Medicine & Life Sciences
Mitochondrial Diseases
100%
Mutation
78%
Mitochondrial DNA
71%
Succinic Acid
62%
Genes
59%
Cell Respiration
54%
Mitochondrial Genome
47%
Mitochondrial Genes
46%
Leigh Disease
45%
Missense Mutation
39%
Hearing Loss
39%
Electron Transport Complex IV
35%
RNA, Transfer, Trp
32%
Transfer RNA
29%
Dilated Cardiomyopathy
27%
Mouth Mucosa
27%
Prodrugs
27%
Cardiomyopathies
25%
RNA, Transfer, Ile
25%
Kearns-Sayre Syndrome
25%
Ataxia with vitamin E deficiency
23%
Electron Transport
22%
Hair Follicle
22%
RNA, Transfer, Ser
21%
Mitochondrial Myopathies
21%
Hypertrophic Cardiomyopathy
21%
Glycogen Storage Disease Type II
18%
Adenosine Triphosphatases
18%
Amiodarone
15%
Energy Metabolism
15%
Methylene Blue
15%
Respiration
14%
Nucleotides
14%
Metformin
13%
Acetaminophen
13%
Cytochromes c
13%
Mitochondria
12%
Hydroxymethylglutaryl-CoA Reductase Inhibitors
12%
Muscular Diseases
12%
Oxidative Phosphorylation
12%
Mitochondrial Proteins
11%
Leukocytes
11%
Tunisia
11%
Proteins
11%
Lactic Acid
11%
Blood Platelets
11%
Valine
10%
Population
10%
Muscle Hypotonia
10%
frataxin
9%
Chemical Compounds
Mutation
65%
Succinate
26%
Disorder
26%
tRNA(Trp)
24%
tRNA(Ser)
24%
tRNA(Ile)
24%
Neuromuscular
22%
Amiodarone
20%
Hydroxymethylglutaryl Coenzyme A Reductase Inhibitor
18%
Secondary Structure
15%
Protein Synthesis
13%
Refractory
13%
Reactive Oxygen Metabolite
12%
Energy
11%
Pharmacological Metabolism
11%
Atorvastatin
11%
tRNA(Leu)
10%
Prodrug
10%
Metabolic
6%
Hydrophobicity
5%
Protein
5%
Glycogen
5%
Cerivastatin
5%