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Revisiting the role of mitochondria in spinal muscular atrophy

Cellular and molecular life sciences : CMLS, 2021-05, Vol.78 (10), p.4785-4804

2021

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Repetitive mild traumatic brain injury in a mouse model produces learning and memory deficits accompanied by histological changes

Journal of neurotrauma, 2012-12, Vol.29 (18), p.2761-2773

2012

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Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7

Molecular therapy. Nucleic acids, 2023-09, Vol.33, p.617-628

2023

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Small junction, big problems: Neuromuscular junction pathology in mouse models of amyotrophic lateral sclerosis (ALS)

Journal of anatomy, 2022-11, Vol.241 (5), p.1089-1107

2022

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The role of survival motor neuron protein (SMN) in protein homeostasis

Cellular and molecular life sciences : CMLS, 2018-11, Vol.75 (21), p.3877-3894

2018

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Excitotoxicity and ALS: New therapy targets an old mechanism

Cell reports. Medicine, 2024-02, Vol.5 (2), p.101423-101423, Article 101423

2024

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A new strategy to increase RNA editing at the Q/R site of GluA2 AMPA receptor subunits by targeting alternative splicing patterns of ADAR2

Journal of neuroscience methods, 2021-12, Vol.364, p.109357-109357, Article 109357

2021

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Spinal muscular atrophy: From approved therapies to future therapeutic targets for personalized medicine

Cell reports. Medicine, 2021-07, Vol.2 (7), p.100346, Article 100346

2021

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Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy

Human molecular genetics, 2020-09, Vol.29 (16), p.2674-2683

2020

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Targeting phosphoglycerate kinase 1 with terazosin improves motor neuron phenotypes in multiple models of amyotrophic lateral sclerosis

EBioMedicine, 2022-09, Vol.83, p.104202-104202, Article 104202

2022

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Neuromuscular junction denervation and terminal Schwann cell loss in the hTDP‐43 overexpression mouse model of amyotrophic lateral sclerosis

Neuropathology and applied neurobiology, 2023-08, Vol.49 (4), p.e12925-n/a

2023

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The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivo

The FEBS journal, 2022-07, Vol.289 (13), p.3894-3914

2022

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Cover Image, Volume 49, Issue 4

Neuropathology and applied neurobiology, 2023-08, Vol.49 (4), p.n/a

2023

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Automated in vivo drug screen in zebrafish identifies synapse-stabilising drugs with relevance to spinal muscular atrophy

Disease models & mechanisms, 2021-04, Vol.14 (4)

2021

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Timing of SMN replacement therapies in mouse models of spinal muscular atrophy: a systematic review and meta-analysis

Brain communications, 2024-08, Vol.6 (4), p.fcae267

2024

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Brain‐derived neurotropic factor polymorphisms, traumatic stress, mild traumatic brain injury, and combat exposure contribute to postdeployment traumatic stress

Brain and behavior, 2016-01, Vol.6 (1), p.e00392-n/a

2016

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Genetics and Other Risk Factors for Past Concussions in Active-Duty Soldiers

Journal of neurotrauma, 2017-02, Vol.34 (4), p.869-875

2017

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Plasma Lipidomic Profiling in a Military Population of Mild Traumatic Brain Injury and Post-Traumatic Stress Disorder with Apolipoprotein E ɛ4-Dependent Effect

Journal of neurotrauma, 2016-07, Vol.33 (14), p.1331-1348

2016

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Development of an Antisense Oligonucleotide Based Method to Manipulate Rna Editing of Ampar Subunits

Chaytow, Helena Anne

2017

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Revisiting the role of mitochondria in spinal muscular atrophy

Repetitive mild traumatic brain injury in a mouse model produces learning and memory deficits accompanied by histological changes

Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7

Small junction, big problems: Neuromuscular junction pathology in mouse models of amyotrophic lateral sclerosis (ALS)

The role of survival motor neuron protein (SMN) in protein homeostasis

Excitotoxicity and ALS: New therapy targets an old mechanism

A new strategy to increase RNA editing at the Q/R site of GluA2 AMPA receptor subunits by targeting alternative splicing patterns of ADAR2

Spinal muscular atrophy: From approved therapies to future therapeutic targets for personalized medicine

Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy

Targeting phosphoglycerate kinase 1 with terazosin improves motor neuron phenotypes in multiple models of amyotrophic lateral sclerosis

Neuromuscular junction denervation and terminal Schwann cell loss in the hTDP‐43 overexpression mouse model of amyotrophic lateral sclerosis

The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivo

Cover Image, Volume 49, Issue 4

Automated in vivo drug screen in zebrafish identifies synapse-stabilising drugs with relevance to spinal muscular atrophy

Timing of SMN replacement therapies in mouse models of spinal muscular atrophy: a systematic review and meta-analysis

Brain‐derived neurotropic factor polymorphisms, traumatic stress, mild traumatic brain injury, and combat exposure contribute to postdeployment traumatic stress

Genetics and Other Risk Factors for Past Concussions in Active-Duty Soldiers

Plasma Lipidomic Profiling in a Military Population of Mild Traumatic Brain Injury and Post-Traumatic Stress Disorder with Apolipoprotein E ɛ4-Dependent Effect

Development of an Antisense Oligonucleotide Based Method to Manipulate Rna Editing of Ampar Subunits

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