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Atherosclerosis|February 10, 1997
Heterozygous hepatic lipase deficiency, due to two missense mutations R186H and L334F, in the HL geneP Knudsen, M Antikainen, M Uusi-Oukari, et al.
The Journal of Biological Chemistry|August 25, 1984
Abnormal lecithin:cholesterol acyltransferase activation by a human apolipoprotein A-I variant in which a single lysine residue is deletedS C Rall, K H Weisgraber, R W Mahley, et al.
The Journal of Clinical Investigation|March 21, 1998
Adenosine(5') oligophospho-(5') guanosines and guanosine(5') oligophospho-(5') guanosines in human plateletsH Schlüter, I Grobeta, J Bachmann, et al.
Nature Genetics|August 4, 1999
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1S Rust, M Rosier, H Funke, et al.
Journal of Lipid Research|June 4, 1998
Plasma and fibroblasts of Tangier disease patients are disturbed in transferring phospholipids onto apolipoprotein A-IA von Eckardstein, A Chirazi, S Schuler-Lüttmann, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 2, 1999
c-erbB-2/EGFR as dominant heterodimerization partners determine a motogenic phenotype in human breast cancer cellsB H Brandt, A Roetger, T Dittmar, et al.
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