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SCN2B
The Mineralocorticoid Receptor Leads to Increased Expression of EGFR
Towards Mutation-Specific Precision Medicine in Atypical Clinical
Transcriptomic Analysis of Native Versus Cultured Human and Mouse Dorsal Root Ganglia Focused on Pharmacological Targets Short
Investigating Unexplained Deaths for Molecular Autopsies
Non-Coding Rnas in the Cardiac Action Potential and Their Impact on Arrhythmogenic Cardiac Diseases
Atrial Fibrillation (ATRIA) Study
72X36 Poster Template
Spatial Distribution of Leading Pacemaker Sites in the Normal, Intact Rat Sinoa
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Pflugers Final
Sodium Channel Mutations in Epilepsy and Other Neurological Disorders
Graded Co-Expression of Ion Channel, Neurofilament, and Synaptic Genes in Fast- Spiking Vestibular Nucleus Neurons
Cardiovascular Diseases Genetic Testing Program Information
Mutations of Voltage-Gated Ionic Channels and Risk of Severe Cardiac Arrhythmias
Genetic Testing for Inherited Cardiomyopathies and Channelopathies AHS – M2025
Scn2b Rabbit Polyclonal Antibody – TA329032 | Origene
GSE50161, (C) GSE66354, (D) GSE74195 and (E) GSE86574
An Enigmatic Case of Cardiac Death in an 18-Years Old Girl
Top View
Binary Architecture of the Nav1.2-B2 Signaling Complex Samir Das1†, John Gilchrist2†, Frank Bosmans2,3*, Filip Van Petegem1*
Supplemental Figures 04 12 2017
Drug Screening in Scn1a Zebrafish Mutant Identifies Clemizole As A
Knockdown of Hnrnpa0, a Del(5Q) Gene, Alters Myeloid Cell Fate In
RT² Profiler PCR Array (Rotor-Gene® Format) Mouse Neuronal Ion Channels
Exclusion of the SCN2B Gene As Candidate for CMT4B
Identification of Genomic Regions Associated with Characters Correlated with the Fertilizing Capacity of Holstein Bulls
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Brugada Syndrome Genereview
Ion Channels Expression and Function Are Strongly Modified in Solid Tumors and Vascular Malformations
Supplementary Data
Ion Channels in the P14 Rat Brain
The Cancer Genome Atlas Dataset-Based Analysis of Aberrantly Expressed Genes by Geneanalytics in Thymoma Associated Myasthenia Gravis: Focusing on T Cells
Single-Cell Transcriptomic Profiling of Progenitors of the Oligodendrocyte Lineage Reveals Transcriptional Convergence During Development
Exploring the Role of Stromal Osmoregulation in Cancer and Disease Using Executable Modelling
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Supplemental Table S18. Cellular Process Enrichment Analysis Output
S41467-018-05074-Y.Pdf