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Impact of inflammatory preconditioning on murine microglial proteome response induced by focal ischemic brain injury.
Front Immunol. 2024 Apr 9;15:1227355. doi: 10.3389/fimmu.2024.1227355. eCollection 2024.
Front Immunol. 2024.
PMID: 38655254
Free PMC article.
Transcriptional regulation of lysosomal acid lipase in differentiating monocytes is mediated by transcription factors Sp1 and AP-2.
Ries S, Büchler C, Langmann T, Fehringer P, Aslanidis C, Schmitz G.
Ries S, et al. Among authors: fehringer p.
J Lipid Res. 1998 Nov;39(11):2125-34.
J Lipid Res. 1998.
PMID: 9799798
Free article.
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Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals.
Ries S, Büchler C, Schindler G, Aslanidis C, Ameis D, Gasche C, Jung N, Schambach A, Fehringer P, Vanier MT, Belli DC, Greten H, Schmitz G.
Ries S, et al. Among authors: fehringer p.
Hum Mutat. 1998;12(1):44-51. doi: 10.1002/(SICI)1098-1004(1998)12:1<44::AID-HUMU7>3.0.CO;2-O.
Hum Mutat. 1998.
PMID: 9633819
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Altered mononuclear phagocyte differentiation associated with genetic defects of the lysosomal acid lipase.
Rothe G, Stöhr J, Fehringer P, Gasche C, Schmitz G.
Rothe G, et al. Among authors: fehringer p.
Atherosclerosis. 1997 Apr;130(1-2):215-21. doi: 10.1016/s0021-9150(97)06065-6.
Atherosclerosis. 1997.
PMID: 9126667
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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.
Ries S, et al. Among authors: fehringer p.
J Lipid Res. 1996 Aug;37(8):1761-5.
J Lipid Res. 1996.
PMID: 8864960
Free article.
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Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity.
Aslanidis C, Ries S, Fehringer P, Büchler C, Klima H, Schmitz G.
Aslanidis C, et al. Among authors: fehringer p.
Genomics. 1996 Apr 1;33(1):85-93. doi: 10.1006/geno.1996.0162.
Genomics. 1996.
PMID: 8617513
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Purification, cloning, and expression of a human enzyme with acyl coenzyme A: cholesterol acyltransferase activity, which is identical to liver carboxylesterase.
Becker A, Böttcher A, Lackner KJ, Fehringer P, Notka F, Aslanidis C, Schmitz G.
Becker A, et al. Among authors: fehringer p.
Arterioscler Thromb. 1994 Aug;14(8):1346-55. doi: 10.1161/01.atv.14.8.1346.
Arterioscler Thromb. 1994.
PMID: 8049197
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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.
Klima H, et al. Among authors: fehringer p.
J Clin Invest. 1993 Dec;92(6):2713-8. doi: 10.1172/JCI116888.
J Clin Invest. 1993.
PMID: 8254026
Free PMC article.
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