| T |
| Targeted disruption of aquaporin-1 leads to impaired recruitment of juxtaglomerular cells in response to chronic stimulation of the renin-angiotensin system |
| *Tinning A., Jensen B., Kurtz A., Madsen K. |
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| Teaching acid-base (patho-) physiology |
| *Alle H. |
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| TGF-receptor mediated NO release induced apoptosis in adult cardiomyocytes of adult rat |
| *Warga B., Heger J., Abdallah Y., Schluter K.-D., Piper H.M., Euler G. |
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| The 1S I/II loop as molecular switch for 1a to enable trafficking of the dihydropyridine receptor (DHPR) |
| Polster A., Pfitzer G., Beam K., *Papadopoulos S. |
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| The activated Mineralocorticoid Receptor interacts with Calcineurin- in respect of CREB signaling |
| *Seiferth A., Ruhs S., Gekle M., Grossmann C. |
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| The afterhyperpolarizing potential following a train of action potentials is reduced in an acute model of epilepsy via protein kinase activation |
| Kernig K., *Kirschstein T., Rohde M., Kohling R. |
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| The analysis of aquaporin-2 regulation by means of the isolated perfused rat kidney |
| *Schurek H.-J., Klokkers J., Pavenstadt H., Schlatter E., Edemir B. |
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| The anesthetic octanol activates CFTR-dependent Cl--secretion in native pulmonary epithelium (Xenopus laevis) |
| *Richter K., Clauss W., Fronius M. |
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| The anion exchanger Slc26a6 functionally interacts and tethers the cytoplasmic carbonic anhydrase II to the apical membrane in murine duodenum |
| *Singh A.K., Riederer B., Soleimani M., Engelhardt R., Seidler U. |
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| The Auxiliary AMPA Receptor Subunit Cornichon - Just a Chaperone? |
| *Harmel N., Mauric V., Klocker N. |
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| The Ca2+-activated potassium channel KCa3.1 shows increased expression in A549 lung carcinoma cells with high metastatic potential |
| *Bulk E., Jungen D., Hascher A., Muller-Tidow C., Schwab A. |
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| The calcium-sensing receptor in the murine renal collecting duct cell line M1 |
| *Himmerkus N., Grussel S., Bleich M. |
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| The cardioprotective effect of brief acidic reperfusion after ischemia in perfused rat hearts is not mimicked by inhibition of the Na+/H+ exchanger NHE1 |
| *Andersen A.-D., Bentzen B.H., Salling H., Klingberg H., Kanneworff M., Grunnet M., Pedersen S.F. |
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| The contractile apparatus but not Ca2+ is the main contributor to compromised force in early pre-fibrotic mdx cardiac muscle with already detectable cardiomyopathy |
| *Wagner S., Weber C., Galmbacher R., Hein S., Schinkel S., Walther A., Martin E., Bekkeredjian R., Muller O.J., Friedrich O. |
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| The differential expression of several mRNA variants of HIF1a during endurance exercise and under normobar hypoxia |
| *Breitbach S., Bohringer A., Simon P., Tug S. |
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| The Dipeptide Isoleucine-Tryptophan (IW) Lowers Blood Pressure in the SHR-Model and Reduce Angiotensin I Conversion in Isolated Rat Aorta |
| *Martin M., Deussen A. |
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| The Effect of Variation artificial Dead Space Volume in Lung Ventilation Gas Exchange: A Model Study |
| *Nasrallah H, Khachab A., Kashefi A, Bernhagen J., Wald B., Mottaghy K. |
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| The electrophysiological effects of chronic application of aldosterone on ventricular myocytes of Gq/11 knock out mice |
| *Pahlavan S., Wiesen K., Oberhofer M., Kaestner L., Lipp P. |
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| The endosomal SNARE protein syntaxin-8 interacts with the K+ channel TASK-1 and modulates its intracellular traffic |
| *Renigunta V.K., Zuzarte M., Siebert K., Schlichthorl G., Preisig-Muller R., Daut J. |
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| The epithelial serine protease trypsin IV activates the human epithelial sodium channel (ENaC) heterologously expressed in Xenopus laevis oocytes |
| *Haerteis S., Krappitz M., Krueger B., Murphy J., Bunnett N.W., Korbmacher C. |
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| The ex vivo perfused lung for assessment of altered lung function during transplantation |
| *Klein S., Dhein S., Bauer L., Vollroth M., Dieterlen M.-T., Mohr F.-W., Bittner H.B. |
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| The importance of the transcriptional factor HIF-1 for dendritic cell function |
| *Wobben R. |
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| The Influence of Lactate on the Proliferation and Differentiation of C2C12 and human primary myoblasts |
| *Willkomm L., Elsen M., Borosch S., Jung R., Bloch W. |
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| The meaning of mechanical strain for vasculogenesis of embryonic stem cells |
| *Behr S., Sauer H. |
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| The non-neuronal cholinergic system in mouse tracheal epithelium: Evidence for the participation of muscarinic M1, M3 receptors and nicotinic receptors |
