Biochemistry, Genetics and Molecular Biology
Allele
15%
Anticipation
12%
Ataxin 3
20%
Autosomal Dominant Inheritance
31%
Base Excision Repair
13%
Binding Protein
23%
Cell Survival
10%
DNA Damage
14%
DNA Damage Response
11%
DNA Glycosylase
24%
DNA Repair
31%
DNA Sequence
14%
DNA Template
11%
Enzyme
11%
Escherichia coli
15%
Gene Expression
33%
Genetic Susceptibility
15%
Genetics
17%
Heart Conduction
10%
Homeostasis
16%
Huntingtin
16%
In Situ Hybridization
11%
Intron
15%
Kinase
45%
Mammalian Cell
16%
MBNL1
10%
Messenger RNA
26%
Mitochondrial Disorder
9%
Mitochondrion
10%
Myotonin-Protein Kinase
12%
Non-Homologous End Joining
16%
Pedigree
12%
Phosphatase
45%
Phosphotransferase
45%
Polyadenylation
9%
Polynucleotide
45%
Reporter Gene
10%
RNA
100%
RNA Polymerase II
16%
RNA-binding Protein
12%
Signal Transduction
14%
SIX5
17%
Skeletal Muscle
14%
Small Molecule
17%
Synapsin I
29%
Transcription
48%
Transgenic Mouse
10%
Translation (Protein Synthesis)
15%
Trinucleotide Repeat Expansion
11%
Wild Type
13%
Keyphrases
3′-untranslated Region (3′-UTR)
12%
ATXN3
33%
Cassette
12%
Cis-acting
16%
CTG Repeat
20%
CUG Repeats
21%
CUG-binding Protein 1 (CUGBP1)
14%
DNA Damage
15%
DNA Damage Repair
29%
DNA Damage Response
11%
DNA Glycosylase
23%
DNA Repair
22%
Gene Expression
19%
Gene Regulation
12%
Human DNA
18%
Huntingtin
12%
Huntington's Disease
31%
Klotho
16%
Mammalian Cells
15%
MBNL1
16%
Mouse Tissue
11%
Myotonic Dystrophy
55%
Myotonic Dystrophy Type 2
33%
NEIL2
25%
Non-homologous End Joining
16%
Overexpression
18%
Oxidized Bases
12%
Pathogenic Mechanism
11%
Pentanucleotide Repeat
18%
Phosphatase
38%
Phosphorylation
13%
Polynucleotide Kinase
40%
Polypyrimidine
16%
Protein Translation
15%
Repair Proteins
15%
Repeat Expansion
21%
RNA Foci
19%
RNA Polymerase II (RNAPII)
13%
RNA Repeats
16%
RNA-binding Protein
13%
SIX5
16%
Small Molecules
19%
Spinocerebellar Ataxia
21%
Spinocerebellar Ataxia Type 10
46%
Spinocerebellar Ataxia Type 3 (SCA3)
28%
Striatal
16%
SUMOylation
16%
Transgenic Mice
15%
ZNF9
16%
β-Galactosidase (β-Gal)
12%
