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Franck K. Kalume, Ph.D. - Publications

Affiliations: 
2004 University of Tennessee Health Science Center, Memphis, TN, United States 
Area:
Neuroscience Biology
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24 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
2023 Mich JK, Ryu J, Wei AD, Gore BB, Guo R, Bard AM, Martinez RA, Bishaw Y, Luber E, Oliveira Santos LM, Miranda N, Ramirez JM, Ting JT, Lein ES, Levi BP, ... Kalume FK, et al. AAV-mediated interneuron-specific gene replacement for Dravet syndrome. Biorxiv : the Preprint Server For Biology. PMID 38168178 DOI: 10.1101/2023.12.15.571820  0.346
2023 Manning A, Han V, Stephens A, Wang R, Bush N, Bard M, Ramirez JM, Kalume F. Elevated susceptibility to exogenous seizure triggers and impaired interneuron excitability in a mouse model of Leigh syndrome epilepsy. Neurobiology of Disease. 106288. PMID 37704057 DOI: 10.1016/j.nbd.2023.106288  0.358
2022 Wei AD, Wakenight P, Zwingman TA, Bard AM, Sahai N, Willemsen MH, Schelhaas HJ, Stegmann APA, Verhoeven JS, de Man SA, Wessels MW, Kleefstra T, Shinde DN, Helbig KL, Basinger A, ... ... Kalume FK, et al. Human KCNQ5 de novo Mutations Underlie Epilepsy and Intellectual Disability. Journal of Neurophysiology. PMID 35583973 DOI: 10.1152/jn.00509.2021  0.318
2021 Roy A, Han VZ, Bard AM, Wehle DT, Smith SEP, Ramirez JM, Kalume F, Millen KJ. Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of -Driven Intractable Epilepsy. Frontiers in Molecular Neuroscience. 14: 772847. PMID 34899181 DOI: 10.3389/fnmol.2021.772847  0.369
2019 Bolea I, Gella A, Sanz E, Prada-Dacasa P, Menardy F, Bard AM, Machuca-Márquez P, Eraso-Pichot A, Mòdol-Caballero G, Navarro X, Kalume F, Quintana A. Defined neuronal populations drive fatal phenotype in a mouse model of Leigh Syndrome. Elife. 8. PMID 31403401 DOI: 10.7554/Elife.47163  0.445
2019 Williams AD, Kalume F, Westenbroek RE, Catterall WA. A More Efficient Conditional Mouse Model of Dravet Syndrome: Implications for Epigenetic Selection and Sex-Dependent Behaviors. Journal of Neuroscience Methods. 108315. PMID 31265868 DOI: 10.1016/J.Jneumeth.2019.108315  0.399
2019 Bolea I, Gella A, Sanz E, Prada-Dacasa P, Menardy F, Bard AM, Machuca-Márquez P, Eraso-Pichot A, Mòdol-Caballero G, Navarro X, Kalume F, Quintana A. Author response: Defined neuronal populations drive fatal phenotype in a mouse model of Leigh syndrome Elife. DOI: 10.7554/Elife.47163.028  0.369
2015 Roy A, Skibo J, Kalume F, Ni J, Rankin S, Lu Y, Dobyns WB, Mills GB, Zhao JJ, Baker SJ, Millen KJ. Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy. Elife. 4. PMID 26633882 DOI: 10.7554/Elife.12703  0.401
2015 Roy A, Ni J, Skibo J, Rankin S, Dobyns WB, Kalume F, Baker SJ, Zhao J, Millen KJ. Modeling human PIK3CA-related congenital brain overgrowth and epilepsy in mice. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 46. PMID 26531452 DOI: 10.1016/J.Ijdevneu.2015.04.131  0.385
2015 Kalume F, Oakley JC, Westenbroek RE, Gile J, de la Iglesia HO, Scheuer T, Catterall WA. Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome. Neurobiology of Disease. 77: 141-54. PMID 25766678 DOI: 10.1016/J.Nbd.2015.02.016  0.331
