Characterization of an abnormal species of apolipoprotein B, apolipoprotein B-37, associated with familial hypobetalipoproteinemia.

Podobne zapisy

• Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.
  od: Young, S G, i wsp.
  Wydane: (1987)
• A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.
  od: Welty, F K, i wsp.
  Wydane: (1991)
• Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in mice.
  od: Homanics, G E, i wsp.
  Wydane: (1993)
• Monoclonal antibody MB19 detects genetic polymorphism in human apolipoprotein B.
  od: Young, S G, i wsp.
  Wydane: (1986)
• Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.
  od: Young, S G, i wsp.
  Wydane: (1990)