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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...

詳細記述

保存先:
書誌詳細
主要な著者: Williamson, Patrick, Halleck, Margaret S., Malowitz, Jonathan, Ng, Susan, Fan, Xiaoxuan, Krahling, Stephen, Remaley, Alan T., Schlegel, Robert A.
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2007
主題:
オンライン・アクセス: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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