"Mice, Inbred C57BL" 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.
One of the first INBRED MOUSE STRAINS to be sequenced. This strain is commonly used as genetic background for transgenic mouse models. Refractory to many tumors, this strain is also preferred model for studying role of genetic variations in development of diseases.
| Descriptor ID |
D008810
|
| MeSH Number(s) |
B01.050.050.199.520.520.420 B01.050.150.900.649.313.992.635.505.500.400.420
|
| Concept/Terms |
Mice, Inbred C57BL- Mice, Inbred C57BL
- C57BL Mice, Inbred
- Inbred C57BL Mice
- Mouse, Inbred C57BL
- C57BL Mouse, Inbred
- Inbred C57BL Mouse
- Mice, C57BL
- C57BL Mice
- Mouse, C57BL
- C57BL Mouse
|
Below are MeSH descriptors whose meaning is more general than "Mice, Inbred C57BL".
Below are MeSH descriptors whose meaning is more specific than "Mice, Inbred C57BL".
This graph shows the total number of publications written about "Mice, Inbred C57BL" by people in this website by year, and whether "Mice, Inbred C57BL" 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 |
|---|
| 1994 | 0 | 3 | 3 |
| 1995 | 0 | 8 | 8 |
| 1996 | 0 | 2 | 2 |
| 1997 | 0 | 4 | 4 |
| 1998 | 0 | 4 | 4 |
| 1999 | 0 | 4 | 4 |
| 2000 | 0 | 5 | 5 |
| 2001 | 0 | 10 | 10 |
| 2002 | 0 | 8 | 8 |
| 2003 | 0 | 11 | 11 |
| 2004 | 0 | 9 | 9 |
| 2005 | 0 | 15 | 15 |
| 2006 | 0 | 14 | 14 |
| 2007 | 0 | 17 | 17 |
| 2008 | 0 | 10 | 10 |
| 2009 | 0 | 15 | 15 |
| 2010 | 0 | 23 | 23 |
| 2011 | 0 | 17 | 17 |
| 2012 | 0 | 24 | 24 |
| 2013 | 0 | 26 | 26 |
| 2014 | 0 | 18 | 18 |
| 2015 | 0 | 23 | 23 |
| 2016 | 0 | 44 | 44 |
| 2017 | 0 | 653 | 653 |
| 2018 | 0 | 607 | 607 |
| 2019 | 0 | 192 | 192 |
| 2020 | 1 | 44 | 45 |
| 2021 | 0 | 47 | 47 |
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Below are the most recent publications written about "Mice, Inbred C57BL" by people in Profiles.
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A human cell-based SARS-CoV-2 vaccine elicits potent neutralizing antibody responses and protects mice from SARS-CoV-2 challenge. Emerg Microbes Infect. 2021 Dec; 10(1):1555-1573.
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Prime-boost vaccination of mice and rhesus macaques with two novel adenovirus vectored COVID-19 vaccine candidates. Emerg Microbes Infect. 2021 Dec; 10(1):1002-1015.
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A novel DNA and protein combination COVID-19 vaccine formulation provides full protection against SARS-CoV-2 in rhesus macaques. Emerg Microbes Infect. 2021 Dec; 10(1):342-355.
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Study on mechanism of matrine in treatment of COVID-19 combined with liver injury by network pharmacology and molecular docking technology. Drug Deliv. 2021 Dec; 28(1):325-342.
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Highly susceptible SARS-CoV-2 model in CAG promoter-driven hACE2-transgenic mice. JCI Insight. 2021 10 08; 6(19).
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The histone methyltransferase Ezh2 restrains macrophage inflammatory responses. FASEB J. 2021 10; 35(10):e21843.
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Coronavirus induces diabetic macrophage-mediated inflammation via SETDB2. Proc Natl Acad Sci U S A. 2021 09 21; 118(38).
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Endothelium-protective, histone-neutralizing properties of the polyanionic agent defibrotide. JCI Insight. 2021 09 08; 6(17).
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Qing-Fei-Pai-Du decoction and wogonoside exert anti-inflammatory action through down-regulating USP14 to promote the degradation of activating transcription factor 2. FASEB J. 2021 09; 35(9):e21870.
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Spike protein of SARS-CoV-2 activates macrophages and contributes to induction of acute lung inflammation in male mice. FASEB J. 2021 09; 35(9):e21801.