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DOC2A
The 16P11.2 Homologs Fam57ba and Doc2a Generate Certain Brain and Body Phenotypes Jasmine M
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
DOC2B (NM 003585) Human Tagged ORF Clone Product Data
Associated 16P11.2 Deletion in Drosophila Melanogaster
Exploring the Relationship Between Gut Microbiota and Major Depressive Disorders
Strong Synaptic Transmission Impact by Copy Number Variations in Schizophrenia
Mechanisms of Membrane Fusion: Disparate Players and Common Principles
P2 Binding Modes of the C2 Domains of Rabphilin 3A and Synaptotagmin 1
Strong Synaptic Transmission Impact by Copy Number Variations in Schizophrenia
DOC2A Sirna (M): Sc-143131
14037 Secretagogin (D4V1Y) XP® Rabbit Mab
Cell-Type-Specific Repression by Methyl-Cpg-Binding Protein 2 Is Biased Toward Long Genes
Prenatal Diagnosis of True Fetal Mosaicism with Small
DOC2 Proteins in Rat Brain: Complementary Distribution and Proposed Function As Vesicular Adapter Proteins in Early Stages of Secretion
Computational Prediction of CRISPR-Impaired Non-Coding
And Post-Synaptic Abnormalities in Schizophrenia Lynsey S
Pervasive Epistasis Modulates Neurodevelopmental Defects of the Autism-Associated 16P11.2 Deletion
Gene Expression Profile in Frontal Cortex in Sporadic Frontotemporal Lobar Degeneration-TDP
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The 16P11.2 Homologs Fam57ba and Doc2a Generate Certain Brain and Body Phenotypes
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16P11.2 Microduplications
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Multi-Locus Genome-Wide Association Analysis Supports the Role of Glutamatergic Synaptic Transmission in the Etiology of Major Depressive Disorder
De Novo Mutations Revealed by Whole-Exome Sequencing Are Strongly Associated with Autism
Unraveling the Cellular Origin and Clinical Prognostic Markers of Infant B-Cell Acute Lymphoblastic Leukemia Using Genome-Wide Analysis
Doc2b Acts As a Calcium Sensor for Vesicle Priming Requiring
Transcriptional Profile of SH-SY5Y Human Neuroblastoma Cells Transfected by Toxoplasma Rhoptry Protein 16
Proteomics and Systems Biology
Neuroscore: a Genome-Wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System
TBX6, LHX1 and Copy Number Variations in the Complex Genetics of Müllerian Aplasia
Transcriptional Signatures of Synaptic Vesicle Genes Define Myotonic Dystrophy Type I
Association of Somatic Mutations of ADAMTS Genes with Improved Chemotherapy Sensitivity and Survival in High-Grade Serous Ovarian Carcinoma
Juul Et Al. – Supplementary Material Explanation of Data Presented In
New Insights on the Genetic Etiology of Alzheimer's and Related Dementia
Related Network and Differential Expression Analyses Identify
Rabbit Anti-Munc13 /FITC Conjugated Antibody