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Apolipoprotein and lipoprotein concentrations in familial apolipoprotein C-II deficiency.
Atherosclerosis, 1982Lipoprotein and apolipoprotein concentrations were determined in 11 homozygous and 9 heterozygous subjects for familial apolipoprotein C-II (Apo C-II) deficiency. Apo C-II was not detectable in the homozygotes, with the exception of 1 subject who possessed immunochemically detectable quantities in one of two samples.
W C, Breckenridge +3 more
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[Apolipoprotein C-II deficiency].
Nihon rinsho. Japanese journal of clinical medicine, 1995Apo C-II has a central role in triglyceride metabolism as a cofactor for lipoprotein lipase (LPL), the enzyme that catalyzes the hydrolysis of triglycerides on plasma lipoproteins. Apo C-II deficiency is a rare genetic disorder that is inherited as an autosomal recessive trait.
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Astrocytes synthesize apolipoprotein E and metabolize apolipoprotein E-containing lipoproteins
Lipids and Lipid Metabolism, 1987R E Pitas, J K Boyles, R W Mahley
exaly
Is Alzheimer's disease an apolipoprotein E amyloidosis?
Lancet, The, 1995Thomas Wisniewski, Maciej Lalowski
exaly
[Apolipoprotein A-II abnormality].
Ryoikibetsu shokogun shirizu, 1998S, Takahashi, I, Miyamori
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Apolipoprotein C-II deficiency
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1984W. Haberbosch +5 more
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