Die Durchblutung aller Organe und Gewebe wird tagtäglich an unterschiedlichste, sich ständig ändernde Bedingungen angepasst. Störungen der adäquaten Anpassung der Durchblutung an einen sich ändernden Bedarf treten bei einer Reihe der am weitesten verbreiteten Erkrankungen, wie Hochdruck und Diabetes, auf. Deshalb befinden sich die Mechanismen, die die Durchblutung regulieren, auch nach vielen Jahren der Erforschung immer noch im Zentrum der Aufmerksamkeit.

 

Die Sektion Kardiovaskuläre Physiologie beschäftigt sich in diesem Zusammenhang mit der Untersuchung der Rolle von verschiedenen Signalmolekülen, insbesondere Ionenkanälen, in glatten Gefäßmuskelzellen und von mechanisch induzierten Signalkaskaden in Endothelzellen verschiedener Gebiete des Kreislaufsystems. Besonderer Fokus liegt dabei auf physiologischen Regulationsvorgängen (myogene und durch perivaskuläres Fett vermittelte Autoregulation, durch mechanische Reize induzierte Signalprozesse, funktionelles Remodelling der Gefäßwand) und damit verbundenen pathophysiologischen Prozessen (Diabetes, Hypertonie, Atherosklerose). Dazu steht ein breites Methodenspektrum vom molekularen über das zelluläre Niveau bis zur Ebene intakter Organe zur Verfügung.

 

Thematisch werden 3 Hauptschwerpunkte verfolgt:

 

  1. Rolle glattmuskulärer Kaliumkanäle in Autoregulationsmechanismen des Kreislaufsystems unter physiologischen und pathophysiologischen Bedingungen.
  2. Mechanismen der funktionellen und strukturellen Plastizität in der Gefäßwand unter Einwirkung mechanischer Kräfte bzw. in der postnatalen Entwicklung. 
  3. Rolle der oberflächlichen Glykokalyx von Endothelzellen bei der Entstehung von pathologischen Situationen wie Entzündungen, Thrombosen und Atherogenese.

 

Längerfristiges Ziel ist es, ein umfassenderes Verständnis der Funktion verschiedener Signalmoleküle durch die Bestimmung ihrer Einbindung in Molekülkomplexe zu entwickeln und dabei detaillierte Kenntnisse über die Regulation der Funktion dieser Signalmolekülen auf subzellulärer Ebene zu erhalten. Damit soll es ermöglicht werden, unter physiologischen und pathophysiologischen Bedingungen das Verständnis autoregulatorischer Prozesse der Kreislaufregulation über akute Mechanismen hinaus zu längerfristig wirkenden Mechanismen des funktionellen bzw. adaptiven Remodellings zu erweitern.

Prof. Dr. Schubert - Publikationen

Rudolf Schubert
2018 | 2017 | 2016 | 2015 | 2013 | 2012 | 2010 | 2009 | 2008 | 2007 | 2006 | 2005 | 2004 | 2002 | 2001 | 2000 | 1999 | 1998 | 1997 | 1996

