Neuroscience
Dystonia
100%
Parkinson's Disease
85%
Synuclein
56%
Cell Nucleus Membrane
47%
Leucine Rich Repeat Kinase 2
34%
Neurodegeneration
26%
In Vivo
24%
Central Nervous System
18%
Striatum
16%
Stereotypic Movement Disorder
16%
Familial Parkinson's Disease
15%
Dopaminergic Neuron
14%
Cholinergic
14%
Cell Death
14%
Parkinsonism
12%
Motor Control
12%
Neurodegenerative Disorder
11%
Oligodendrocyte
11%
Chaperone-Mediated Autophagy
11%
Extracellular Matrix
11%
Envelope Protein
11%
Endoplasmic reticulum
10%
Brainstem
10%
Dopaminergic
10%
Epileptic Absence
9%
Polypeptide
9%
Kinase
8%
Behavior (Neuroscience)
8%
Basal Ganglia
7%
Thalamotomy
7%
Substantia nigra
7%
Tractography
7%
Lysosome
7%
Neuropeptide
7%
Cerebellum
7%
Proteasome
7%
Nitric Oxide
7%
Midbrain
6%
Neurotransmitter Release
6%
Loss of Function Mutation
6%
Diffusion Tensor Imaging
6%
Neurotoxin
6%
Mitochondrial Permeability Transition Pore
6%
Tetracycline
6%
Synaptic Plasticity
6%
Tremor
5%
Small Hairpin RNA
5%
Neurogenesis
5%
Neuromuscular Disorder
5%
Peripheral Nerve
5%
Biochemistry, Genetics and Molecular Biology
Nuclear Membrane
88%
Kinase
57%
Phosphotransferase
57%
Mouse
54%
Leucine-Rich Repeat
48%
Synuclein
35%
Genetics
27%
THAP1
22%
Maturation
20%
Skeletal Muscle
15%
Hepatocyte
13%
Emerin
13%
Oligodendrocyte
12%
Knockout Mouse
12%
Chaperone-Mediated Autophagy
11%
Secretion (Process)
11%
Gene Function
11%
Fish Model
11%
Mouse Model
11%
Cell Death
11%
Wild Type
10%
Myelination
9%
Nuclear Pore
8%
Facilitated Diffusion
8%
Dopaminergic
8%
Glutamic Acid
7%
Gene Mutation
7%
Lysosome
7%
Animal Model
7%
Lipid Metabolism
7%
Lipid Liver Level
7%
Lamin
7%
Nitric Oxide
7%
AAA Protein
6%
Neurotransmitter Release
6%
YY1
6%
Nerve Cell Plasticity
6%
Transgenic Mouse
6%
Proteasome
6%
WD40 Repeat
6%
Protein Interaction
5%
Mouse Mutant
5%
Postnatal Development
5%
Protein Phosphatase 1
5%
Nervous System Development
5%
Normal Human
5%
Gene Product
5%
Mitochondrial DNA
5%
Volume
5%
Zebra Fish
5%
Keyphrases
TorsinA
61%
Parkinson's Disease
56%
Leucine-rich Repeat Kinase 2 (LRRK2)
36%
Dystonia
33%
Polypeptide 1
32%
Lamina-associated
32%
DYT1 Dystonia
30%
Alpha-synuclein (α-syn)
25%
DYT1
24%
Nuclear Envelope
22%
Mouse Model
20%
THAP1
17%
Neurodegeneration
16%
Disease-related Proteins
14%
TOR1A
13%
Sympathetic Neurons
12%
Ciliary Neurotrophic Factor
11%
Leukemia Inhibitory Factor
11%
Neurodevelopmental Disorders
11%
Disease Pathogenesis
10%
Nuclear Envelope Proteins
10%
ATP13A2
9%
Central Nervous System
9%
Idiopathic Parkinson's Disease
9%
Nuclear Membrane
9%
Choline Acetyltransferase (ChAT)
9%
Cell Death
8%
Overexpression
8%
Striated muscle
8%
Nuclear Envelopathies
8%
Steatosis
7%
Genetic Causes
7%
Membrane Budding
7%
DYT-THAP1
7%
Neurotoxicity
7%
Neurodegenerative Diseases
7%
Genetic Background
7%
FEOBV
7%
Dopaminergic Neurons
7%
Disease-causing mutations
6%
Death Signals
6%
Non-cell Autonomous
6%
Human Brain
6%
Mesencephalic
6%
Parkinson's Disease Model
6%
Apoptosis
6%
Glial Cell Line-derived Neurotrophic Factor
6%
Kinase Domain
6%
WD40 Domain
6%
Substantia Nigra
6%
