A Novel Abetalipoproteinemia Genotype

This publication has 12 references indexed in Scilit:

• A 30-Amino Acid Truncation of the Microsomal Triglyceride Transfer Protein Large Subunit Disrupts Its Interaction with Protein Disulfide-isomerase and Causes Abetalipoproteinemia
  Published by Elsevier ,1995
• Secretion of apolipoprotein B-containing lipoproteins from HeLa cells is dependent on expression of the microsomal triglyceride transfer protein and is regulated by lipid availability.
  Proceedings of the National Academy of Sciences, 1994
• Human microsomal triglyceride transfer protein large subunit gene structure
  Biochemistry, 1994
• Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein
  Human Molecular Genetics, 1993
• Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia
  Nature, 1993
• Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia
  Science, 1992
• Simple and efficient oligonucleotide-directed mutagenesis using one primer and circular plasmid DNA template
  Gene Analysis Techniques, 1989
• Localization of intracellular triacylglycerol and cholesteryl ester transfer activity in rat tissues
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1986
• Sequence of protein disulphide isomerase and implications of its relationship to thioredoxin
  Nature, 1985
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970