2015 Roy A, Skibo J, Kalume F, Ni J, Rankin S, Lu Y, Dobyns WB, Mills GB, Zhao JJ, Baker SJ, Millen KJ. Author response: Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy Elife. DOI: 10.7554/Elife.12703.026  0.368
2013 Cheah CS, Westenbroek RE, Roden WH, Kalume F, Oakley JC, Jansen LA, Catterall WA. Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome. Channels (Austin, Tex.). 7: 468-72. PMID 23965409 DOI: 10.4161/Chan.26023  0.427
2013 Kalume F. Sudden unexpected death in Dravet syndrome: respiratory and other physiological dysfunctions. Respiratory Physiology & Neurobiology. 189: 324-328. PMID 23850567 DOI: 10.1016/J.Resp.2013.06.026  0.445
2013 Kalume F, Westenbroek RE, Cheah CS, Yu FH, Oakley JC, Scheuer T, Catterall WA. Sudden unexpected death in a mouse model of Dravet syndrome. The Journal of Clinical Investigation. 123: 1798-808. PMID 23524966 DOI: 10.1172/Jci66220  0.446
2012 Cheah CS, Yu FH, Westenbroek RE, Kalume FK, Oakley JC, Potter GB, Rubenstein JL, Catterall WA. Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome. Proceedings of the National Academy of Sciences of the United States of America. 109: 14646-51. PMID 22908258 DOI: 10.1073/Pnas.1211591109  0.502
2011 Dutton SB, Sawyer NT, Kalume F, Jumbo-Lucioni P, Borges K, Catterall WA, Escayg A. Protective effect of the ketogenic diet in Scn1a mutant mice. Epilepsia. 52: 2050-6. PMID 21801172 DOI: 10.1111/J.1528-1167.2011.03211.X  0.39
2011 Oakley JC, Kalume F, Catterall WA. Insights into pathophysiology and therapy from a mouse model of Dravet syndrome. Epilepsia. 52: 59-61. PMID 21463282 DOI: 10.1111/J.1528-1167.2011.03004.X  0.481
2010 Catterall WA, Kalume F, Oakley JC. NaV1.1 channels and epilepsy. The Journal of Physiology. 588: 1849-59. PMID 20194124 DOI: 10.1113/Jphysiol.2010.187484  0.47
2009 Oakley JC, Kalume F, Yu FH, Scheuer T, Catterall WA. Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy. Proceedings of the National Academy of Sciences of the United States of America. 106: 3994-9. PMID 19234123 DOI: 10.1073/Pnas.0813330106  0.39
2007 Kalume F, Yu FH, Westenbroek RE, Scheuer T, Catterall WA. Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 11065-74. PMID 17928448 DOI: 10.1523/Jneurosci.2162-07.2007  0.446
2007 Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, Spain WJ, McKnight GS, Scheuer T, Catterall WA. Erratum: Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy Nature Neuroscience. 10: 134-134. DOI: 10.1038/Nn0107-134B  0.416
2006 Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, Spain WJ, McKnight GS, Scheuer T, Catterall WA. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy. Nature Neuroscience. 9: 1142-9. PMID 16921370 DOI: 10.1038/Nn1754  0.454
2004 Kalume F, Lee SM, Morcos Y, Callaway JC, Levin MC. Molecular mimicry: cross-reactive antibodies from patients with immune-mediated neurologic disease inhibit neuronal firing. Journal of Neuroscience Research. 77: 82-9. PMID 15197740 DOI: 10.1002/Jnr.20137  0.542
2002 Levin MC, Lee SM, Kalume F, Morcos Y, Dohan FC, Hasty KA, Callaway JC, Zunt J, Desiderio D, Stuart JM. Autoimmunity due to molecular mimicry as a cause of neurological disease. Nature Medicine. 8: 509-13. PMID 11984596 DOI: 10.1038/Nm0502-509  0.538
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