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Leonard Petrucelli, PhD

Neuroscience Research Mayo Clinic Jacksonville, Jacksonville, FL, United States 
"Leonard Petrucelli"

Mean distance: 18.04 (cluster 28)
Cross-listing: Alzheimer's Tree


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Joseph W Paul research assistant 2011-2013 Mayo Clinc (Cell Biology Tree)
Mercedes Prudencio post-doc Mayo Clinic Jacksonville
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Goodman LD, Prudencio M, Kramer NJ, et al. (2019) Toxic expanded GGGGCC repeat transcription is mediated by the PAF1 complex in C9orf72-associated FTD. Nature Neuroscience
Goodman LD, Prudencio M, Srinivasan AR, et al. (2019) eIF4B and eIF4H mediate GR production from expanded G4C2 in a Drosophila model for C9orf72-associated ALS. Acta Neuropathologica Communications. 7: 62
Zhang YJ, Guo L, Gonzales PK, et al. (2019) Heterochromatin anomalies and double-stranded RNA accumulation underlie poly(PR) toxicity. Science (New York, N.Y.). 363
Jiang L, Ash PEA, Maziuk BF, et al. (2018) TIA1 regulates the generation and response to toxic tau oligomers. Acta Neuropathologica
Hanna Al Shaikh R, Caulfield T, Strongosky AJ, et al. (2018) TRIO gene segregation in a family with cerebellar ataxia. Neurologia I Neurochirurgia Polska
Ebbert MTW, Farrugia SL, Sens JP, et al. (2018) Long-read sequencing across the C9orf72 'GGGGCC' repeat expansion: implications for clinical use and genetic discovery efforts in human disease. Molecular Neurodegeneration. 13: 46
Mordes DA, Prudencio M, Goodman LD, et al. (2018) Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients. Acta Neuropathologica Communications. 6: 55
Zhang YJ, Gendron TF, Ebbert MTW, et al. (2018) Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis. Nature Medicine
Pottier C, Zhou X, Perkerson RB, et al. (2018) Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. The Lancet. Neurology
Lee CW, Stankowski JN, Chew J, et al. (2017) The lysosomal protein cathepsin L is a progranulin protease. Molecular Neurodegeneration. 12: 55
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