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Apolipoprotein and lipoprotein concentrations in familial apolipoprotein C-II deficiency.

Atherosclerosis, 1982
Lipoprotein 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
openaire   +1 more source

[Apolipoprotein C-II deficiency].

Nihon rinsho. Japanese journal of clinical medicine, 1995
Apo 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.
openaire   +1 more source

Astrocytes synthesize apolipoprotein E and metabolize apolipoprotein E-containing lipoproteins

Lipids and Lipid Metabolism, 1987
R E Pitas, J K Boyles, R W Mahley
exaly  

Is Alzheimer's disease an apolipoprotein E amyloidosis?

Lancet, The, 1995
Thomas Wisniewski, Maciej Lalowski
exaly  

[Apolipoprotein A-II abnormality].

Ryoikibetsu shokogun shirizu, 1998
S, Takahashi, I, Miyamori
openaire   +1 more source

Apolipoprotein C-II deficiency

Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1984
W. Haberbosch   +5 more
openaire   +1 more source

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