Apolipoprotein O 抗体
(Apolipoprotein O (APOO))
This gene is a member of the apolipoprotein family. Members of this protein family are involved in the transport and metabolism of lipids. The encoded protein associates with HDL, LDL and VLDL lipoproteins and is characterized by chondroitin-sulfate glycosylation. This protein may be involved in preventing lipid accumulation in the myocardium in obese and diabetic patients. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 4, 5, 12 and 16.[provided by RefSeq, Sep 2009].
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Latest Publications for our Apolipoprotein O 抗体
: "QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease. ..." in: eLife, Vol. 5, (2016) (PubMed).: "QIL1 is a novel mitochondrial protein required for MICOS complex stability and cristae morphology." in: eLife, Vol. 4, (2015) (PubMed).
: "ApoO, a novel apolipoprotein, is an original glycoprotein up-regulated by diabetes in human heart." in: The Journal of biological chemistry, Vol. 281, Issue 47, pp. 36289-302, (2006) (PubMed).
: "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. ..." in: Genome research, Vol. 13, Issue 10, pp. 2265-70, (2003) (PubMed).
Aliases for Apolipoprotein O 抗体
apolipoprotein O, a (apooa) 抗体apolipoprotein O (apoo) 抗体
apolipoprotein O (APOO) 抗体
apolipoprotein O (Apoo) 抗体
apolipoprotein O L homeolog (apoo.L) 抗体
apolipoprotein O, b (apoob) 抗体
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