2018

Li Youhai, Lapina Natalia, Weinzierl Nina, Bonde Lisbeth, Boedtkjer Ebbe, Schubert Rudolf, Moshage Han, Wohlfart Paulus, Schilling Lothar. A novel method to isolate retinal and brain microvessels from individual rats: Microscopic and molecular biological characterization and application in hyperglycemic animals. https://doi.org/10.1016/j.vph.2018.07.001
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Mochalov S. V., Tarasova N. V., Kudryashova T. V., Gaynullina D. K., Kalenchuk V. U., Borovik A. S., Vorotnikov A. V., Tarasova O. S., Schubert Rudolf. Higher Ca2+-sensitivity of arterial contraction in 1-week-old rats is due to a greater Rho-kinase activity. https://doi.org/10.1111/apha.13044
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Braun Diana, Zollbrecht Christa, Dietze Stefanie, Schubert Rudolf, Golz Stefan, Summer Holger, Persson Pontus B., Carlström Mattias, Ludwig Marion, Patzak Andreas. Hypoxia/Reoxygenation of Rat Renal Arteries Impairs Vasorelaxation via Modulation of Endothelium-Independent sGC/cGMP/PKG Signaling. https://doi.org/10.3389/fphys.2018.00480
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Shvetsova Anastasia A., Gaynullina Dina K., Tarasova Olga S., Schubert Rudolf. Negative feedback regulation of vasocontraction by potassium channels in 10- to 15-day-old rats: Dominating role of Kv 7 channels. https://doi.org/10.1111/apha.13176
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Gollasch Maik, Welsh Donald G., Schubert Rudolf. Perivascular adipose tissue and the dynamic regulation of Kv 7 and Kir channels: Implications for resistant hypertension. https://doi.org/10.1111/micc.12434
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Krämer Bernhard K, Mang Johannes F, Schubert Rudolf. The Effect of Microgravity on Central Aortic Blood Pressure. https://doi.org/10.1093/ajh/hpy133
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Schmid Johannes, Müller Bettina, Heppeler David, Gaynullina Dina, Kassmann Mario, Gagov Hristo, Mladenov Mitko, Gollasch Maik, Schubert Rudolf. The Unexpected Role of Calcium‐Activated Potassium Channels: Limitation of NO‐Induced Arterial Relaxation. https://doi.org/10.1161/jaha.117.007808
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Lubomirov L. T., Papadopoulos S., Filipova D., Baransi Sufian, Todorović D., Lake P., Metzler D., Hilsdorf S., Schubert Rudolf, Schroeter M. M., Pfitzer G.. The involvement of phosphorylation of myosin phosphatase targeting subunit 1 (MYPT1) and MYPT1 isoform expression in NO/cGMP mediated differential vasoregulation of cerebral arteries compared to systemic arteries. https://doi.org/10.1111/apha.13079
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Schubert Rudolf. The second life of ion transporters as signal transducers. https://doi.org/10.1111/apha.13155
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2017

Liu Z. Z., Mathia S., Pahlitzsch T., Wennysia I. C., Persson P. B., Lai E. Y., Högner A., Xu M. Z., Schubert Rudolf, Rosenberger C., Patzak A.. Myoglobin facilitates angiotensin II-induced constriction of renal afferent arterioles. https://doi.org/10.1152/ajprenal.00394.2016
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Gagov Hristo, Emilova Radoslava, Dimitrova Daniela, Mladenov Mitko, Schubert Rudolf. Perivascular adipose tissue as regulator of the force of artery contractions in health and disease. https://doi.org/10.3897/biodiscovery.20.e19831
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Zavaritskaya Olga, Lubomirov Lubomir T., Altay Serdar, Schubert Rudolf. Src tyrosine kinases contribute to serotonin-mediated contraction by regulating calcium-dependent pathways in rat skeletal muscle arteries. https://doi.org/10.1007/s00424-017-1949-3
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2016

Schubert Rudolf, Grozdanova Radslava Emilova, Dimitrova Daniela, Mladenov Mitko, Hadzi-Petrushev Nikola, Daneva Teodora, Padeshki Plamen, Chichova Mariela, Lubomirov L., Simeonovska-Nokolova Daniela, Gagov Hristo. Diabetes Converts Arterial Regulation by Perivascular Adipose Tissue From Relaxation Into H2O2-Mediated Contraction.
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Schubert Rudolf. Relaxation and contraction rates: underestimated parameters of vascular contractility?. https://doi.org/10.1111/apha.12810
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Schubert Rudolf, Heumann Philipp, Koenen Anna, Zavaritskaya Olga, Schütze Konrad, Ramm André, Schlüter Torsten, Steinbach Antje, Rettig Rainer, Grisk Olaf. Sympathetic denervation facilitates L-type Ca2+ channel activation in renal but not in mesenteric resistance arteries. https://doi.org/10.1097/HJH.0000000000000856
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Tsvetkov Dmitry, Tano Jean-Yves, Kassmann Mario, Wang Ning, Schubert Rudolf, Gollasch Maik. The Role of DPO-1 and XE991-Sensitive Potassium Channels in Perivascular Adipose Tissue-Mediated Regulation of Vascular Tone. https://doi.org/10.3389/fphys.2016.00335
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2015

