Keyphrases
Parkinson's Disease
100%
Alpha-synuclein (α-syn)
53%
Huntington's Disease
40%
Glucocerebrosidase
38%
Neurodegenerative Diseases
26%
Neurodegeneration
25%
Lysosomal Disease
23%
Induced Pluripotent Stem Cells (iPSCs)
22%
Mitochondrial Dysfunction
21%
Mutant Huntingtin
19%
ATP13A2
17%
Parkin
16%
Parkinson Patients
16%
Dopaminergic Neurons
15%
Idiopathic Parkinson's Disease
15%
Synucleinopathy
14%
Huntingtin
13%
Glucocerebrosidase Activity
13%
Lysosome
13%
Lysosomal Function
13%
GBA1
13%
Mitochondria-lysosome Contacts
11%
Transcription Factor
10%
Gaucher Disease
10%
Patient-derived
10%
Disease Pathogenesis
10%
PARK9
9%
Parkinson's Disease Model
9%
Stem Cell-derived
9%
Autophagy
8%
PGC-1
8%
Human Dopaminergic Neuron
8%
Dopamine
8%
Movement Disorders
8%
Dystonia
8%
Midbrain Dopaminergic Neurons
8%
Rab7
8%
Mitochondria
7%
Neuroprotection
7%
Genetic Risk
7%
Neurological Disorders
7%
Dopamine Metabolism
7%
Leucine-rich Repeat Kinase 2 (LRRK2)
7%
Lysosomal Storage Disease
7%
Synaptic Dysfunction
7%
Dysregulation
6%
Mendelian Randomization
6%
Human Neurons
6%
Integral Membrane Protein
6%
Gene Expression
6%
Biochemistry, Genetics and Molecular Biology
Synuclein
46%
Glucocerebrosidase
35%
Glucosylceramidase
35%
Dopaminergic
26%
Genetics
25%
Induced Pluripotent Stem Cell
25%
Huntingtin
23%
Lysosome
20%
Mitochondrion
18%
ATP13A2
13%
Fibroblast
11%
Enzyme
11%
Transcription Factors
10%
Dynamics
9%
Mitochondrial Disorder
9%
Homeostasis
9%
Autosomal Recessive Inheritance
8%
Wild Type
8%
Gene Expression
8%
Oxidative Stress
8%
Gaucher's Disease
7%
PINK1
7%
Promoter Region
7%
Autophagy
7%
Genetic Risk
7%
Secretion (Process)
6%
Mendelian Randomization
6%
Enzymatic Hydrolysis
6%
Mitophagy
6%
Integral Membrane Protein
6%
Guanosine Triphosphate
6%
Missense
6%
Binding Protein
6%
Lysine
5%
Penetrance
5%
Nerve Cell Differentiation
5%
Single-Nucleotide Polymorphism
5%
Progerin
5%
Lysosomal Storage Disease
5%
Epigenetics
5%
Neuroscience
Parkinson's Disease
75%
Glucosylceramidase
37%
Synuclein
32%
Huntington's Disease
30%
Neurodegeneration
27%
Huntingtin
23%
Neurodegenerative Disorder
21%
Dopaminergic Neuron
19%
Stem Cell
17%
Lysosomes
14%
Transcription Factors
10%
Parkin
10%
Midbrain
9%
Autophagy
9%
Stereotypic Movement Disorder
9%
Dystonia
9%
Gene Expression
8%
Dopaminergic
7%
Neuroprotection
7%
Parkinsonism
7%
Metabolic Pathway
6%
Fibroblast
6%
Synapsin I
6%
Synaptic Vesicle
6%
Mitochondrion
6%
Carboxy-Lyases
6%
Integral Membrane Protein
6%
Receptor
6%
Polyglutamine
5%
Lysosome Enzyme
5%
Alpha-Synuclein
5%
Familial Parkinson's Disease
5%
Alzheimer's Disease
5%
Amyloid Precursor Protein
5%