"COS Cells" 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.
CELL LINES derived from the CV-1 cell line by transformation with a replication origin defective mutant of SV40 VIRUS, which codes for wild type large T antigen (ANTIGENS, POLYOMAVIRUS TRANSFORMING). They are used for transfection and cloning. (The CV-1 cell line was derived from the kidney of an adult male African green monkey (CERCOPITHECUS AETHIOPS).)
| Descriptor ID |
D019556
|
| MeSH Number(s) |
A11.251.210.172.500 A11.329.228.220
|
| Concept/Terms |
COS Cells- COS Cells
- COS Cell
- Cell, COS
- Cells, COS
COS-7 Cells- COS-7 Cells
- COS 7 Cells
- COS-7 Cell
- Cell, COS-7
- Cells, COS-7
COS-1 Cells- COS-1 Cells
- COS 1 Cells
- COS-1 Cell
- Cell, COS-1
- Cells, COS-1
|
Below are MeSH descriptors whose meaning is more general than "COS Cells".
Below are MeSH descriptors whose meaning is more specific than "COS Cells".
This graph shows the total number of publications written about "COS Cells" by people in this website by year, and whether "COS Cells" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "COS Cells" by people in Profiles.
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Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy. Invest Ophthalmol Vis Sci. 2019 11 01; 60(14):4811-4819.
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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nat Genet. 2015 Aug; 47(8):926-32.