Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome
出版年份 2020 全文链接
标题
Scn8a
Antisense Oligonucleotide Is Protective in Mouse Models of
SCN8A
Encephalopathy and Dravet Syndrome
作者
关键词
-
出版物
ANNALS OF NEUROLOGY
Volume 87, Issue 3, Pages 339-346
出版商
Wiley
发表日期
2020-01-15
DOI
10.1002/ana.25676
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Therapeutic Antisense Oligonucleotides Are Coming of Age
- (2019) C. Frank Bennett Annual Review of Medicine
- Is Targeting of Compensatory Ion Channel Gene Expression a Viable Therapeutic Strategy for Dravet Syndrome?
- (2019) Lori L. Isom Epilepsy Currents
- Antisense Oligonucleotide Therapies for Neurodegenerative Diseases
- (2019) C. Frank Bennett et al. Annual Review of Neuroscience
- Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders
- (2018) Amanda S. Lindy et al. EPILEPSIA
- Antisense oligonucleotides extend survival and reverse decrement in muscle response in ALS models
- (2018) Alex McCampbell et al. JOURNAL OF CLINICAL INVESTIGATION
- Selective targeting of Scn8a prevents seizure development in a mouse model of mesial temporal lobe epilepsy
- (2018) Jennifer C. Wong et al. Scientific Reports
- A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome
- (2018) Morgana Favero et al. JOURNAL OF NEUROSCIENCE
- The phenotype of SCN8A developmental and epileptic encephalopathy
- (2018) Elena Gardella et al. NEUROLOGY
- Prominent role of forebrain excitatory neurons in SCN8A encephalopathy
- (2018) Rosie K A Bunton-Stasyshyn et al. BRAIN
- Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
- (2018) Yuanyuan Liu et al. BRAIN
- The therapeutic potential of RNA regulation in neurological disorders
- (2018) Jolien Roovers et al. EXPERT OPINION ON THERAPEUTIC TARGETS
- Huntingtin suppression restores cognitive function in a mouse model of Huntington’s disease
- (2018) Amber L. Southwell et al. Science Translational Medicine
- ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology
- (2017) Ingrid E. Scheffer et al. EPILEPSIA
- Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice
- (2017) Lindsay A. Becker et al. NATURE
- Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
- (2017) Richard S. Finkel et al. NEW ENGLAND JOURNAL OF MEDICINE
- SCN8Aencephalopathy: Research progress and prospects
- (2016) Miriam H. Meisler et al. EPILEPSIA
- The phenotypic spectrum of SCN8A encephalopathy
- (2015) J. Larsen et al. NEUROLOGY
- Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy
- (2015) Jacy L. Wagnon et al. Frontiers in Neurology
- Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy
- (2014) Jacy L. Wagnon et al. HUMAN MOLECULAR GENETICS
- Semaphorin 5A inhibits synaptogenesis in early postnatal- and adult-born hippocampal dentate granule cells
- (2014) Yuntao Duan et al. eLife
- Mapping genetic modifiers of survival in a mouse model of Dravet syndrome
- (2013) A. R. Miller et al. GENES BRAIN AND BEHAVIOR
- Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
- (2010) Anne T. Berg et al. EPILEPSIA
- Exaggerated emotional behavior in mice heterozygous null for the sodium channelScn8a(Nav1.6)
- (2008) B. C. McKinney et al. GENES BRAIN AND BEHAVIOR
- Analyzing real-time PCR data by the comparative CT method
- (2008) Thomas D Schmittgen et al. Nature Protocols
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