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Epilepsia
|
January 7, 2020
SCN8A encephalopathy: Mechanisms and models
Miriam H Meisler
Gene
|
April 23, 2003
TSRC1, a widely expressed gene containing seven thrombospondin type I repeats
David A Buchner, Miriam H Meisler
Frontiers in Neurology
|
June 2, 2015
Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy
Jacy 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 disability
Janelle 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 mice
Guy 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 Disorders
Sophie F Hill, Miriam H Meisler
The Journal of Clinical Investigation
|
August 3, 2005
Sodium channel mutations in epilepsy and other neurological disorders
Miriam H Meisler, Jennifer A Kearney
Genesis (New York, N.Y. : 2000)
|
November 30, 2013
Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8a
Julie M Jones, Miriam H Meisler
Methods in Enzymology
|
December 24, 2013
Mouse models of PI(3,5)P2 deficiency with impaired lysosome function
Guy M Lenk, Miriam H Meisler
Page
of 14
Search research articles
Search
Showing results (1-10 of 131) with videos related to
Sort By:
Page
of 14
Epilepsia
|
January 7, 2020
SCN8A encephalopathy: Mechanisms and models
Miriam H Meisler
Gene
|
April 23, 2003
TSRC1, a widely expressed gene containing seven thrombospondin type I repeats
David A Buchner, Miriam H Meisler
Frontiers in Neurology
|
June 2, 2015
Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy
Jacy 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 disability
Janelle 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 mice
Guy 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 Disorders
Sophie F Hill, Miriam H Meisler
The Journal of Clinical Investigation
|
August 3, 2005
Sodium channel mutations in epilepsy and other neurological disorders
Miriam H Meisler, Jennifer A Kearney
Genesis (New York, N.Y. : 2000)
|
November 30, 2013
Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8a
Julie M Jones, Miriam H Meisler
Methods in Enzymology
|
December 24, 2013
Mouse models of PI(3,5)P2 deficiency with impaired lysosome function
Guy M Lenk, Miriam H Meisler
Page
of 14