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SCN3A
The Mineralocorticoid Receptor Leads to Increased Expression of EGFR
Phenotypic Spectrum and Long-Term Outcome in Children with Genetic Causes of Early-Onset Epileptic Encephalopathy
An Advance About the Genetic Causes of Epilepsy
Spatial Distribution of Leading Pacemaker Sites in the Normal, Intact Rat Sinoa
Identifying Genes in Monoamine Nuclei That May Determine Stress Vulnerability and Depressive Behavior in Wistar–Kyoto Rats
Sodium Channel Mutations in Epilepsy and Other Neurological Disorders
Oestrogen Receptor Β Mediates the Actions of Bisphenol-A on Ion Channel Expression in Mouse Pancreatic Beta Cells
Original Article ITGA8 Accelerates Migration and Invasion of Myeloma Cells in Multiple Myelomas
Genetic Variations Associated with Pharmacoresistant Epilepsy (Review)
Graded Co-Expression of Ion Channel, Neurofilament, and Synaptic Genes in Fast- Spiking Vestibular Nucleus Neurons
Insensitivity to Pain Upon Adult-Onset Deletion of Nav1.7 Or Its Blockade with Selective Inhibitors
Epilepsy Next-Generation Sequencing Guide
Single-Cell Rnaseq Reveals Cell Adhesion Molecule Profiles in Electrophysiologically Defined Neurons
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
Supplemental Figures 04 12 2017
RT² Profiler PCR Array (Rotor-Gene® Format) Mouse Neuronal Ion Channels
SCN3A Deficiency Associated with Increased Seizure Susceptibility Tyra Lamar, Emory University Carlos G
Ion Channels Expression and Function Are Strongly Modified in Solid Tumors and Vascular Malformations
Top View
Paralogue Annotation Identifies Novel Pathogenic Variants in Patients With
Ion Channels in the P14 Rat Brain
Gene Expression Signatures of Sporadic ALS Motor Neuron Populations
Heterozygous Deletion of SCN2A and SCN3A in a Patient with Autism
Ion Channels As Therapeutic Targets in High Grade Gliomas
Single-Cell Rnaseq Reveals Cell Adhesion Molecule Profiles
Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle
Membrane Channel Gene Expression in Human Costal and Articular Chondrocytes A
Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
Investigating the Expression of Sodium Channels in Retinal Ganglion Cells Bailey Mooney, Marnie Rechtzigel, Lauren Laboissonniere, Jeff Trimarchi
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Mutations in SCN3A Cause Early Infantile Epileptic Encephalopathy
Differential Roles of Nav1.2 and Nav1.6 in Regulating Neuronal
KCNMA1 Mutation in Children with Paroxysmal Dyskinesia and Epilepsy: Case Report and Literature Review
Gene Profiling of Embryonic Skeletal Muscle Lacking Type I Ryanodine
List of Gene Panels Used for Epilepsy Diagnosis in Different Companies
Blueprint Genetics Epileptic Encephalopathy Panel
Heterozygous Variants in KCNC2 Cause a Broad Spectrum of Epilepsy Phenotypes 2 Associated with Characteristic Functional Alterations 3