Gaynullina Dina, Dweep Harsh, Gloe Torsten, Tarasova Olga S., Sticht Carsten, Gretz Norbert, Schubert Rudolf. Alteration of mRNA and microRNA expression profiles in rat muscular type vasculature in early postnatal development. https://doi.org/10.1038/srep11106
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Schubert Rudolf. Are microRNAs opening up a new world of regulation?. https://doi.org/10.1111/apha.12564
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Emilova Radoslava, Dimitrova Daniela, Mladenov Mitko, Daneva Teodora, Schubert Rudolf, Gagov Hristo. Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery. https://doi.org/10.1080/13102818.2014.991565
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2013

Gaynullina Dina, Lubomirov Lubomir T., Sofronova Svetlana I., Kalenchuk Vyacheslav U., Gloe Torsten, Pfitzer Gabriele, Tarasova Olga S., Schubert Rudolf. Functional remodelling of arterial endothelium during early postnatal development in rats. https://doi.org/10.1093/cvr/cvt138
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Sazdova Iliyana V., Ilieva Bilyana M., Shkodrova Milena, Milusheva Alexandra, Chichova Mariela, Schubert Rudolf, Fülüp Ferenc, Lubomirov Lubomir T., Gagov Hristo S.. Obestatin Signalling in Excised Frog Heart. https://doi.org/10.7546/cr-2013-66-6-13101331-10
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Iozzi D., Schubert Rudolf, Kalenchuk V. U., Neri A., Sgaragli G., Fusi F., Saponara S.. Quercetin relaxes rat tail main artery partlyviaa PKG-mediated stimulation of KCa1.1 channels. https://doi.org/10.1111/apha.12083
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Zavaritskaya Olga, Zhuravleva Nadezda, Schleifenbaum Johanna, Gloe Torsten, Devermann Lena, Kluge Reinhart, Mladenov Mitko, Frey Manfred, Gagov Hristo, Fésüs Gabor, Gollasch Maik, Schubert Rudolf. Role of KCNQ Channels in Skeletal Muscle Arteries and Periadventitial Vascular Dysfunction. https://doi.org/10.1161/hypertensionaha.112.197566
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Abramochkin Denis V., Kuzmin Vladislav S., Mitrochin Vadim M., Kalugin Leonid, Dvorzhak Anton, Makarenko Ekaterina Y., Schubert Rudolf, Kamkin Andre. TNF-α provokes electrical abnormalities in rat atrial myocardium via a NO-dependent mechanism. https://doi.org/10.1007/s00424-013-1320-2
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2012

Lidington Darcy, Schubert Rudolf, Bolz Steffen-Sebastian. Capitalizing on diversity: an integrative approach towards the multiplicity of cellular mechanisms underlying myogenic responsiveness. https://doi.org/10.1093/cvr/cvs345
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Seker Fatih, Hesser Jürgen, Neumaier-Probst Eva, Groden Christoph, Brockmann Marc A., Schubert Rudolf, Brockmann Carolin. Dose–response relationship of locally applied nimodipine in an ex vivo model of cerebral vasospasm. https://doi.org/10.1007/s00234-012-1079-8
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Climent Belén, Schubert Rudolf, Stankevicius Edgaras, García-Sacristán Albino, Simonsen Ulf, Rivera Luis. Large conductance Ca2+-activated K+ channels modulate endothelial cell outward currents and nitric oxide release in the intact rat superior mesenteric artery. https://doi.org/10.1016/j.bbrc.2011.12.076
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2010

Schubert Rudolf, Sazdova Ilyana V., Ilieva Bilyana M., Shkodrova Milena, Fulop Ferenc, Gagov Hristo. Mechanism of the positive inotropic effect of dimethyl sulfoxide at low doses in excised frog heart preparations.
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Schleifenbaum Johanna, Köhn Carolin, Voblova Nedzda, Dubrovska Galyna, Zavarirskaya Olga, Gloe Torsten, Crean Christopher S., Luft Friedrich C., Huang Yu, Schubert Rudolf, Gollasch Maik. Systemic peripheral artery relaxation by KCNQ channel openers and hydrogen sulfide. https://doi.org/10.1097/HJH.0b013e32833c20d5
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2009

