Výsledky vyhledávání - Massimo Carella

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  1. 1
    The Emerging Role of Altered d-Aspartate Metabolism in Schizophrenia: New Insights From Preclinical Models and Human Studies

    The Emerging Role of Altered d-Aspartate Metabolism in Schizophrenia: New Insights From Preclinical Models and Human Studies Autor Francesco Errico, Tommaso Nuzzo, Massimo Carella, Alessandro Bertolino, Alessandro Usiello

    Vydáno 2018
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  2. 2
    High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE

    High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE Autor Stefano Castellana, Caterina Fusilli, Gianluigi Mazzoccoli, Tommaso Biagini, Daniele Capocefalo, Massimo Carella, Angelo L. Vescovi, Tommaso Mazza

    Vydáno 2017
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  3. 3
    Emery‐Dreifuss muscular dystrophy type 4: A new SYNE1 mutation associated with hypertrophic cardiomyopathy masked by a perinatal distress‐related spastic diplegia

    Emery‐Dreifuss muscular dystrophy type 4: A new SYNE1 mutation associated with hypertrophic cardiomyopathy masked by a perinatal distress‐related spastic diplegia Autor Sandra, Mastroianno, Maria Pia, Leone, Stefano, Castellana, Pietro, Palumbo, Crociani, Paola, Aldo, Russo, Giuseppe, Di Stolfo, Massimo, Carella

    Vydáno 2019
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  4. 4
    The Common −866G/A Polymorphism in the Promoter Region of the UCP-2 Gene Is Associated with Reduced Risk of Type 2 Diabetes in Caucasians from Italy

    The Common −866G/A Polymorphism in the Promoter Region of the UCP-2 Gene Is Associated with Reduced Risk of Type 2 Diabetes in Caucasians from Italy Autor Angela Bulotta, Ornella Ludovico, Angelo Coco, Rosa Di Paola, Alessandro Quattrone, Massimo Carella, Fabio Pellegrini, Sabrina Prudente, Vincenzo Trischitta

    Vydáno 2005
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  5. 5
    On the statistical assessment of classifiers using DNA microarray data

    On the statistical assessment of classifiers using DNA microarray data Autor Nicola Ancona, Rosalia Maglietta, Ada Piepoli, A. D’Addabbo, Rosa Cotugno, Michelangelo Savino, Sabino Liuni, Massimo Carella, Graziano Pesole, Francesco Perri

    Vydáno 2006
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  6. 6
    Mitochondrial dysregulation and oxidative stress in patients with chronic kidney disease

    Mitochondrial dysregulation and oxidative stress in patients with chronic kidney disease Autor Simona Granata, Gianluigi Zaza, Simona Simone, Gaetano Villani, Dominga Latorre, Paola Pontrelli, Massimo Carella, Francesco Paolo Schena, Giuseppe Grandaliano, Giovanni Pertosa

    Vydáno 2009
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  7. 7
    Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

    Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome Autor Alessandro Mussa, Cristina Molinatto, Flavia Cerrato, Orazio Palumbo, Massimo Carella, Giuseppina Baldassarre, Diana Carli, Clementina Peris, Andrea Riccio, Giovanni Battista Ferrero

    Vydáno 2017
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  8. 8
    Juvenile Hemochromatosis Locus Maps to Chromosome 1q

    Juvenile Hemochromatosis Locus Maps to Chromosome 1q Autor Antonella Roetto, Antonio Totaro, Mario Cazzola, M. Cicilano, S. Bosio, Giuseppe D'Ascola, Massimo Carella, L. Zelante, Alison Kelly, Timothy M. Cox, Paolo Gasparini, Clara Camaschella

    Vydáno 1999
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  9. 9
    BEAT: Bioinformatics Exon Array Tool to store, analyze and visualize Affymetrix GeneChip Human Exon Array data from disease experiments

    BEAT: Bioinformatics Exon Array Tool to store, analyze and visualize Affymetrix GeneChip Human Exon Array data from disease experiments Autor Arianna Consiglio, Massimo Carella, De Giorgio, Gianfranco Delle Foglie, Candida Giovannelli, Giorgio Grillo, Massimo Ianigro, Flavio Licciulli, Orazio Palumbo, Ada Piepoli, Elena Ranieri, Sabino Liuni

    Vydáno 2012
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  10. 10
    Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits

    Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits Autor Carmela Fusco, Lucia Micale, Bartolomeo Augello, Maria Teresa Pellico, Deny Menghini, Paolo Alfieri, M. Cristina Digilio, Barbara Mandriani, Massimo Carella, Orazio Palumbo, Stefano Vicari, Giuseppe Merla

