Biochemistry, Genetics and Molecular Biology
Mutation
100%
Lipid Storage
97%
Nested Gene
44%
Protein
42%
Lipid Droplet
34%
ABHD5
28%
Adipose Triglyceride Lipase
28%
Genetics
24%
Dehydrogenase
18%
Missense Mutation
17%
Frameshift Mutation
15%
Phenotype
14%
Riboflavin
14%
Age
13%
Lipase
13%
Patatin-Like Phospholipase
13%
Induced Pluripotent Stem Cell
13%
Acyl CoA Dehydrogenase
13%
Flavoprotein
11%
Fibroblast
11%
Wild Type
10%
Fatty Acid
9%
Lysozyme
8%
Enzymatic Hydrolysis
8%
Reduction (Chemistry)
8%
Transactivation
7%
ETFDH
7%
Lipid Metabolism
7%
Electron Transport
7%
Cyclin-Dependent Kinase
6%
Long Noncoding RNA
6%
Skeletal Muscle
6%
Genetic Disorder
6%
Ubiquinone
6%
Endorphin
6%
Molecular Weight
6%
Bioinformatics
6%
Mutant
6%
Mutant Protein
6%
Autosomal Recessive Inheritance
5%
Gene Mutation
5%
Lipid
5%
Exercise
5%
BAP1
5%
Transcription Factor EZH2
5%
Oxidoreductase
5%
Electron Transfer
5%
Sample
5%
Transcription Factor
5%
Medicine and Dentistry
Myopathy
36%
Patient
30%
Syndrome
28%
Lipid Storage
16%
Neutral Lipid Storage Disease
15%
Gene
15%
Lipid
11%
Diagnosis
9%
Muscle
9%
Therapeutic Procedure
9%
ABHD5
8%
Child
7%
Riboflavin
7%
Congenital Ichthyosiform Erythroderma
6%
Liver
6%
microRNA
5%
Family
5%
Biological Marker
5%
Analysis
5%
Parent
5%
Fatty Liver
5%
Neuroscience
Gene
20%
Brain-Derived Neurotrophic Factor
20%
Bipolar Disorder
19%
Polymorphism
16%
Muscle Disorder
12%
Genotype
11%
5-HTTLPR
9%
Depression
8%
Face
7%
Spectrum Disorder
6%
Substance Abuse and Dependence
6%
Irisin
6%
Adiponectin
6%
Oligomer
6%
Cortisol
5%
