Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Laura Herlan"'
Autor:
Angela Schulz, Nicola Victoria Müller, Nina Anne van de Lest, Andreas Eisenreich, Martina Schmidbauer, Andrei Barysenka, Bettina Purfürst, Anje Sporbert, Theodor Lorenzen, Alexander M Meyer, Laura Herlan, Anika Witten, Frank Rühle, Weibin Zhou, Emile de Heer, Marion Scharpfenecker, Daniela Panáková, Monika Stoll, Reinhold Kreutz
Publikováno v:
eLife, Vol 8 (2019)
Unraveling the genetic susceptibility of complex diseases such as chronic kidney disease remains challenging. Here, we used inbred rat models of kidney damage associated with elevated blood pressure for the comprehensive analysis of a major albuminur
Externí odkaz:
https://doaj.org/article/3ce65e8761e146108e0f630955c54002
Autor:
Katja Grabowski, Laura Herlan, Anika Witten, Fatimunnisa Qadri, Andreas Eisenreich, Diana Lindner, Martin Schädlich, Angela Schulz, Jana Subrova, Ketaki Nitin Mhatre, Uwe Primessnig, Ralph Plehm, Sophie van Linthout, Felicitas Escher, Michael Bader, Monika Stoll, Dirk Westermann, Frank R. Heinzel, Reinhold Kreutz
Publikováno v:
Hypertension Research
Hypertension Research, 45(2), 292-307. Nature Publishing Group
Hypertension Research, 45(2), 292-307. Nature Publishing Group
Treatment of hypertension-mediated cardiac damage with left ventricular (LV) hypertrophy (LVH) and heart failure remains challenging. To identify novel targets, we performed comparative transcriptome analysis between genetic models derived from strok
Autor:
Anika Witten, Martina Schmidbauer, Marion Scharpfenecker, Anje Sporbert, Weibin Zhou, Daniela Panáková, Nina A. van de Lest, Emile de Heer, Reinhold Kreutz, Nicola Victoria Müller, Andrei Barysenka, Laura Herlan, Frank Rühle, Alexander M Meyer, Angela Schulz, Monika Stoll, Andreas Eisenreich, Bettina Purfürst, Theodor Lorenzen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c2cca0785022be13863bd0603a3bef8
https://doi.org/10.7554/elife.42068.040
https://doi.org/10.7554/elife.42068.040
Publikováno v:
Journal of Hypertension. 34:323-331
Angiotensin (Ang)II is involved in induction of proteinuria, renal injury, and apoptosis and thus a major contributor to the development of chronic kidney disease. Podocytes are of major importance for the pathogenesis of several kidney diseases. Dec
Autor:
Angela, Schulz, Nicola Victoria, Müller, Nina Anne, van de Lest, Andreas, Eisenreich, Martina, Schmidbauer, Andrei, Barysenka, Bettina, Purfürst, Anje, Sporbert, Theodor, Lorenzen, Alexander M, Meyer, Laura, Herlan, Anika, Witten, Frank, Rühle, Weibin, Zhou, Emile, de Heer, Marion, Scharpfenecker, Daniela, Panáková, Monika, Stoll, Reinhold, Kreutz
Publikováno v:
eLife
Unraveling the genetic susceptibility of complex diseases such as chronic kidney disease remains challenging. Here, we used inbred rat models of kidney damage associated with elevated blood pressure for the comprehensive analysis of a major albuminur
Autor:
Herbert Schulz, Reinhold Kreutz, Norbert Hubner, Leonard Schulte, Angela Schulz, Laura Herlan
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 42:1051-1058
Defects in nephrogenesis can have detrimental effects on cardiovascular and renal health in adult life. This is confirmed by observations in the Munich Wistar Fromter (MWF) rat that exhibits a congenital nephron deficit and renal failure with age. He
Autor:
Peter Kossmehl, Leonard Schulte, Concha F. García-Prieto, Angela Schulz, Sabrina Schütten, Johannes Unland, Sebastian Langer, Reinhold Kreutz, María S. Fernández-Alfonso, Laura Herlan
Publikováno v:
Physiological Genomics. 47:281-289
Munich Wistar Frömter (MWF) rats develop spontaneous albuminuria that is linked to autosomal genetic loci and inherit a nephron deficit in both female and male animals, respectively. However, albuminuria and kidney damage are clearly more pronounced
Publikováno v:
Hypertension. 62
We previously confirmed in the Munich Wistar Frömter (MWF) rat a functional role of a major quantitative trait locus (QTL) on rat chromosome (RNO)6 for both albuminuria development and an inherited nephron deficit in the consomic strain MWF-6SHR. W
Autor:
Angela Schulz, Ralph Plehm, Laura Herlan, Reinhold Kreutz, Michael Bader, Andreas Eisenreich, K. Grabowski, Dominik N. Müller
Publikováno v:
Journal of Hypertension. 34:e102