    Vydáno 2013
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  11. 11
    Pathogenetic role of the deafness-related M34T mutation of Cx26

    Pathogenetic role of the deafness-related M34T mutation of Cx26 Autor Massimiliano Bicego, Martina Beltramello, Salvatore Melchionda, Massimo Carella, Valeria Piazza, Leopoldo Zelante, Feliksas F. Bukauskas, Edoardo Arslan, Elona Cama, Sergio Pantano, Roberto Bruzzone, Paola D’Andrea, Fabio Mammano

    Vydáno 2006
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  12. 12
    Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patients

    Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patients Autor Tommaso Nuzzo, Silvia Sacchi, Francesco Errico, Simona Keller, Orazio Palumbo, Ermanno Florio, Daniela Punzo, Francesco Napolitano, Massimiliano Copetti, Massimo Carella, Lorenzo Chiariotti, Alessandro Bertolino, Loredano Pollegioni, Alessandro Usiello

    Vydáno 2017
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  13. 13
    Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

    Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports Autor Laura Bernardini, Stefania Gimelli, Cristina Gervasini, Massimo Carella, Anwar Baban, Giada Frontino, Giancarlo Barbano, Maria Teresa Divizia, Luigi Fedele, Antonio Novelli, Frédérique Béna, Faustina Lalatta, Monica Miozzo, Bruno Dallapiccola

    Vydáno 2009
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  14. 14
    Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations

    Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations Autor Ilaria Gandin, Flavio Faletra, Francesca Faletra, Massimo Carella, Vanna Pecile, Giovanni Battista Ferrero, Elisa Biamino, Pietro Palumbo, Orazio Palumbo, Paolo Bosco, Corrado Romano, Chiara Belcaro, Diego Vozzi, Pio D’Adamo

    Vydáno 2014
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  15. 15
    Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like Cells

    Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like Cells Autor Elena Binda, Alberto Visioli, Fabrizio Giani, Nadia Trivieri, Orazio Palumbo, Silvia Restelli, Fabio Dezi, Tommaso Mazza, Caterina Fusilli, Federico Legnani, Massimo Carella, Francesco Di Meco, Rohit Duggal, Angelo L. Vescovi

    Vydáno 2016
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  16. 16
    MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

    MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss Autor Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, María L. Arbonés, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella, Leopoldo Zelante, Xavier Estivill, Karen B. Avraham, Paolo Gasparini

    Vydáno 2001
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  17. 17
    A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2

    A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 Autor Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, Elvira Grandone, Pietro Palumbo, Alessandro Salina, Concetta Aloi, Pietro Buono, Antonella Izzo, Giuseppe d’Annunzio, Gennaro Vecchione, Ada Orrico, Rita Genesio, Francesca Simonelli, Adriana Franzese

    Vydáno 2014
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  18. 18
    Differences in Gene Expression and Cytokine Release Profiles Highlight the Heterogeneity of Distinct Subsets of Adipose Tissue-Derived Stem Cells in the Subcutaneous and Visceral Adipose Tissue in Humans

    Differences in Gene Expression and Cytokine Release Profiles Highlight the Heterogeneity of Distinct Subsets of Adipose Tissue-Derived Stem Cells in the Subcutaneous and Visceral A... Autor Sebastio Perrini, Romina Ficarella, Ernesto Picardi, Angelo Cignarelli, Maria Pia Foschino Barbaro, Pasquale Nigro, Alessandro Peschechera, Orazio Palumbo, Massimo Carella, Michele De Fazio, Annalisa Natalicchio, Luigi Laviola, Graziano Pesole, Francesco Giorgino

    Vydáno 2013
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  19. 19
    APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

    APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants Autor Salvatore Daniele Bianco, Luca Parca, Francesco Petrizzelli, Tommaso Biagini, Agnese Giovannetti, Niccolò Liorni, Alessandro Napoli, Massimo Carella, Vincent Procaccio, Marie T. Lott, Shiping Zhang, Angelo L. Vescovi, Douglas C. Wallace, Viviana Caputo, Tommaso Mazza

    Vydáno 2023
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  20. 20
    Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

    Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment Autor Howard T. Jacobs, Timothy Hutchin, Timo Käppi, Greta Gillies, Kia Minkkinen, John Walker, Karen Thompson, Anja T. Rovio, Massimo Carella, Salvatore Melchionda, Leopoldo Zelante, Paolo Gasparini, Ilmari Pyykkö, Zahid H. Shah, Massimo Zeviani, Robert F. Mueller

    Vydáno 2004
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