Homozygous familial hypercholesterolemia mutant with a defect in internalization of low density lipoprotein.

Podobne knjige/članki

• Defects of receptor-mediated low density lipoprotein catabolism in homozygous familial hypercholesterolemia and hypothyroidism in vivo.
  od: Thompson, G R, et al.
  Izdano: (1981)
• Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis
  od: Fahed, Akl C., et al.
  Izdano: (2012)
• Binding, internalization, and degradation of low density lipoprotein by normal human fibroblasts and by fibroblasts from a case of homozygous familial hypercholesterolemia.
  od: Stein, O, et al.
  Izdano: (1976)
• Degradation of cationized low density lipoprotein and regulation of cholesterol metabolism in homozygous familial hypercholesterolemia fibroblasts.
  od: Basu, S K, et al.
  Izdano: (1976)
• Esterification of Low Density Lipoprotein Cholesterol in Human Fibroblasts and Its Absence in Homozygous Familial Hypercholesterolemia
  od: Goldstein, Joseph L., et al.
  Izdano: (1974)