Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sabine Neudecker"'
Autor:
Frank G Zöllner, Daniel Schock-Kusch, Sandra Bäcker, Sabine Neudecker, Norbert Gretz, Lothar R Schad
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79992 (2013)
Glomerular filtration rate (GFR) is an essential parameter of kidney function which can be measured by dynamic contrast enhanced magnetic resonance imaging (MRI-GFR) and transcutaneous approaches based on fluorescent tracer molecules (optical-GFR). I
Externí odkaz:
https://doaj.org/article/61a6db549bdd4fbaab3c86ce60dc6c87
Autor:
Daniel Schock-Kusch, Stefania Geraci, Esther Ermeling, Yury Shulhevich, Carsten Sticht, Juergen Hesser, Dzmitry Stsepankou, Sabine Neudecker, Johannes Pill, Roland Schmitt, Anette Melk
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e71519 (2013)
Measuring renal function in laboratory animals using blood and/or urine sampling is not only labor-intensive but puts also a strain on the animal. Several approaches for fluorescence based transcutaneous measurement of the glomerular filtration rate
Externí odkaz:
https://doaj.org/article/59478e21424b4ccda58b31867968dc3f
Autor:
Annemarie Pucci, Arthur Schönhals, Bettina Kränzlin, Sabine Neudecker, A. Regenscheit, Wolfgang Petrich, Niels Kröger-Lui, Katharina Haase, Norbert Gretz
Publikováno v:
The Analyst. 140:2086-2092
Changes in the volume covered by mucin-secreting goblet cell regions within colon thin sections may serve as a means to differentiate between ulcerative colitis and infectious colitis. Here we show that rapid, quantum cascade laser-based mid-infrared
Autor:
Sabine Neudecker, Anatoli Shmarlouski, Jürgen Hesser, Jochen Friedemann, Yury Shulhevich, Dzmitry Stsepankou, Stefania Geraci, Norbert Gretz
Publikováno v:
Biomedical Signal Processing and Control. 14:30-41
Measurement of renal function in awake rats or mice can be accomplished by an intelligent plaster device that fits on the back of animals. The device performs a percutaneous measurement of the kinetics of a labeled fluorescent dye exclusively elimina
Autor:
Susanne N.E. Boehn, Norbert Gretz, Sabine Neudecker, Bettina Kränzlin, M. T. Bihoreau, Li Li, Sonja Spahn, Sigrid Hoffmann, Priyanka Pandey, Vicente E. Torres, Andrea Keppler, Hermann Josef Gröne
Publikováno v:
Nephrology Dialysis Transplantation. 28:2045-2058
Background Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common human inherited diseases. Modifier genes seem to modulate the disease progression and might therefore be promising drug targets. Although a number of modifier l
Autor:
Sabine Neudecker, Norbert Gretz
Publikováno v:
Polycystic Kidney Disease: from Bench to Bedside. :6-16
Autor:
Sabine Neudecker, Raffi Kalayciyan, Friedrich Wetterling, Norbert Gretz, Lothar R. Schad, Stefan Haneder
Publikováno v:
Journal of Magnetic Resonance Imaging. 38:564-572
Purpose: To develop a sodium-MRI (23Na-MRI) method for bilateral renal sodium concentration (RSC) measurements in rat kidneys at 9.4 Tesla (T). Materials and Methods: To simultaneously achieve high B1-field homogeneity and high receive sensitivity a
Autor:
Wilhelm Kriz, Ivo Wolf, Carsten Sticht, Daniel Schock-Kusch, John F. Bertram, Melanie Heilmann, Lina Gubhaju, Norbert Gretz, Lothar R. Schad, Sabine Neudecker
Publikováno v:
Nephrology Dialysis Transplantation. 27:100-107
Background Glomerular number and size are important risk factors for chronic kidney disease (CKD) and cardiovascular disease and have traditionally been estimated using invasive techniques. Here, we report a novel technique to count and size every gl
Autor:
Elena Maier, Sabine Neudecker, Bettina Kränzlin, Sigrid Hoffmann, Marie-Thérèse Bihoreau, Kiran Menon, Norbert Gretz, Rebecca Walz, Nicholas Obermüller
Publikováno v:
The American Journal of Pathology. 177:3000-3009
The PKD/Mhm(cy/+) rat is a widely used animal model for the study of human autosomal dominant polycystic kidney disease, one of the most common genetic disorders, affecting one in 1000 individuals. We identified a new gene, Anks6, which is mutated (A
Publikováno v:
Medizinische Genetik. 22:332-338
Zusammenfassung Polyzystische Nierenerkrankungen (PKD) sind der häufigste genetische Grund für ein terminales Nierenversagen. Flüssigkeitsgefüllte Zysten bilden sich im Nierenparenchym und beeinträchtigen die Nierenfunktion mit zunehmender Anzah