Biochemistry, Genetics and Molecular Biology
Motor Neuron
86%
Antisense
74%
Exon
69%
Exon Skipping
62%
Dystrophin
52%
Skeletal Muscle
46%
Oligonucleotide
42%
Tamsulosin
34%
Genomics
33%
Upper Motor Neuron
32%
Lower Motor Neuron
32%
Dysferlin
29%
Morpholino
22%
Cell Death
21%
Gene Expression
21%
Molecular Interaction
19%
Fibroblast
19%
Tissue Culture
19%
Transcriptomics
18%
Gene Ontology
17%
Stem Cell
17%
Quality Control
15%
Genetics
14%
Secretome
14%
Protein Homeostasis
14%
RNA Metabolism
14%
Microvesicles
14%
Glutamic Acid
14%
Normal Human
14%
Biogenesis
14%
Messenger RNA
13%
Induced Pluripotent Stem Cell
12%
Genome-Wide Association Study
12%
Astrocyte
12%
Cell Membrane
11%
Secretion (Process)
11%
Bioinformatics
11%
Functional Genomics
10%
Protein-Protein Interaction
9%
RNA Sequencing
9%
Reprogramming
9%
Subcellular Localization
9%
Wild Type
9%
Methylation
9%
Annexin A2
9%
Ultracentrifugation
9%
Cell Cycle
9%
Arabidopsis
9%
Arabidopsis thaliana
9%
Oxygen Tension
9%
Medicine and Dentistry
Amyotrophic Lateral Sclerosis
38%
Duchenne Muscular Dystrophy
34%
Diseases
30%
Exon
29%
Dystrophin
28%
Neuromuscular Disease
25%
Tamsulosin
21%
Muscular Dystrophy
21%
Motor Neuron Disease
20%
Interaction Network
19%
Antisense
19%
Skeletal Muscle
19%
Neuromuscular Disorder
17%
Gene Expression
16%
Antisense Oligonucleotide
15%
Myotube
14%
Myoblast
13%
Transcriptomics
11%
Exon Skipping
10%
Myopathy
10%
Cohort Effect
9%
Personalized Medicine
9%
Sphingomyelin
9%
Ceramide
9%
Systematic Review
9%
Cellular Mechanism
9%
Cell Death
9%
Facioscapulohumeral Muscular Dystrophy
9%
Hyperplasia
9%
Hypotrophy
9%
Bromodeoxyuridine
9%
Fibroblast
9%
Dysferlin
9%
Dysferlinopathy
9%
Cell Line
9%
Cell Cycle
9%
Biological Marker
8%
Muscle Protein
8%
Tissue (Anatomy)
8%
Neurodegeneration
7%
In Vitro
7%
Cell Signaling Pathway
6%
Muscle Growth
6%
Myonecrosis
6%
Postnatal Growth
6%
Necrosis
6%
Prevalence
6%
Cell Function
5%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Motor Neuron Disease
33%
Neuromuscular
29%
Neuromuscular Disorder
27%
Tamsulosin
24%
Exosome
19%
Gene Expression
12%
Muscular Dystrophy
12%
Myoblast
11%
Cell Death
10%
Skeletal Muscle
10%
Transcriptomics
10%
Neurofilament
9%
Progressive Muscular Atrophy
9%
Primary Lateral Sclerosis
9%
RNA-Seq
9%
Sphingomyelin
9%
Ceramide
9%
Functional Genomics
9%
Cell Line
9%
Cell Cycle
9%
Dystrophin
9%
Systematic Review
9%
Neurotoxicity
9%
Neurodegeneration
7%
Cell Function
7%
Genome-Wide Association Study
7%
Neurodegenerative Disorder
6%
Transcription Factors
6%
Sphingolipid
5%
Muscle Atrophy
5%