Biochemistry, Genetics and Molecular Biology
TSC2
100%
Tuberous Sclerosis
90%
TSC1
80%
Missense Mutation
32%
RNA Splicing
28%
Mutation Rate
28%
Fibroblast
24%
Gene Expression
24%
Genetic Screening
23%
Transcriptome
23%
RNA Sequence
23%
Stress Granule
21%
Lysosome
21%
Phosphatidylinositol Phosphate
21%
Genome Sequencing
21%
SPRED1
21%
Penetrance
21%
Accessible Surface Area
21%
Amino Acids
21%
Subependymal Giant Cell Astrocytoma
21%
Somatic Mutation
21%
Gene Expression Profiling
20%
RNA
16%
RNA Sequencing
14%
Genetic Disorder
13%
Mental Retardation
10%
Alpha Helix
10%
GTPase-activating Protein
7%
Protein Function
7%
Transposable Element
7%
Point Mutation
7%
Missense
6%
Oligomerization
6%
Next Generation Sequencing
6%
Mosaicism
6%
Cycloheximide
6%
Neuroscience
Tuberous Sclerosis
47%
TSC1
29%
Astrocytoma
21%
Mammalian Target of Rapamycin
21%
Epileptic Seizure
21%
Cortical Malformation
21%
Lysosome
21%
Missense Mutation
21%
Gene Expression
21%
Somatics
21%
Mammalian Target of Rapamycin Complex 1
21%
Hyperactivity
21%
Chromosome 16
21%
Intellectual and Developmental Disabilities
11%
Pulsed-Field Gel Electrophoresis
8%
Amino Acid Substitution
7%
Autosomal Dominant Disorder
7%
Medicine and Dentistry
Tuberous Sclerosis
26%
Hyperactivation
21%
Mutation Rate
21%
Somatic Mutation
21%
Gene Expression
21%
Penetrance
21%
Pathogenicity
21%
Subependymal Giant Cell Astrocytoma
21%
Diagnosis
6%
Prenatal Screening
6%
Nonsense Mediated mRNA Decay
6%
Donor Site
6%
