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Author Report for: Aslanidis C

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    Title: Lipoprotein (a) downregulates lysosomal acid lipase and induces interleukin-6 in human blood monocytes
    Buechler C, Ullrich H, Aslanidis C, Bared SM, Lingenhel A, Ritter M, Schmitz G
    Ref: Biochimica & Biophysica Acta, 1642:25, 2003 : PubMed

            

    Title: High-speed detection of the two common paraoxonase polymorphisms Leu55-->Met and Gln192-->Arg by real-time fluorescence PCR and melting curves
    Harangi M, Aslanidis C, Paragh G, Schmitz G
    Ref: Clinical Chemistry & Laboratory Medicine, 40:337, 2002 : PubMed

            

    Title: Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals
    Ries S, Buchler C, Schindler G, Aslanidis C, Ameis D, Gasche C, Jung N, Schambach A, Fehringer P and Schmitz G <3 more author(s)>
    Ref: Hum Mutat, 12:44, 1998 : PubMed

            

    Title: Transcriptional regulation of lysosomal acid lipase in differentiating monocytes is mediated by transcription factors Sp1 and AP-2
    Ries S, Buchler C, Langmann T, Fehringer P, Aslanidis C, Schmitz G
    Ref: J Lipid Res, 39:2125, 1998 : PubMed

            

    Title: A novel variant of lysosomal acid lipase in cholesteryl ester storage disease associated with mild phenotype and improvement on lovastatin
    Gasche C, Aslanidis C, Kain R, Exner M, Helbich T, Dejaco C, Schmitz G, Ferenci P
    Ref: Journal of Hepatology, 27:744, 1997 : PubMed

            

    Title: Differentiation-dependent expression of a human carboxylesterase in monocytic cells and transcription factor binding to the promoter
    Langmann T, Aslanidis C, Schuierer M, Schmitz G
    Ref: Biochemical & Biophysical Research Communications, 230:215, 1997 : PubMed

            

    Title: Structural organization and characterization of the promoter region of a human carboxylesterase gene
    Langmann T, Becker A, Aslanidis C, Notka F, Ullrich H, Schwer H, Schmitz G
    Ref: Biochimica & Biophysica Acta, 1350:65, 1997 : PubMed

            

    Title: Molecular cloning and characterization of a novel putative carboxylesterase, present in human intestine and liver
    Schwer H, Langmann T, Daig R, Becker A, Aslanidis C, Schmitz G
    Ref: Biochemical & Biophysical Research Communications, 233:117, 1997 : PubMed

            

    Title: Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity
    Aslanidis C, Ries S, Fehringer P, Buchler C, Klima H, Schmitz G
    Ref: Genomics, 33:85, 1996 : PubMed

            

    Title: A new mutation in the gene for lysosomal acid lipase leads to Wolman disease in an African kindred
    Ries S, Aslanidis C, Fehringer P, Carel JC, Gendrel D, Schmitz G
    Ref: J Lipid Res, 37:1761, 1996 : PubMed

            

    Title: Genomic organization of the human lysosomal acid lipase gene (LIPA)
    Aslanidis C, Klima H, Lackner KJ, Schmitz G
    Ref: Genomics, 20:329, 1994 : PubMed

            

    Title: Purification, cloning, and expression of a human enzyme with acyl coenzyme A: cholesterol acyltransferase activity, which is identical to liver carboxylesterase
    Becker A, Bottcher A, Lackner KJ, Fehringer P, Notka F, Aslanidis C, Schmitz G
    Ref: Arterioscler Thromb, 14:1346, 1994 : PubMed

            

    Title: A splice junction mutation causes deletion of a 72-base exon from the mRNA for lysosomal acid lipase in a patient with cholesteryl ester storage disease
    Klima H, Ullrich K, Aslanidis C, Fehringer P, Lackner KJ, Schmitz G
    Ref: J Clinical Investigation, 92:2713, 1993 : PubMed

            


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