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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2004 | 2 |
2006 | 1 |
2008 | 1 |
2010 | 1 |
2011 | 1 |
2024 | 0 |
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Large-scale mutagenesis of the mouse to understand the genetic bases of nervous system structure and function.
Brain Res Mol Brain Res. 2004 Dec 20;132(2):105-15. doi: 10.1016/j.molbrainres.2004.09.016.
Brain Res Mol Brain Res. 2004.
PMID: 15582151
Free PMC article.
Review.
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination.
Patton BL, Wang B, Tarumi YS, Seburn KL, Burgess RW.
Patton BL, et al.
J Cell Sci. 2008 May 15;121(Pt 10):1593-604. doi: 10.1242/jcs.015354. Epub 2008 Apr 22.
J Cell Sci. 2008.
PMID: 18430779
Item in Clipboard
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
Kearney JA, Yang Y, Beyer B, Bergren SK, Claes L, Dejonghe P, Frankel WN.
Kearney JA, et al.
Hum Mol Genet. 2006 Mar 15;15(6):1043-8. doi: 10.1093/hmg/ddl019. Epub 2006 Feb 7.
Hum Mol Genet. 2006.
PMID: 16464983
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A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice.
Tokuda S, Mahaffey CL, Monks B, Faulkner CR, Birnbaum MJ, Danzer SC, Frankel WN.
Tokuda S, et al.
Hum Mol Genet. 2011 Mar 1;20(5):988-99. doi: 10.1093/hmg/ddq544. Epub 2010 Dec 15.
Hum Mol Genet. 2011.
PMID: 21159799
Free PMC article.
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Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13.
Buchner DA, Seburn KL, Frankel WN, Meisler MH.
Buchner DA, et al.
Mamm Genome. 2004 May;15(5):344-51. doi: 10.1007/s00335-004-2332-1.
Mamm Genome. 2004.
PMID: 15170223
Free article.
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