"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 |
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1995 | 0 | 5 | 5 |
1996 | 0 | 4 | 4 |
1997 | 0 | 7 | 7 |
1998 | 0 | 8 | 8 |
1999 | 0 | 6 | 6 |
2000 | 0 | 8 | 8 |
2001 | 0 | 5 | 5 |
2002 | 0 | 9 | 9 |
2003 | 0 | 13 | 13 |
2004 | 0 | 14 | 14 |
2005 | 0 | 20 | 20 |
2006 | 0 | 20 | 20 |
2007 | 0 | 27 | 27 |
2008 | 0 | 31 | 31 |
2009 | 0 | 27 | 27 |
2010 | 0 | 41 | 41 |
2011 | 0 | 39 | 39 |
2012 | 0 | 47 | 47 |
2013 | 0 | 55 | 55 |
2014 | 0 | 60 | 60 |
2015 | 0 | 49 | 49 |
2016 | 0 | 53 | 53 |
2017 | 0 | 48 | 48 |
2018 | 0 | 55 | 55 |
2019 | 0 | 51 | 51 |
2020 | 0 | 56 | 56 |
2021 | 0 | 57 | 57 |
2022 | 0 | 18 | 18 |
2023 | 0 | 11 | 11 |
2024 | 7 | 34 | 41 |
2025 | 3 | 25 | 28 |
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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-mouse atlas of intrarenal myeloid cells identifies conserved disease-associated macrophages in lupus nephritis. J Exp Med. 2025 Nov 03; 222(11).
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Tropism and Retinal Transduction Efficiency of Adeno-Associated Virus Serotypes in Mice. Invest Ophthalmol Vis Sci. 2025 Sep 02; 66(12):18.
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RIPK3 Contributes to Thyroid Hormone-Induced Photoreceptor Degeneration. Int J Mol Sci. 2025 Aug 22; 26(17).
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Unconventional myosin VI is involved in regulation of muscle energy metabolism. Am J Physiol Cell Physiol. 2025 Oct 01; 329(4):C1004-C1021.
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Role of MiR-204 in controlling metabolic functions of the subretinal microglia. Theranostics. 2025; 15(17):8952-8963.
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Cutting edge: Extrinsic and intrinsic sex effects differentially regulate pulmonary ILC2 numbers, phenotype, and function. J Immunol. 2025 Aug 01; 214(8):1891-1897.
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Vagal Stimulation Rescues HFpEF by Altering Cardiac Resident Macrophage Function. Circ Res. 2025 Aug 15; 137(5):664-681.
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CYP1B1 knockout enhanced IFN-? production is required but not sufficient for protection of cigarette smoke-exposed mice against lethal influenza virus infection. Front Immunol. 2025; 16:1600025.
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Dhdds T206A and Dhdds K42E knock-in mouse models of retinitis pigmentosa 59 are phenotypically similar. Dis Model Mech. 2025 Jul 01; 18(7).
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S1PR1 regulates lymphatic valve development and tertiary lymphoid organ formation in the ileum. J Exp Med. 2025 Sep 01; 222(9).