Search results (12)
« Back to PublicationsCellular and axonal transport phenotypes due to the C9ORF72 HRE in iPSC motor and sensory neurons
Journal article
Scaber J. et al, (2024), Stem Cell Reports, 19, 957 - 972
C9orf72-ALS human iPSC microglia are pro-inflammatory and toxic to co-cultured motor neurons via MMP9
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Vahsen BF. et al, (2023), Nature Communications, 14
dvantages of routine next‐generation sequencing over standard genetic testing in the amyotrophic lateral sclerosis clinic
Journal article
Scaber J. et al, (2023), European Journal of Neurology, 30, 2240 - 2249
Human iPSC co-culture model to investigate the interaction between microglia and motor neurons
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Vahsen BF. et al, (2022), Scientific Reports, 12
case of SOD1 deficiency: implications for clinical trials.
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Farrimond L. and Talbot K., (2022), Brain, 145, 805 - 806
Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chain
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Thompson AG. et al, (2022), Brain Communications, 4
Impairment of mitochondrial calcium buffering links mutations in C9orf72 and TARDBP in iPS-derived motor neurons from patients with ALS/FTD
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DAFINCA R. et al, (2020), Stem Cell Reports
Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunction
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Gordon D. et al, (2019), Neurobiology of Disease, 121, 148 - 162
Initial Identification of a Blood-Based Chromosome Conformation Signature for Aiding in the Diagnosis of Amyotrophic Lateral Sclerosis
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Salter M. et al, (2018), EBioMedicine, 33, 169 - 184
TARDBP pathogenic mutations increase cytoplasmic translocation of TDP-43 and cause reduction of endoplasmic reticulum Ca2+ signaling in motor neurons
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Mutihac R. et al, (2015), Neurobiology of Disease, 75, 64 - 77
Memantine and cholinesterase inhibitor combination therapy for Alzheimer's disease: a systematic review
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Farrimond LE. et al, (2012), BMJ Open, 2, e000917 - e000917