Keyphrases
Valosin-containing Protein
100%
Limb-girdle muscular Dystrophy
78%
Myopathy
75%
Autophagy
65%
Multisystem Proteinopathy
65%
Frontotemporal Dementia
57%
Inclusion Body Myopathy
54%
Paget's Disease of Bone
42%
Inclusion Body Myositis
42%
DNAJB6
39%
Skeletal muscle
39%
IBMPFD
35%
Amyotrophic Lateral Sclerosis
34%
TAR DNA-binding Protein 43 (TDP-43)
33%
SQSTM1
28%
Protein Aggregates
27%
ATP Synthase
25%
Idiopathic Inflammatory Myopathies
25%
Sporadic Inclusion Body Myositis (sIBM)
25%
Autophagic
24%
Motor Neuron
21%
Mouse Model
21%
Lysosome
20%
Muscular Dystrophy
19%
Protein Aggregation
19%
Clinical Preparedness
18%
Autophagosome
18%
Protein-coding Genes
18%
Disease-causing mutations
18%
VCP mutation
18%
Muscle Biopsy
17%
Autosomal Dominant
17%
Autophagic Flux
17%
Disease-associated
17%
Rapamycin
16%
Hsp40
16%
Knock-in Mouse Model
16%
Degenerative Disease
16%
Clinical Trials
15%
AAA+ ATPase
15%
Mouse Skeletal muscle
15%
Phenotypic Spectrum
15%
Hereditary Myopathy
15%
Heat Shock Protein 70 (HSP70)
14%
Diagnostic Criteria
14%
Mammalian Target of Rapamycin (mTOR)
14%
Distal Myopathy
14%
Lysophagy
14%
Macrophages
13%
R155H mutation
13%
Biochemistry, Genetics and Molecular Biology
Valosin-Containing Protein
83%
Autophagy
67%
P97
64%
Skeletal Muscle
62%
Proteinopathy
58%
Genetics
50%
ATPase
35%
Transactive Response Dna Binding Protein-43
31%
Mouse Model
28%
Motor Neuron
28%
Protein Aggregation
27%
Autophagosome
22%
Ubiquitin
21%
Autosomal Dominant Inheritance
21%
Prion Protein
20%
Exome Sequencing
19%
Missense
19%
Wild Type
18%
Lysosome
18%
Clinical Trial
16%
Induced Pluripotent Stem Cell
14%
Clinical Classification
13%
Presenilin
13%
Genetic Divergence
12%
Programmed Cell Death
12%
Stress Granule
11%
Autosomal Recessive Inheritance
11%
Missense Mutation
11%
Cell Function
11%
Isoform
10%
RNA-binding Protein
10%
Protein Homeostasis
10%
Fibroblast
10%
Macrophage
10%
Hsp70
10%
Proteomics
10%
Mechanistic Target of Rapamycin
10%
Catenin
10%
Homeostasis
10%
Ubiquitination
9%
Mitochondrion
9%
Desmin
9%
Amino Acids
9%
AAA+
9%
Heat Shock Protein
9%
Molecular Genetics
9%
Proband
9%
Crystallin
9%
Mass Spectrometry
8%
Knockout Mouse
8%
Medicine and Dentistry
Myopathy
54%
Diseases
52%
Valosin Containing Protein
39%
Limb Girdle Muscular Dystrophy
32%
Autophagy
29%
Inclusion Body Myositis
23%
Skeletal Muscle
23%
Weakness
17%
Vacuolization
16%
Muscle Disease
15%
Clinical Trial
15%
Diagnostic Criterion
14%
Amyotrophic Lateral Sclerosis
13%
Muscle Biopsy
13%
Adenosine Triphosphatase
12%
Frontotemporal Lobar Degeneration
12%
Paget Bone Disease
12%
Mitophagy
11%
Autophagosome
11%
Distal Myopathy
11%
Muscular Dystrophy
11%
Rapamycin
10%
Copper Deficiency
9%
Protein Diet
9%
Cardiovascular Risk
9%
Transactive Response Dna Binding Protein-43
9%
Fronto-Temporal Lobar Degeneration
9%
Macrophage
9%
Desmin
9%
Myositis
9%
Genotype Phenotype Correlation
8%
Cell Function
8%
5' Nucleotidase
8%
Neuromuscular Disorder
7%
TAR DNA Binding Protein
6%
Magnetic Resonance Imaging
6%
DeJerine-Sottas Disease
6%
Neuropathy
6%
Quality of Life
6%
Duchenne Muscular Dystrophy
6%
Genetic Screening
6%
Autosomal Dominant Inheritance
5%
Loss of Function Mutation
5%
Motor Neuron Disease
5%
Pathogenicity
5%
Knockout Mouse
5%
Colchicine
5%
Autosomal Recessive Inheritance
5%
Disease
5%
Ubiquitin
5%
