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39篇 您的检索式:作者名="Hollborn"
    题名 作者 年代 出处 被引量
1Early activation of inflammatory and immune response-related genes after experimental detachment of the porcine retina显示文摘Hollborn M Francke M landiev I 2008Invest Ophthalmol Via Sci2008,49,3:1
2Proliferative gliosis causes misloeation and inactivation of inwardly rectifying K^+ (Kir) channels in rabbit retinal glial cells 显示文摘Ulbricht E Pannicke T Hollborn M 2008Exp Eye Res2008,86,2:1
3Epression of LRPI in retinal pigment epithelial cells and its regulation by growth factors显示文摘Hollborn M Birkenmeier G Saalbach A 2004Invest Ophthalnol Vis Sci2004,45,6:1
4Transcriptional regulation of aquaporin-3 in hu- man retinal pigment epithelial cells 显示文摘Hollborn M Ulbricht E Reichenbach A 2012Mol Biol Rep2012,39,8:1
5Expression of LRP1 in retinal pigment epithelial cells and its regulation by growth factors显示文摘Hollborn M Birkenmeier G Saalbach A 2004Invest Ophthalmol Vis Sci2004,45,:1
6Induction of cytokines in glial cells surrounding cortical β-amyloid plaques in transgenic Tg2576 mice with Alzheimer pathology显示文摘Gaby Mehlhorn Margrit Hollborn Reinhard Schliebs 2000International Journal of Developmental Neuroscience2000,,4:1
7Retinal gene expression and Müller cell responses after branch retinal vein occlusion in the rat显示文摘Rehak M Hollborn M Iandiev I 2009Invest Ophthalmol Vis Sei2009,50,:1
8Cellular signaling and factors involved in Müller cell gliosis: Neuroprotective and detrimental effects显示文摘Andreas Bringmann Ianors Iandiev Thomas Pannicke Antje Wurm Margrit Hollborn Peter Wiedemann Neville N. Osborne Andreas Reichenbach 2009Progress in Retinal and Eye Research2009,,6:1
9Positive feedback regulation between MMP-9 and VEGF in human RPE cells显示文摘Hollborn M Stathopoulos C Steffen A 2007Invest Ophthalmol Vis Sci2007,48,9:1
10Human retinal epithelium produces and responds to placenta growth factor 显示文摘Hollborn M Tenckhoff S Seifert M 2006Graefes Arch Clin Exp Ophthalmol2006,244,6:1
11Expression of LRP1 in retinal pigment epithelial cells and its regulation by growth factors显示文摘Hollborn M Birkenmeier G Saalbach A 2004Invest Ophthalmol Vis Sci2004,45,6:1
12Effective chemokines and cytokines in the rejection of human retinal pigment epithelium (RPE) cell grafts 显示文摘Enzmann V Kaufmann A Hollborn M Wiedemann P Gemsa D Kohen L 1999Transpl Immunol1999,7,1:1
13Retinal gene expression andMuller cell responses after branch retinal vein occlusion in the ra显示文摘Rehak M Hollborn M Iandiev I 2009Invest Ophthalmol Vis Sci2009,50,:1
14Glial cell expression of hepatocyte growth factor in vitreoretinal proliferative disease显示文摘Hollborn M Krausse C Iandiev I 2004Lab Invest2004,84,8:1
15The influence of proinflammatory cytokines on human retinal pigment epithelium cell receptors显示文摘Hollborn M Kohen L Wiedemann P 2001Greafe''s Arch Clin Exp Ophthalmol2001,239,4:1
16Minor influence of the immunosuppressive cytokines IL-10 and TGF-beta on the proliferation and apoptosis of human retinal pigment epithelial (RPE) cells in vitro 显示文摘Enzmann V Hollborn M Wiedemann P 2001Ocul Immunol Inflamm2001,9,4:1
17Expression of LRP1 in retinal pigment epithelial cells and its regulation by growth factors显示文摘Hollborn M Birkenmeier G Saalbach A 2004Invest Ophthalmol Vis Sci2004,45,6:1
18Characterixation of the basic fibroblast growth factor-evoked proliferation of the human Muller cell line,MIO-M1显示文摘Hollborn M Jahn K Limb GA 2004Graefes Arch Clin Exp Ophthalmol2004,242,5:1
19Positive feedback regulation between MMP-9 and VEGF in human RPE cells 显示文摘Hollborn M Stathopoulos C Steffen A 2007Invest Ophthalmol Visual Sci2007,48,9:1
20NOD2-and disease-specific gene expression profiles of peripheral blood mononuclear cells from Crohn's disease patients显示文摘AIM To investigate disease-specific gene expression profiles of peripheral blood mononuclear cells(PBMCs) from Crohn's disease(CD) patients in clinical remission.METHODS Patients with CD in clinical remission or with very low disease activity according to the Crohn's disease activity index were genotyped regarding nucleotidebinding oligomerization domain 2(NOD2),and PBMCs from wild-type(WT)-NOD2 patients,patients with homozygous or heterozygous NOD2 mutations and healthy donors were isolated for further analysis.The cells were cultured with vitamin D,peptidoglycan(PGN) and lipopolysaccharide(LPS) for defined periods of time before RNA was isolated and subjected to microarray analysis using Clariom S assays and quantitative realtime PCR.NOD2-and disease-specific gene expression profiles were evaluated with repeated measure ANOVA by a general linear model.RESULTS Employing microarray assays,a total of 267 genes were identified that were significantly up-or downregulated in PBMCs of WT-NOD2 patients,compared to healthy donors after challenge with vitamin D and/or a combination of LPS and PGN(P < 0.05;threshold:≥ 2-fold change).For further analysis by real-time PCR,genes with known impact on inflammation and immunity were selected that fulfilled predefined expression criteria.In a larger cohort of patients and controls,a disease-associated expression pattern,with higher transcript levels in vitamin D-treated PBMCs from patients,was observed for three of these genes,CLEC5 A(P < 0.030),lysozyme(LYZ;P < 0.047) and TREM1(P < 0.023).Six genes were found to be expressed in a NOD2-dependent manner(CD101,P < 0.002;CLEC5 A,P < 0.020;CXCL5,P < 0.009;IL-24,P < 0.044;ITGB2,P < 0.041;LYZ,P < 0.042).Interestingly,the highest transcript levels were observed in patients with heterozygous NOD2 mutations.CONCLUSION Our data identify CLEC5 A and LYZ as CD-and NOD2-associated genes of PBMCs and encourage further studies on their pathomechanistic roles.Holger Schufler Maria Rohde Sarah Rohde Astrid Huth Nicole Gittel Hannes Hollborn Dirk Koczan Ane Glass Georg Lamprecht Robert Jaster 2018World Journal of Gastroenterology2018,24,11:1
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