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KIF5A
Supplemental Material Table of Contents
Genome-Wide Analyses Identify KIF5A As a Novel ALS Gene
Disrupted Neuronal Trafficking in Amyotrophic Lateral Sclerosis
The Universal Mechanism of Intermediate Filament Transport
Neurofilaments and Neurofilament Proteins in Health and Disease
Drosophila and Human Transcriptomic Data Mining Provides Evidence for Therapeutic
Supplementary Table 1
Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis
Molecular Diagnosis of Inherited Peripheral Neuropathies by Targeted Next-Generation Sequencing: Molecular Spectrum Delineation
Mrna Transport in Dendrites: RNA Granules, Motors, and Tracks
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Regional Collapsing of Rare Variation Implicates Specific Genic Regions
KIF5C, a Novel Neuronal Kinesin Enriched in Motor Neurons
Increased Expression of Plakoglobin Is Associated with Upregulated MAPK and PI3K/AKT Signalling Pathways in Early Resectable Pancreatic Ductal Adenocarcinoma
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
Distal Axonal Proteins and Their Related Mirnas in Cultured Cortical Neurons
Unique Function of Kinesin Kif5a in Localization of Mitochondria in Axons
Top View
Neurofilaments at a Glance
A Novel Mutation in the Stalk Domain of KIF5A Causes a Slowly Progressive Atypical Motor Syndrome
Integrating Lung Tissue and Lavage Proteomes Reveals Unique Pathways in Allergen
Disease Mechanisms in Inherited Neuropathies
Large Scale Molecular Studies of Pituitary Neuroendocrine Tumors: Novel Markers, Mechanisms and Translational Perspectives
Genome-Wide Scan for Common Variants Associated With
Morphological Neurite Changes Induced by Porcupine Inhibition Are Rescued by Wnt Ligands Juan A
A New Approach for Rare Variation Collapsing on Functional Protein Domains Implicates Specific Genic Regions in ALS
A Missense Mutation in the Coiled-Coil Domain of the KIF5A Gene and Late-Onset Hereditary Spastic Paraplegia
The KIF1A Homolog Unc-104 Is Important for Spontaneous
Manser Charlotte 2020 Thesis.Pdf
KIF5A and KLC1 Expression in Alzheimer's Disease
Sensors and Effectors 4 1
Supplemental Data
Specific Interaction of KIF11 with ZBP1 Regulates the Transport of B-Actin
Investigation of an Amyotrophic Lateral Sclerosis-Associated Profilin 1 Mutant
Genome-Wide Methylomic Analysis of Monozygotic Twins Discordant for Adolescent Depression
Proteome Profile of Peripheral Myelin in Healthy Mice and in a Neuropathy