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Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2a.
Epilepsia. 2016 Jun;57(6):e103-7. doi: 10.1111/epi.13390. Epub 2016 Apr 25.
Epilepsia. 2016.
PMID: 27112236
Free PMC article.
Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
Hawkins NA, Zachwieja NJ, Miller AR, Anderson LL, Kearney JA.
Hawkins NA, et al. Among authors: zachwieja nj.
PLoS Genet. 2016 Oct 21;12(10):e1006398. doi: 10.1371/journal.pgen.1006398. eCollection 2016 Oct.
PLoS Genet. 2016.
PMID: 27768696
Free PMC article.
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Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome.
Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA.
Calhoun JD, et al. Among authors: zachwieja nj.
Epilepsia. 2017 Aug;58(8):e111-e115. doi: 10.1111/epi.13811. Epub 2017 May 28.
Epilepsia. 2017.
PMID: 28556246
Free PMC article.
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Loss of Adipocyte VEGF Impairs Endurance Exercise Capacity in Mice.
Zachwieja NJ, O'Connell GC, Stricker JC, Allen J, Vona-Davis L, Bryner R, Mandler W, Olfert IM.
Zachwieja NJ, et al.
Med Sci Sports Exerc. 2015 Nov;47(11):2329-39. doi: 10.1249/MSS.0000000000000663.
Med Sci Sports Exerc. 2015.
PMID: 25785931
Free PMC article.
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