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RAB39B
Reframing Psychiatry for Precision Medicine
The C9orf72-Interacting Protein Smcr8 Is a Negative Regulator of Autoimmunity and Lysosomal Exocytosis
Autosomal Recessive Ataxias and with the Early-Onset Parkinson’S Disease That We Identified Here As Overlapping with the SFARI Autism Gene
Prediction of Human Disease Genes by Human-Mouse Conserved Coexpression Analysis
Systematic Elucidation of Neuron-Astrocyte Interaction in Models of Amyotrophic Lateral Sclerosis Using Multi-Modal Integrated Bioinformatics Workflow
Rab39a and Rab39b Display Different Intracellular Distribution and Function in Sphingolipids and Phospholipids Transport
Mutations in RAB39B in Individuals with Intellectual Disability, Autism Spectrum Disorder, and Macrocephaly Marc Woodbury-Smith1,2* , Eric Deneault2, Ryan K
WO 2016/040794 Al 17 March 2016 (17.03.2016) P O P C T
RAB39B Gene Mutations Are Not Linked to Familial Parkinson's
Supplementary Table 1 Double Treatment Vs Single Treatment
Microarray Bioinformatics and Its Applications to Clinical Research
High Functioning Autism with Missense
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
A Comprehensive Genetic Database of Parkinson's Disease
Cystatin A, a Potential Common Link for Mutant Myocilin Causative Glaucoma
The Int22h1/Int22h2-Mediated Xq28 Duplication Syndrome: an Intersection Between Neurodevelopment, Immunology, and Cancer
Rab Gtpases: Switching to Human Diseases
216141 2 En Bookbackmatter 461..490
Top View
RAB39B-Mediated Trafficking of the Glua2-AMPAR Subunit Controls
Supplementary Methods
Mutations in RAB39B in Individuals with Intellectual Disability, Autism Spectrum Disorder, and Macrocephaly
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
An Atlas of Tissue-Specific Conserved Coexpression for Functional
Transcriptomics-Based Phenotypic Screening Supports Drug Discovery in Human Glioblastoma Cells
Mutations in the Small Gtpase Gene RAB39B Are Responsible for X-Linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
Genes with High Penetrance for Syndromic and Non-Syndromic Autism Typically Function Within the Nucleus and Regulate Gene Expression Emily L
Genes by Expressed Sequence Tag Profiling Genome-Wide Analysis Of
Tissue-Specific Conserved Coexpression for Disease Gene
Mouse Rab39b Knockout Project (CRISPR/Cas9)