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Transbilayer Phospholipid Movements in ABCA1-Deficient Cells

Tangier disease is an inherited disorder that results in a deficiency in circulating levels of HDL. Although the disease is known to be caused by mutations in the ABCA1 gene, the mechanism by which lesions in the ABCA1 ATPase effect this outcome is not known. The inability of ABCA1 knockout mice (AB...

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Détails bibliographiques
Auteurs principaux: Williamson, Patrick, Halleck, Margaret S., Malowitz, Jonathan, Ng, Susan, Fan, Xiaoxuan, Krahling, Stephen, Remaley, Alan T., Schlegel, Robert A.
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2007
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1939730/
https://ncbi.nlm.nih.gov/pubmed/17710129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0000729
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