Gillian P. Bates

Affiliations: 
King's College London, London, UK 
Area:
Genetics, Huntington's disease
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"Gillian Bates"
Mean distance: 18.25 (cluster 32)
 
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Publications

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Sogorb-Gonzalez M, Landles C, Caron NS, et al. (2024) Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington disease models. Brain : a Journal of Neurology
Hoschek F, Natan J, Wagner M, et al. (2024) Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues. Molecular Medicine (Cambridge, Mass.). 30: 36
Aldous SG, Smith EJ, Landles C, et al. (2024) A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease. Brain : a Journal of Neurology
Bondulich MK, Phillips J, Cañibano-Pico M, et al. (2024) Translatable plasma and CSF biomarkers for use in mouse models of Huntington's disease. Brain Communications. 6: fcae030
Smith EJ, Sathasivam K, Landles C, et al. (2023) Early detection of exon 1 huntingtin aggregation in zQ175 brains by molecular and histological approaches. Brain Communications. 5: fcad010
Geijtenbeek KW, Janzen J, Bury AE, et al. (2022) Reduction in PA28αβ activation in HD mouse brain correlates to increased mHTT aggregation in cell models. Plos One. 17: e0278130
Fienko S, Landles C, Sathasivam K, et al. (2022) Alternative processing of human HTT mRNA with implications for Huntington's disease therapeutics. Brain : a Journal of Neurology
Gu X, Richman J, Langfelder P, et al. (2022) Uninterrupted CAG repeat drives striatum-selective transcriptionopathy and nuclear pathogenesis in human Huntingtin BAC mice. Neuron
Schulze-Krebs A, Canneva F, Stemick J, et al. (2021) Transglutaminase 6 Is Colocalized and Interacts with Mutant Huntingtin in Huntington Disease Rodent Animal Models. International Journal of Molecular Sciences. 22
Schindler F, Praedel N, Neuendorf N, et al. (2021) Small, Seeding-Competent Huntingtin Fibrils Are Prominent Aggregate Species in Brains of zQ175 Huntington's Disease Knock-in Mice. Frontiers in Neuroscience. 15: 682172
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