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Miriam H Meisler

Showing results (1-10 of 131) with videos related to

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Epilepsia|January 7, 2020
SCN8A encephalopathy: Mechanisms and modelsMiriam H Meisler
Gene|April 23, 2003
TSRC1, a widely expressed gene containing seven thrombospondin type I repeatsDavid A Buchner, Miriam H Meisler
Frontiers in Neurology|June 2, 2015
Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic EncephalopathyJacy L Wagnon, Miriam H Meisler
Frontiers in Genetics|November 7, 2013
Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disabilityJanelle E O'Brien, Miriam H Meisler
Molecular Genetics and Metabolism|November 26, 2022
Chloroquine corrects enlarged lysosomes in FIG4 null cells and reduces neurodegeneration in Fig4 null miceGuy M Lenk, Miriam H Meisler
Genesis (New York, N.Y. : 2000)|August 3, 2004
Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6)Stephen I Levin, Miriam H Meisler
Developmental Neuroscience|August 19, 2021
Antisense Oligonucleotide Therapy for Neurodevelopmental DisordersSophie F Hill, Miriam H Meisler
The Journal of Clinical Investigation|August 3, 2005
Sodium channel mutations in epilepsy and other neurological disordersMiriam H Meisler, Jennifer A Kearney
Genesis (New York, N.Y. : 2000)|November 30, 2013
Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8aJulie M Jones, Miriam H Meisler
Methods in Enzymology|December 24, 2013
Mouse models of PI(3,5)P2 deficiency with impaired lysosome functionGuy M Lenk, Miriam H Meisler
Pageof 14

Showing results (1-10 of 131) with videos related to

Sort By:
Pageof 14
Epilepsia|January 7, 2020
SCN8A encephalopathy: Mechanisms and modelsMiriam H Meisler
Gene|April 23, 2003
TSRC1, a widely expressed gene containing seven thrombospondin type I repeatsDavid A Buchner, Miriam H Meisler
Frontiers in Neurology|June 2, 2015
Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic EncephalopathyJacy L Wagnon, Miriam H Meisler
Frontiers in Genetics|November 7, 2013
Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disabilityJanelle E O'Brien, Miriam H Meisler
Molecular Genetics and Metabolism|November 26, 2022
Chloroquine corrects enlarged lysosomes in FIG4 null cells and reduces neurodegeneration in Fig4 null miceGuy M Lenk, Miriam H Meisler
Genesis (New York, N.Y. : 2000)|August 3, 2004
Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6)Stephen I Levin, Miriam H Meisler
Developmental Neuroscience|August 19, 2021
Antisense Oligonucleotide Therapy for Neurodevelopmental DisordersSophie F Hill, Miriam H Meisler
The Journal of Clinical Investigation|August 3, 2005
Sodium channel mutations in epilepsy and other neurological disordersMiriam H Meisler, Jennifer A Kearney
Genesis (New York, N.Y. : 2000)|November 30, 2013
Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8aJulie M Jones, Miriam H Meisler
Methods in Enzymology|December 24, 2013
Mouse models of PI(3,5)P2 deficiency with impaired lysosome functionGuy M Lenk, Miriam H Meisler
Pageof 14