Re-expression of SynGAP protein in adulthood improves translatable measures of brain function and behavior
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Re-expression of SynGAP protein in adulthood improves translatable measures of brain function and behavior
Authors
Keywords
-
Journal
eLife
Volume 8, Issue -, Pages -
Publisher
eLife Sciences Publications, Ltd
Online
2019-04-26
DOI
10.7554/elife.46752
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The first international conference on SYNGAP1-related brain disorders: a stakeholder meeting of families, researchers, clinicians, and regulators
- (2018) Monica Weldon et al. Journal of Neurodevelopmental Disorders
- Experience-dependent trends in CA1 theta and slow gamma rhythms in freely behaving mice
- (2018) Brian J. Gereke et al. JOURNAL OF NEUROPHYSIOLOGY
- Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders
- (2018) Murat Kilinc et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- SYNGAP1 heterozygosity disrupts sensory processing by reducing touch-related activity within somatosensory cortex circuits
- (2018) Sheldon D. Michaelson et al. NATURE NEUROSCIENCE
- SYNGAP1 encephalopathy
- (2018) Danique R.M. Vlaskamp et al. NEUROLOGY
- ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology
- (2017) Ingrid E. Scheffer et al. EPILEPSIA
- Autism genetics: opportunities and challenges for clinical translation
- (2017) Jacob A. S. Vorstman et al. NATURE REVIEWS GENETICS
- Translational use of event-related potentials to assess circuit integrity in ASD
- (2017) Meera E. Modi et al. Nature Reviews Neurology
- Interictal spikes and epileptic seizures: their relationship and underlying rhythmicity
- (2016) Philippa J. Karoly et al. BRAIN
- Electrical status epilepticus in sleep (ESES)/continuous spikes and waves during slow sleep (CSWS) syndrome in children: An electroclinical evaluation according to the EEG patterns
- (2016) Pinar Gencpinar et al. EPILEPSY & BEHAVIOR
- Genetic and neurodevelopmental spectrum ofSYNGAP1-associated intellectual disability and epilepsy
- (2016) Cyril Mignot et al. JOURNAL OF MEDICAL GENETICS
- Adult restoration of Shank3 expression rescues selective autistic-like phenotypes
- (2016) Yuan Mei et al. NATURE
- Developmental timing and critical windows for the treatment of psychiatric disorders
- (2016) Oscar Marín NATURE MEDICINE
- Rhythms of the hippocampal network
- (2016) Laura Lee Colgin NATURE REVIEWS NEUROSCIENCE
- De novo, heterozygous, loss-of-function mutations inSYNGAP1cause a syndromic form of intellectual disability
- (2015) Michael J. Parker et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Syngap1 Haploinsufficiency Damages a Postnatal Critical Period of Pyramidal Cell Structural Maturation Linked to Cortical Circuit Assembly
- (2015) Massimiliano Aceti et al. BIOLOGICAL PSYCHIATRY
- Electrophysiological biomarkers of diagnosis and outcome in neurodevelopmental disorders
- (2015) Shafali S. Jeste et al. CURRENT OPINION IN NEUROLOGY
- Autism Spectrum Disorder and Epilepsy
- (2015) Shafali Spurling Jeste et al. JOURNAL OF CHILD NEUROLOGY
- Input-specific regulation of hippocampal circuit maturation by non-muscle myosin IIB
- (2015) Emin D. Ozkan et al. JOURNAL OF NEUROCHEMISTRY
- SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG
- (2015) Claudia Funke et al. NEUROPEDIATRICS
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- Large-scale discovery of novel genetic causes of developmental disorders
- (2014) T. W. Fitzgerald et al. NATURE
- Prioritization of neurodevelopmental disease genes by discovery of new mutations
- (2014) Alexander Hoischen et al. NATURE NEUROSCIENCE
- One gene, many neuropsychiatric disorders: lessons from Mendelian diseases
- (2014) Xiaolin Zhu et al. NATURE NEUROSCIENCE
- Reduced Cognition in Syngap1 Mutants Is Caused by Isolated Damage within Developing Forebrain Excitatory Neurons
- (2014) Emin D. Ozkan et al. NEURON
- Recurrent de novo mutations implicate novel genes underlying simplex autism risk
- (2014) B. J. O'Roak et al. Nature Communications
- SYNGAP1 Links the Maturation Rate of Excitatory Synapses to the Duration of Critical-Period Synaptic Plasticity
- (2013) J. P. Clement et al. JOURNAL OF NEUROSCIENCE
- Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
- (2013) Gemma L Carvill et al. NATURE GENETICS
- Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses
- (2012) James P. Clement et al. CELL
- Mutations inSYNGAP1Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency
- (2012) Martin H. Berryer et al. HUMAN MUTATION
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
- (2012) Anita Rauch et al. LANCET
- Molecular and behavioral changes associated with adult hippocampus-specific SynGAP1 knockout
- (2012) M. Muhia et al. LEARNING & MEMORY
- Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities
- (2012) H. Y. Zoghbi et al. Cold Spring Harbor Perspectives in Biology
- De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism
- (2011) Fadi F. Hamdan et al. BIOLOGICAL PSYCHIATRY
- Dendritic spine pathology in neuropsychiatric disorders
- (2011) Peter Penzes et al. NATURE NEUROSCIENCE
- Trends in the Prevalence of Developmental Disabilities in US Children, 1997-2008
- (2011) C. A. Boyle et al. PEDIATRICS
- Disruption of hippocampus-regulated behavioural and cognitive processes by heterozygous constitutive deletion of SynGAP
- (2010) Mary Muhia et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Reduced Expression of the NMDA Receptor-Interacting Protein SynGAP Causes Behavioral Abnormalities that Model Symptoms of Schizophrenia
- (2009) Xiaochuan Guo et al. NEUROPSYCHOPHARMACOLOGY
- Mutations inSYNGAP1in Autosomal Nonsyndromic Mental Retardation
- (2009) Fadi F. Hamdan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Neurofibromin Regulation of ERK Signaling Modulates GABA Release and Learning
- (2008) Yijun Cui et al. CELL
- Reversal of learning deficits in a Tsc2 +/− mouse model of tuberous sclerosis
- (2008) Dan Ehninger et al. NATURE MEDICINE
- Reversing Neurodevelopmental Disorders in Adults
- (2008) Dan Ehninger et al. NEURON
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now