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Search results (17)

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Aberrant dynein function promotes TDP-43 aggregation and upregulation of p62 in male mice harboring transgenic human TDP-43.

Christoforidou E. et al, (2023), Amyotrophic lateral sclerosis & frontotemporal degeneration, 1 - 10

An ALS-linked mutation in TDP-43 disrupts normal protein interactions in the motor neuron response to oxidative stress

Feneberg E. et al, (2020), Neurobiology of Disease, 144, 105050 - 105050

Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes.

Sleigh JN. et al, (2020), Cell reports, 30, 3655 - 3662.e2

Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivo

Williamson MG. et al, (2019), Human Molecular Genetics, 28, 3584 - 3599

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

Gordon D. et al, (2019), Neurobiology of Disease, 121, 148 - 162

The interactome of human TDP-43 in a cellular model of amyotrophic lateral sclerosis

Feneberg E. et al, (2019), EUROPEAN JOURNAL OF NEUROLOGY, 26, 221 - 222

TDP-43 is cytoplasmically mislocalized and associated with impaired stress responses and survival of primary neurons from symptomatic amyotrophic lateral sclerosis (ALS) mice

Farrimond L. et al, (2016), EUROPEAN JOURNAL OF NEUROLOGY, 23, 390 - 391

Absence of wide-spread mis-splicing in the preclinical phase of a native promoter driven TDP-43 mouse model of ALS

Scaber J. et al, (2016), EUROPEAN JOURNAL OF NEUROLOGY, 23, 797 - 797

Absence of wide-spread mis-splicing in the preclinical phase of a native promoter driven TDP-43 mouse model of ALS

Scaber J. et al, (2016), NEUROMUSCULAR DISORDERS, 26, S31 - S31

TARDBP pathogenic mutations increase cytoplasmic translocation of TDP-43 and cause reduction of endoplasmic reticulum Ca2+ signaling in motor neurons

Mutihac R. et al, (2015), Neurobiology of Disease, 75, 64 - 77

Motor disorders

Gordon D. and Talbot K., (2014), 63 - 78

Fusion between human mesenchymal stem cells and rodent cerebellar Purkinje cells

Kemp K. et al, (2011), Neuropathology and Applied Neurobiology, 37, 166 - 178

Human Mesenchymal Stem Cells Infiltrate the Spinal Cord, Reduce Demyelination, and Localize to White Matter Lesions in Experimental Autoimmune Encephalomyelitis

Gordon D. et al, (2010), Journal of Neuropathology & Experimental Neurology, 69, 1087 - 1095

Human mesenchymal stem cells abrogate experimental allergic encephalomyelitis after intraperitoneal injection, and with sparse CNS infiltration

Gordon D. et al, (2008), Neuroscience Letters, 448, 71 - 73

Antisense suppression of tau in cultured rat oligodendrocytes inhibits process formation

Gordon D. et al, (2008), Journal of Neuroscience Research, 86, 2591 - 2601

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