Keyphrases
Duchenne muscular Dystrophy
100%
Limb-girdle muscular Dystrophy
82%
DNAJB6
68%
Dystrophin
59%
Muscle Disease
50%
Idiopathic Inflammatory Myopathies
46%
Muscular Dystrophy
45%
Myopathy
42%
Exon Duplication
36%
Skipping
36%
Exon
36%
Dermatomyositis
33%
Genetic Basis
27%
Exon Skipping
26%
Heat Shock Protein 70 (HSP70)
25%
Dystrophinopathy
25%
Missense mutation
25%
Mouse Model
24%
Treatment Strategy
22%
Knockdown
22%
Clinical Trials
22%
Duplication
22%
Myopathology
22%
Clinical Phenotype
21%
Polymyositis
21%
Disease Onset
21%
Multisystem Proteinopathy
21%
Therapeutic Potential
20%
Exome Sequencing
20%
Therapeutic Approaches
20%
Myotubes
19%
Gene Therapy
18%
Tetrahymena
18%
DNAJB4
18%
Congenital Myopathy
18%
Camptocormia
18%
Manifesting Carriers
18%
6-methylmercaptopurine
18%
Adenine Phosphoribosyltransferase
18%
Isoform-specific
18%
Respiratory Failure
18%
Clinical Utility
18%
Lithium Chloride
18%
Z-domain
18%
Cytosolic 5′-nucleotidase 1A
18%
Phenotypic Spectrum
18%
Valosin-containing Protein
18%
Natural History
18%
Patient-derived Cell Line
18%
Phenotypic Diversity
18%
Biochemistry, Genetics and Molecular Biology
Exon
72%
Mouse Model
52%
Dystrophin
49%
Isoform
39%
Skeletal Muscle
38%
Exome Sequencing
27%
Genetics
24%
Proteinopathy
21%
Missense Mutation
20%
Mass Spectrometry
20%
Immunoblotting
20%
Genotyping
19%
Clinical Trial
18%
Oligonucleotide
18%
Tetrahymena
18%
Antisense
18%
Mutant Protein
18%
Genetic Carrier
18%
Heterozygote
18%
Adenine Phosphoribosyltransferase
18%
Adenine
18%
Small Molecule
18%
Valosin-Containing Protein
18%
Internal Ribosome Entry Site
18%
Disease Registry
18%
Grip Strength
18%
Cas9
18%
Isotope Labeling
18%
Catenin
18%
Glycogen Synthase Kinase
18%
ATPase
18%
Protein Quality Control
18%
Exon Skipping
17%
Wild Type
17%
Dystroglycan
15%
Messenger RNA
14%
Paromomycin
12%
Reading Frame
12%
Fibroblast
12%
RNAI
12%
Co-Chaperone
11%
Missense
9%
Knockout Mouse
9%
Disease Burden
9%
Rigidity
9%
Fungal Cell Culture
9%
Chaperone (Protein)
9%
Heat Shock
9%
Observational Study
9%
Cell Death
9%
Medicine and Dentistry
Duchenne Muscular Dystrophy
60%
Myopathy
60%
Diseases
48%
Exon
36%
Dermatomyositis
27%
Exome Sequencing
22%
Camptocormia
18%
Polymyositis
18%
Valosin Containing Protein
18%
Limb Girdle Muscular Dystrophy
18%
Muscular Dystrophy
18%
5' Nucleotidase
18%
Myositis
18%
Cell Line
18%
Inclusion Body Myositis
18%
Antisense Oligonucleotide
18%
Adenosine Triphosphatase
18%
Exon Skipping
17%
Muscle Biopsy
16%
Disease
15%
Messenger RNA
14%
Ophthalmoparesis
13%
Vacuolization
13%
Weakness
12%
Genetic Screening
12%
Gene Therapy
12%
Muscle Disease
12%
Dystrophin
11%
Histopathology
10%
Muscle Weakness
10%
Heterozygote
9%
Antisynthetase Syndrome
9%
Onset Age
7%
Patient Registry
7%
Clinical Research
6%
Clinical Feature
6%
Immunosuppressive Drug
6%
Clinical Trial
6%
Haploinsufficiency
6%
Nosology
6%
Cohort Effect
6%
Medicine
6%
Drive
6%
Neuromuscular Disorder
6%
Paget Bone Disease
5%
Skeletal Muscle
5%
Genotype Phenotype Correlation
5%
