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Results: 1-14 |
Results: 14
The zinc finger protein 202 (ZNF202) is a transcriptional repressor of ATPbinding cassette transporter A1 (ABCA1) and ABCG1 gene expression and a modulator of cellular lipid efflux
Authors: Porsch-Ozcurumez, M Langmann, T Heimerl, S Borsukova, H Kaminski, WE Drobnik, W Honer, C Schumacher, C Schmitz, G
Citation: M. Porsch-ozcurumez et al., The zinc finger protein 202 (ZNF202) is a transcriptional repressor of ATPbinding cassette transporter A1 (ABCA1) and ABCG1 gene expression and a modulator of cellular lipid efflux, J BIOL CHEM, 276(15), 2001, pp. 12427-12433
ATP-binding cassette transporter A1 (ABCA1) affects total body sterol metabolism
Authors: Drobnik, W Lindenthal, B Lieser, B Ritter, M Weber, TC Liebisch, G Giesa, U Igel, M Borsukova, H Buchler, C Fung-Leung, WP Von Bergmann, K Schmitz, G
Citation: W. Drobnik et al., ATP-binding cassette transporter A1 (ABCA1) affects total body sterol metabolism, GASTROENTY, 120(5), 2001, pp. 1203-1211
Lipopolysaccharide and ceramide docking to CD14 provokes ligand-specific receptor clustering in rafts
Authors: Pfeiffer, A Bottcher, A Orso, E Kapinsky, M Nagy, P Bodnar, A Spreitzer, I Liebisch, G Drobnik, W Gempel, K Horn, M Holmer, S Hartung, T Multhoff, G Schutz, G Schindler, H Ulmer, AJ Heine, H Stelter, F Schutt, C Rothe, G Szollosi, J Damjanovich, S Schmitz, G
Citation: A. Pfeiffer et al., Lipopolysaccharide and ceramide docking to CD14 provokes ligand-specific receptor clustering in rafts, EUR J IMMUN, 31(11), 2001, pp. 3153-3164
Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice
Authors: Orso, E Broccardo, C Kaminski, WE Bottcher, A Liebisch, G Drobnik, W Gotz, A Chambenoit, O Diederich, W Langmann, T Spruss, T Luciani, MF Rothe, G Lackner, KJ Chimini, G Schmitz, G
Citation: E. Orso et al., Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice, NAT GENET, 24(2), 2000, pp. 192-196
ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport
Authors: Klucken, J Buchler, C Orso, E Kaminski, WE Porsch-Ozcurumez, M Liebisch, C Kapinsky, M Diederich, W Drobnik, W Dean, M Allikmets, R Schmitz, G
Citation: J. Klucken et al., ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport, P NAS US, 97(2), 2000, pp. 817-822
Mutation analysis of the human adipocyte-specific apM-I gene
Authors: Schaffler, A Barth, N Palitzsch, KD Drobnik, W Scholmerich, J Schmitz, G
Citation: A. Schaffler et al., Mutation analysis of the human adipocyte-specific apM-I gene, EUR J CL IN, 30(10), 2000, pp. 879-887
Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7)
Authors: Kaminski, WE Orso, E Diederich, W Klucken, J Drobnik, W Schmitz, G
Citation: We. Kaminski et al., Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7), BIOC BIOP R, 273(2), 2000, pp. 532-538
Growth and cell cycle abnormalities of fibroblasts from Tangier disease patients
Authors: Drobnik, W Liebisch, G Biederer, C Trumbach, B Rogler, G Muller, P Schmitz, G
Citation: W. Drobnik et al., Growth and cell cycle abnormalities of fibroblasts from Tangier disease patients, ART THROM V, 19(1), 1999, pp. 28-38
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangierdisease
Authors: Bodzioch, M Orso, E Klucken, T Langmann, T Bottcher, L Diederich, W Drobnik, W Barlage, S Buchler, C Porsch-Ozcurumez, M Kaminski, WE Hahmann, HW Oette, K Rothe, G Aslanidis, C Lackner, KJ Schmitz, G
Citation: M. Bodzioch et al., The gene encoding ATP-binding cassette transporter 1 is mutated in Tangierdisease, NAT GENET, 22(4), 1999, pp. 347-351
ATP-binding cassette transporter A1 (ABCA1) in macrophages: A dual function in inflammation and lipid metabolism?
Authors: Schmitz, G Kaminski, WE Porsch-Ozcurumez, M Klucken, J Orso, E Bodzioch, M Buchler, C Drobnik, W
Citation: G. Schmitz et al., ATP-binding cassette transporter A1 (ABCA1) in macrophages: A dual function in inflammation and lipid metabolism?, PATHOBIOLOG, 67(5-6), 1999, pp. 236-240
Soluble thrombomodulin and endothelial dysfunction in early atherosclerosis
Authors: John, S Drobnik, W Lackner, K Schmieder, RE
Citation: S. John et al., Soluble thrombomodulin and endothelial dysfunction in early atherosclerosis, LANCET, 354(9190), 1999, pp. 1647-1647
Quantitative measurement of different ceramide species from crude cellularextracts by electrospray ionization tandem mass spectrometry (ESI-MS/MS)
Authors: Liebisch, G Drobnik, W Reil, M Trumbach, B Arnecke, R Olgemoller, B Roscher, A Schmitz, G
Citation: G. Liebisch et al., Quantitative measurement of different ceramide species from crude cellularextracts by electrospray ionization tandem mass spectrometry (ESI-MS/MS), J LIPID RES, 40(8), 1999, pp. 1539-1546
Frequency and significance of the A -> G (-3826) polymorphism in the promoter of the gene for uncoupling protein-I with regard to metabolic parameters and adipocyte transcription factor binding in a large population-based Caucasian cohort
Authors: Schaffler, A Palitzsch, KD Watzlawek, E Drobnik, W Schwer, H Scholmerich, J Schmitz, G
Citation: A. Schaffler et al., Frequency and significance of the A -> G (-3826) polymorphism in the promoter of the gene for uncoupling protein-I with regard to metabolic parameters and adipocyte transcription factor binding in a large population-based Caucasian cohort, EUR J CL IN, 29(9), 1999, pp. 770-779
The human apM-1, an adipocyte-specific gene linked to the family of TNF's and to genes expressed in activated T cells, is mapped to chromosome 1q21.3-q23, a susceptibility locus identified for familial combined hyperlipidaemia (FCH)
Authors: Schaffer, A Orso, E Palitzsch, KD Buchler, C Drobnik, W Furst, A Scholmerich, J Schmitz, G
Citation: A. Schaffer et al., The human apM-1, an adipocyte-specific gene linked to the family of TNF's and to genes expressed in activated T cells, is mapped to chromosome 1q21.3-q23, a susceptibility locus identified for familial combined hyperlipidaemia (FCH), BIOC BIOP R, 260(2), 1999, pp. 416-425
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