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CNTNAP2
The Untold Stories of the Speech Gene, the FOXP2 Cancer Gene
Blood Biomarkers for Memory: Toward Early Detection of Risk for Alzheimer Disease, Pharmacogenomics, and Repurposed Drugs
CNTNAP2 Gene in High Functioning Autism
FEATURED ARTICLES Pair of a Kind Neuroscience Gateway (January 2008) | Doi:10.1038/Aba1803
Whole-Exome Sequencing Supports Genetic Heterogeneity in Childhood
FOXP2 and Language Alterations in Psychiatric Pathology Salud Mental, Vol
An Introduction to Neurogenetics
Variation in Neurodevelopmental Outcomes in Children with Sex Chromosome Trisomies: Testing the Double Hit Hypothesis [Version 2; Peer Review: 2 Approved]
Caspr2 (CNTNAP2) (NM 014141) Human Tagged ORF Clone Lentiviral Particle Product Data
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population
CNTNAP2 Ectodomain, Detected in Neuronal and CSF Sheddomes, Modulates Ca2+ Dynamics and Network Synchrony
CNTNAP2) Reveals the Presence of Two Caspr2 Isoforms with Overlapping Interactomes☆
Disruption of the CNTNAP2 Gene in a T(7;15) Translocation Family Without Symptoms of Gilles De La Tourette Syndrome
INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
Foxp2 and Vocalization
CNTNAP2 Polymorphisms and Structural Brain Connectivity: a Diffusion-Tensor Imaging Study
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-Like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
Mouse CNTNAP2 / CASPR2 Protein (His Tag)
Top View
CNTNAP2 Monoclonal Antibody, Clone FF19 (Streptavidin)
Genetic Characteristics of Non-Familial Epilepsy
Role of CNTNAP2 in Autism Manifestation Outlines the Regulation of Signaling Between Neurons at the Synapse Swati Agarwala1 and Nallur B
Caspr2) in Multiple Levels of Sensory Systems
CNTN6 Mutations Are Risk Factors for Abnormal Auditory Sensory Perception in Autism Spectrum Disorders
Altered Auditory Processing, Filtering, and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders
Replication of CNTNAP2 Association with Nonword Repetition and Support for FOXP2 Association with Timed Reading and Motor Activities in a Dyslexia Family Sample
Caspr2/CNTNAP2 Rabbit Mab
Novel Candidate Genes and Regions for Childhood Apraxia of Speech Identified by Array Comparative Genomic Hybridization
CNTNAP2) and Its Interaction with Contactin 2 (CNTN2
Single Nucleotide Polymorphisms in the CNTNAP2 Gene in Brazilian Patients with Autistic Spectrum Disorder
A Functional Genetic Link Between Distinct Developmental Language Disorders
Genetic Differences Between Humans and Other Hominins Contribute To
Gene on Chromosome 7 Associated with Autism
Comprehensive Cross-Disorder Analyses of CNTNAP2 Suggest It Is Unlikely to Be A