Item Type | Name |
Concept
|
Acetylcholinesterase
|
Concept
|
Adenylyl Cyclases
|
Concept
|
Algorithms
|
Concept
|
Bordetella pertussis
|
Concept
|
Calmodulin
|
Concept
|
Analysis of Variance
|
Concept
|
Dipeptides
|
Concept
|
Atrophy
|
Concept
|
Carbon Monoxide
|
Concept
|
Clostridium botulinum
|
Concept
|
Blood-Brain Barrier
|
Concept
|
Homozygote
|
Concept
|
DNA Mutational Analysis
|
Concept
|
Dogs
|
Concept
|
Depression
|
Concept
|
Enzyme Activation
|
Concept
|
Gene Expression Regulation
|
Concept
|
Nitrogen
|
Concept
|
Hippocampus
|
Concept
|
DNA, Viral
|
Concept
|
Hydrogen-Ion Concentration
|
Concept
|
Lobeline
|
Concept
|
Housing, Animal
|
Concept
|
Hydrocortisone
|
Concept
|
Phosphatidylcholines
|
Concept
|
Extremities
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Mutation
|
Concept
|
Myoglobin
|
Concept
|
Hot Temperature
|
Concept
|
Nucleic Acid Conformation
|
Concept
|
Oocytes
|
Concept
|
Pedigree
|
Concept
|
Probability
|
Concept
|
Pressure
|
Concept
|
Protein Processing, Post-Translational
|
Concept
|
Pyridines
|
Concept
|
Gangliosides
|
Concept
|
Receptor, Insulin
|
Concept
|
Spasms, Infantile
|
Concept
|
Cohort Studies
|
Concept
|
Sexual Maturation
|
Concept
|
Humans
|
Concept
|
Protein Engineering
|
Concept
|
Sodium Channels
|
Concept
|
Transduction, Genetic
|
Concept
|
Vacuolar Proton-Translocating ATPases
|
Concept
|
Principal Component Analysis
|
Concept
|
Rats, Sprague-Dawley
|
Concept
|
Sequence Alignment
|
Concept
|
In Situ Hybridization
|
Concept
|
Treatment Outcome
|
Concept
|
Mice, Knockout
|
Concept
|
Crystallography, X-Ray
|
Concept
|
Mutation, Missense
|
Concept
|
Genetic Association Studies
|
Concept
|
Proteomics
|
Concept
|
COS Cells
|
Concept
|
Mice
|
Concept
|
Receptors, Nicotinic
|
Concept
|
Radioimmunoassay
|
Concept
|
Rats
|
Concept
|
High-Throughput Nucleotide Sequencing
|
Concept
|
Temperature
|
Concept
|
Models, Statistical
|
Concept
|
Lysosomal-Associated Membrane Protein 1
|
Concept
|
Botulinum Toxins, Type A
|
Concept
|
Kv1.2 Potassium Channel
|
Concept
|
Nanofibers
|
Concept
|
Cations
|
Concept
|
Chromatin
|
Concept
|
Cloning, Molecular
|
Concept
|
Heterozygote
|
Concept
|
Kinetics
|
Concept
|
Longitudinal Studies
|
Concept
|
Microscopy, Fluorescence
|
Concept
|
Recombinant Fusion Proteins
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Genetic Loci
|
Academic Article
|
Intermediate state trapping of a voltage sensor.
|
Academic Article
|
Functional role of ATP binding to synapsin I in synaptic vesicle trafficking and release dynamics.
|
Academic Article
|
Temperature Accelerated Molecular Dynamics with Soft-Ratcheting Criterion Orients Enhanced Sampling by Low-Resolution Information.
|
Academic Article
|
Comparison between Mean Forces and Swarms-of-Trajectories String Methods.
|
Academic Article
|
Free energy and kinetics of conformational transitions from Voronoi tessellated milestoning with restraining potentials.
|
Academic Article
|
Molecular Dynamics Simulations of Ion Selectivity in a Claudin-15 Paracellular Channel.
|
Academic Article
|
Closed-Locked and Apo-Resting State Structures of the Human a7 Nicotinic Receptor: A Computational Study.
|
Academic Article
|
Synapsins are expressed at neuronal and non-neuronal locations in Octopus vulgaris.
|
Academic Article
|
Neuronal firing modulation by a membrane-targeted photoswitch.
|
Academic Article
|
Engineering REST-Specific Synthetic PUF Proteins to Control Neuronal Gene Expression: A Combined Experimental and Computational Study.
|
Academic Article
|
Thermodynamics and Kinetics of Ion Permeation in Wild-Type and Mutated Open Active Conformation of the Human a7 Nicotinic Receptor.
|
Academic Article
|
Isobaric Labeling Proteomics Allows a High-Throughput Investigation of Protein Corona Orientation.
|
Academic Article
|
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
|
Academic Article
|
Structural Mechanism of ?-Currents in a Mutated Kv7.2 Voltage Sensor Domain from Molecular Dynamics Simulations.
|
Academic Article
|
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants.
|
Academic Article
|
Free energy and kinetics of cAMP permeation through connexin26 via applied voltage and milestoning.
|
Academic Article
|
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
|
Academic Article
|
Computational Assessment of Different Structural Models for Claudin-5 Complexes in Blood-Brain Barrier Tight Junctions.
|
Academic Article
|
Computational study of ion permeation through claudin-4 paracellular channels.
|
Academic Article
|
Computational methods and theory for ion channel research.
|
Academic Article
|
Non-Markov-Type Analysis and Diffusion Map Analysis for Molecular Dynamics Trajectory of Chignolin at a High Temperature.
|
Academic Article
|
Ca2+ binding to synapsin I regulates resting Ca2+ and recovery from synaptic depression in nerve terminals.
|
Academic Article
|
Editorial: Recent advancements in modeling and simulations of ion channels.
|
Academic Article
|
In Silico Conformational Features of Botulinum Toxins A1 and E1 According to Intraluminal Acidification.
|
Academic Article
|
Multiscale modelling of claudin-based assemblies: A magnifying glass for novel structures of biological interfaces.
|
Concept
|
Voltage-Gated Sodium Channels
|
Concept
|
NAV1.2 Voltage-Gated Sodium Channel
|
Concept
|
Optogenetics
|
Concept
|
alpha7 Nicotinic Acetylcholine Receptor
|
Academic Article
|
The intramembrane COOH-terminal domain of PRRT2 regulates voltage-dependent Na+ channels.
|
Academic Article
|
Molecular Dynamics Simulations of Ion Permeation in Human Voltage-Gated Sodium Channels.
|
Academic Article
|
The impact of pathogenic and artificial mutations on Claudin-5 selectivity from molecular dynamics simulations.
|
Academic Article
|
Missense mutations in the membrane domain of PRRT2 affect its interaction with Nav1.2 voltage-gated sodium channels.
|
Academic Article
|
Charting Nanocluster Structures via Convolutional Neural Networks.
|
Academic Article
|
Case Report: Novel biallelic moderately damaging variants in RTTN in a patient with cerebellar dysplasia.
|