Identification of an Alternative Transcript of ABCA1 Gene in Different Human Cell Types
- 1 May 2001
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 283 (3), 590-597
- https://doi.org/10.1006/bbrc.2001.4823
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- Complete genomic sequence of the human ABCA1 gene: Analysis of the human and mouse ATP-binding cassette A promoterProceedings of the National Academy of Sciences, 2000
- Analysis of hABC1 Gene 5′ End: Additional Peptide Sequence, Promoter Region, and Four PolymorphismsBiochemical and Biophysical Research Communications, 2000
- An inventory of the human ABC proteinsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1999
- The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathwayJournal of Clinical Investigation, 1999
- Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol effluxThe Lancet, 1999
- Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyNature Genetics, 1999
- The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier diseaseNature Genetics, 1999
- Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1Nature Genetics, 1999
- Cellular Cholesterol Transport and Efflux in Fibroblasts Are Abnormal in Subjects With Familial HDL DeficiencyArteriosclerosis, Thrombosis, and Vascular Biology, 1999
- Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease.Journal of Clinical Investigation, 1995