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NLGN3
Screening of a Clinically and Biochemically Diagnosed SOD Patient Using Exome Sequencing: a Case Report with a Mutations/Variations Analysis Approach
Environmental and Genetic Factors in Autism Spectrum Disorders: Special Emphasis on Data from Arabian Studies
Excess of Rare Novel Loss-Of-Function Variants in Synaptic Genes in Schizophrenia and Autism Spectrum Disorders
Mouse Nlgn3 Knockout Project (CRISPR/Cas9)
Neuroligin3 Splice Isoforms Shape Mouse Hippocampal Inhibitory Synaptic Function
Advances in Autism Genetics: on the Threshold of a New Neurobiology
Mirna Regulons Associated with Synaptic Function
No Evidence for Involvement of Genetic Variants in the X-Linked
Mutations in Neuroligin-3 in Male Mice Impact Behavioral Flexibility but Not Relational Memory in a Touchscreen Test of Visual Transitive Inference Rebecca H
With Autism Spectrum Disorders in a Chinese Han Cohort Jindan Yu1, Xue He1, Dan Yao1, Zhongyue Li2, Hui Li3 and Zhengyan Zhao1*
Dimerization of Postsynaptic Neuroligin Drives Synaptic Assembly Via Transsynaptic Clustering of Neurexin
Behavioral Profiles of Mouse Models for Autism Spectrum Disorders Elodie Ey, Claire S
X-Linked Mental Retardation: a Clinical Guide
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
Autism-Associated Mutation Inhibits Protein Kinase C-Mediated Neuroligin-4X Enhancement of Excitatory Synapses
Significance of Neurexin and Neuroligin Polymorphisms in Regulating Risk of Hirschsprung’S Disease Yanhong Li, Hui Liu, Yubin Dong
Identification and Characterization of the TRIP8 and REEP3 Genes on Chromosome 10Q21.3 As Novel Candidate Genes for Autism
Top View
Using Gene Ontology to Describe the Role of the Neurexin-Neuroligin-SHANK Complex in Human, Mouse and Rat and Its Relevance to Autism Patel Et Al
UNIVERSITY of CALIFORNIA RIVERSIDE a Comparison of Gene
Specific Neuroligin3–Aneurexin1 Signaling Regulates Gabaergic Synaptic Function in Mouse Hippocampus
Familial Deletion Within NLGN4 Associated with Autism and Tourette Syndrome
XLMR Genes: Update 2007
INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
Autistic Phenotypes and Genetic Testing: State-Of-The- Art for the Clinical Geneticist C Lintas, a M Persico
216141 2 En Bookbackmatter 461..490
Prognostic Significance of Esterase Gene Expression in Multiple Myeloma
Autism Candidate Genes Via Mouse Phenomics ⇑ Terrence F
"The Genetics of Autism" In: Encyclopedia of Life Sciences
Recombinant Human Neuroligin 3/NLGN3 Catalog Number: 9069-NL
Human Neuroligin-3 / NLGN3 Protein (His Tag)
The Role of Neuroligins in the Cerebellum Highlights the Diversity of Synapse-Specifying Molecules
Autism Genetics
Original Article the Single Nucleotide Polymorphism Study on the SHANK3 and NLGN3 Gene in Association with Autism in Wenzhou Children
Autism Candidate Genes Via Mouse Phenomics ⇑ Terrence F
Synaptic Proteins and Receptors Defects in Autism Spectrum Disorders
Systematic Phenomics Analysis of Autism-Associated Genes Reveals Parallel Networks Underlying Reversible Impairments in Habituation
Stagewise Identification of Significantly Mutated and Dysregulated Gene Clusters in Major
Integrative Analysis Identified Key Schizophrenia Risk Factors from An
Genetic Basis of Autism Spectrum Disorder
Global Analysis of Protein Expression of Inner Ear Hair Cells
(NLGN3) (NM 018977) Human Recombinant Protein Product Data
Snapshot: Neuroligin-Neurexin Complexes Stéphane Baudouin and Peter Scheiffele Biozentrum of the University of Basel, 4056 Basel, Switzerland
Analysis of the Neuroligin 3 and 4 Genes in Autism and Other
Mutations of the X-Linked Genes Encoding Neuroligins NLGN3 and NLGN4 Are Associated with Autism
1 Abnormal Social Behaviors and Dysfunction of Autism-Related Genes
Assessing the Role of Drosophila Melanogaster Neuroligin 3 on Social Spacing and Climbing Behaviour
Comparative Analysis of Autosomal and X-Linked Genes Involved in Nonspecific Cognitive Impairment