Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets von Izzo, Antonella, Mollo, Nunzia, Nitti, Maria, Paladino, Simona, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Barbato, Maria, Sarnataro, Viviana, Conti, Anna, Nitsch, Lucio

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The hand that has forgotten its cunning-Lessons from musicians' hand dystonia von Conti, Anna M., Pullman, Seth, Frucht, Steven J.

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Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression von De Rosa, Laura, Fasano, Dominga, Zerillo, Lucrezia, Valente, Valeria, Izzo, Antonella, Mollo, Nunzia, Amodio, Giuseppina, Polishchuk, Elena, Polishchuk, Roman, Melone, Mariarosa Anna Beatrice, Criscuolo, Chiara, Conti, Anna, Nitsch, Lucio, Remondelli, Paolo, Pierantoni, Giovanna Maria, Paladino, Simona

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Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells von Mollo, Nunzia, Nitti, Maria, Zerillo, Lucrezia, Faicchia, Deriggio, Micillo, Teresa, Accarino, Rossella, Secondo, Agnese, Petrozziello, Tiziana, Calì, Gaetano, Cicatiello, Rita, Bonfiglio, Ferdinando, Sarnataro, Viviana, Genesio, Rita, Izzo, Antonella, Pinton, Paolo, Matarese, Giuseppe, Paladino, Simona, Conti, Anna, Nitsch, Lucio

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Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation von Mollo, Nunzia, Esposito, Matteo, Aurilia, Miriam, Scognamiglio, Roberta, Accarino, Rossella, Bonfiglio, Ferdinando, Cicatiello, Rita, Charalambous, Maria, Procaccini, Claudio, Micillo, Teresa, Genesio, Rita, Cali, Gaetano, Secondo, Agnese, Paladino, Simona, Matarese, Giuseppe, De Vita, Gabriella, Conti, Anna, Nitsch, Lucio, Izzo, Antonella

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Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy von Conti, Anna, Fabbrini, Floriana, D'Agostino, Paola, Negri, Rosa, Greco, Dario, Genesio, Rita, D'Armiento, Maria, Olla, Carlo, Paladini, Dario, Zannini, Mariastella, Nitsch, Lucio

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Identification of novel Pax8 targets in FRTL-5 thyroid cells by gene silencing and expression microarray analysis von Di Palma, Tina, Conti, Anna, de Cristofaro, Tiziana, Scala, Serena, Nitsch, Lucio, Zannini, Mariastella

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The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines von BEGHINI, Alessandro, MAGNANI, Ivana, LARIZZA, Lidia, ROVERSI, Gaia, PIEPOLI, Tiziana, DI TERLIZZI, Simona, MORONI, Ramona F, POLLO, Bianca, FUHRMAN CONTI, Anna M, COWELL, John K, FINOCCHIARO, Gaetano

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Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses von Conti, Anna, Nitsch, Lucio, Zannini, Mariastella, Martino, Marco De, Mollo, Nunzia, Cicatiello, Rita, Bonfiglio, Ferdinando, Cristofaro, Tiziana de, Manco, Rosanna, Izzo, Antonella, Genesio, Rita

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Exploring Burial and Dietary Patterns at the Copper Age Necropolis of Selvicciola (Viterbo, Italy): New Perspectives from 14C and Stable Isotope Data von di Cicco, Maria Rosa, Altieri, Simona, Mantile, Noemi, Petitti, Patrizia, Persiani, Carlo, Conti, Anna Maria, Allegrezza, Luciana, Cavazzuti, Claudio, Lubritto, Carmine

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Wide gene expression profiling of ischemia‐reperfusion injury in human liver transplantation von Conti, Anna, Scala, Simona, D'Agostino, Paola, Alimenti, Elena, Morelli, Daniele, Andria, Barbara, Tammaro, Angela, Attanasio, Chiara, Ragione, Floriana Della, Scuderi, Vincenzo, Fabbrini, Floriana, D'Esposito, Maurizio, Di Florio, Ernesto, Nitsch, Lucio, Calise, Fulvio, Faiella, Antonio

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Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype von Genesio, Rita, Melis, Daniela, Gatto, Sole, Izzo, Antonella, Ronga, Valentina, Cappuccio, Gerarda, Lanzo, Ambra, Andria, Generoso, D'Esposito, Maurizio, Matarazzo, Maria R., Conti, Anna, Nitsch, Lucio

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Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells von Izzo, Antonella, Nitti, Maria, Mollo, Nunzia, Paladino, Simona, Procaccini, Claudio, Faicchia, Deriggio, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Polishchuk, Elena, Polishchuk, Roman, Pinton, Paolo, Matarese, Giuseppe, Conti, Anna, Nitsch, Lucio

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Suppression of neurite outgrowth by high-dose nerve growth factor is independent of functional p75NTR receptors von Conti, Anna M., Brimijoin, Stephen, Miller, Laurence J., Windebank, Anthony J.

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Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects von Piccoli, Claudia, Izzo, Antonella, Scrima, Rosella, Bonfiglio, Ferdinando, Manco, Rosanna, Negri, Rosa, Quarato, Giovanni, Cela, Olga, Ripoli, Maria, Prisco, Marina, Gentile, Flaviana, Calì, Gaetano, Pinton, Paolo, Conti, Anna, Nitsch, Lucio, Capitanio, Nazzareno

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Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund‐Thomson syndrome von Miozzo, Monica, Castorina, Pierangela, Riva, Paola, Dalprà, Leda, Fuhrman Conti, Anna Maria, Volpi, Ludovica, Hoe, Tuck S., Khoo, Alan, Wiegant, Joop, Rosenberg, Carla, Larizza, Lidia

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Exploring Burial and Dietary Patterns at the Copper Age Necropolis of Selvicciola : New Perspectives from [sup.14]C and Stable Isotope Data von di Cicco, Maria Rosa, Altieri, Simona, Mantile, Noemi, Petitti, Patrizia, Persiani, Carlo, Conti, Anna Maria, Allegrezza, Luciana, Cavazzuti, Claudio, Lubritto, Carmine

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Nanostructured TiO2 films with 2 eV optical gaps von Barborini, Emanuele, Conti, Anna Maria, Kholmanov, Iskandar, Piseri, Paolo, Podestd, Alessandro, Milani, Paolo, Cepek, Cinzia, Sakho, Omar, Macovez, Roberto, Sancrotti, Massimo

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Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype von Rita, Genesio, Daniele, De Brasi, Anna, Conti, Annamaria, Borghese, Pasqua, Di Micco, Pasquale, Di Costanzo, Dario, Paladini, Paola, Ungaro, Lucio, Nitsch

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Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region von Fusco, Francesca, Paciolla, Mariateresa, Chen, Emily, Li, Xu, Genesio, Rita, Conti, Anna, Jones, Julie, Poeta, Loredana, Lioi, Maria Brigida, Ursini, Matilde Valeria, Miano, Maria Giuseppina

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