"Collagen Type VII" 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.
A non-fibrillar collagen involved in anchoring the epidermal BASEMENT MEMBRANE to underlying tissue. It is a homotrimer comprised of C-terminal and N-terminal globular domains connected by a central triple-helical region.
| Descriptor ID |
D024143
|
| MeSH Number(s) |
D12.776.860.300.250.400.300
|
| Concept/Terms |
Procollagen Type VII- Procollagen Type VII
- Type VII, Procollagen
- Type VII Procollagen
- Procollagen, Type VII
|
Below are MeSH descriptors whose meaning is more general than "Collagen Type VII".
Below are MeSH descriptors whose meaning is more specific than "Collagen Type VII".
This graph shows the total number of publications written about "Collagen Type VII" by people in this website by year, and whether "Collagen Type VII" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 3 | 0 | 3 |
| 2018 | 1 | 1 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Collagen Type VII" by people in Profiles.
-
Genotype-Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care Centre. Acta Derm Venereol. 2018 Oct 10; 98(9):873-879.
-
Autoimmune Subepidermal Bullous Diseases of the Skin and Mucosae: Clinical Features, Diagnosis, and Management. Clin Rev Allergy Immunol. 2018 Feb; 54(1):26-51.
-
Identical COL71A1 heterozygous mutations resulting in different dystrophic epidermolysis bullosa phenotypes. Pediatr Dermatol. 2018 Mar; 35(2):e94-e98.
-
Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis. Br J Dermatol. 2017 12; 177(6):1683-1692.
-
High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well-matched antibody panel. Australas J Dermatol. 2018 Feb; 59(1):73-76.
-
Prospective studies on the routine use of a novel multivariant enzyme-linked immunosorbent assay for the diagnosis of autoimmune bullous diseases. J Am Acad Dermatol. 2017 May; 76(5):889-894.e5.
-
TALEN-based gene correction for epidermolysis bullosa. Mol Ther. 2013 Jun; 21(6):1151-9.