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Author Details
Full Name
Laura Ferraiuolo
Affiliation
Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield
ORCID
Career Start Year
2007
Papers
60
H Index
28
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36857431
A cell-penetrant peptide blocking <i>C9ORF72</i>-repeat RNA nuclear export reduces the neurotoxic effects of dipeptide repeat proteins.
Sci Transl Med
2023
34767256
Biological and methodological complexities of beta-amyloid peptide: Implications for Alzheimer's disease research.
J Neurochem
2022
35568435
<i>C9ORF72</i>-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons.
Life Sci Alliance
2022
35628601
Towards 3D Bioprinted Spinal Cord Organoids.
Int J Mol Sci
2022
36619668
Loss of TMEM106B exacerbates C9ALS/FTD DPR pathology by disrupting autophagosome maturation.
Front Cell Neurosci
2022
36499600
Blood-Brain Barrier Disruption and Its Involvement in Neurodevelopmental and Neurodegenerative Disorders.
Int J Mol Sci
2022
36497181
Micro-RNAs Shuttled by Extracellular Vesicles Secreted from Mesenchymal Stem Cells Dampen Astrocyte Pathological Activation and Support Neuroprotection in In-Vitro Models of ALS.
Cells
2022
36241425
Low expression of EXOSC2 protects against clinical COVID-19 and impedes SARS-CoV-2 replication.
Life Sci Alliance
2022
35291294
Low expression of EXOSC2 protects against clinical COVID-19 and impedes SARS-CoV-2 replication.
bioRxiv
2022
35224690
Defective repair of topoisomerase I induced chromosomal damage in Huntington's disease.
Cell Mol Life Sci
2022
33440662
Mitochondrial Dysfunction in Alzheimer's Disease: A Biomarker of the Future?
Biomedicines
2021
33732769
A Parkinson's Disease-relevant Mitochondrial and Neuronal Morphology High-throughput Screening Assay in LUHMES Cells.
Bio Protoc
2021
33869658
Adipose-derived stem cells protect motor neurons and reduce glial activation in both <i>in vitro</i> and <i>in vivo</i> models of ALS.
Mol Ther Methods Clin Dev
2021
33892003
Mini-Review: Induced pluripotent stem cells and the search for new cell-specific ALS therapeutic targets.
Neurosci Lett
2021
34975412
Emerging Mechanisms Underpinning Neurophysiological Impairments in <i>C9ORF72</i> Repeat Expansion-Mediated Amyotrophic Lateral Sclerosis/Frontotemporal Dementia.
Front Cell Neurosci
2021
34963475
Astrocytic C-X-C motif chemokine ligand-1 mediates β-amyloid-induced synaptotoxicity.
J Neuroinflammation
2021
34376242
SRSF1-dependent inhibition of C9ORF72-repeat RNA nuclear export: genome-wide mechanisms for neuroprotection in amyotrophic lateral sclerosis.
Mol Neurodegener
2021
34173837
DNA damage as a mechanism of neurodegeneration in ALS and a contributor to astrocyte toxicity.
Cell Mol Life Sci
2021
34314817
NRF2 as a therapeutic opportunity to impact in the molecular roadmap of ALS.
Free Radic Biol Med
2021
33314575
Directly converted astrocytes retain the ageing features of the donor fibroblasts and elucidate the astrocytic contribution to human CNS health and disease.
Aging Cell
2021
32365522
Deficits in Mitochondrial Spare Respiratory Capacity Contribute to the Neuropsychological Changes of Alzheimer's Disease.
J Pers Med
2020
32058042
Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease.
Prog Neurobiol
2020
32968089
Oxidative switch drives mitophagy defects in dopaminergic parkin mutant patient neurons.
Sci Rep
2020
32669685
Applications of machine learning to diagnosis and treatment of neurodegenerative diseases.
Nat Rev Neurol
2020
30698736
Astrocyte adenosine deaminase loss increases motor neuron toxicity in amyotrophic lateral sclerosis.
Brain
2019
31647549
C9orf72 expansion within astrocytes reduces metabolic flexibility in amyotrophic lateral sclerosis.
Brain
2019
31579294
A High-throughput and Pathophysiologically Relevant Astrocyte-motor Neuron Co-culture Assay for Amyotrophic Lateral Sclerosis Therapeutic Discovery.
Bio Protoc
2019
30711519
Micro-RNAs secreted through astrocyte-derived extracellular vesicles cause neuronal network degeneration in C9orf72 ALS.
EBioMedicine
2019
30169589
Lost in translation: microRNAs mediate pathological cross-talk between motor neurons and astrocytes.
Brain
2018
30171839
Ursodeoxycholic Acid Improves Mitochondrial Function and Redistributes Drp1 in Fibroblasts from Patients with Either Sporadic or Familial Alzheimer's Disease.
J Mol Biol
2018
30195799
Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS.
Mol Ther Nucleic Acids
2018
27965018
High content analysis in amyotrophic lateral sclerosis.
Mol Cell Neurosci
2017
28168207
Additive amelioration of ALS by co-targeting independent pathogenic mechanisms.
Ann Clin Transl Neurol
2017
28677678
SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits.
Nat Commun
2017
28840555
Can Astrocytes Be a Target for Precision Medicine?
Adv Exp Med Biol
2017
26928464
Major histocompatibility complex class I molecules protect motor neurons from astrocyte-induced toxicity in amyotrophic lateral sclerosis.
Nat Med
2016
27688759
Oligodendrocytes contribute to motor neuron death in ALS via SOD1-dependent mechanism.
Proc Natl Acad Sci U S A
2016
27716798
MicroNeurotrophins Improve Survival in Motor Neuron-Astrocyte Co-Cultures but Do Not Improve Disease Phenotypes in a Mutant SOD1 Mouse Model of Amyotrophic Lateral Sclerosis.
PLoS One
2016
27334615
The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy.
EMBO J
2016
26780562
New In Vitro Models to Study Amyotrophic Lateral Sclerosis.
Brain Pathol
2016
25085783
Differences in protein quality control correlate with phenotype variability in 2 mouse models of familial amyotrophic lateral sclerosis.
Neurobiol Aging
2015
26621731
Translational profiling identifies a cascade of damage initiated in motor neurons and spreading to glia in mutant SOD1-mediated ALS.
Proc Natl Acad Sci U S A
2015
26528138
Lysosomal and phagocytic activity is increased in astrocytes during disease progression in the SOD1 (G93A) mouse model of amyotrophic lateral sclerosis.
Front Cell Neurosci
2015
25358252
Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates.
Mol Ther
2015
24379375
Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALS.
Proc Natl Acad Sci U S A
2014
25411487
Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortex.
J Neurosci
2014
25233402
The non-cell-autonomous component of ALS: new in vitro models and future challenges.
Biochem Soc Trans
2014
24750229
Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones.
Neuropathol Appl Neurobiol
2014
24607225
Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis.
Neuron
2014
23449106
Neural stem cells as a therapeutic approach for amyotrophic lateral sclerosis.
Mol Ther
2013
1 - 50 of 60
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University of California San Francisco
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Co-authored papers
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Jan Rehwinkel
MRC Weatherall Institute of Molecular Medicine, University of Oxford
Co-authored papers
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Wenbin Wei
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Harvard Medical School
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1
Calum Harvey
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Andrew Peden
University of Sheffield
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1
Michael P Snyder
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David E Gordon
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