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Proteolytic shedding of the prion protein via activation of metallopeptidase ADAM10 reduces cellular binding and toxicity of amyloid-β oligomers.

Journal article

Jarosz-Griffiths HH. et al, (2019), The Journal of biological chemistry, 294, 7085 - 7097

Molecular genetic overlap between migraine and major depressive disorder

Journal article

Yang Y. et al, (2018), European Journal of Human Genetics, 26, 1202 - 1216

Engineered method for directional growth of muscle sheets on electrospun fibers

Journal article

Soliman E. et al, (2018), Journal of Biomedical Materials Research Part A, 106, 1165 - 1176

Small vessels, dementia and chronic diseases – molecular mechanisms and pathophysiology

Journal article

Horsburgh K. et al, (2018), Clinical Science, 132, 851 - 868

Aligned electrospun fibers for neural patterning

Journal article

Soliman E. et al, (2018), Biotechnology Letters, 40, 601 - 607

HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth disease

Journal article

Benoy V. et al, (2018), Brain, 141, 673 - 687

Neurovascular dysfunction in dementia – human cellular models and molecular mechanisms

Journal article

Parkes I. et al, (2018), Clinical Science, 132, 399 - 418

Plexin-Semaphorin Signaling Modifies Neuromuscular Defects in a Drosophila Model of Peripheral Neuropathy

Journal article

Grice SJ. et al, (2018), Frontiers in Molecular Neuroscience, 11

Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused byGarsmutations

Journal article

Sleigh JN. et al, (2017), Proceedings of the National Academy of Sciences, 114, E3324 - E3333

Mitophagy and Alzheimer’s Disease: Cellular and Molecular Mechanisms

Journal article

Kerr JS. et al, (2017), Trends in Neurosciences, 40, 151 - 166

Multiplex High-Throughput Targeted Proteomic Assay To Identify Induced Pluripotent Stem Cells

Journal article

Baud A. et al, (2017), Analytical Chemistry, 89, 2440 - 2448

Most brain disease-associated and eQTL haplotypes are not located within transcription factor DNase-seq footprints in brain

Journal article

Handel AE. et al, (2017), Human Molecular Genetics, ddw369 - ddw369

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Journal article

Gormley P. et al, (2016), Nature Genetics, 48, 1296 - 1296

DOMINANT GARS MUTATIONS CAUSE A DEVELOPMENTAL PERTURBATION OF SENSORY NEURON FATE IN CHARCOT-MARIE-TOOTH TYPE 2D MICE

Conference paper

Sleigh JN. et al, (2016), JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 21, 302 - 302

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