Pinggera A - Search Results

1

AMPA receptor anchoring at CA1 synapses is determined by N-terminal domain and TARP γ8 interactions.

Watson JF, Pinggera A, Ho H, Greger IH. Watson JF, et al. Among authors: pinggera a. Nat Commun. 2021 Aug 23;12(1):5083. doi: 10.1038/s41467-021-25281-4. Nat Commun. 2021. PMID: 34426577 Free PMC article.

2

Biology of AMPA receptor interacting proteins - From biogenesis to synaptic plasticity.

Matthews PM, Pinggera A, Kampjut D, Greger IH. Matthews PM, et al. Among authors: pinggera a. Neuropharmacology. 2021 Oct 1;197:108709. doi: 10.1016/j.neuropharm.2021.108709. Epub 2021 Jul 13. Neuropharmacology. 2021. PMID: 34271020 Review.

3

Allosteric coupling of sub-millisecond clamshell motions in ionotropic glutamate receptor ligand-binding domains.

Rajab S, Bismin L, Schwarze S, Pinggera A, Greger IH, Neuweiler H. Rajab S, et al. Among authors: pinggera a. Commun Biol. 2021 Sep 9;4(1):1056. doi: 10.1038/s42003-021-02605-0. Commun Biol. 2021. PMID: 34504293 Free PMC article.

4

Stabilization of negative activation voltages of Cav1.3 L-Type Ca²⁺-channels by alternative splicing.

Hofer NT, Pinggera A, Nikonishyna YV, Tuluc P, Fritz EM, Obermair GJ, Striessnig J. Hofer NT, et al. Among authors: pinggera a. Channels (Austin). 2021 Dec;15(1):38-52. doi: 10.1080/19336950.2020.1859260. Channels (Austin). 2021. PMID: 33380256 Free PMC article.

5

Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy.

Rinné S, Stallmeyer B, Pinggera A, Netter MF, Matschke LA, Dittmann S, Kirchhefer U, Neudorf U, Opp J, Striessnig J, Decher N, Schulze-Bahr E. Rinné S, et al. Among authors: pinggera a. Int J Mol Sci. 2022 Nov 17;23(22):14215. doi: 10.3390/ijms232214215. Int J Mol Sci. 2022. PMID: 36430690 Free PMC article.

6

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.

7

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.

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

Aldosterone-Producing Adenomas: Histopathology-Genotype Correlation and Identification of a Novel CACNA1D Mutation.

Tan GC, Negro G, Pinggera A, Tizen Laim NMS, Mohamed Rose I, Ceral J, Ryska A, Chin LK, Kamaruddin NA, Mohd Mokhtar N, A Jamal AR, Sukor N, Solar M, Striessnig J, Brown MJ, Azizan EA. Tan GC, et al. Among authors: pinggera a. Hypertension. 2017 Jul;70(1):129-136. doi: 10.1161/HYPERTENSIONAHA.117.09057. Epub 2017 Jun 5. Hypertension. 2017. PMID: 28584016

10

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.

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