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Alexandra Koschak

Showing results (31-40 of 39) with videos related to

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The Journal of Biological Chemistry|October 15, 2011
Functional properties of a newly identified C-terminal splice variant of Cav1.3 L-type Ca2+ channelsGabriella Bock, Mathias Gebhart, Anja Scharinger, et al.
Bioconjugate Chemistry|May 16, 2002
Synthesis, characterization, and application of cy-dye- and alexa-dye-labeled hongotoxin(1) analogues. The first high affinity fluorescence probes for voltage-gated K+ channelsBernt Pragl, Alexandra Koschak, Maria Trieb, et al.
Molecular & Cellular Proteomics : MCP|November 12, 2025
Quantitative Proteomics Identifies Potential Molecular Adaptations in Mouse Models of Congenital Stationary Night Blindness Type 2Matthias Ganglberger, Lucia Zanetti, Anna-Sophia Egger, et al.
Biochimica Et Biophysica Acta|May 7, 2014
Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2Verena Burtscher, Klaus Schicker, Elena Novikova, et al.
Channels (Austin, Tex.)|September 21, 2013
Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2Dagmar Knoflach, Vasily Kerov, Simone B Sartori, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 24, 2014
Differential neuronal targeting of a new and two known calcium channel β4 subunit splice variants correlates with their regulation of gene expressionSolmaz Etemad, Gerald J Obermair, Daniel Bindreither, et al.
The Journal of Clinical Investigation|May 18, 2004
Isoform-specific regulation of mood behavior and pancreatic beta cell and cardiovascular function by L-type Ca 2+ channelsMartina J Sinnegger-Brauns, Alfred Hetzenauer, Irene G Huber, et al.
Frontiers in Cellular Neuroscience|September 18, 2015
Cell-type-specific tuning of Cav1.3 Ca(2+)-channels by a C-terminal automodulatory domainAnja Scharinger, Stephanie Eckrich, David H Vandael, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
The Journal of Biological Chemistry|October 15, 2011
Functional properties of a newly identified C-terminal splice variant of Cav1.3 L-type Ca2+ channelsGabriella Bock, Mathias Gebhart, Anja Scharinger, et al.
Bioconjugate Chemistry|May 16, 2002
Synthesis, characterization, and application of cy-dye- and alexa-dye-labeled hongotoxin(1) analogues. The first high affinity fluorescence probes for voltage-gated K+ channelsBernt Pragl, Alexandra Koschak, Maria Trieb, et al.
Molecular & Cellular Proteomics : MCP|November 12, 2025
Quantitative Proteomics Identifies Potential Molecular Adaptations in Mouse Models of Congenital Stationary Night Blindness Type 2Matthias Ganglberger, Lucia Zanetti, Anna-Sophia Egger, et al.
Biochimica Et Biophysica Acta|May 7, 2014
Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2Verena Burtscher, Klaus Schicker, Elena Novikova, et al.
Channels (Austin, Tex.)|September 21, 2013
Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2Dagmar Knoflach, Vasily Kerov, Simone B Sartori, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 24, 2014
Differential neuronal targeting of a new and two known calcium channel β4 subunit splice variants correlates with their regulation of gene expressionSolmaz Etemad, Gerald J Obermair, Daniel Bindreither, et al.
The Journal of Clinical Investigation|May 18, 2004
Isoform-specific regulation of mood behavior and pancreatic beta cell and cardiovascular function by L-type Ca 2+ channelsMartina J Sinnegger-Brauns, Alfred Hetzenauer, Irene G Huber, et al.
Frontiers in Cellular Neuroscience|September 18, 2015
Cell-type-specific tuning of Cav1.3 Ca(2+)-channels by a C-terminal automodulatory domainAnja Scharinger, Stephanie Eckrich, David H Vandael, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
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