Analysis of hABC1 Gene 5′ End: Additional Peptide Sequence, Promoter Region, and Four Polymorphisms

This publication has 17 references indexed in Scilit:

• Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice
  Nature Genetics, 2000
• An inventory of the human ABC proteins
  Biochimica et Biophysica Acta (BBA) - Biomembranes, 1999
• Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred
  Proceedings of the National Academy of Sciences, 1999
• The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway
  Journal of Clinical Investigation, 1999
• Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux
  The Lancet, 1999
• Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
  Nature Genetics, 1999
• The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
  Nature Genetics, 1999
• Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
  Nature Genetics, 1999
• Molecular Cloning of the Human ATP-Binding Cassette Transporter 1 (hABC1): Evidence for Sterol-Dependent Regulation in Macrophages
  Biochemical and Biophysical Research Communications, 1999
• ABC1, an ATP Binding Cassette Transporter Required for Phagocytosis of Apoptotic Cells, Generates a Regulated Anion Flux after Expression in Xenopus laevis Oocytes
  Journal of Biological Chemistry, 1997