MARVEL Domain-Containing Proteins
"MARVEL Domain-Containing Proteins" 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 family of proteins that share a domain with a four transmembrane-helix architecture referred to as the MARVEL domain. The MARVEL domain proteins play important role in vesicular trafficking and in the formation of TIGHT JUNCTIONS.
| Descriptor ID |
D062792
|
| MeSH Number(s) |
D12.776.543.488
|
| Concept/Terms |
MARVEL Domain-Containing Proteins- MARVEL Domain-Containing Proteins
- Domain-Containing Proteins, MARVEL
- MARVEL Domain Containing Proteins
- Proteins, MARVEL Domain-Containing
- Mal and Related Proteins for Vesicle Trafficking and Membrane Link Domain Proteins
- MARVEL Domain Proteins
|
Below are MeSH descriptors whose meaning is more general than "MARVEL Domain-Containing Proteins".
Below are MeSH descriptors whose meaning is more specific than "MARVEL Domain-Containing Proteins".
This graph shows the total number of publications written about "MARVEL Domain-Containing Proteins" by people in this website by year, and whether "MARVEL Domain-Containing Proteins" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
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Below are the most recent publications written about "MARVEL Domain-Containing Proteins" by people in Profiles.
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Energy status dictates PD-L1 protein abundance and anti-tumor immunity to enable checkpoint blockade. Mol Cell. 2021 06 03; 81(11):2317-2331.e6.
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Co-expression of sperm membrane proteins CMTM2A and CMTM2B is essential for ADAM3 localization and male fertility in mice. J Cell Sci. 2018 10 08; 131(19).
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Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. Circ Cardiovasc Genet. 2010 Jun; 3(3):248-55.
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Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect. Ann Neurol. 2006 Feb; 59(2):398-403.