DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» SYNGAP1
SYNGAP1
Genetic and Neurodevelopmental Spectrum Of
Translational Regulation of Syngap1 by FMRP Modulates NMDAR Mediated Signalling
SYNGAP1 Resource Guide
Endogenous Sirnas and Noncoding RNA-Derived Small Rnas Are Expressed in Adult Mouse Hippocampus and Are Up-Regulated in Olfactory Discrimination Training
Syngap Families Welcome Packet Welcome
The First International Conference on SYNGAP1-Related Brain Disorders
Characterization of Intellectual Disability and Autism Comorbidity Through Gene Panel Sequencing
Twenty Years of Syngap Research: from Synapses to Cognition
Tiratha Raj Singh.Pdf
SYNGAP1 Controls the Maturation of Dendrites, Synaptic Function, and Network Activity in Developing Human Neurons
SYNGAP1: Mind the Gap
Syngap Splice Isoforms Differentially Regulate Synaptic Plasticity and Dendritic Development
Genetic and Neurodevelopmental Spectrum Of
Syngap Isoforms Differentially Regulate Synaptic Plasticity And
Multi-Parametric Analysis of 58 SYNGAP1 Variants Reveal Impacts on Gtpase Signaling
Human SYNGAP1 Regulates the Development of Neuronal Activity by Controlling Dendritic and Synaptic Maturation
SYNGAP1 Encephalopathy a Distinctive Generalized Developmental and Epileptic Encephalopathy
Audiogenic Seizures in the Fmr1 Knockout Mouse Are Induced By
Top View
SYNGAP1 Controls the Maturation of Dendrites, Synaptic Function, and Network Activity in Developing Human Neurons
SYNGAP1-Related Intellectual Disability Syndrome
Altered TAOK2 Activity Causes Autism-Related Neurodevelopmental and Cognitive Abnormalities Through Rhoa Signaling
SYNGAP1-Related Intellectual Disability
Post-Transcriptionally Impaired De Novo Mutations Contribute to The
Intellectual Disability, the Long Way from Genes to Biological Mechanisms
Genetic and Neurodevelopmental Spectrum of SYNGAP1-Associated Intellectual Disability and Epilepsy
SYNGAP1 Syndrome FTNW
De Novo, Heterozygous, Loss-Of-Function Mutations in SYNGAP1 Cause a Syndromic Form of Intellectual Disability
Syngap1-Related Nsid
1 Sleep Abnormalities in the Synaptopathies – SYNGAP1-Related Intellectual Disability and Phelan-Mcdermid Syndrome Constance S
Juul Et Al. – Supplementary Material Explanation of Data Presented In
Lys05 – a Promising Autophagy Inhibitor in the Radiosensitization
Reactions from the 2020 SYNGAP1 Scientific Conference
Reduced Cognition in Syngap1 Mutants Is Caused by Isolated Damage Within Developing Forebrain Excitatory Neurons
SYNGAP1 Gene Synaptic Ras Gtpase Activating Protein 1
Long Non-Coding RNA (Lncrna) Roles in Cell Biology, Neurodevelopment and Neurological Disorders
SYNGAP1-Related Syndrome