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Mitochondrial calcium uniporter Mcu controls excitotoxicity and is transcriptionally repressed by neuroprotective nuclear calcium signals

Nature communications, 2013-06, Vol.4 (1), p.2034, Article 2034

2013

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Initial characterisation of adult human ovarian cell populations isolated by DDX4 expression and aldehyde dehydrogenase activity

Scientific reports, 2018-05, Vol.8 (1), p.6953-11, Article 6953

2018

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Loss of cerebellar glutamate transporters EAAT4 and GLAST differentially affects the spontaneous firing pattern and survival of Purkinje cells

Human molecular genetics, 2018-08, Vol.27 (15), p.2614-2627

2018

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Extracellular Localisation of the C-Terminus of DDX4 Confirmed by Immunocytochemistry and Fluorescence-Activated Cell Sorting

Cells (Basel, Switzerland), 2019-06, Vol.8 (6), p.578

2019

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Temporal Profiling of the Cortical Synaptic Mitochondrial Proteome Identifies Ageing Associated Regulators of Stability

Cells (Basel, Switzerland), 2021-12, Vol.10 (12), p.3403

2021

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Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus Toxin

Biomolecules (Basel, Switzerland), 2021-10, Vol.11 (10), p.1499

2021

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The Role of Extracellular Regulated Kinases I/II in Late-Phase Long-Term Potentiation

The Journal of neuroscience, 2002-07, Vol.22 (13), p.5432-5441

2002

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Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy

The Journal of clinical investigation, 2014-04, Vol.124 (4), p.1821-1834

2014

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Functional assessment of triheteromeric NMDA receptors containing a human variant associated with epilepsy

The Journal of physiology, 2019-03, Vol.597 (6), p.1691-1704

2019

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Endomicroscopy and electromyography of neuromuscular junctions in situ

Annals of clinical and translational neurology, 2014-11, Vol.1 (11), p.867-883

2014

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β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations

Human molecular genetics, 2014-07, Vol.23 (14), p.3875-3882

2014

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Microarray profiling emphasizes transcriptomic differences between hippocampal in vivo tissue and in vitro cultures

Brain communications, 2021-01, Vol.3 (3), p.fcab152-fcab152

2021

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The human NMDA receptor GluN2A N615K variant influences channel blocker potency

Pharmacology research & perspectives, 2019-08, Vol.7 (4), p.e00495

2019

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The human NMDA receptor GluN2AN615K variant influences channel blocker potency

Pharmacology research & perspectives, 2019-08, Vol.7 (4), p.n/a

2019

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A VAMP-Binding Protein from Aplysia Required for Neurotransmitter Release

Science (American Association for the Advancement of Science), 1995-09, Vol.269 (5230), p.1580-1583

1995

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Spinal cord neurone loss and foot placement changes in a rat knock-in model of amyotrophic lateral sclerosis Type 8

Brain communications, 2024-05, Vol.6 (3), p.fcae184

2024

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The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells

Human molecular genetics, 2006-02, Vol.15 (4), p.625-635

2006

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Aplysia CREB2 represses long-term facilitation: Relief of repression converts transient facilitation into long-term functional and structural change

Cell, 1995-12, Vol.83 (6), p.979-992

1995

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Dysregulation of ubiquitin homeostasis and [beta]-catenin signaling promote spinal muscular atrophy.(Research article)

The Journal of clinical investigation, 2014-04, Vol.124 (4), p.1821

2014

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The neuroprotective Wld super(S) gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells

Human molecular genetics, 2006-02, Vol.15 (4), p.625-635

2006

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Characterization of a Y-Box factor from Aplysia californica

Gene, 1994-08, Vol.145 (2), p.231-235

1994

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Architecture of eukaryotic mRNA 3′-end processing machinery

Science (American Association for the Advancement of Science), 2017-11, Vol.358 (6366), p.1056-1059

2017

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A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis

American journal of human genetics, 2004-11, Vol.75 (5), p.822-831

2004

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CLICK: one-step generation of conditional knockout mice

BMC genomics, 2018-05, Vol.19 (1), p.318-318, Article 318

2018

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A Bi-fluorescence complementation system to detect associations between the Endoplasmic reticulum and mitochondria

Scientific reports, 2017-12, Vol.7 (1), p.17467-12, Article 17467

2017

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Mitochondrial calcium uniporter Mcu controls excitotoxicity and is transcriptionally repressed by neuroprotective nuclear calcium signals

Initial characterisation of adult human ovarian cell populations isolated by DDX4 expression and aldehyde dehydrogenase activity

Loss of cerebellar glutamate transporters EAAT4 and GLAST differentially affects the spontaneous firing pattern and survival of Purkinje cells

Extracellular Localisation of the C-Terminus of DDX4 Confirmed by Immunocytochemistry and Fluorescence-Activated Cell Sorting

Temporal Profiling of the Cortical Synaptic Mitochondrial Proteome Identifies Ageing Associated Regulators of Stability

Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus Toxin

The Role of Extracellular Regulated Kinases I/II in Late-Phase Long-Term Potentiation

Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy

Functional assessment of triheteromeric NMDA receptors containing a human variant associated with epilepsy

Endomicroscopy and electromyography of neuromuscular junctions in situ

β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations

Microarray profiling emphasizes transcriptomic differences between hippocampal in vivo tissue and in vitro cultures

The human NMDA receptor GluN2A N615K variant influences channel blocker potency

The human NMDA receptor GluN2AN615K variant influences channel blocker potency

A VAMP-Binding Protein from Aplysia Required for Neurotransmitter Release

Spinal cord neurone loss and foot placement changes in a rat knock-in model of amyotrophic lateral sclerosis Type 8

The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells

Aplysia CREB2 represses long-term facilitation: Relief of repression converts transient facilitation into long-term functional and structural change

Dysregulation of ubiquitin homeostasis and [beta]-catenin signaling promote spinal muscular atrophy.(Research article)

The neuroprotective Wld super(S) gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells

Characterization of a Y-Box factor from Aplysia californica

Architecture of eukaryotic mRNA 3′-end processing machinery

A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis

CLICK: one-step generation of conditional knockout mice

A Bi-fluorescence complementation system to detect associations between the Endoplasmic reticulum and mitochondria

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