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Jump to: 2018 | 2017 | 2016 | 2015 | 2014
Number of items: 29.

2018

Lubomirov, L. T., Papadopoulos, S., Filipova, D., Baransi, S., Todorovic, D., Lake, P., Metzler, D., Hilsdorf, S., Schubert, R., Schroeter, M. M. and Pfitzer, G. (2018). 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. Acta Physiol., 224 (1). HOBOKEN: WILEY. ISSN 1748-1716

2017

Filipova, D., Walter, A., Gaspar, J., Brunn, A., Deckert, M., Sachinidis, A., Pfitzer, G. and Papadopoulos, S. (2017). Transcriptomic changes during skeletal muscle development in the presence and absence of the type 1 ryanodine receptor (RYR1). Acta Physiol., 219. S. 38 - 39. HOBOKEN: WILEY. ISSN 1748-1716

Lubomirov, L. T., Schroeter, M. M., Metzler, D., Zittrich, S., Kock-Hauser, C., Ardestani, M. A., Schmitz, C., Papadopoulos, S. and Pfitzer, G. (2017). Regulation of murine basilar artery tone: Importance of MYPT1(T696) phosphorylation, and unimportance of PKG-dependent MYPT1(S695) phosphorylation, which only occurs in the nucleus. Acta Physiol., 219. S. 56 - 58. HOBOKEN: WILEY. ISSN 1748-1716

Pfitzer, G., Schroeter, M. M. and Lubomirov, L. T. (2017). Ca2+-independent regulators of vascular smooth muscle tone: Myosin light chain phosphatase and actin dynamics. Acta Physiol., 219. S. 17 - 18. HOBOKEN: WILEY. ISSN 1748-1716

2016

Barthel, S. L., Frohn, M., Metzler, D., Trunschke, O., Puetz, S., Koch, M., Neiss, W. F., Schroeter, M. M. and Pfitzer, G. (2016). Besides its effect on bladder contractility, caldesmon deficiency leads to a triad of morphological features: umbilical hernia, split lower part of the sternum and white liver areas. Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Cimiotti, D., Kostareva, A., Smolina, N., Majchrzak, M., Moehner, D., Wies, A., Milting, H., Stehle, R., Pfitzer, G., Muegge, A. and Jaquet, K. (2016). Modulation of Ca2+-regulatory function by three novel mutations in TNNI3 associated with severe infant restrictive cardiomyopathy. Cardiovasc. Res., 111. S. S37 - 1. OXFORD: OXFORD UNIV PRESS. ISSN 1755-3245

Cimiotti, D., Kostareva, A., Smolina, N., Majchrzak, M., Moehner, D., Wies, A., Milting, H., Stehle, R., Pfitzer, G., Muegge, A. and Jaquet, K. (2016). Modulation of Ca2+-regulatory function by three novel mutations in TNNI3 associated with severe infant restrictive cardiomyopathy. Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Diermeier, S., Haug, M., Reischl, B., Buttgereit, A., Schuermann, S., Spoerrer, M., Goldmann, W. H., Fabry, B., Elhimine, F., Stehle, R., Pfitzer, G., Winter, L., Clemen, C., Schroeder, R. and Friedrich, O. (2016). DesR349P Mutation Results in Ultrastructural Disruptions and Compromise of Skeletal Muscle Biomechanics Already at Preclinical Stages in Young Mice before the Onset of Protein Aggregation. Biophys. J., 110 (3). S. 303A - 304. CAMBRIDGE: CELL PRESS. ISSN 1542-0086

Filipova, D., Walter, A. M., Gasper, J. A., Brunn, A., Deckert, M., Sachinidis, A., Pfitzer, G. and Papadopoulos, S. (2016). Profound changes in the gene expression of skeletal muscle lacking the type 1 ryanodine receptor (RYR1). Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Lubomirov, L. T., Schroeter, M. M., Hilsdorf, S., Filipova, D., Baransi, S., Papadopoulos, S. and Pfitzer, G. (2016). The role of alternative mRNA splicing and threonine 696/853-phosphorylation of myosin phosphatase regulatory subunit (MYPT1) in the regulation of tone of murine brain vasculature. Acta Physiol., 216. HOBOKEN: WILEY. ISSN 1748-1716

Moehner, D., Elhamine, F., Stehle, R. and Pfitzer, G. (2016). The troponin I mutation Delta K184 blunts the effects of PKA-mediated phosphorylation on contraction and relaxation kinetics but not on Ca2+-sensitivity. Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Trunschke, O., Papadopoulos, S., Frohn, M., Barthel, S. L., Naumann, S., Metzler, D., Pfitzer, G. and Schroeter, M. M. (2016). The actin cytoskeleton in embryonic fibroblasts from caldesmon deficient mice. Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

2015

Diermeier, S., Iberl, J., Vetter, K., Haug, M., Reischl, B., Buttgereit, A., Schuermann, S., Spoerrer, M., Goldmann, W. H., Fabry, B., Elhimine, F., Stehle, R., Pfitzer, G., Winter, L., Clemen, C., Schroeder, R. and Friedrich, O. (2015). DesR349P mutation results in ultrastructural disruptions and compromise of skeletal muscle biomechanics already at preclinical stages in young mice before the onset of protein aggregation. Mol. Biol. Cell, 26. BETHESDA: AMER SOC CELL BIOLOGY. ISSN 1939-4586

