Keyphrases
3′-untranslated Region (3′-UTR)
20%
Active Intervention
20%
Allelic Series
20%
Amyotrophic Lateral Sclerosis
20%
Antisense Oligonucleotides
20%
C9orf72
20%
Cas9 Protein
20%
Cellular Pathways
20%
Clinical Biomarkers
80%
CTG Expansion
80%
CTG Repeat
20%
Developmental Regulation
20%
Disease Biomarker
20%
Disease Mechanisms
20%
Disease Status
20%
DMPK Gene
20%
Effective Therapy
20%
Expansion mutation
20%
Frontotemporal Dementia
20%
Functional Impairment
20%
FXTAS
20%
Genetic Modification
20%
Heart muscle
20%
Knock-in Mouse Model
20%
Knockdown
20%
Late-onset
20%
Lateral Sclerosis
10%
Length-dependent
20%
Loss Function
20%
MicroRNA
20%
Microsatellite Disorders
20%
Mouse Experimental Model
20%
Mouse Model
20%
Multiple Strategies
20%
Muscle Structure
20%
Myotonic Dystrophy
80%
Neuromuscular Disease
20%
Non-AUG Translation
20%
Pathomechanism
20%
Pre-mRNA Processing
20%
Preclinical Therapy
80%
RAN Translation
20%
Relative Contribution
20%
Repeat Expansion Diseases
10%
Repeat Length
20%
RNA in Disease
20%
RNA Localization
20%
RNA Processing
20%
RNA Splicing Defects
40%
RNA-binding Protein
20%
Rolling Circle Amplification
20%
Small Molecules
40%
Splicing Defect
40%
Therapeutic Approaches
20%
Therapeutic Intervention
20%
Therapeutic Response
20%
Transcriptome Analysis
20%
Biochemistry, Genetics and Molecular Biology
Antisense
25%
C9orf72
20%
CRISPR/Cas9
25%
Experimental Model
25%
Gene Expression Profiling
25%
Messenger RNA
25%
MicroRNA
25%
Microsatellite DNA
20%
Mouse
50%
Mouse Model
20%
Oligonucleotide
25%
Precursor mRNA
25%
RNA
75%
RNA Processing
45%
RNA Splicing
50%
RNA-binding Protein
25%
Rolling Circle Amplification
20%
Small Molecule
45%
Splicing Defect
100%
Transcription
50%
Untranslated Region
20%
Pharmacology, Toxicology and Pharmaceutical Science
Amyotrophic Lateral Sclerosis
20%
Antisense Oligonucleotide
20%
Ataxia
20%
Biological Marker
80%
Disease
60%
Experimental Mouse
20%
Frontotemporal Dementia
20%
Functional Disease
20%
Messenger RNA Precursor
20%
microRNA
20%
Mouse
20%
Mouse Model
20%
Myotonic Dystrophy
80%
Neuromuscular Disease
20%
RNA Binding Protein
20%
Sclerosis
5%
Syndrome
20%
Transcriptome
20%