"Mice, Neurologic Mutants" 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 which carry mutant genes for neurologic defects or abnormalities.
| Descriptor ID |
D008818
|
| MeSH Number(s) |
B01.050.150.900.649.313.992.635.505.500.550.480
|
| Concept/Terms |
Mice, Neurologic Mutants- Mice, Neurologic Mutants
- Mouse, Neurological Mutant
- Mouse, Neurologic Mutant
- Mutant Mouse, Neurologic
- Neurologic Mutant Mouse
- Neurologic Mutant Mice
- Mice, Neurologic Mutant
- Mutant Mice, Neurologic
- Mice, Neurological Mutants
- Neurological Mutant Mouse
Lurcher Mice- Lurcher Mice
- Mice, Lurcher
- Lurcher Mouse
- Mouse, Lurcher
Weaver Mouse- Weaver Mouse
- Mouse, Weaver
- Weaver Mice
- Mice, Weaver
Reeler Mice- Reeler Mice
- Mice, Reeler
- Reeler Mouse
- Mouse, Reeler
Staggerer Mice- Staggerer Mice
- Mice, Staggerer
- Staggerer Mouse
- Mouse, Staggerer
Chakragati Mice- Chakragati Mice
- Mice, Chakragati
- Chakragati Mouse
- Mouse, Chakragati
- ckr Mutant Mice
- Mice, ckr Mutant
- Mutant Mice, ckr
Nervous Mice- Nervous Mice
- Mice, Nervous
- Nervous Mouse
- Mouse, Nervous
|
Below are MeSH descriptors whose meaning is more general than "Mice, Neurologic Mutants".
Below are MeSH descriptors whose meaning is more specific than "Mice, Neurologic Mutants".
This graph shows the total number of publications written about "Mice, Neurologic Mutants" by people in this website by year, and whether "Mice, Neurologic Mutants" 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 |
|---|
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 1 | 1 |
| 2001 | 1 | 2 | 3 |
| 2004 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Mice, Neurologic Mutants" by people in Profiles.
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Freeman MR. Signaling mechanisms regulating Wallerian degeneration. Curr Opin Neurobiol. 2014 Aug; 27:224-31.
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Musiek ES, Lim MM, Yang G, Bauer AQ, Qi L, Lee Y, Roh JH, Ortiz-Gonzalez X, Dearborn JT, Culver JP, Herzog ED, Hogenesch JB, Wozniak DF, Dikranian K, Giasson BI, Weaver DR, Holtzman DM, Fitzgerald GA. Circadian clock proteins regulate neuronal redox homeostasis and neurodegeneration. J Clin Invest. 2013 Dec; 123(12):5389-400.
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Jiang Y, Matevossian A, Guo Y, Akbarian S. Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice. Neuropharmacology. 2011 Jun; 60(7-8):1088-97.
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Pedrini S, Sau D, Guareschi S, Bogush M, Brown RH, Naniche N, Kia A, Trotti D, Pasinelli P. ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2. Hum Mol Genet. 2010 Aug 01; 19(15):2974-86.
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Li X, Sapp E, Chase K, Comer-Tierney LA, Masso N, Alexander J, Reeves P, Kegel KB, Valencia A, Esteves M, Aronin N, Difiglia M. Disruption of Rab11 activity in a knock-in mouse model of Huntington's disease. Neurobiol Dis. 2009 Nov; 36(2):374-83.
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Low HP, Gr?co B, Tanahashi Y, Gallant J, Jones SN, Billings-Gagliardi S, Recht LD, Schwartz WJ. Embryonic stem cell rescue of tremor and ataxia in myelin-deficient shiverer mice. J Neurol Sci. 2009 Jan 15; 276(1-2):133-7.
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Rios M, Lambe EK, Liu R, Teillon S, Liu J, Akbarian S, Roffler-Tarlov S, Jaenisch R, Aghajanian GK. Severe deficits in 5-HT2A -mediated neurotransmission in BDNF conditional mutant mice. J Neurobiol. 2006 Mar; 66(4):408-20.
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Kim YJ, Sapp E, Cuiffo BG, Sobin L, Yoder J, Kegel KB, Qin ZH, Detloff P, Aronin N, DiFiglia M. Lysosomal proteases are involved in generation of N-terminal huntingtin fragments. Neurobiol Dis. 2006 May; 22(2):346-56.
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Schafer DP, Bansal R, Hedstrom KL, Pfeiffer SE, Rasband MN. Does paranode formation and maintenance require partitioning of neurofascin 155 into lipid rafts? J Neurosci. 2004 Mar 31; 24(13):3176-85.
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Nystuen A, Legare ME, Shultz LD, Frankel WN. A null mutation in inositol polyphosphate 4-phosphatase type I causes selective neuronal loss in weeble mutant mice. Neuron. 2001 Oct 25; 32(2):203-12.