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UNC13B
The Role of Molecular Scaffolds at the Active Zone in Synaptic Vesicle Distribution and Release Probability
Pharmacological Mechanisms Underlying the Hepatoprotective Effects of Ecliptae Herba on Hepatocellular Carcinoma
Primepcr™Assay Validation Report
Reduced Insulin Secretion Correlates with Decreased Expression of Exocytotic Genes in Pancreatic Islets from Patients with Type 2 Diabetes
Genomic and Transcriptome Analysis Revealing an Oncogenic Functional Module in Meningiomas
Whole-Genome Sequencing Reveals Genetic Variation in the Asian House Rat
The Association of UNC13B Gene Polymorphisms and Diabetic
Starting a Molecular Systems View of Endocytosis
Snareopathies: Diversity in Mechanisms and Symptoms
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Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Oxidized Phospholipids Regulate Amino Acid Metabolism Through MTHFD2 to Facilitate Nucleotide Release in Endothelial Cells
A Potential Target Gene of 9P13.3 Amplicon in Prostate Cancer
Patterns of Sequence Conservation in Presynaptic Neural Genes
Exome Sequencing for Bipolar Disorder Points to Roles of De Novo Loss-Of-Function and Protein-Altering Mutations
Original Article Gene Expression Profiling Based on Microarray
Identification of Novel Genetic Variations for Amyotrophic Lateral Sclerosis (ALS)
There Are 1393 Genes Significant by SAM with 90Th Percentile Confidence, the False Discovery Rate Among the 1393 Significant Genes Is 0.09968
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Genome-Wide Identification of the Genetic Basis of Amyotrophic Lateral Sclerosis
Association Between Regulating Synaptic Membrane Exocytosis 2 Gene Polymorphisms and Degenerative Lumbar Scoliosis
Common ALS/FTD Risk Variants in UNC13A Exacerbate Its Cryptic Splicing 2 and Loss Upon TDP-43 Mislocalization
SUPPLEMENTARY APPENDIX Transcriptional Activities of DUX4 Fusions in B-Cell Acute Lymphoblastic Leukemia
Stable Positioning of Unc13 Restricts Synaptic Vesicle Fusion to Defined Release Sites to Promote Synchronous Neurotransmission
A G/T Substitution in Intron-1 of UNC13B Gene Is Associated with Increased Risk of Nephropathy in Patients with Type 1 Diabetes
Whole Genome Microarray Analysis of Gene Expression in Subjects with Fragile X Syndrome Douglas C
Adipose Liver Muscle Brain
Flexible Model-Based Joint Probabilistic Clustering of Binary and Continuous Inputs and Its Application to Genetic Regulation and Cancer
Snapshot: Mammalian Rab Proteins in Endocytic Trafficking Thierry Galvez, Jérôme Gilleron, Marino Zerial, and Gregory A
Analysis of RIM Expression and Function at Mouse Photoreceptor Ribbon Synapses
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With
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
STAT Autism and Intellectual Disability Panel
Transcriptional Maturation of the Mouse Auditory Forebrain Troy A
Anti-UNC13B Antibody (ARG54991)
Supplemental Figure 1. Gene Ontology Analysis of SAHA Dose-Responsive Genes