An oily competition: role of β subunit palmitoylation for Ca(2+) channel modulation by fatty acids

por Striessnig, Jörg
Publicado 2009

Lonely but diverse: Cav1.3 L-type Ca(2+) channels in cochlear inner hair cells

por Striessnig, Jörg
Publicado 2013

Voltage‐gated calcium channels – from basic mechanisms to disease

por Striessnig, Jörg
Publicado 2016

Voltage-Gated Ca(2+)-Channel α1-Subunit de novo Missense Mutations: Gain or Loss of Function – Implications for Potential Therapies

por Striessnig, Jörg
Publicado 2021

Ca(v)1.3 (CACNA1D) L‐type Ca(2+) channel dysfunction in CNS disorders

por Pinggera, Alexandra, Striessnig, Jörg
Publicado 2016

L-type calcium channels as drug targets in CNS disorders

por Ortner, Nadine J, Striessnig, Jörg
Publicado 2015

C-Terminal Modulatory Domain Controls Coupling of Voltage-Sensing to Pore Opening in Ca(v)1.3 L-type Ca(2+) Channels

por Lieb, Andreas, Ortner, Nadine, Striessnig, Jörg
Publicado 2014

Channelopathies in Ca(v)1.1, Ca(v)1.3, and Ca(v)1.4 voltage-gated L-type Ca(2+) channels

por Striessnig, Jörg, Bolz, Hanno Jörn, Koschak, Alexandra
Publicado 2010

Pharmacology of L-type Calcium Channels: Novel Drugs for Old Targets?

por Striessnig, Jörg, Ortner, Nadine J., Pinggera, Alexandra
Publicado 2015

Regulation of Ca(V)1.3 Ca(2+) channels in cochlear inner hair cells

por Pinggera, Alexandra, Brandt, Niels, Kaur, Gurjot, Engel, Jutta, Striessnig, Jörg
Publicado 2012

L-type Ca(2+) channels in heart and brain

por Striessnig, Jörg, Pinggera, Alexandra, Kaur, Gurjot, Bock, Gabriella, Tuluc, Petronel
Publicado 2014

De novo CACAN1D Ca(2+) channelopathies: clinical phenotypes and molecular mechanism

por Ortner, Nadine J., Kaserer, Teresa, Copeland, J. Nathan, Striessnig, Jörg
Publicado 2020

Structural determinants of Ca(V)1.3 L-type calcium channel gating

por Lieb, Andreas, Scharinger, Anja, Sartori, Simone, Sinnegger-Brauns, Martina J., Striessnig, Jörg
Publicado 2012

Gating defects of disease-causing de novo mutations in Ca(v)1.3 Ca(2+) channels

por Pinggera, Alexandra, Negro, Giulia, Tuluc, Petronel, Brown, Morris J., Lieb, Andreas, Striessnig, Jörg
Publicado 2018

New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy

por Pinggera, Alexandra, Mackenroth, Luisa, Rump, Andreas, Schallner, Jens, Beleggia, Filippo, Wollnik, Bernd, Striessnig, Jörg
Publicado 2017

Structural determinants of Ca(V)1.3 L-type calcium channel gating

por Lieb, Andreas, Scharinger, Anja, Hechenblaickner, Florian, Gebhart, Mathias, Koschak, Alexandra, Sinnegger-Brauns, Martina J, Striessnig, Jörg
Publicado 2011

RIM modulates Ca(V)1.3 Ca(2+ )channels

por Gebhart, Mathias, Juhasz-Vedres, Gabriella, Trockenbacher, Alexander, Obermair, Gerald J, Engel, Jutta, Koschak, Alexandra, Striessnig, Jörg
Publicado 2008

Splice variants of the Ca(V)1.3 L-type calcium channel regulate dendritic spine morphology

por Stanika, Ruslan, Campiglio, Marta, Pinggera, Alexandra, Lee, Amy, Striessnig, Jörg, Flucher, Bernhard E., Obermair, Gerald J.
Publicado 2016

CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium Channels

por Pinggera, Alexandra, Lieb, Andreas, Benedetti, Bruno, Lampert, Michaela, Monteleone, Stefania, Liedl, Klaus R., Tuluc, Petronel, Striessnig, Jörg
Publicado 2015

Stabilization of negative activation voltages of Cav1.3 L-Type Ca(2+)-channels by alternative splicing

por Hofer, Nadja T., Pinggera, Alexandra, Nikonishyna, Yuliia V., Tuluc, Petronel, Fritz, Eva M., Obermair, Gerald J., Striessnig, Jörg
Publicado 2020