Biochemistry, Genetics and Molecular Biology
Fibroblast
100%
Biotin
94%
Amnion Fluid
71%
Enzyme
66%
Oxidoreductase
59%
Dehydrogenase
51%
Metabolic Pathway
46%
Metabolite
46%
Dilution
43%
Holocarboxylase Synthetase
36%
Amino Acids
31%
Propionic Acidemia
26%
Leucine
25%
Gas Chromatography-Mass Spectrometry
25%
Acyl-CoA
24%
Mevalonate Kinase
23%
Hypoxanthine-Guanine Phosphoribosyltransferase
22%
Chemical Ionization
21%
Valine
20%
Liquid
20%
Selected Ion Monitoring
20%
Enzyme Activity
20%
Methylcrotonyl-CoA Carboxylase
19%
Anabolism
19%
Globotriaosylceramide
19%
Coenzyme A
18%
Mouse
17%
Newborn Screening
17%
Fabry Disease
15%
HMG-CoA
15%
Precursor
15%
Methylmalonic Acidemia
14%
Newborn Period
14%
Lipid
14%
Thiolase
14%
Isoleucine
14%
Propionyl-CoA Carboxylase
13%
Lymphoblast
13%
Carnitine-Acylcarnitine Translocase Deficiency
12%
Amnion Cell
12%
Inborn Error of Metabolism
12%
Autosomal Recessive Inheritance
12%
Lymphocyte
11%
Beta Oxidation
10%
Dried Blood Spot
10%
Creatinine
10%
Succinic Semialdehyde
10%
Succinate-Semialdehyde Dehydrogenase
10%
Extract
10%
Short-Chain Fatty Acid
9%
Keyphrases
Biotin
54%
Amniotic Fluid
52%
Carboxylase
44%
Multiple Carboxylase Deficiency
39%
Prenatal Diagnosis
39%
Biotin-responsive
38%
Propionic Acidemia
36%
Fibroblasts
34%
Organic Acids
29%
Leucine
29%
Stable Isotope Analysis
29%
Cultured Fibroblasts
29%
Organic Acidemia
26%
Metabolism
26%
3-methylglutaconic Aciduria
23%
Methylmalonic Acidemia
22%
Coenzyme A
22%
Biotin Deficiency
22%
Hydratase
22%
Carboxylase Deficiency
22%
Holocarboxylase Synthetase
21%
3-hydroxy-3-methylglutaryl-coenzyme A
19%
Hypoxanthine-guanine Phosphoribosyltransferase
18%
Lyase
18%
Propionyl-CoA Carboxylase
17%
Skin Fibroblasts
17%
Chemical Ionization
17%
Lactic Acidosis
17%
Pyruvate Carboxylase
16%
Hyperammonemia
16%
Methyl
15%
Valine Metabolism
14%
Purine Metabolism
14%
Reye Syndrome
14%
Methylcrotonylglycinuria
14%
Branched-chain α-ketoacid Dehydrogenase Complex
14%
Mevalonate Kinase Deficiency
14%
Cardiomyopathy
14%
Uric Acid
14%
L-carnitine
14%
Short-chain Fatty Acids
14%
Gas Chromatography-mass Spectrometry
14%
Fetus
14%
Metabolic Acidosis
14%
Dehydrogenase
13%
Hyperuricemia
12%
Enzyme Activity
12%
3-hydroxyisovaleric Acid
12%
Inherited Disorders
12%
Partition Chromatography
12%
Pharmacology, Toxicology and Pharmaceutical Science
Disease
86%
Reye Syndrome
29%
Propionic Acidemia
29%
Carboxylase
27%
Purine
26%
Biotin
26%
Fatty Acid
26%
Hypoxanthine Phosphoribosyltransferase
25%
Ammonium
24%
Methylmalonic Acidemia
22%
Carbon 14
20%
Succinate Semialdehyde Dehydrogenase
20%
Carnitine
19%
Globotriaosylceramide
19%
Disorders of Carbohydrate Metabolism
18%
Uric Acid
18%
Purine Derivative
18%
Aciduria
17%
Stable Isotope
17%
Short Chain Fatty Acid
17%
Acetyl Coenzyme A Acetyltransferase
17%
Triheptanoin
16%
Hypoxanthine
16%
Cardiomyopathy
16%
Acidemia
15%
Heart Disease
14%
Isoleucine
14%
Mouse
14%
2 Oxoisovalerate Dehydrogenase (Lipoamide)
14%
4 Aminobutyric Acid
14%
Carboxylate
13%
Amino Acid
13%
Fabry Disease
12%
Metabolic Acidosis
12%
Hyperammonemia
12%
Valine
12%
Succinic Semialdehyde
12%
Hyperuricemia
11%
Allopurinol
11%
Acylcarnitine
11%
Symptom
10%
Chemical Ionization
10%
Leucine
9%
3 Hydroxybutyric Acid
9%
Propionic Acid
9%
Gamma-Hydroxybutyric Acid
9%
High Performance Liquid Chromatography
9%
Long Chain Acyl Coenzyme A Dehydrogenase
9%
Acyl-CoA
9%
Hydroxymethylglutaryl Coenzyme A Lyase
8%