Roberta Marongiu, PhD

Affiliations: 
2009- Neurosurgery Weill Cornell Medical College, New York, NY, United States 
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"Roberta Marongiu"
Mean distance: 15.49 (cluster 11)
 
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Publications

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Kelm-Nelson CA, Brauer AFL, Barth KJ, et al. (2017) Characterization of early-onset motor deficits in the Pink1 -/- mouse model of Parkinson disease. Brain Research
Marongiu R, Arango-Lievano M, Francardo V, et al. (2016) Gene therapy blockade of dorsal striatal p11 improves motor function and dyskinesia in parkinsonian mice. Proceedings of the National Academy of Sciences of the United States of America
Schintu N, Zhang X, Alvarsson A, et al. (2016) p11 modulates L-DOPA therapeutic effects and dyskinesia via distinct cell types in experimental Parkinsonism. Proceedings of the National Academy of Sciences of the United States of America
Gürsel DB, Banu MA, Berry N, et al. (2015) Tight regulation between cell survival and programmed cell death in GBM stem-like cells by EGFR/GSK3b/PP2A signaling. Journal of Neuro-Oncology. 121: 19-29
Arango-Lievano M, Schwarz JT, Vernov M, et al. (2014) Cell-type specific expression of p11 controls cocaine reward. Biological Psychiatry. 76: 794-801
Lenzi P, Marongiu R, Falleni A, et al. (2012) A subcellular analysis of genetic modulation of PINK1 on mitochondrial alterations, autophagy and cell death. Archives Italiennes De Biologie. 150: 194-217
Morgenstern PF, Marongiu R, Musatov SA, et al. (2011) Adeno-associated viral gene delivery in neurodegenerative disease. Methods in Molecular Biology (Clifton, N.J.). 793: 443-55
Michiorri S, Gelmetti V, Giarda E, et al. (2010) The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy. Cell Death and Differentiation. 17: 962-74
Marongiu R, Spencer B, Crews L, et al. (2009) Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux. Journal of Neurochemistry. 108: 1561-74
Marongiu R, Ferraris A, Ialongo T, et al. (2008) PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum. Human Mutation. 29: 565
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