Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells

Thromb Haemost. 1999 Feb;81(2):322-3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Amino Acid Substitution*
  • Biological Transport
  • Blood Coagulation Disorders / enzymology*
  • Blood Coagulation Disorders / genetics
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Cell Membrane / metabolism
  • DNA Mutational Analysis
  • DNA, Complementary / genetics
  • Female
  • Gene Expression
  • Gene Frequency
  • Genes, Recessive
  • Genotype
  • Humans
  • Male
  • Membrane Lipids / physiology
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics*
  • Mutation, Missense*
  • Phosphatidylserines / physiology
  • Phospholipid Transfer Proteins*
  • Point Mutation*
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics
  • Syndrome

Substances

  • Carrier Proteins
  • DNA, Complementary
  • Membrane Lipids
  • Membrane Proteins
  • Phosphatidylserines
  • Phospholipid Transfer Proteins
  • RNA, Messenger