"Mice, Mutant Strains" 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.
Mice bearing mutant genes which are phenotypically expressed in the animals.
| Descriptor ID |
D008817
|
| MeSH Number(s) |
B01.050.150.900.649.313.992.635.505.500.550
|
| Concept/Terms |
Mice, Mutant Strains- Mice, Mutant Strains
- Mutant Strains Mice
- Strains Mice, Mutant
- Mutant Mouse Strain
- Mouse Strain, Mutant
- Mouse Strains, Mutant
- Mutant Mouse Strains
- Strain, Mutant Mouse
- Strains, Mutant Mouse
- Mutant Strains of Mice
- Mice Mutant Strain
- Mice Mutant Strains
- Mouse, Mutant Strain
- Mutant Strain Mouse
- Strain Mouse, Mutant
- Mutant Strain of Mouse
- Mouse Mutant Strain
- Mouse Mutant Strains
|
Below are MeSH descriptors whose meaning is more general than "Mice, Mutant Strains".
Below are MeSH descriptors whose meaning is more specific than "Mice, Mutant Strains".
- Mice, Mutant Strains
- Mice, 129 Strain
- Mice, Biozzi
- Mice, Hairless
- Mice, Inbred mdx
- Mice, Jimpy
- Mice, Knockout
- Mice, Neurologic Mutants
- Mice, Nude
- Mice, Obese
- Mice, Quaking
- Mice, SCID
This graph shows the total number of publications written about "Mice, Mutant Strains" by people in this website by year, and whether "Mice, Mutant Strains" 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 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 1 | 2 |
| 2008 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Mice, Mutant Strains" by people in Profiles.
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Pain insensitivity: distal S6-segment mutations in NaV1.9 emerge as critical hotspot. Neurogenetics. 2017 07; 18(3):179-181.
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Specification of tissue-resident macrophages during organogenesis. Science. 2016 09 09; 353(6304).
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Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina. Hum Mol Genet. 2015 Mar 15; 24(6):1584-601.
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Loss of p19Arf in a Rag1(-/-) B-cell precursor population initiates acute B-lymphoblastic leukemia. Blood. 2011 Jul 21; 118(3):544-53.
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Interference with PPARgamma signaling causes cerebral vascular dysfunction, hypertrophy, and remodeling. Hypertension. 2008 Apr; 51(4):867-71.
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Crosstalk between keratinocytes and adaptive immune cells in an IkappaBalpha protein-mediated inflammatory disease of the skin. Immunity. 2007 Aug; 27(2):296-307.
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One step generation of fully chimeric antibodies using Cgamma1- and Ckappa mutant mice. J Immunother. 2007 Apr; 30(3):338-49.
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Expression of the basic helix-loop-factor Olig2 in the developing retina: Olig2 as a new marker for retinal progenitors and late-born cells. Gene Expr Patterns. 2007 Jan; 7(1-2):57-65.
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Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice. J Neurochem. 1999 Apr; 72(4):1580-5.
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Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J Biol Chem. 1996 Jan 05; 271(1):283-8.
MeSH information
