Resultados da pesquisa - G. Assmann

Isolation of human serum HDL1 by zonal ultracentrifugation Por G Schmitz, G Assmann

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Isoproteins of human apolipoprotein A-II: isolation and characterization. Por G Schmitz, K Ilsemann, B Melnik, G Assmann

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One-step screening method for the polymorphism of apolipoproteins A-I, A-II, and A-IV Por H J Menzel, R G Kladetzky, G Assmann

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High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins. Por H U Jabs, G Assmann, D Greifendorf, A Benninghoven

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Lipid binding properties of the Tangier apolipoprotein A-I and its isoproteins. Por M Rosseneu, G Assmann, M J Taveirne, G Schmitz

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Interaction of Tangier lipoproteins with cholesteryl ester-laden mouse peritoneal macrophages. Por G Schmitz, G Assmann, B Brennhausen, H J Schaefer

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Site-specific methionine sulfoxide formation is the structural basis of chromatographic heterogeneity of apolipoproteins A-I, C-II, and C-III. Por A von Eckardstein, M Walter, H Holz, A Benninghoven, G Assmann

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Structural and functional properties of reconstituted high density lipoprotein discs prepared with six apolipoprotein A-I variants. Por A Jonas, A von Eckardstein, KE Kézdy, A Steinmetz, G Assmann

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A new molecular defect in the lecithin: cholesterol acyltransferase (LCAT) gene associated with fish eye disease. Por C Contacos, D R Sullivan, K A Rye, H Funke, G Assmann

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Characterization of very low density lipoproteins and intermediate density lipoproteins of normo- and hyperlipidemic apolipoprotein E-2 homozygotes. Por G Schmitz, G Assmann, J Augustin, A Dirkes-Kersting, B Brennhaüsen, C Karoff

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The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes Por J A Kuivenhoven, H Pritchard, J Hill, J Frohlich, G Assmann, J Kastelein

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Accumulation of oxygenated steryl esters in Wolman's disease Por G. Assmann, D.S. Fredrickson, H.R. Sloan, H.M. Fales, R.J. Highet

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Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass... Por T P Leren, K S Bakken, U Daum, L Ose, K Berg, G Assmann, A von Eckardstein

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Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45–>Asn), in a Turkish patient. Por S Lüttmann, A von Eckardstein, W Wei, H Funke, E Köhler, R W Mahley, G Assmann

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Normolipemic dysbetalipoproteinemia and hyperlipoproteinemia type III in subjects homozygous for a rare genetic apolipoprotein E variant (apoE1). Por A Steinmetz, N Assefbarkhi, C Eltze, K Ehlenz, H Funke, A Pies, G Assmann, H Kaffarnik

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An improved method for quantification of cholesterol and cholesteryl esters in human monocyte-derived macrophages by high performance liquid chromatography with identification of u... Por P Cullen, M Fobker, K Tegelkamp, K Meyer, F Kannenberg, A Cignarella, A Benninghoven, G Assmann

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A natural apolipoprotein A-I variant, apoA-I (L141R)Pisa, interferes with the formation of alpha-high density lipoproteins (HDL) but not with the formation of pre beta 1-HDL and in... Por R Miccoli, Y Zhu, U Daum, J Wessling, Y Huang, R Navalesi, G Assmann, A von Eckardstein

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