Consiglia Pacelli

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2011-2015 Clinical and experiemtal medicine Universita di Foggia 
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"Consiglia Pacelli"
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Fortin GM, Ducrot C, Giguère N, et al. (2018) Segregation of dopamine and glutamate release sites in dopamine neuron axons: regulation by striatal target cells. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201800713RR
Giguere N, Pacelli C, Saumure C, et al. (2018) Comparative analysis of Parkinson's disease-associated genes reveals altered survival and bioenergetics of parkin-deficient dopamine neurons in mice. The Journal of Biological Chemistry
Doucet-Beaupré H, Gilbert C, Profes MS, et al. (2016) Lmx1a and Lmx1b regulate mitochondrial functions and survival of adult midbrain dopaminergic neurons. Proceedings of the National Academy of Sciences of the United States of America
Selleri S, Bifsha P, Civini S, et al. (2016) Human mesenchymal stromal cell-secreted lactate induces M2-macrophage differentiation by metabolic reprogramming. Oncotarget
Samuel F, Flavin WP, Iqbal S, et al. (2015) Effects of Serine 129 phosphorylation on α-synuclein aggregation, membrane association, and internalization. The Journal of Biological Chemistry
Pacelli C, Giguère N, Bourque MJ, et al. (2015) Elevated Mitochondrial Bioenergetics and Axonal Arborization Size Are Key Contributors to the Vulnerability of Dopamine Neurons. Current Biology : Cb. 25: 2349-60
Lippolis R, Siciliano RA, Pacelli C, et al. (2015) Altered protein expression pattern in skin fibroblasts from parkin-mutant early-onset Parkinson's disease patients. Biochimica Et Biophysica Acta
Vergara D, Ferraro MM, Cascione M, et al. (2015) Cytoskeletal Alterations and Biomechanical Properties of parkin-Mutant Human Primary Fibroblasts. Cell Biochemistry and Biophysics. 71: 1395-404
De Rasmo D, Signorile A, Larizza M, et al. (2012) Activation of the cAMP cascade in human fibroblast cultures rescues the activity of oxidatively damaged complex I. Free Radical Biology & Medicine. 52: 757-64
Arnoldi A, Tonelli A, Crippa F, et al. (2008) A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia. Human Mutation. 29: 522-31
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