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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...
Tallennettuna:
| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2007
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| Aiheet: | |
| Linkit: | 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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