Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Jochen R. Hirsch"'
Publikováno v:
Translational Neuroscience. 2:246-251
Natriuretic peptides (NPs) regulate salt and water homeostasis by inducing natriuresis and diuresis in the kidney. These actions in addition to those via the heart and vascular system play important roles in the regulation of blood pressure. In the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f04f61de31b247472eae721512ae66a
https://doi.org/10.2478/s13380-011-0029-y
https://doi.org/10.2478/s13380-011-0029-y
Autor:
Bayram Edemir, Ana Velic, Gert Gabriëls, Rita Schröter, Eberhard Schlatter, Jochen R. Hirsch, Sandra Paasche
Publikováno v:
American Journal of Transplantation. 5:1276-1285
Renal transplantation is associated with alterations of tubular functions and of the renin-angiotensin-aldosterone system. The underlying cellular and molecular mechanisms are unclear. We used an allogeneic rat renal transplantation model of acute re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f9515a3f6a53600dda28f57260a505
https://doi.org/10.1111/j.1600-6143.2005.00890.x
https://doi.org/10.1111/j.1600-6143.2005.00890.x
Autor:
Eberhard Schlatter, Bayram Edemir, Ana Velic, Heike Stegemann, Jasmin Bartel, Jochen R. Hirsch, Rita Schröter, Christian August, Regina Thomas, Gert Gabriëls
Publikováno v:
Journal of the American Society of Nephrology. 15:967-977
Kidney transplantation often leads to disturbances of solute and volume maintenance in humans. To investigate underlying mechanisms, expression and function of renal transporters and receptors of the proximal tubule (PT) were analyzed in an acute rej
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dd2ac795441aea146a5d100c16248b3
https://doi.org/10.1097/01.asn.0000117287.74203.89
https://doi.org/10.1097/01.asn.0000117287.74203.89
Autor:
Eberhard Schlatter, Giuliano Ciarimboli, Jochen R. Hirsch, Valentin Gorboulev, Katja Struwe, Petra Arndt, Hermann Koepsell
Publikováno v:
Journal of Cellular Physiology. 201:420-428
The human organic cation transporter type 1 (hOCT1) is an important transport system for small organic cations in the liver. Organic cation transporters are regulated by different signaling pathways, but the regulation of hOCT1 has not yet been studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca3c8bc859462276794de86d11c13bed
https://doi.org/10.1002/jcp.20081
https://doi.org/10.1002/jcp.20081
Autor:
Thomas Mehrens, V. Mönnich, Eberhard Schlatter, Giuliano Ciarimboli, C. Popp, Ibrahim Çetinkaya, Hermann Koepsell, Jochen R. Hirsch
Publikováno v:
Journal of Membrane Biology. 189:237-244
The electrogenic cation transporters OCT1 and OCT2 in the basolateral membrane of renal proximal tubules mediate the first step during secretion of organic cations. Previously we demonstrated stimulation and change of selectivity for rat OCT1 (rOCT1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a0db20b5b3a656bd056f34b5e00cfd
https://doi.org/10.1007/s00232-002-1023-7
https://doi.org/10.1007/s00232-002-1023-7
Autor:
Eberhard Schlatter, Erik Harms, Robert Kleta, Ibrahim Çetinkaya, Peter Herter, Jochen R. Hirsch
Publikováno v:
Journal of the American Society of Nephrology. 13:2085-2093
Cystinosis is the most common cause of the renal Fanconi syndrome in children, leading to severe electrolyte disturbances and growth failure. A defective lysosomal transporter, cystinosin, results in intralysosomal accumulation of cystine. Loading ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce316689a11f02a4af4173a304b3e80d
https://doi.org/10.1097/01.asn.0000023681.13865.25
https://doi.org/10.1097/01.asn.0000023681.13865.25
Autor:
Andreas Karschin, Ortrud K. Steinlein, Wenli Gu, Christian Derst, Jochen R. Hirsch, Jürgen Daut, Günter Schlichthörl, Hartmut Engels, Christine Karschin
Publikováno v:
The Journal of Physiology. 539:657-668
Two novel alternatively spliced isoforms of the human two-pore-domain potassium channel TREK-2 were isolated from cDNA libraries of human kidney and fetal brain. The cDNAs of 2438 base pairs (bp) (TREK-2b) and 2559 bp (TREK-2c) encode proteins of 508
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1200240e4ae3a55b53d14ddbb17fd752
https://doi.org/10.1113/jphysiol.2001.013432
https://doi.org/10.1113/jphysiol.2001.013432
Autor:
Eberhard Schlatter, Hans-Jürgen Piechota, Ibrahim Çetinkaya, Gesine Pietig, Jochen R. Hirsch, Thomas Mehrens
Publikováno v:
Journal of Biological Chemistry. 276:33741-33746
The kidney, and more specifically the proximal tubule, is the main site of elimination of cationic endogenous metabolites and xenobiotics. Although numerous studies exist on renal organic cation transport of rat and rabbit, no information is availabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a4cf31280600af17041f6d9ec58b88
https://doi.org/10.1074/jbc.m104617200
https://doi.org/10.1074/jbc.m104617200
Autor:
Andreas Karschin, Eberhard Schlatter, Erhard Wischmeyer, Achim Thomzig, Jürgen Daut, Frank Döring, Rüdiger W. Veh, Regina Preisig-Müller, Jochen R. Hirsch, Wolfgang Kummer, Christian Derst
Publikováno v:
Kidney International. 59(6):2197-2205
Cellular localization of the potassium channel Kir7.1 in guinea pig and human kidney. Background K + channels have important functions in the kidney, such as maintenance of the membrane potential, volume regulation, recirculation, and secretion of po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30a82a2435dcf724931c35807b0f421
Autor:
Karl-Heinz Grzeschik, Andreas Karschin, Erhard Wischmeyer, Regina Preisig-Müller, Jochen R. Hirsch, Hartmut Engel, Sindhu Rajan, Christian Derst, Christine Karschin, Jürgen Daut
Publikováno v:
FEBS Letters. 491:305-311
We have identified several cDNAs for the human Kir5.1 subunit of inwardly rectifying K+ channels. Alternative splicing of exon 3 and the usage of two alternative polyadenylation sites contribute to cDNA diversity. The hKir5.1 gene KCNJ16 is assigned
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969bae461b71c31e1aa40edb571415bc
https://doi.org/10.1016/s0014-5793(01)02202-5
https://doi.org/10.1016/s0014-5793(01)02202-5