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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Detalles Bibliográficos
Autores principales: Williamson, Patrick, Halleck, Margaret S., Malowitz, Jonathan, Ng, Susan, Fan, Xiaoxuan, Krahling, Stephen, Remaley, Alan T., Schlegel, Robert A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939730/
https://www.ncbi.nlm.nih.gov/pubmed/17710129
http://dx.doi.org/10.1371/journal.pone.0000729

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939730/
https://www.ncbi.nlm.nih.gov/pubmed/17710129
http://dx.doi.org/10.1371/journal.pone.0000729

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