Medicine and Dentistry
Dystrophin
98%
Exon
96%
Duchenne Muscular Dystrophy
53%
Exon Skipping
48%
Antisense Oligonucleotide
42%
Diseases
40%
Oligomer
36%
Protein
31%
Messenger RNA Precursor
22%
Muscular Dystrophy
22%
Morpholino Oligonucleotide
21%
Induced Pluripotent Stem Cell
18%
Antisense
18%
In Vitro
17%
Phenotype
16%
Fibroblast
16%
Reading Frame
15%
Pluripotent Stem Cell Line
14%
Retinitis pigmentosa
14%
Nonsense Mutation
13%
Usher Syndrome
13%
Messenger RNA
12%
Rare Disease
12%
Stargardt Disease
10%
RNA Processing
10%
Nucleic Acid
9%
Muscle Atrophy
9%
Amyotrophic Lateral Sclerosis
8%
Inclusion Body Myositis
8%
Pathogenesis
8%
Epithelial Cell
8%
Cell Penetrating Peptide
8%
Phosphorothioic Acid
8%
Autosomal Recessive Inheritance
7%
Genotype
7%
Karyotype
7%
Kruppel Like Factor 4
7%
Episome
6%
Visual Impairment
6%
Glycogen Storage Disease Type II
6%
Retinal Specific ATP Binding Cassette Transporter
6%
Becker Muscular Dystrophy
6%
Cell Lineage
6%
Skeletal Muscle
6%
Parkinson's Disease
5%
Element
5%
RNA
5%
Wasting Syndrome
5%
Retina Dystrophy
5%
Short Hairpin RNA
5%
Agricultural and Biological Sciences
Dystrophin
100%
Exon
95%
Mutation
95%
Proteins
45%
Oligonucleotide
31%
Cell Lines
22%
Clinical Trials
22%
Fibroblast
22%
Phenotype
18%
Induced Pluripotent Stem Cell
16%
Golden Retriever
15%
ABCA4
14%
Genomics
13%
Gene Expression
13%
Nonsense Mutation
13%
Cell-Penetrating Peptide
10%
Intron
10%
Genotype
9%
Inclusion Bodies
8%
Epithelial Cells
8%
Allele
8%
Polymerase Chain Reaction
7%
Animal Models
7%
Stakeholders
6%
LIN28
6%
Bioinformatics
6%
SMN2
6%
RNA
6%
Retina
6%
Molecular Biology
5%
DNA
5%
Retinal Pigment Epithelium
5%
Gene Therapy
5%
Alternative Splicing
5%
Heritability
5%
Progerin
5%
Biochemistry, Genetics and Molecular Biology
Nested Gene
42%
Antisense
38%
Dystrophin
38%
Exon Skipping
35%
Mutation
35%
Oligonucleotide
34%
RNA Processing
12%
Gene Expression
11%
Morpholino
10%
Phosphorothioates
10%
Allele
10%
Golden Retriever
9%
Genotyping
9%
Cell-Penetrating Peptide
9%
Fibroblast
8%
RNA Splicing
7%
Intron
7%
Polymerase Chain Reaction
7%
Pregnancy
7%
SMN2
6%
Phenotype
6%
Skeletal Muscle
6%
Progerin
5%