Kirschstein Timo, Dammann Fabian, Klostermann Jenny, Rehberg Mirko, Tokay Tursonjan, Schubert Rudolf, Köhling Rüdiger. Dopamine induces contraction in the proximal, but relaxation in the distal rat isolated small intestine. https://doi.org/10.1016/j.neulet.2009.08.080
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Anschütz Stephanie, Schubert Rudolf. Modulation of the myogenic response by neurogenic influences in rat small arteries. https://doi.org/10.1038/sj.bjp.0706323
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Sazdova Iliyana, Ilieva Bilyana, Minkov Ignat, Schubert Rudolf, Gagov Hristo. Obestatin as contractile mediator of excised frog heart. https://doi.org/10.2478/s11535-009-0023-3
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Tarasova O.S., Puzdrova V.A., Tarasova N.V., Mochalov S.V., Vorotnikov A.V., Schubert Rudolf. P3.11 Rapid contractile phenotype of vascular smooth muscle is controlled by trophic influence of sympathetic nerves. https://doi.org/10.1016/j.autneu.2009.05.159
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Schubert Rudolf, Leuner Kristina, Heiser J.H., Derksen S., Mladenov Mitko, Fehske C:J:, Gollasch M., Schneider G., Harteneck C., Müller W.E., Chatterjee Shyam Sunder. Simple 2,4-Diacylphloroglucinols as Classic Transient Receptor Potential-6 Activators-Identification of a Novel Pharmacophore. https://doi.org/10.1124/mol.109.057513
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2008

Mladenov Mitko, Hristov Kiril, Dimitriova D. Z., Schubert Rudolf, Lubomirov L. T., Gjorgoski Icko, Duridanova D. B., Gagov Hristo. Ghrelin signalling in guinea-pig femoral artery smooth muscle cells. https://doi.org/10.1111/j.1748-1716.2008.01880.x
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2007

Ivanova Iliyana V., Schubert Rudolf, Duridanova Dessislava B., Bolton Thomas B., Lubomirov Lubomir T., Gagov Hristo S.. Cocaine- and amphetamine-regulated transcript (CART) peptide as anin vivoregulator of cardiac function inRana ridibundafrog. https://doi.org/10.1113/expphysiol.2007.038935
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Schubert Rudolf, Lidington D., Bolz S.. The emerging role of Ca2+ sensitivity regulation in promoting myogenic vasoconstriction. https://doi.org/10.1016/j.cardiores.2007.07.018
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2006

Köhler Ralf, Heyken Willm-Thomas, Heinau Philipp, Schubert Rudolf, Si Han, Kacik Michael, Busch Christoph, Grgic Ivica, Maier Tanja, Hoyer Joachim. Evidence for a Functional Role of Endothelial Transient Receptor Potential V4 in Shear Stress–Induced Vasodilatation. https://doi.org/10.1161/01.atv.0000225698.36212.6a
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Si Han, Heyken Willm-Thomas, Wölfle Stephanie E., Tysiac Marcin, Schubert Rudolf, Grgic Ivica, Vilianovich Larisa, Giebing Günter, Maier Tanja, Gross Volkmar, Bader Michael, de Wit Cor, Hoyer Joachim, Köhler Ralf. Impaired Endothelium-Derived Hyperpolarizing Factor-Mediated Dilations and Increased Blood Pressure in Mice Deficient of the Intermediate-Conductance Ca2+-Activated K+Channel. https://doi.org/10.1161/01.res.0000238377.08219.0c
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Rust Marco B., Faulhaber Jörg, Budack Mareike K., Pfeffer Carsten, Maritzen Tanja, Didié Michael, Beck Franz-Xaver, Boettger Thomas, Schubert Rudolf, Ehmke Heimo, Jentsch Thomas J., Hübner Christian A.. Neurogenic Mechanisms Contribute to Hypertension in Mice With Disruption of the K-Cl Cotransporter KCC3. https://doi.org/10.1161/01.res.0000204449.83861.22
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Pfitzer G., Lubomirov L. T., Reimann K., Gagov H., Schubert Rudolf. Regulation of the crossbridge cycle in vascular smooth muscle by cAMP signalling. https://doi.org/10.1007/s10974-006-9097-y
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Schubert Rudolf. Sphingosine-1-phosphate in the circulatory system: Cause and therapeutic target for vascular dysfunction?. https://doi.org/10.1016/j.cardiores.2006.02.012
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Lubomirov L. T., Schubert Rudolf, Gagov Hristo, Duridanova D. B., Pfitzer G.. Urocortin increases the intracellular cAMP concentration and thus decreases the degree of phosphorylation of MYPT1 and increases the myosin phosphatase activity. https://doi.org/10.1134/s0006350906050010
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Lubomirov Lubomir T., Reimann Katrin, Metzler Doris, Hasse Veronika, Stehle Robert, Ito Masaaki, Hartshorne David J., Gagov Hristo, Pfitzer Gabriele, Schubert Rudolf. Urocortin-Induced Decrease in Ca2+ Sensitivity of contraction in Mouse Tail Arteries is Attributable to cAMP-Dependent Dephosphorylation of MYPT1 and Activation of Myosin Light Chain Phosphatase. https://doi.org/10.1161/01.res.0000219904.43852.3e
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2005

