"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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1995 | 1 | 15 | 16 |
1996 | 1 | 21 | 22 |
1997 | 0 | 17 | 17 |
1998 | 0 | 16 | 16 |
1999 | 0 | 35 | 35 |
2000 | 1 | 43 | 44 |
2001 | 0 | 40 | 40 |
2002 | 1 | 64 | 65 |
2003 | 0 | 88 | 88 |
2004 | 0 | 64 | 64 |
2005 | 0 | 62 | 62 |
2006 | 1 | 94 | 95 |
2007 | 0 | 98 | 98 |
2008 | 0 | 94 | 94 |
2009 | 0 | 110 | 110 |
2010 | 0 | 128 | 128 |
2011 | 0 | 151 | 151 |
2012 | 0 | 138 | 138 |
2013 | 0 | 163 | 163 |
2014 | 0 | 174 | 174 |
2015 | 0 | 176 | 176 |
2016 | 0 | 148 | 148 |
2017 | 0 | 136 | 136 |
2018 | 0 | 156 | 156 |
2019 | 0 | 135 | 135 |
2020 | 0 | 161 | 161 |
2021 | 0 | 131 | 131 |
2022 | 0 | 29 | 29 |
2023 | 0 | 39 | 39 |
2024 | 23 | 86 | 109 |
2025 | 1 | 13 | 14 |
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Below are the most recent publications written about "Mice, Inbred C57BL" by people in Profiles.
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Non-invasive real-time pulsed Doppler assessment of blood flow in mouse ophthalmic artery. Cell Rep Methods. 2025 Feb 24; 5(2):100983.
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In vivo expansion of gene-targeted hepatocytes through transient inhibition of an essential gene. Sci Transl Med. 2025 Feb 12; 17(785):eadk3920.
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Neuronal Network Activation Induced by Forniceal Deep Brain Stimulation in Mice. Genes (Basel). 2025 Feb 09; 16(2).
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Targeting Tiam1 Enhances Hippocampal-Dependent Learning and Memory in the Adult Brain and Promotes NMDA Receptor-Mediated Synaptic Plasticity and Function. J Neurosci. 2025 Feb 05; 45(6).
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Moderating carbohydrate digestion rate in mice promotes fat oxidation and metabolic flexibility revealed through a new approach to assess metabolic substrate utilization. Eur J Nutr. 2025 Feb 04; 64(2):83.
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Altered thermal preference by preoptic estrogen receptor alpha neurons in postpartum females. Mol Metab. 2025 Mar; 93:102108.
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Comparative Single-Cell Analysis Reveals Tendon Progenitor Dysfunction by Age-Associated Oxidative Stress and Its Restoration by Antioxidant Treatments. J Cell Physiol. 2025 Feb; 240(2):e70016.
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Rational design of a Lfng-enhancer AAV construct drives specific and efficient gene expression in inner ear supporting cells. Hear Res. 2025 Mar; 458:109203.
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Sex Differences in Response to Diet Enriched With Glutathione Precursors in the Aging Heart. J Gerontol A Biol Sci Med Sci. 2025 Jan 16; 80(2).
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ACE2 Enhances Sensitivity to PD-L1 Blockade by Inhibiting Macrophage-Induced Immunosuppression and Angiogenesis. Cancer Res. 2025 Jan 15; 85(2):299-313.