Biochemistry, Genetics and Molecular Biology
RNA
100%
Transcription
48%
Phosphotransferase
45%
Polynucleotide
45%
Kinase
45%
Phosphatase
45%
Gene Expression
33%
Autosomal Dominant Inheritance
31%
DNA Repair
31%
Synapsin I
29%
Messenger RNA
26%
DNA Glycosylase
24%
Binding Protein
23%
Ataxin 3
20%
Small Molecule
17%
Genetics
17%
SIX5
17%
Huntingtin
16%
Non-Homologous End Joining
16%
Mammalian Cell
16%
Homeostasis
16%
RNA Polymerase II
16%
Escherichia coli
15%
Allele
15%
Translation (Protein Synthesis)
15%
Genetic Susceptibility
15%
Intron
15%
DNA Sequence
14%
Skeletal Muscle
14%
Signal Transduction
14%
DNA Damage
14%
Wild Type
13%
Base Excision Repair
13%
Pedigree
12%
Anticipation
12%
Myotonin-Protein Kinase
12%
RNA-binding Protein
12%
DNA Damage Response
11%
Trinucleotide Repeat Expansion
11%
Enzyme
11%
In Situ Hybridization
11%
DNA Template
11%
MBNL1
10%
Reporter Gene
10%
Heart Conduction
10%
Transgenic Mouse
10%
Cell Survival
10%
Mitochondrion
10%
Mitochondrial Disorder
9%
Polyadenylation
9%
Keyphrases
Myotonic Dystrophy
55%
Spinocerebellar Ataxia Type 10
46%
Polynucleotide Kinase
40%
Phosphatase
38%
Myotonic Dystrophy Type 2
33%
ATXN3
33%
Huntington's Disease
31%
Spinocerebellar Ataxia Type 3 (SCA3)
28%
NEIL2
25%
DNA Glycosylase
23%
CUG Repeats
21%
Spinocerebellar Ataxia
21%
Repeat Expansion
21%
DNA Damage Repair
20%
CTG Repeat
20%
Small Molecules
19%
RNA Foci
19%
Overexpression
18%
Human DNA
18%
Pentanucleotide Repeat
18%
DNA Repair
17%
RNA Repeats
16%
Polypyrimidine
16%
MBNL1
16%
Striatal
16%
Cis-acting
16%
Non-homologous End Joining
16%
Klotho
16%
ZNF9
16%
SUMOylation
16%
SIX5
16%
Gene Expression
16%
Mammalian Cells
15%
Transgenic Mice
15%
Protein Translation
15%
CUG-binding Protein 1 (CUGBP1)
14%
RNA Polymerase II (RNAPII)
13%
RNA-binding Protein
13%
Cassette
12%
Gene Regulation
12%
β-Galactosidase (β-Gal)
12%
Oxidized Bases
12%
Huntingtin
12%
Repair Proteins
12%
3′-untranslated Region (3′-UTR)
12%
Pathogenic Mechanism
11%
Mouse Tissue
11%
Neurodegenerative Diseases
11%
Apoptosis
11%
Skeletal muscle
11%
