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SHANK3
The Human Gene Connectome As a Map of Short Cuts for Morbid Allele Discovery
A 29 Mainland Chinese Cohort of Patients with Phelan–Mcdermid
Genetic Findings As the Potential Basis of Personalized Pharmacotherapy in Phelan-Mcdermid Syndrome
Network Impact of the SERT Ala56 Coding Variant
Prevalence of SHANK3 Variants in Patients with Different Subtypes of Autism Spectrum Disorders
Synaptic Pathways Related to Shank3 and Its Interaction Partner Prosapip1
Analysis of Genotype, Phenotype, and Age Progression in Phelan-Mcdermid Syndrome Sara Sarasua Clemson University,
[email protected]
FMR1 and Autism, an Intriguing Connection Revisited
Contribution of SHANK3 Mutations to Autism Spectrum Disorder
Apparent Genetic Rescue of Adult Shank3 Exon 21 Insertion Mutation Mice Tempered by Appropriate Control Experiments
Identification of 22Q13 Genes Most Likely to Contribute to Phelan
INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
Phelan-Mcdermid Syndrome (22Q13 Deletions)
A Common Cause for Phelan-Mcdermid Syndrome and Neurofibromatosis Type 2: One Ring to Bind Them Ariel M
SHANK Proteins: Roles at the Synapse and in Autism Spectrum Disorder
Shank3 Modulates Sleep and Expression of Circadian
Delineation of the Genetic and Clinical Spectrum of Phelan-Mcdermid Syndrome Caused by SHANK3 Point Mutations Silvia De Rubeis1,2† , Paige M
SHANK3 Gene SH3 and Multiple Ankyrin Repeat Domains 3
Top View
Neuropsychiatric Decompensation in Adolescents and Adults with Phelan
De Novo Mutations in the Gene Encoding the Synaptic Scaffolding Protein SHANK3 in Patients Ascertained for Schizophrenia
Complex Genetic Network Underlying the Convergent of Rett Syndrome Like (RTT-L) Phenotype in Neurodevelopmental Disorders
Interstitial 22Q13 Deletions: Genes Other Than SHANK3 Have Major Effects on Cognitive and Language Development
A Recurrent SHANK3 Frameshift Variant in Autism Spectrum Disorder
Supplemental Information
SHANK3 Blocking Peptide (CDBP6094) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
22Q13.2Q13.32 Genomic Regions Associated with Severity of Speech Delay, Developmental Delay, and Physical Features in Phelan–Mcdermid Syndrome