Elhamine, F., Winter, L., Wiche, G., Pfitzer, G. and Stehle, R. (2015). Contractile properties of myofibrillar bundles isolated from plectin-deficient mouse psoas muscle. Acta Physiol., 213. S. 188 - 190. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Elhamine, F., Winter, L., Wiche, G., Pfitzer, G. and Stehle, R. (2015). Contractile properties of myofibrillar bundles isolated from plectin-deficient mouse psoas muscle. Acta Physiol., 213. S. 188 - 190. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Filipova, D., Walter, A., Gaspar, J. A., Pfitzer, G., Sachinidis, A. and Papadopoulos, S. (2015). Genomic profiling of ryanodine receptor type 1 (RYR1)-deficient skeletal muscle. Acta Physiol., 213. S. 152 - 153. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Filipova, D., Walter, A., Gaspar, J. A., Pfitzer, G., Sachinidis, A. and Papadopoulos, S. (2015). Genomic profiling of ryanodine receptor type 1 (RYR1)-deficient skeletal muscle. Acta Physiol., 213. S. 152 - 153. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Lubomirov, L. T., Papadopoulos, S., Welter, J., Puetz, S., Ardestani, M., Filipova, D., Schroeter, M., Gagov, H. and Pfitzer, G. (2015). Age related changes in the contribution of eNOS, nNOS and reactive oxygen species (ROS) to regulation of vascular tone of murine basilar arteries. Acta Physiol., 213. S. 178 - 179. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Lubomirov, L. T., Papadopoulos, S., Welter, J., Puetz, S., Ardestani, M., Filipova, D., Schroeter, M., Gagov, H. and Pfitzer, G. (2015). Age related changes in the contribution of eNOS, nNOS and reactive oxygen species (ROS) to regulation of vascular tone of murine basilar arteries. Acta Physiol., 213. S. 178 - 179. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Pfitzer, G., Schroeter, M. M., Frohn, M., Puetz, S., Metzler, D., Lubomirov, L. T., Trunschke, O., Koch, M. and Neiss, W. F. (2015). Gene targeting of CALD1 which encodes caldesmon: effect on murine development and smooth muscle contractility. Acta Physiol., 213. S. 189 - 191. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Pfitzer, G., Schroeter, M. M., Frohn, M., Puetz, S., Metzler, D., Lubomirov, L. T., Trunschke, O., Koch, M. and Neiss, W. F. (2015). Gene targeting of CALD1 which encodes caldesmon: effect on murine development and smooth muscle contractility. Acta Physiol., 213. S. 189 - 191. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Stehle, R., Juengst, C., Zittrich, S., Elhamine, F., Papadopoulos, S., Winter, L., Schauss, A. and Pfitzer, G. (2015). Plectin and desmin architecture in psoas myofibrillar bundles resolved by stimulated emission depletion (STED) and ground state depletion (GSD) microscopy. Acta Physiol., 213. S. 65 - 66. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Stehle, R., Juengst, C., Zittrich, S., Elhamine, F., Papadopoulos, S., Winter, L., Schauss, A. and Pfitzer, G. (2015). Plectin and desmin architecture in psoas myofibrillar bundles resolved by stimulated emission depletion (STED) and ground state depletion (GSD) microscopy. Acta Physiol., 213. S. 65 - 66. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

2014

Bitzer, M., Eckhardt, J., Habermann, A., Schroeter, M., Papadopoulos, S., Frangakis, A., Pfitzer, G. and Stehle, R. (2014). Characterisation of CapZ deficient zebrafish larvae utilising a novel force measurement technique. Acta Physiol., 210. S. 160 - 162. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Elhamine, F., Eckhardt, J., Brockmeier, K., Bennink, G., Stehle, R. and Pfitzer, G. (2014). Postnatal development of myofibrillar protein expression and function in humans with congenital right ventricular outflow tract obstruction. Acta Physiol., 210. S. 26 - 27. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Elhamine, F., Groen, M., Iorga, B., Radke, M., Gotthardt, M., Pfitzer, G. and Stehle, R. (2014). Cardiomyopathy related changes in myofibrillar force kinetics. Acta Physiol., 210. S. 42 - 43. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Pfitzer, G. (2014). Biomechanical adaptation to hindlimb suspension: it involves not only transcriptional mechanisms but also post-translational modification of the molecular motor, myosin. Acta Physiol., 212 (4). S. 263 - 267. HOBOKEN: WILEY. ISSN 1748-1716

Rippl, S., Bitzer, M., Papadopoulos, S., Schroeter, M., Pfitzer, G. and Stehle, R. (2014). The role of the actin capping protein (CapZ) for force development and force kinetics in skeletal myofibrils. Acta Physiol., 210. S. 102 - 103. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716

Stehle, R., Papadopoulos, S. and Pfitzer, G. (2014). Muscle sound during macroscale skeletal muscle relaxation: is it linked to processes on the microscale sarcomere level? Acta Physiol., 211 (1). S. 8 - 11. HOBOKEN: WILEY. ISSN 1748-1716

This list was generated on Fri Mar 29 01:40:55 2024 CET.