Biochemistry, Genetics and Molecular Biology
Allele
15%
Anticipation
12%
Ataxin 3
20%
Autosomal Dominant Inheritance
30%
Base Excision Repair
13%
Binding Protein
21%
Cell Survival
10%
DNA Damage
14%
DNA Damage Response
11%
DNA Glycosylase
25%
DNA Repair
31%
DNA Sequence
14%
DNA Template
11%
Enzyme
11%
Escherichia coli
16%
Gene Expression
34%
Genetic Susceptibility
15%
Genetics
17%
Heart Conduction
10%
Homeostasis
11%
Huntingtin
17%
in Situ Hybridization
11%
Intron
15%
Kinase
45%
Mammalian Cell
16%
MBNL1
10%
Messenger RNA
26%
Mitochondrion
10%
Mouse
46%
Myotonin-Protein Kinase
11%
Non-Homologous End Joining
17%
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
12%
SIX5
15%
Skeletal Muscle
13%
Small Molecule
18%
Synapsin I
29%
Transcription
41%
Transgenic Mouse
10%
Translation (Protein Synthesis)
15%
Trinucleotide Repeat Expansion
11%
Wild Type
13%
Keyphrases
3′-untranslated Region (3′-UTR)
12%
Apoptosis
11%
ATXN3
34%
Cassette
13%
Cis-acting
17%
CTG Repeat
20%
CUG Repeats
22%
CUG-binding Protein 1 (CUGBP1)
14%
DNA Damage Repair
20%
DNA Glycosylase
23%
DNA Repair
14%
Gene Expression
16%
Gene Regulation
13%
Human DNA
18%
Huntingtin
12%
Huntington's Disease
32%
Klotho
17%
Mammalian Cells
16%
MBNL1
17%
Mouse Tissue
11%
Myotonic Dystrophy
56%
Myotonic Dystrophy Type 2
34%
NEIL2
25%
Neurodegenerative Diseases
11%
Non-homologous End Joining
17%
Overexpression
18%
Oxidized Bases
13%
Pathogenic Mechanism
12%
Pentanucleotide Repeat
18%
Phosphatase
38%
Polynucleotide Kinase
41%
Polypyrimidine
17%
Protein Translation
15%
Repair Proteins
12%
Repeat Expansion
21%
RNA Foci
19%
RNA Polymerase II (RNAPII)
13%
RNA Repeats
17%
RNA-binding Protein
13%
SIX5
16%
Skeletal muscle
11%
Small Molecules
19%
Spinocerebellar Ataxia
21%
Spinocerebellar Ataxia Type 10
46%
Spinocerebellar Ataxia Type 3 (SCA3)
28%
Striatal
17%
SUMOylation
17%
Transgenic Mice
15%
ZNF9
17%
β-Galactosidase (β-Gal)
13%
