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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).
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Papers共 342 篇Author StatisticsCo-AuthorSimilar Experts
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Kyung-Hee Kim,Eun Pyo Hong, Yukyeong Lee,Zachariah L McLean, Emanuela Elezi,Ramee Lee,Seung Kwak,Branduff McAllister,Thomas H Massey,Sergey Lobanov,Peter Holmans,Michael Orth,
Proceedings of the National Academy of Sciences of the United States of Americano. 16 (2024): e2322924121-e2322924121
Zachariah L McLean,Dadi Gao,Kevin Correia,Jennie C L Roy,Shota Shibata,Iris N Farnum, Zoe Valdepenas-Mellor,Marina Kovalenko, Manasa Rapuru,Elisabetta Morini,Jayla Ruliera,Tammy Gillis,
Nature communicationsno. 1 (2024): 3182-3182
Journal of Huntington's diseaseno. 1 (2024): 33-40
Human molecular genetics (2024)
Zachariah L. McLean,Dadi Gao,Kevin Correia,Jennie C. L. Roy,Shota Shibata,Iris N. Farnum, Zoe Valdepenas-Mellor,Marina Kovalenko, Manasa Rapuru,Elisabetta Morini,Jayla Ruliera,Tammy Gillis,
Nature Communicationsno. 1 (2024): 1-17
Human molecular geneticsno. 1 (2023): 30-45
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)
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