor. Genome Res. 2015 Nov; 25(11):1646-55.

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Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing. Mol Genet Metab. 2014 Nov; 113(3):230-5.

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Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies. Arthritis Rheumatol. 2014 Apr; 66(4):940-9.

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Collagen type XI a1 facilitates head and neck squamous cell cancer growth and invasion. Br J Cancer. 2013 Dec 10; 109(12):3049-56.

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Induction of high temperature requirement A1, a serine protease, by TGF-beta1 in articular chondrocytes of mouse models of OA. Histol Histopathol. 2014 May; 29(5):609-18.

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Hearing impairment in Stickler syndrome: a systematic review. Orphanet J Rare Dis. 2012 Oct 30; 7:84.

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