"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 3 | 3 |
| 1997 | 0 | 14 | 14 |
| 1998 | 0 | 10 | 10 |
| 1999 | 0 | 12 | 12 |
| 2000 | 0 | 21 | 21 |
| 2001 | 0 | 11 | 11 |
| 2002 | 0 | 12 | 12 |
| 2003 | 0 | 19 | 19 |
| 2004 | 0 | 19 | 19 |
| 2005 | 0 | 15 | 15 |
| 2006 | 0 | 11 | 11 |
| 2007 | 0 | 11 | 11 |
| 2008 | 0 | 7 | 7 |
| 2009 | 0 | 7 | 7 |
| 2010 | 0 | 6 | 6 |
| 2011 | 0 | 7 | 7 |
| 2012 | 0 | 7 | 7 |
| 2013 | 0 | 4 | 4 |
| 2014 | 0 | 3 | 3 |
| 2015 | 0 | 5 | 5 |
| 2016 | 0 | 5 | 5 |
| 2017 | 0 | 3 | 3 |
| 2018 | 0 | 6 | 6 |
| 2019 | 0 | 3 | 3 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 2 | 2 |
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click here.
Below are the most recent publications written about "COS Cells" by people in Profiles.
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Molecular determinants for a-tubulin methylation by SETD2. J Biol Chem. 2021 07; 297(1):100898.
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Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension. Nat Commun. 2021 03 04; 12(1):1444.
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Nuclear receptor SHP dampens transcription function and abrogates mitotic chromatin association of PXR and ERa via intermolecular interactions. Biochim Biophys Acta Gene Regul Mech. 2021 03; 1864(3):194683.
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LRRTM4 is a member of the transsynaptic complex between rod photoreceptors and bipolar cells. J Comp Neurol. 2021 01; 529(1):221-233.
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Early prediction of phenotypic severity in Citrullinemia Type 1. Ann Clin Transl Neurol. 2019 09; 6(9):1858-1871.
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Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling. Clin Sci (Lond). 2019 01 31; 133(2):225-238.
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Thrombospondin-3 augments injury-induced cardiomyopathy by intracellular integrin inhibition and sarcolemmal instability. Nat Commun. 2019 01 08; 10(1):76.
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Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Nat Commun. 2018 10 26; 9(1):4455.
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De novo design of a fluorescence-activating ?-barrel. Nature. 2018 09; 561(7724):485-491.
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?IV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy. Am J Hum Genet. 2018 06 07; 102(6):1158-1168.