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Quantitative gene expression analysis of fractalkine using laser microdissection in biopsies from kidney allografts with acute rejection
Pietrzyk, M. C., Banas, B., Wolf, K., Rümmele, P., Woenckhaus, M., Hoffmann, U., Krämer, B. K. und Fischereder, M. (2004) Quantitative gene expression analysis of fractalkine using laser microdissection in biopsies from kidney allografts with acute rejection. Transplantation proceedings 36 (9), S. 2659-2661.Veröffentlichungsdatum dieses Volltextes: 05 Aug 2009 13:27
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.1298
Zusammenfassung
Percutaneous biopsy of the kidney remains the gold standard to establish a diagnosis in renal diseases. Only semiquantitative assessments of gene expression on biopsies have been possible so far. We studied gene expression of the chemokine fractalkine (FKN) in 12 biopsies from laser microdissected kidney allografts that showed histologic signs of acute rejection and 10 controls. As quantified by ...
Percutaneous biopsy of the kidney remains the gold standard to establish a diagnosis in renal diseases. Only semiquantitative assessments of gene expression on biopsies have been possible so far. We studied gene expression of the chemokine fractalkine (FKN) in 12 biopsies from laser microdissected kidney allografts that showed histologic signs of acute rejection and 10 controls. As quantified by real-time PCR, the relative tubular FKN expression increased from 1.0 [0.81 to 2.95] (median [range]) in controls to 12.44 [0.90 to 191.0] in acute rejection (P < .01); glomerular FKN expression from 1.3 [0.07 to 27.44] to 12.22 [1.32 to 50.23] (P < .05); and vascular expression, from 0.72 [0.37 to 5.11] to 7.07 [1.19 to 73.49] (P < .01). Furthermore, there was a trend toward higher glomerular FKN expression among patients with more severe rejection. Our results suggest a role of FKN in acute renal allograft rejection.
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| Dokumentenart | Artikel | ||||||
| Titel eines Journals oder einer Zeitschrift | Transplantation proceedings | ||||||
| Verlag: | ELSEVIER SCIENCE INC | ||||||
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| Ort der Veröffentlichung: | NEW YORK | ||||||
| Band: | 36 | ||||||
| Nummer des Zeitschriftenheftes oder des Kapitels: | 9 | ||||||
| Seitenbereich: | S. 2659-2661 | ||||||
| Datum | November 2004 | ||||||
| Institutionen | Medizin > Lehrstuhl für Innere Medizin II | ||||||
| Identifikationsnummer |
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| Stichwörter / Keywords | DYSFUNCTION; CHEMOKINES; CX(3)CR1; TISSUE; CELLS; | ||||||
| Dewey-Dezimal-Klassifikation | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||||
| Status | Veröffentlicht | ||||||
| Begutachtet | Ja, diese Version wurde begutachtet | ||||||
| An der Universität Regensburg entstanden | Ja | ||||||
| Dokumenten-ID | 1298 |
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