Medicine & Life Sciences
11-beta-Hydroxysteroid Dehydrogenases
100%
Congenital Generalized Lipodystrophy
95%
Lipodystrophy
85%
1-Acylglycerol-3-Phosphate O-Acyltransferase
80%
Lamin Type A
68%
Mutation
58%
Isoenzymes
48%
Genes
44%
Apparent Mineralocorticoid Excess Syndrome
38%
Adipose Tissue
34%
prelamin A
32%
Enzymes
31%
Liver
31%
Kidney
30%
Protein Isoforms
30%
Hydrocortisone
30%
Acyltransferases
28%
Complementary DNA
27%
Oxidoreductases
27%
Familial Partial Lipodystrophy
26%
Triglycerides
24%
Mineralocorticoid Receptors
23%
NAD
22%
Lipid Droplets
22%
Phosphatidic Acids
21%
Progeria
21%
Cortisone
21%
Organism Cloning
19%
Glycerides
19%
Pedigree
18%
Adipocytes
18%
Apparent mineralocorticoid excess
18%
Hypertension
17%
Insulin Resistance
17%
Hypertriglyceridemia
16%
NADP
16%
lysophosphatidic acid
15%
Exons
14%
Genetic Heterogeneity
14%
Mineralocorticoids
14%
Proteins
14%
Tissue Distribution
14%
Aldosterone
14%
1-Acylglycerophosphocholine O-Acyltransferase
13%
Fats
13%
Phospholipids
13%
Missense Mutation
12%
Loss of Function Mutation
12%
Phosphates
12%
Werner Syndrome
12%
Chemical Compounds
Mutation
47%
Mineralocorticoid
44%
Complementary DNA
34%
Fat
25%
Cortisol
20%
Enzyme Activity
19%
Insulin Derivative
19%
Disorder
15%
Lysophosphatidic Acid
14%
Protein
14%
Cortisone
14%
Phosphatidic Acid
14%
Heterogeneity
11%
Metabolic
10%
Transferase Inhibitor
9%
Leptin
8%
Cofactor
8%
Glycerophospholipid
8%
Steroid
7%
Nucleotide
7%
Troglitazone
7%
Blum Aziridine Synthesis
6%
Peroxisome Proliferator
6%
Lipid
6%
Resistance
6%
Acyl-CoA
6%
Forskolin
5%
Prenylation
5%
Triglyceride
5%
Hypertensive
5%
Receptor Binding Affinity
5%
Tamoxifen
5%
Aldosterone
5%
Glucocorticoid
5%
Adrenal Cortex Hormone
5%