Felix Aigner

Prof. Felix Aigner

Barmherzige Brüder Hospital Graz
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 September 2008 in International Journal of Colorectal Disease
Verified
Journal Article
Closed access
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FAFelix Aigner
Felix Aigner
HGHannes Gruber
Hannes Gruber
FCFriedrich Conrad
Friedrich Conrad
JEJasmin Eder
Jasmin Eder
TWThilo Wedel
Thilo Wedel
HFHelga Fritsch
Helga Fritsch

1 January 2004 in The American Journal of Surgery
Verified
Journal Article
Closed access
FAFelix Aigner
Felix Aigner
GBGerd Bodner
Gerd Bodner
FCFriedrich Conrad
Friedrich Conrad
GMGodwin Mbaka
Godwin Mbaka
AKAlfons Kreczy
Alfons Kreczy
HFHelga Fritsch
Helga Fritsch

1 July 2006 in Journal of Gastrointestinal Surgery
Verified
Journal Article
Closed access
FAFelix Aigner
Felix Aigner
GBGerd Bodner
Gerd Bodner
HGHannes Gruber
Hannes Gruber
FCFriedrich Conrad
Friedrich Conrad
HFHelga Fritsch
Helga Fritsch
HBHugo Bonatti
Hugo Bonatti

1 February 2004 in Diseases of the Colon & Rectum
Verified
Journal Article
Closed access
FAFelix Aigner
Felix Aigner
AZAndrew P. Zbar
Andrew P. Zbar
BLBarbara Ludwikowski
Barbara Ludwikowski
AKAlfons Kreczy
Alfons Kreczy
PKPeter Kovacs
Peter Kovacs
HFHelga Fritsch
Helga Fritsch
PURPOSE:The rectogenital septum (known in clinical literature as Denonvilliers' fascia) forms an incomplete partition between the rectum and the urogenital organs in both men and women. It is composed of collagenous and elastic fibers and smooth muscle cells intermingled with nerve fibers emerging f

26 March 2007 in American Journal of Transplantation
Verified
Journal Article
Open access
PDF file
FAFelix Aigner
Felix Aigner
HMH. T. Maier
H. T. Maier
HSH. G. Schwelberger
H. G. Schwelberger
EWE. A. Wallnöfer
E. A. Wallnöfer
AAA. Amberger
A. Amberger
Jakob TroppmairJakob Troppmair
Jakob Troppmair
Ischemia and reperfusion (IR) are known to negatively affect early allograft function following solid organ transplantation. Lipocalin‐2 (Lcn‐2) has been described as a marker and potential positive modulator of acute inflammation during these processes. Using a heterotopic murine heart transplant model we previously found that IR resulted in a pronounced upregulation of Lcn‐2 mRNA in the heart at 12 (22.7‐fold increase) and 24 h (9.8‐fold increase) of reperfusion. We now confirm this increase at the protein level and provide evidence for infiltrating polymorphonuclear cells as the primary source of Lcn‐2 protein. Lcn‐2 levels are increased 6.6‐fold at 12 h, 11.4‐fold at 24 h and 6.4 fold at 48 h after reperfusion. In Lcn‐2−/− grafts the number of infiltrating granulocytes is reduced by 54% (p < 0.05) at 2 h, 79% (p < 0.01) at 12 h, 72% (p < 0.01) at 24 h and 52% (p < 0.01) at 48 h after reperfusion compared to Lcn‐2+/+ grafts, without any differences in cardiomyocyte apoptosis. These data suggest a function of Lcn‐2 in the initiation of the inflammatory response. Moreover, an increase in Lcn‐2 is not only restricted to the transplanted heart, but is also observed in the kidney, hinting at a possible involvement of Lcn‐2 in the systemic response to IR.

1 April 2006 in Arthroscopy
Verified
Journal Article
Closed access
FKFranz Kralinger
Franz Kralinger
FAFelix Aigner
Felix Aigner
SLStefano Longato
Stefano Longato
MRMichael Rieger
Michael Rieger
MWMarkus Wambacher
Markus Wambacher