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SHANK1
Deciphering the Molecular Profile of Plaques, Memory Decline And
Supplementary Table 1. Mutated Genes That Contain Protein Domains Identified Through Mutation Enrichment Analysis
Rare Gene Deletions in Genetic Generalized and Rolandic Epilepsies
Whole Genome Sequencing Puts Forward Hypotheses on Metastasis Evolution and Therapy in Colorectal Cancer
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Disentangling the Role of SHANK1 in a Mouse Model for Autism Spectrum Disorder: from Brain to Behavior
Protein Family Members. the GENE.FAMILY
Synaptic Pathways Related to Shank3 and Its Interaction Partner Prosapip1
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
Mouse Shank1 Conditional Knockout Project (CRISPR/Cas9)
Towards a Gene-Level Map of Resilience to Genetic Variants Associated with Autism Thomas Rolland1*, Freddy Cliquet1, Richard
SHANK1 Deletions in Males with Autism Spectrum Disorder
Exploratory Neuroimmune Profiling Identifies CNS-Specific Alterations in COVID-19 Patients with Neurological Involvement
Networking of Shank and Tsc1 Protein in Autistic Disorder
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
SHANK Proteins: Roles at the Synapse and in Autism Spectrum Disorder
SHANK1 Deletions in Males with Autism Spectrum Disorder
Changes in Contractile Protein Expression Are Linked to Ventricular Stiffness in Infants with Pulmonary Hypertension Or Right Ve
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Abundance of Regulatory T Cell (Treg) As a Predictive Biomarker for Neoadjuvant Chemotherapy in Triple-Negative Breast Cancer
Article Concentration (A), Mode Sizes (B) and Size Distribution Curves (C) Were Assessed by Nanoparticle Tracking Analysis
Irsp53/BAIAP2 in Dendritic Spine Development, NMDA Receptor Regulation, and Psychiatric Disorders
ATP11C Is a Major Flippase in Human Erythrocytes and Its Defect Causes Congenital Hemolytic Anemia
Meta-Analysis of SHANK Mutations in Autism Spectrum Disorders: a Gradient of Severity in Cognitive Impairments
Transcriptional Signatures of Synaptic Vesicle Genes Define Myotonic Dystrophy Type I
Rabbit Anti-BAIAP2/FITC Conjugated Antibody-SL0242R-FITC
Gene by Environment Interaction Mouse Model Reveals a Functional Role for 5-Hydroxymethylcytosine in Neurodevelopmental Disorders
Integrative Analysis Identified Key Schizophrenia Risk Factors from An
Whole Exome Sequencing to Identify Disease-Causing Mutations in Lower Motor Neuron Disease and Peripheral Neuropathy
Case-Control Study of Six Genes Asymmetrically Expressed in The
ANTIBODIES for NEUROSCIENCE 2 Antibodies for Neuroscience