Clapcote SJ - Search Results

1

Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood.

Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. Kirshenbaum GS, et al. Among authors: clapcote sj. Neurogenetics. 2016 Jan;17(1):57-63. doi: 10.1007/s10048-015-0461-1. Epub 2015 Oct 13. Neurogenetics. 2016. PMID: 26463346 Free PMC article.

2

Survey of embryonic stem cell line source strains in the water maze reveals superior reversal learning of 129S6/SvEvTac mice.

Clapcote SJ, Roder JC. Clapcote SJ, et al. Behav Brain Res. 2004 Jun 4;152(1):35-48. doi: 10.1016/j.bbr.2003.09.030. Behav Brain Res. 2004. PMID: 15135967

3

Simplex PCR assay for sex determination in mice.

Clapcote SJ, Roder JC. Clapcote SJ, et al. Biotechniques. 2005 May;38(5):702, 704, 706. doi: 10.2144/05385BM05. Biotechniques. 2005. PMID: 15945368 Free article. No abstract available.

4

NIH Swiss and Black Swiss mice have retinal degeneration and performance deficits in cognitive tests.

Clapcote SJ, Lazar NL, Bechard AR, Wood GA, Roder JC. Clapcote SJ, et al. Comp Med. 2005 Aug;55(4):310-6. Comp Med. 2005. PMID: 16158906

5

Effects of the rd1 mutation and host strain on hippocampal learning in mice.

Clapcote SJ, Lazar NL, Bechard AR, Roder JC. Clapcote SJ, et al. Behav Genet. 2005 Sep;35(5):591-601. doi: 10.1007/s10519-005-5634-5. Behav Genet. 2005. PMID: 16184487

6

Novel strategies for the development of animal models of refractory epilepsy.

Snead OC 3rd, Clapcote SJ, Roder JC, Boulianne GL. Snead OC 3rd, et al. Among authors: clapcote sj. Adv Neurol. 2006;97:155-71. Adv Neurol. 2006. PMID: 16383125 Review. No abstract available.

7

Deletion polymorphism of Disc1 is common to all 129 mouse substrains: implications for gene-targeting studies of brain function.

Clapcote SJ, Roder JC. Clapcote SJ, et al. Genetics. 2006 Aug;173(4):2407-10. doi: 10.1534/genetics.106.060749. Epub 2006 Jun 4. Genetics. 2006. PMID: 16751659 Free PMC article. Review.

8

Methods to rapidly and accurately screen a large number of ENU mutagenized mice for abnormal motor phenotypes.

Abramow-Newerly W, Lipina T, Abramow-Newerly M, Kim D, Bechard AR, Xie G, Clapcote SJ, Roder JC. Abramow-Newerly W, et al. Among authors: clapcote sj. Amyotroph Lateral Scler. 2006 Jun;7(2):112-8. doi: 10.1080/14660820500443000. Amyotroph Lateral Scler. 2006. PMID: 16753976

9

Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.

Xie G, Clapcote SJ, Nieman BJ, Tallerico T, Huang Y, Vukobradovic I, Cordes SP, Osborne LR, Rossant J, Sled JG, Henderson JT, Roder JC. Xie G, et al. Among authors: clapcote sj. Genes Brain Behav. 2007 Nov;6(8):717-27. doi: 10.1111/j.1601-183X.2007.00302.x. Epub 2007 Mar 21. Genes Brain Behav. 2007. PMID: 17376154 Free article.

10

Behavioral phenotypes of Disc1 missense mutations in mice.

Clapcote SJ, Lipina TV, Millar JK, Mackie S, Christie S, Ogawa F, Lerch JP, Trimble K, Uchiyama M, Sakuraba Y, Kaneda H, Shiroishi T, Houslay MD, Henkelman RM, Sled JG, Gondo Y, Porteous DJ, Roder JC. Clapcote SJ, et al. Neuron. 2007 May 3;54(3):387-402. doi: 10.1016/j.neuron.2007.04.015. Neuron. 2007. PMID: 17481393 Free article.

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