Pinggera A - Search Results

1

A Polybasic Plasma Membrane Binding Motif in the I-II Linker Stabilizes Voltage-gated CaV1.2 Calcium Channel Function.

Kaur G, Pinggera A, Ortner NJ, Lieb A, Sinnegger-Brauns MJ, Yarov-Yarovoy V, Obermair GJ, Flucher BE, Striessnig J. Kaur G, et al. Among authors: pinggera a. J Biol Chem. 2015 Aug 21;290(34):21086-21100. doi: 10.1074/jbc.M115.645671. Epub 2015 Jun 22. J Biol Chem. 2015. PMID: 26100638 Free PMC article.

2

L-type Ca²⁺ channels in heart and brain.

Striessnig J, Pinggera A, Kaur G, Bock G, Tuluc P. Striessnig J, et al. Among authors: pinggera a. Wiley Interdiscip Rev Membr Transp Signal. 2014 Mar 1;3(2):15-38. doi: 10.1002/wmts.102. Wiley Interdiscip Rev Membr Transp Signal. 2014. PMID: 24683526 Free PMC article.

3

CACNA1D de novo mutations in autism spectrum disorders activate Cav1.3 L-type calcium channels.

Pinggera A, Lieb A, Benedetti B, Lampert M, Monteleone S, Liedl KR, Tuluc P, Striessnig J. Pinggera A, et al. Biol Psychiatry. 2015 May 1;77(9):816-22. doi: 10.1016/j.biopsych.2014.11.020. Epub 2014 Dec 8. Biol Psychiatry. 2015. PMID: 25620733 Free PMC article.

4

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

Striessnig J, Ortner NJ, Pinggera A. Striessnig J, et al. Among authors: pinggera a. Curr Mol Pharmacol. 2015;8(2):110-22. doi: 10.2174/1874467208666150507105845. Curr Mol Pharmacol. 2015. PMID: 25966690 Free PMC article. Review.

5

Ca_v 1.3 (CACNA1D) L-type Ca²⁺ channel dysfunction in CNS disorders.

Pinggera A, Striessnig J. Pinggera A, et al. J Physiol. 2016 Oct 15;594(20):5839-5849. doi: 10.1113/JP270672. Epub 2016 Feb 29. J Physiol. 2016. PMID: 26842699 Free PMC article. Review.

6

Splice variants of the Ca_V1.3 L-type calcium channel regulate dendritic spine morphology.

Stanika R, Campiglio M, Pinggera A, Lee A, Striessnig J, Flucher BE, Obermair GJ. Stanika R, et al. Among authors: pinggera a. Sci Rep. 2016 Oct 6;6:34528. doi: 10.1038/srep34528. Sci Rep. 2016. PMID: 27708393 Free PMC article.

7

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

Pinggera A, Mackenroth L, Rump A, Schallner J, Beleggia F, Wollnik B, Striessnig J. Pinggera A, et al. Hum Mol Genet. 2017 Aug 1;26(15):2923-2932. doi: 10.1093/hmg/ddx175. Hum Mol Genet. 2017. PMID: 28472301 Free PMC article.

8

Mechanisms Responsible for ω-Pore Currents in Ca_v Calcium Channel Voltage-Sensing Domains.

Monteleone S, Lieb A, Pinggera A, Negro G, Fuchs JE, Hofer F, Striessnig J, Tuluc P, Liedl KR. Monteleone S, et al. Among authors: pinggera a. Biophys J. 2017 Oct 3;113(7):1485-1495. doi: 10.1016/j.bpj.2017.08.010. Biophys J. 2017. PMID: 28978442 Free PMC article.

9

Gating defects of disease-causing de novo mutations in Ca_v1.3 Ca²⁺ channels.

Pinggera A, Negro G, Tuluc P, Brown MJ, Lieb A, Striessnig J. Pinggera A, et al. Channels (Austin). 2018;12(1):388-402. doi: 10.1080/19336950.2018.1546518. Channels (Austin). 2018. PMID: 30465465 Free PMC article.

10

RBP2 stabilizes slow Cav1.3 Ca²⁺ channel inactivation properties of cochlear inner hair cells.

Ortner NJ, Pinggera A, Hofer NT, Siller A, Brandt N, Raffeiner A, Vilusic K, Lang I, Blum K, Obermair GJ, Stefan E, Engel J, Striessnig J. Ortner NJ, et al. Among authors: pinggera a. Pflugers Arch. 2020 Jan;472(1):3-25. doi: 10.1007/s00424-019-02338-4. Epub 2019 Dec 17. Pflugers Arch. 2020. PMID: 31848688 Free PMC article.

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