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J Ortner

Showing results (81-90 of 87) with videos related to

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Pflugers Archiv : European Journal of Physiology|December 19, 2019
RBP2 stabilizes slow Cav1.3 Ca<sup>2+</sup> channel inactivation properties of cochlear inner hair cellsNadine J Ortner, Alexandra Pinggera, Nadja T Hofer, et al.
Molecular Psychiatry|January 9, 2026
Aberrant calcium signaling and neuronal activity in the L271H CACNA1D (Cav1.3) iPSC model of neurodevelopmental diseaseMarcel Tisch, Stefanie M Geisler, Elisa Gabassi, et al.
The Journal of General Physiology|March 29, 2022
Calcium current modulation by the γ1 subunit depends on alternative splicing of CaV1.1Yousra El Ghaleb, Nadine J Ortner, Wilfried Posch, et al.
Neurology. Genetics|September 9, 2024
A Novel De Novo Gain-of-Function <i>CACNA1D</i> Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and HypotoniaFabian Dannenberg, Arpad Von Moers, Petra Bittigau, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 9, 2017
Lower Affinity of Isradipine for L-Type Ca<sup>2+</sup> Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's DiseaseNadine J Ortner, Gabriella Bock, Antonios Dougalis, et al.
Gut|December 13, 2002
Time gated fluorescence spectroscopy in Barrett's oesophagusM-A E J Ortner, B Ebert, E Hein, et al.
JCI Insight|September 12, 2023
The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome-like phenotype in miceNadine J Ortner, Anupam Sah, Enrica Paradiso, et al.
Pageof 9

Showing results (81-90 of 87) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 87 results.
Pflugers Archiv : European Journal of Physiology|December 19, 2019
RBP2 stabilizes slow Cav1.3 Ca<sup>2+</sup> channel inactivation properties of cochlear inner hair cellsNadine J Ortner, Alexandra Pinggera, Nadja T Hofer, et al.
Molecular Psychiatry|January 9, 2026
Aberrant calcium signaling and neuronal activity in the L271H CACNA1D (Cav1.3) iPSC model of neurodevelopmental diseaseMarcel Tisch, Stefanie M Geisler, Elisa Gabassi, et al.
The Journal of General Physiology|March 29, 2022
Calcium current modulation by the γ1 subunit depends on alternative splicing of CaV1.1Yousra El Ghaleb, Nadine J Ortner, Wilfried Posch, et al.
Neurology. Genetics|September 9, 2024
A Novel De Novo Gain-of-Function <i>CACNA1D</i> Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and HypotoniaFabian Dannenberg, Arpad Von Moers, Petra Bittigau, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 9, 2017
Lower Affinity of Isradipine for L-Type Ca<sup>2+</sup> Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's DiseaseNadine J Ortner, Gabriella Bock, Antonios Dougalis, et al.
Gut|December 13, 2002
Time gated fluorescence spectroscopy in Barrett's oesophagusM-A E J Ortner, B Ebert, E Hein, et al.
JCI Insight|September 12, 2023
The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome-like phenotype in miceNadine J Ortner, Anupam Sah, Enrica Paradiso, et al.
Pageof 9