MARIANI, ELISA

MARIANI, ELISA  

DIPARTIMENTO DI SCIENZE PER LA QUALITA' DELLA VITA  

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Risultati 1 - 7 di 7 (tempo di esecuzione: 0.01 secondi).
Titolo Autore(i) Anno Periodico Editore Tipo File
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi...; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli. 2009-01-01 HUMAN MUTATION - 1.01 Articolo in rivista -
Characterization of human gene locus CYYR1: a complex multi-transcript system Raffaella Casadei;Maria Chiara Pelleri;Lorenza Vitale;Federica Facchin;Silvia Canaider;Pierluigi ...Strippoli;Matteo Vian;Allison Piovesan;Eva Bianconi;Elisa Mariani;Francesco Piva;Flavia Frabetti 2014-01-01 MOLECULAR BIOLOGY REPORTS - 1.01 Articolo in rivista -
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. Bartoletti-Stella A;Mariani E;Kurelac I;Maresca A;Caratozzolo MF;Iommarini L;Carelli V;Eusebi LH;...Guido A;Cenacchi G;Fuccio L;Rugolo M;Tullo A;Porcelli AM;Gasparre G 2013-01-01 CELL DEATH & DISEASE - 1.01 Articolo in rivista cddis2013187.pdf
Meta-analysis of Parkinson's disease transcriptome data using TRAM software: Whole substantia nigra tissue and single dopamine neuron differential gene expression Mariani, Elisa; Frabetti, Flavia; Tarozzi, Andrea; Pelleri, Maria Chiara; Pizzetti, Fabrizio; Cas...adei, Raffaella 2016-01-01 PLOS ONE - 1.01 Articolo in rivista journal.pone.0161567.PDF
META-ANALYSIS OF SUBSTANTIA NIGRA TRANSCRIPTOME DATA: SEARCHING FOR NEW BIOMARKERS OF PD Mariani, E.; Pelleri, M.C.; Frabetti, F.; Tarozzi, A.; Casadei, R. 2015-01-01 NEURODEGENERATIVE DISEASES - 1.06 Abstract in rivista -
Sex-Specific Transcriptome Differences in Substantia Nigra Tissue: A Meta-Analysis of Parkinson's Disease Data Mariani, Elisa; Lombardini, Lorenza; Facchin, Federica; Pizzetti, Fabrizio; Frabetti, Flavia; Tar...ozzi, Andrea; Casadei, Raffaella 2018-01-01 GENES - 1.01 Articolo in rivista genes-09-00275.pdf
Where Birt-Hogg-Dubé meets Cowden Syndrome: Mirrored genetic defects in two cases of syndromic oncocytic tumours Pradella L.M.; Lang M.; Kurelac I.; Mariani E.; Guerra F.; Zuntini R.; Tallini G.; MacKay A.; Rei...s-Filho J.S.; Seri M.; Turchetti D.; Gasparre G. 2013-01-01 EUROPEAN JOURNAL OF HUMAN GENETICS - 1.01 Articolo in rivista -