Alexandra Pinggera

Francis Crick Avenue
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

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

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

Journal: International journal of molecular sciences

Published: September 22, 2022

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

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

Journal: Communications biology

Published: April 15, 2021

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

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

Journal: Neuropharmacology

Published: March 30, 2021

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

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

Journal: Channels (Austin, Tex.)

Published: December 31, 2020

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

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

Journal: Nature communications

Published: July 09, 2020

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

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

Journal: Pflugers Archiv : European journal of physiology

Published: July 23, 2019

Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels.

Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels.

Journal: Channels (Austin, Tex.)

Published: November 23, 2018

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

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

Journal: Human molecular genetics

Published: March 26, 2017

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

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

Journal: Biophysical journal

Published: March 16, 2017

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

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

Journal: Hypertension (Dallas, Tex. : 1979)

Published: January 09, 2017

Splice variants of the CaV1.3 L-type calcium channel regulate dendritic spine morphology.

Splice variants of the CaV1.3 L-type calcium channel regulate dendritic spine morphology.

Journal: Scientific reports

Published: March 09, 2016

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

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

Journal: The Journal of physiology

Published: September 24, 2015

Showing 1-12 of 16

Last Updated: 09/26/2026