"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.
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Year | Major Topic | Minor Topic | Total |
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1993 | 0 | 4 | 4 |
1994 | 0 | 6 | 6 |
1995 | 0 | 6 | 6 |
1996 | 0 | 3 | 3 |
1997 | 0 | 4 | 4 |
1998 | 0 | 6 | 6 |
1999 | 0 | 3 | 3 |
2000 | 0 | 6 | 6 |
2001 | 0 | 4 | 4 |
2002 | 0 | 10 | 10 |
2003 | 0 | 13 | 13 |
2004 | 0 | 16 | 16 |
2005 | 0 | 20 | 20 |
2006 | 0 | 23 | 23 |
2007 | 0 | 28 | 28 |
2008 | 0 | 29 | 29 |
2009 | 0 | 27 | 27 |
2010 | 0 | 43 | 43 |
2011 | 0 | 39 | 39 |
2012 | 0 | 56 | 56 |
2013 | 0 | 50 | 50 |
2014 | 0 | 53 | 53 |
2015 | 0 | 48 | 48 |
2016 | 0 | 51 | 51 |
2017 | 0 | 53 | 53 |
2018 | 0 | 48 | 48 |
2019 | 0 | 47 | 47 |
2020 | 0 | 54 | 54 |
2021 | 0 | 54 | 54 |
2022 | 0 | 20 | 20 |
2023 | 0 | 6 | 6 |
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Below are the most recent publications written about "Mice, Inbred C57BL" by people in Profiles.
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Progressive cognitive impairment after recovery from neuroinvasive and non-neuroinvasive Listeria monocytogenes infection. Front Immunol. 2023; 14:1146690.
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The Role of C-X-C Chemokines in Staphylococcus aureus Endophthalmitis. Invest Ophthalmol Vis Sci. 2023 Mar 01; 64(3):10.
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Combining ASBT inhibitor and FGF15 treatments enhances therapeutic efficacy against cholangiopathy in female but not male Cyp2c70 KO mice. J Lipid Res. 2023 03; 64(3):100340.
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Wheat Germ Supplementation Reduces Inflammation and Gut Epithelial Barrier Dysfunction in Female Interleukin-10 Knockout Mice Fed a Pro-Atherogenic Diet. J Nutr. 2023 03; 153(3):870-879.
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Osteopontin contributes to virus resistance associated with type I IFN expression, activation of downstream ifn-inducible effector genes, and CCR2+CD115+CD206+ macrophage infiltration following ocular HSV-1 infection of mice. Front Immunol. 2022; 13:1028341.
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Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Lab Invest. 2021 10; 101(10):1382-1393.
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Cardiomyocyte PAI-1 influences the cardiac transcriptome and limits the extent of cardiac fibrosis in response to left ventricular pressure overload. Cell Signal. 2023 04; 104:110555.
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Prolactin-Induced Protein facilitates corneal wound healing. Exp Eye Res. 2022 Dec; 225:109300.
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Localized ablative immunotherapy drives de novo CD8+ T-cell responses to poorly immunogenic tumors. J Immunother Cancer. 2022 Oct; 10(10).
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Melanocortin receptor agonist melanotan-II microinjected in the nucleus accumbens decreases appetitive and consumptive responding for food. Neuropeptides. 2022 Dec; 96:102289.