Biochemistry, Genetics and Molecular Biology
Rett Syndrome
100%
Mutation
70%
Protein
63%
Corepressor
46%
Defense Mechanism
46%
Ubiquitin
46%
Transcription
34%
DNA
34%
Nested Gene
34%
Silencing Mediator of Retinoid and Thyroid Hormone Receptor
28%
Chromatin
27%
Methylation
26%
MECP2
24%
DNA Methylation
23%
Missense Mutation
23%
AT Hook Motif
23%
Luciferase
23%
Nuclear Localization Sequence
23%
Phosphorylation
23%
Wild Type
23%
DNA Binding
23%
MBD1
23%
Development
23%
Luminescence
23%
Small Molecule
23%
Protein Inhibitor of Activated STAT
23%
Regulatory Mechanism
23%
Histone Deacetylase
23%
Phenotype
22%
Mouse
20%
Nuclear Protein
18%
Sumoylation
18%
WD40 Repeat
17%
Methyl-CpG-Binding Domain
17%
DNA-binding Domain
16%
Aptitude
14%
Cytosine
14%
Histone
13%
Mouse Model
12%
Screening
11%
Brain Function
11%
Protein Kinase A
11%
Comprehension
11%
Animal Models
11%
Peptide
11%
Spectrum
11%
Conjugation
11%
Neuronal Activity
10%
SETDB1
9%
Amino Acid Substitution
7%
Neuroscience
Rett Syndrome
47%
DNA
23%
Nuclear Localization Signal
23%
Silencing Mediator of Retinoid and Thyroid Hormone Receptor
23%
Ubiquitin
23%
Phosphorylation
23%
Protein
20%
Sumoylation
15%
Nervous System Disorder
7%
Nuclear Protein
7%
Chromatin
6%
Missense Mutation
5%
Gene
5%
