Sophie R. Thomson

发表

Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome

Giles E. Hardingham, Owen Dando, P. Kind, 2017, Neuron.

Examining mechanisms underlying the selective vulnerability of motor units in a mouse model of Spinal Muscular Atrophy

Sophie R. Thomson, 2014 .

Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome

J. Darnell, P. Kind, K. Li, 2022, Nature Communications.

Excess ribosomal protein production unbalances translation in Fragile X Syndrome

J. Darnell, P. Kind, K. Li, 2022, bioRxiv.

Using induced pluripotent stem cells (iPSC) to model human neuromuscular connectivity: promise or reality?

S. Chandran, T. Gillingwater, T. Wishart, 2012, Journal of anatomy.

Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy

Rachael A. Powis, Ewout J. N. Groen, J. Highley, 2017, PLoS genetics.

Explorer Morphological characteristics of motor neurons do not determine their relative susceptibility to degeneration in a mouse model of severe spinal muscular atrophy

G. Hamilton, T. Gillingwater, Sophie R. Thomson, 2016 .

Morphological Characteristics of Motor Neurons Do Not Determine Their Relative Susceptibility to Degeneration in a Mouse Model of Severe Spinal Muscular Atrophy

G. Hamilton, T. Gillingwater, Sophie R. Thomson, 2012, PloS one.

FMRP and the Pathophysiology of Fragile X Syndrome

P. Kind, Emily K. Osterweil, Sophie R. Thomson, 2016 .