Alexandra Koschak
Innsbruck, Austria
Last Updated: 09/26/2026
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Found 20 publications
Quantitative Proteomics Identifies Potential Molecular Adaptations in Mouse Models of Congenital Stationary Night Blindness Type 2.
Journal: Molecular & cellular proteomics : MCP
Published: May 26, 2025
Exploring the potential for gene therapy in Cav1.4-related retinal channelopathies.
Journal: Channels (Austin, Tex.)
Published: March 25, 2025
Characterization of two pathological gating-charge substitutions in Cav1.4 L-type calcium channels.
Journal: Channels (Austin, Tex.)
Published: March 21, 2023
A novel calcium channel Cavβ2 splice variant with unique properties predominates in the retina.
Journal: The Journal of biological chemistry
Published: August 19, 2022
Knockout of CaV1.3 L-type calcium channels in a mouse model of retinitis pigmentosa.
Journal: Scientific reports
Published: May 06, 2021
Cav1.4 dysfunction and congenital stationary night blindness type 2.
Journal: Pflugers Archiv : European journal of physiology
Published: January 04, 2021
Function of cone and cone-related pathways in CaV1.4 IT mice.
Journal: Scientific reports
Published: August 21, 2020
Assessment of the Retina of Plp-α-Syn Mice as a Model for Studying Synuclein-Dependent Diseases.
Journal: Investigative ophthalmology & visual science
Published: June 06, 2020
Protein kinase N1 critically regulates cerebellar development and long-term function.
Journal: The Journal of clinical investigation
Published: July 07, 2017
Relevance of tissue specific subunit expression in channelopathies.
Journal: Neuropharmacology
Published: March 01, 2017
The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential.
Journal: Pharmacological reviews
Published: September 13, 2015
Gain-of-function nature of Cav1.4 L-type calcium channels alters firing properties of mouse retinal ganglion cells.
Journal: Channels (Austin, Tex.)
Published: August 15, 2015
Last Updated: 09/26/2026