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个人简介
We are using molecular genetic approaches in humans and knock-in mice, with precisely targeted gene mutations, to understand the basis of inherited human neurodegenerative diseases. Two major interests, where we have identified the underlying gene defects and have made genetically accurate mouse and neuronal cell models, are Huntington’s disease (HD) and Neuronal Ceroid Lipofuscinosis (NCLs).
研究兴趣
论文共 273 篇作者统计合作学者相似作者
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biorxiv(2023)
Zenodo (CERN European Organization for Nuclear Research) (2023)
Zachariah L McLean,Dadi Gao,Kevin Correia,Jennie C L Roy, Shota Shibata, Iris N Farnum, Zoe Valdepenas-Mellor, Manasa Rapuru,Elisabetta Morini,Jayla Ruliera,Tammy Gillis,Diane Lucente,
bioRxiv : the preprint server for biology (2023)
Branduff McAllister,Jasmine Donaldson,Caroline S. Binda,Sophie Powell, Uroosa Chughtai,Gareth Edwards,Joseph Stone,Sergey Lobanov, Linda Elliston,Laura-Nadine Schuhmacher,Elliott Rees,Georgina Menzies,
biorxiv(2022)
Branduff McAllister,Jasmine Donaldson,Caroline S. Binda,Sophie Powell, Uroosa Chughtai,Gareth Edwards,Joseph Stone,Sergey Lobanov, Linda Elliston,Laura-Nadine Schuhmacher,Elliott Rees,Georgina Menzies,
biorxiv(2021)
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