Ruth Peter, Bucurenciu Iancu, Zhao Hong, Zhou Xiao-Bo, Sausbier Ulrike, Arntz Claudia, Feil Susi, Essin Kyrill, Feil Robert, Hofmann Franz, Knaus Hans-Günther, Shipston Michael J, Storm Johan, Korth Michael, Schubert Rudolf, Gollasch Maik, Sausbier Matthias. Analysis of BKCa channel deficient mice. https://doi.org/10.1186/1471-2210-5-s1-s39
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Sausbier Matthias, Arntz Claudia, Bucurenciu Iancu, Zhao Hong, Zhou Xiao-Bo, Sausbier Ulrike, Feil Susanne, Kamm Simone, Essin Kyrill, Sailer Claudia A., Abdullah Usamah, Krippeit-Drews Peter, Feil Robert, Hofmann Franz, Knaus Hans-Günther, Kenyon Chris, Shipston Michael J., Storm Johan F., Neuhuber Winfried, Korth Michael, Schubert Rudolf, Gollasch Maik, Ruth Peter. Elevated Blood Pressure Linked to Primary Hyperaldosteronism and Impaired Vasodilation in BK Channel–Deficient Mice. https://doi.org/10.1161/01.cir.0000156448.74296.fe
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Sausbier Matthias, Zhao Hong, Schubert Rudolf, Sausbier Ulrike, Abdullah U, Huber Andrea, Feil Susi, Feil Robert, Hofmann Franz, Neuhuber Winfried, Allescher Hans-Dieter, Ruth Peter. Enhanced vascular cGMP/cGK I signaling and hypotonia in cysteine-rich-protein 2-deficient mice. https://doi.org/10.1186/1471-2210-5-s1-p48
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Schubert Rudolf. Non-capacitative calcium entry—Extension of the possibilities for calcium entry in vascular tissue. https://doi.org/10.1016/j.cardiores.2005.07.018
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2004

Schubert Rudolf, Krien Ulrike, Wulfsen Iris, Schiemann Dorrit, Lehmann Gernot, Ulfig Norbert, Veh Ruediger W., Schwarz Jürgen R., Gago Hristo. Nitric Oxide Donor Sodium Nitroprusside Dilates Rat Small Arteries by Activation of Inward Rectifier Potassium Channels. https://doi.org/10.1161/01.hyp.0000121882.42731.6b
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2002

Schubert Rudolf, Kalentchuk Vjatscheslav U., Krien Ulrike. Rho kinase inhibition partly weakens myogenic reactivity in rat small arteries by changing calcium sensitivity. https://doi.org/10.1152/ajpheart.00549.2002
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2001

Schubert Rudolf, Nelson Mark T.. Protein kinases: tuners of the BKCa channel in smooth muscle. https://doi.org/10.1016/s0165-6147(00)01775-2
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Schubert Rudolf, Krien Ulrike, Gagov Hristo. Protons Inhibit the BKCa Channel of Rat Small Artery Smooth Muscle Cells. https://doi.org/10.1159/000051027
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Lubomirov Lubomir, Gagov Hristo, Petkova-Kirova Polina, Duridanova Dessislava, Kalentchuk Vjatscheslav U., Schubert Rudolf. Urocortin relaxes rat tail arteries by a PKA-mediated reduction of the sensitivity of the contractile apparatus for calcium. https://doi.org/10.1038/sj.bjp.0704418
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Strauss Ulf, Herbrik Martin, Mix Eilhard, Schubert Rudolf, Rolfs Arndt. Whole-cell patch-clamp: true perforated or spontaneous conventional recordings?. https://doi.org/10.1007/s004240100578
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2000

