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Bio
Gillian Bates studies the molecular and genetic underpinnings of Huntington’s disease, a late-onset brain disorder that leads to uncontrolled movements, emotional problems and cognitive difficulties. Gillian’s research highlights include her role in first mapping then cloning the huntingtin gene, together with the creation of the first mouse model of the disease.
Her work is helping to reveal novel therapeutic targets for the treatment of Huntington’s disease — one such possible target being histone deacetylase 4, the effectiveness of which Gillian first demonstrated using her mouse model.
Gillian has received a number of awards in recognition of her work, including the Society’s GlaxoSmithKline Prize in 1998 for her part in discovering the cause of Huntington’s disease. In addition to being a Fellow of the Society, she was also elected as a Fellow of the Academy of Medical Sciences in 1999 and as a member of EMBO, the European Molecular Biology Organisation, in 2002.
Research Interests
Papers共 330 篇Author StatisticsCo-AuthorSimilar Experts
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Nikolaos Tataridas-Pallas,Yahyah Aman,Rhianna Williams, Hannah Chapman, Kevin J.H. Cheng,Casandra Gomez-Paredes,Gillian P. Bates,John Labbadia
Franziska Hoschek,Julia Natan, Maximilian Wagner,Kirupa Sathasivam,Alshaimaa Abdelmoez, Björn von Einem,Gillian P. Bates,G. Bernhard Landwehrmeyer,Andreas Neueder
Brain communicationsno. 1 (2023): fcad010-fcad010
Brainno. 5 (2023): 1784-1798
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Karlijne W. Geijtenbeek, Jolien Janzen, Aleksandra Bury,Alicia Sanz-Sanz,Ron A. Hoebe,Marie K. Bondulich,Gillian P. Bates,Eric Reits,Sabine Schipper-Krom
PLOS ONEno. 12 (2022): e0278130-e0278130
Karlijne W. Geijtenbeek, Jolien Janzen, Aleksandra E. Bury,Alicia Sanz-Sanz,Ron A. Hoebe,Marie K. Bondulich,Gillian P. Bates,Eric A. J. Reits,Sabine Schipper-Krom
A: Pathogenic mechanisms (2022): A1-A2
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