A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice
Boumil, Rebecca M, Letts, Verity A, Roberts, Monica C, Lenz, Christine, Mahaffey, Connie L, Zhang, Zhong-Wei, Moser, Tobias, Frankel, Wayne N
Published in PLoS genetics (01.08.2010)
Published in PLoS genetics (01.08.2010)
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Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy
Asinof, Samuel K, Sukoff Rizzo, Stacey J, Buckley, Alexandra R, Beyer, Barbara J, Letts, Verity A, Frankel, Wayne N, Boumil, Rebecca M
Published in PLoS genetics (01.06.2015)
Published in PLoS genetics (01.06.2015)
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Modes and regulation of endocytic membrane retrieval in mouse auditory hair cells
Neef, Jakob, Jung, Sangyong, Wong, Aaron B, Reuter, Kirsten, Pangrsic, Tina, Chakrabarti, Rituparna, Kügler, Sebastian, Lenz, Christine, Nouvian, Régis, Boumil, Rebecca M, Frankel, Wayne N, Wichmann, Carolin, Moser, Tobias
Published in The Journal of neuroscience (15.01.2014)
Published in The Journal of neuroscience (15.01.2014)
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Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4
Beyer, Barbara, Deleuze, Charlotte, Letts, Verity A., Mahaffey, Connie L., Boumil, Rebecca M., Lew, Timothy A., Huguenard, John R., Frankel, Wayne N.
Published in Human molecular genetics (15.06.2008)
Published in Human molecular genetics (15.06.2008)
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Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis
Dhindsa, Ryan S, Bradrick, Shelton S, Yao, Xiaodi, Heinzen, Erin L, Petrovski, Slave, Krueger, Brian J, Johnson, Michael R, Frankel, Wayne N, Petrou, Steven, Boumil, Rebecca M, Goldstein, David B
Published in Neurology. Genetics (01.06.2015)
Published in Neurology. Genetics (01.06.2015)
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The roles of MAD1 , MAD2 and MAD3 in meiotic progression and the segregation of nonexchange chromosomes
Dawson, Dean S, Cheslock, Peter S, Kemp, Benedict J, Boumil, Rebecca M
Published in Nature genetics (01.07.2005)
Published in Nature genetics (01.07.2005)
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Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy: e1005347
Asinof, Samuel K, Rizzo, Stacey JSukoff, Buckley, Alexandra R, Beyer, Barbara J, Letts, Verity A, Frankel, Wayne N, Boumil, Rebecca M
Published in PLoS genetics (01.06.2015)
Published in PLoS genetics (01.06.2015)
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Journal Article
A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice: e1001046
Boumil, Rebecca M, Letts, Verity A, Roberts, Monica C, Lenz, Christine, Mahaffey, Connie L, Zhang, Zhong-wei, Moser, Tobias, Frankel, Wayne N
Published in PLoS genetics (01.08.2010)
Published in PLoS genetics (01.08.2010)
Get full text
Journal Article