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Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
Eur J Neurosci. 2011 Oct;34(8):1268-75. doi: 10.1111/j.1460-9568.2011.07826.x. Epub 2011 Aug 22.
Eur J Neurosci. 2011.
PMID: 21864321
Free PMC article.
Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.
Volkers L, Rook MB, Das JH, Verbeek NE, Groenewegen WA, van Kempen MJ, Lindhout D, Koeleman BP.
Volkers L, et al. Among authors: das jh.
Neurosci Lett. 2009 Oct 2;462(1):24-9. doi: 10.1016/j.neulet.2009.06.064. Epub 2009 Jun 25.
Neurosci Lett. 2009.
PMID: 19559753
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Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation.
Volkers L, Kahlig KM, Das JH, van Kempen MJ, Lindhout D, Koeleman BP, Rook MB.
Volkers L, et al. Among authors: das jh.
J Gen Physiol. 2013 Dec;142(6):641-53. doi: 10.1085/jgp.201311042.
J Gen Physiol. 2013.
PMID: 24277604
Free PMC article.
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Structure of the cyclic-AMP-responsive exchange factor Epac2 in its auto-inhibited state.
Rehmann H, Das J, Knipscheer P, Wittinghofer A, Bos JL.
Rehmann H, et al.
Nature. 2006 Feb 2;439(7076):625-8. doi: 10.1038/nature04468.
Nature. 2006.
PMID: 16452984
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Differential Neuroproteomic and Systems Biology Analysis of Spinal Cord Injury.
Moghieb A, Bramlett HM, Das JH, Yang Z, Selig T, Yost RA, Wang MS, Dietrich WD, Wang KK.
Moghieb A, et al. Among authors: das jh.
Mol Cell Proteomics. 2016 Jul;15(7):2379-95. doi: 10.1074/mcp.M116.058115. Epub 2016 May 5.
Mol Cell Proteomics. 2016.
PMID: 27150525
Free PMC article.
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