| *Hollenhorst M., Lips K., Kummer W., Clauss W., Fronius M. |
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| The novel gasotransmitter hydrogen sulfide impairs pulmonary transepithelial ion transport |
| *Erb A., Fronius M., Clauss W., Althaus M. |
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| The organic anion transporter 1 is a pharmacological target for inhibitors of prolyl hydroxylases |
| *Hagos Y., Krick W., Willam C., Burckhardt G., Burckhardt B.C. |
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| The polarity protein Scribble is a negative regulator of endothelial shear stress signalling |
| *Kruse C.K.G., Wandzioch K., Brandes R.P., Michaelis U.R. |
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| The protection against reperfusion injury through uncoupling of the mitochondrial respiratory chain at the start of reperfusion |
| *Raffenberg S., Woste A., Shahzad T., Johnson V., Abdallah Y., Iraqi W. |
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| The role of adenosine and ATP in tubuloglomerular feedback and RBF autoregulation |
| *Dautzenberg M., Just A. |
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| The role of phospolipase2 signaling in the enhancement of sodium transport elicited by hypotonicity in A6 cells |
| *Polyankina A., Steels P., Bleich M. |
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| The Role of TGFb for Renin Cell Recruitment under chronic Stimulation of the RAS |
| *Gerl M., Kurtz A., Wagner C. |
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| The Role of the C-Terminus in Functional Expression of Rat Connexin46 |
| *Schlingmann B., Busko S., Hemmerling F., Ngezahayo A. |
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| The sialyltransferase ST3Gal-IV regulates eosinophil recruitment in vivo |
| *Frommhold D., Doerner A., Abisch J., Huber S., Mall M., Vohringer D., Sperandio M. |
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| The structural basis of silencing of acid-sensing ion channel (ASIC) 3 by the integral membrane protein stomatin |
| *Siebertz H., Kadurin I., Polleichtner G., Grunder S. |
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| The TNF-receptor-subtype 1 is responsible for ischemia/reperfusion induced endothelial dysfunction in vivo |
| Chaudhry D., *Pircher J., Mannell H., Sohn H., Pohl U., Krotz F. |
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| The Wilms tumor transcription factor, WT1, stimulates expression of the ADAMTS16 gene |
| *Jacobi C., Kirschner K., Scholz H. |
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| Thymoquinone-induced platelet apoptosis |
| *Towhid S., Gehring E.-M., Qadri S., Schmid E., Munzer P., Borst O., Lang F. |
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| Tight junctions of human pleura mesothelium: structure, function and pathophysiological aspects |
| *Amasheh S., Markov A.G., Volgin G.N., Voronkova M.A., Yablonsky P.K., Fromm M. |
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| Time dependent activation of myeloid cells by different conditions of hypoxia |
| *Schwartz M., Winning S., Fandrey J. |
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| TNF enhances the vasoconstrictor potential of serotonin and thromboxane through impairment of endothelial function |
| *Kleinbongard P., Schoner S., Leineweber K., Bose D., Konorza T., Eggebrecht H., Haude M., Erbel R., Heusch G. |
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| Transcriptional regulation of the Ca2+ channel Orai1/STIM1 by the serum- and glucocorticoid-inducible kinase SGK1 |
| *Eylenstein A., Regel I., Lang F. |
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| Transfection of cystic fibrosis airway epithelial cells with wtCFTR-mRNA restores CFTR function |
| Bangel-Ruland N., *Knieper Y., Sobczak K., Leier G., Rosenecker J., Weber W.-M. |
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| Translation of ligand binding to activation in CNGA2:A4:B1b channels |
| *Nache V., Zimmer T., Kusch J., Biskup C., Schmauder R., Schulz E., Seifert R., Boenigk W., Schwede F., Benndorf K. |
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| Transport activity of the sodium bicarbonate cotransporter NBCe1 is increased by a functional interaction with different carbonic anhydrase isoforms |
| *Schler C., Becker H.M., McKenna R., Deitmer J.W. |
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| Transport rate of the p-glycoprotein (Pgp) is depending on chirality of the substrate |
| *Thews O., Biesalski B., Yilmaz B., Rosch F., Fellner M. |
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| TRPC6 channels are functionally expressed in mouse skeletal muscle and seem to counteract fatigue development during repetitive stimulation of the soleus muscle |
| *Zhang Y., Pritschow B., Sinnhofer C., Brinkmeier H. |
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| Tryptophan scanning analysis of the second transmembrane helix of barttin reveals two sites of interaction with ClC-K chloride channels |
| *Wojciechowski D., Fischer M., Fahlke C. |
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| Two different pathways contribute to cytotoxicity of mouse cytotoxic T lymphocytes |
| *Dudenhffer-Pfeifer M., Krause E., Hoth M., Rettig J. |
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| Two independent cGMP-mediated pathways mediate nitrergic relaxation in ICC and SMC: Studies in mice lacking NO-sensitive guanylyl cyclase |
| *Groneberg D., Lies B., Konig P., Friebe A. |
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