Leonard Petrucelli, PhD
Affiliations: | Neuroscience Research | Mayo Clinic Jacksonville, Jacksonville, FL, United States |
Area:
http://www.biomedexperts.com/Profile.bme/1110907/Leonard_PetrucelliWebsite:
http://mayoresearch.mayo.edu/mayo/research/staff/petrucelli_l.cfmGoogle:
"Leonard Petrucelli"Bio:
http://mayoresearch.mayo.edu/petrucelli_lab/
http://www.alzforum.org/com/res/detail.asp?id={6FC44417-BF30-4883-A2A1-95E498E8F852}
http://www.molecularneurodegeneration.com/edboard/start.asp?id=730361
Mean distance: 18.04 (cluster 28)
Cross-listing: Alzheimer's Tree
Children
Sign in to add traineeJoseph W Paul | research assistant | 2011-2013 | Mayo Clinc (Cell Biology Tree) |
Mercedes Prudencio | post-doc | Mayo Clinic Jacksonville |
BETA: Related publications
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Publications
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Seddighi S, Qi YA, Brown AL, et al. (2024) Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD. Science Translational Medicine. eadg7162 |
Marks JD, Ayuso VE, Carlomagno Y, et al. (2024) TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science Translational Medicine. 16: eadf9735 |
Li Z, Weller CA, Shah S, et al. (2023) ProtPipe: A Multifunctional Data Analysis Pipeline for Proteomics and Peptidomics. Biorxiv : the Preprint Server For Biology |
Cabrera GT, Meijboom KE, Abdallah A, et al. (2023) Artificial microRNA suppresses C9ORF72 variants and decreases toxic dipeptide repeat proteins in vivo. Gene Therapy |
Pickles S, Zanetti Alepuz D, Koike Y, et al. (2023) CRISPR interference to evaluate modifiers of -mediated toxicity in FTD. Frontiers in Cell and Developmental Biology. 11: 1251551 |
Estades Ayuso V, Pickles S, Todd T, et al. (2023) TDP-43-regulated cryptic RNAs accumulate in Alzheimer's disease brains. Molecular Neurodegeneration. 18: 57 |
Koike Y, Pickles S, Ayuso VE, et al. (2023) Correction: TDP-43 and other hnRNPs regulate cryptic exon inclusion of a key ALS/FTD risk gene, UNC13A. Plos Biology. 21: e3002228 |
Dulski J, Koga S, Prudencio M, et al. (2023) Perry syndrome: Novel DCTN1 mutation in a large kindred and first observation of prodromal disease. Parkinsonism & Related Disorders. 112: 105481 |
Dulski J, Al-Shaikh RH, Prudencio M, et al. (2023) First families with spinocerebellar ataxia type 7 in Poland. Neurologia I Neurochirurgia Polska. 57: 310-313 |
Abdelhak A, Barba L, Romoli M, et al. (2023) Prognostic performance of blood neurofilament light chain protein in hospitalized COVID-19 patients without major central nervous system manifestations: an individual participant data meta-analysis. Journal of Neurology |