Characterization of the peripheral neuropathy in neonatal and adult mice that are homozygous for the fatty liver dystrophy (fld) mutation

Medicine & Life Sciences

• Fatty Liver 100%
• Peripheral Nervous System Diseases 98%
• Mutation 52%
• Sciatic Nerve 28%
• Myelin Sheath 20%
• Hypertriglyceridemia 15%
• Lipase 14%
• Myelin P2 Protein 12%
• Neutral Glycosphingolipids 11%
• apolipoprotein A-IV 10%
• Myelin P0 Protein 10%
• Apolipoproteins C 10%
• Liver 10%
• Neurofilament Proteins 9%
• GAP-43 Protein 9%
• Lipids 8%
• Cholesterol Esters 8%
• Lipoprotein Lipase 8%
• Nerve Regeneration 8%
• Thin Layer Chromatography 8%
• Schwann Cells 7%
• Homozygote 7%
• Weaning 7%
• Apolipoproteins E 7%
• Demyelinating Diseases 7%
• Cell Nucleus 6%
• Animals 6%
• Dyslipidemias 6%
• Peripheral Nerves 6%
• Lipid Metabolism 6%
• Gait 6%
• Phospholipids 6%
• Axons 5%
• Mitochondria 5%
• Electrons 5%

Chemical Compounds

• Mutation 79%
• Lipid 48%
• Protein 38%
• Glycosphingolipid 30%
• Apolipoprotein 28%
• Developmental 28%
• Lipoprotein 25%
• Thin Layer Chromatography 21%
• Cholesterol 20%
• Phospholipid 19%
• Pharmacological Metabolism 18%
• Ester 14%
• Electron Particle 12%
• Reduction 10%