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Xi Du - Publications

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Neuroscience, Epilepsy, Neurogenesis
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9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Szabo GG, Du X, Oijala M, Varga C, Parent JM, Soltesz I. Extended Interneuronal Network of the Dentate Gyrus. Cell Reports. 20: 1262-1268. PMID 28793251 DOI: 10.1016/J.Celrep.2017.07.042  0.399
2017 Du X, Zhang H, Parent JM. Rabies Tracing of Birthdated Dentate Granule Cells in Rat Temporal Lobe Epilepsy. Annals of Neurology. PMID 28470680 DOI: 10.1002/Ana.24946  0.408
2016 Du X, Parent J. Mini-Brains Make Big Leaps for Studying Human Neural Development and Disease. Epilepsy Currents. 16: 402-404. PMID 27857624 DOI: 10.5698/1535-7511-16.6.402  0.394
2015 Du X, Parent JM. Using Patient-Derived Induced Pluripotent Stem Cells to Model and Treat Epilepsies. Current Neurology and Neuroscience Reports. 15: 588. PMID 26319172 DOI: 10.1007/s11910-015-0588-3  0.362
2014 Hoshi M, Du XX, Shinlapawittayatorn K, Liu H, Chai S, Wan X, Ficker E, Deschênes I. Brugada syndrome disease phenotype explained in apparently benign sodium channel mutations. Circulation. Cardiovascular Genetics. 7: 123-31. PMID 24573164 DOI: 10.1161/Circgenetics.113.000292  0.401
2011 Shinlapawittayatorn K, Dudash LA, Du XX, Heller L, Poelzing S, Ficker E, Deschênes I. A novel strategy using cardiac sodium channel polymorphic fragments to rescue trafficking-deficient SCN5A mutations. Circulation. Cardiovascular Genetics. 4: 500-9. PMID 21840964 DOI: 10.1161/Circgenetics.111.960633  0.576
2011 Shinlapawittayatorn K, Du XX, Liu H, Ficker E, Kaufman ES, Deschênes I. A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 455-62. PMID 21109022 DOI: 10.1016/J.Hrthm.2010.11.034  0.571
2010 Shinlapawittayatorn K, Du X, Liu H, Ficker E, Deschenes I. Do Sodium Channel α - α Interactions Contribute to Loss-of-Function Observed in Brugada Syndrome? Biophysical Journal. 98: 311a. DOI: 10.1016/J.Bpj.2009.12.1691  0.562
2009 Shinlapawittayatorn K, Du X, Liu H, Kaufman ES, Deschenes I. A Common SCN5A Polymorphism Restores the Biophysical Defects of LQT3 Mutations Biophysical Journal. 96: 249a. DOI: 10.1016/J.Bpj.2008.12.1227  0.578
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