Petkova-Kirova Polina, Gagov Hristo, Krien Ulrike, Duridanova Dessislava, Noack Thomas, Schubert Rudolf. 4-Aminopyridine affects rat arterial smooth muscle BKCacurrents by changing intracellular pH. https://doi.org/10.1038/sj.bjp.0703742
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Sausbier Matthias, Schubert Rudolf, Voigt Viktor, Hirneiss Christoph, Pfeifer Alexander, Korth Michael, Kleppisch Thomas, Ruth Peter, Hofmann Franz. Mechanisms of NO/cGMP-Dependent Vasorelaxation. https://doi.org/10.1161/01.res.87.9.825
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1999

Schubert Rudolf, Noack Thomas, Serebryakov Vladimir N.. Protein kinase C reduces the KCa current of rat tail artery smooth muscle cells. https://doi.org/10.1152/ajpcell.1999.276.3.c648
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Schubert Rudolf, Mulvany Michael J.. The myogenic response: established facts and attractive hypotheses. https://doi.org/10.1042/cs19980403
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Schubert Rudolf, Lehmann Gernot, Serebryakov Vladimir N., Mewes Hartmut, Hopp Hans-Heinrich. cAMP-dependent protein kinase is in an active state in rat small arteries possessing a myogenic tone. https://doi.org/10.1152/ajpheart.1999.277.3.h1145
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1998

Schubert Rudolf, Strauss Ulf, Jung S., Mix E.. K+ currents of encephalitogenic memory T cells decrease with encephalitogenicity while interleukin-2 (IL-2) receptor expression remains stable during IL-2 dependent cell expansion.
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Stimulation of vascular smooth muscle cell K-Ca current by iloprost is smaller in SHR than in WKY rats. https://doi.org/10.1159/000025584
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1997

Schubert Rudolf, Serebryakov V. N., Mewes H., Hopp H. H.. Iloprost dilates rat small arteries: role of K(ATP)- and K(Ca)-channel activation by cAMP-dependent protein kinase. https://doi.org/10.1152/ajpheart.1997.272.3.h1147
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Wesselman J. P., Schubert Rudolf, VanBavel E. D., Nilsson H., Mulvany M. J.. KCa-channel blockade prevents sustained pressure-induced depolarization in rat mesenteric small arteries. https://doi.org/10.1152/ajpheart.1997.272.5.h2241
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Schubert Rudolf, Serebryankov V. N.. The iloprost-induced increase of calcium-activated potassium currents is smaller in hypertensive compared to normotensive rat tail artery smooth muscle cells.
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1996

Fischer Jörg-Gerald, Mewes Hartmut, Hopp Hans-Heinrich, Schubert Rudolf. Analysis of pressurized resistance vessel diameter changes with a low cost digital image processing device. https://doi.org/10.1016/0169-2607(96)01726-9
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Strauß Ulf, Wittstock Ute, Schubert Rudolf, Teuscher Eberhard, Jung Stefan, Mix Eilhard. Cicutoxin from Cicuta virosa: a New and Potent Potassium Channel Blocker in T Lymphocytes. https://doi.org/10.1006/bbrc.1996.0233
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Schubert Rudolf, Serebryakov V. N., Engel H., Hopp H. H.. Iloprost activates KCa channels of vascular smooth muscle cells: role of cAMP-dependent protein kinase. https://doi.org/10.1152/ajpcell.1996.271.4.c1203
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Schubert Rudolf. Multiple Ligand-Ion Solutions: A Guide for Solution Preparation and Computer Program Understanding. https://doi.org/10.1159/000159136
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Schubert Rudolf, Wesselman Jos P. M., Nilsson Holger, Mulvany Michael J.. Noradrenaline-induced depolarization is smaller in isobaric compared to isometric preparations of rat mesenteric small arteries. https://doi.org/10.1007/bf02253846
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