PP2A regulates HDAC4 nuclear import von Paroni, Gabriela, Cernotta, Nadia, Dello Russo, Claudio, Gallinari, Paola, Pallaoro, Michele, Foti, Carmela, Talamo, Fabio, Orsatti, Laura, Steinkühler, Christian, Brancolini, Claudio

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Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome von Mucciolo, Mafalda, Dello Russo, Claudio, D'Emidio, Laura, Mesoraca, Alvaro, Giorlandino, Claudio

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Loss of Histone Deacetylase 4 Causes Segregation Defects during Mitosis of p53-Deficient Human Tumor Cells von CADOT, Bruno, BRUNETTI, Mirko, COPPARI, Sabina, FEDELI, Silvia, DE RINALDIS, Emanuele, DELLO RUSSO, Claudio, GALLINARI, Paola, DE FRANCESCO, Raffaele, STEINKÜHLER, Christian, FILOCAMO, Gessica

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Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience von Margiotti, Katia, Cesta, Anthony, Dello Russo, Claudio, Cima, Antonella, Barone, Maria Antonietta, Viola, Antonella, Sparacino, Davide, Mesoraca, Alvaro, Giorlandino, Claudio

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Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene von Fabiani, Marco, Libotte, Francesco, Margiotti, Katia, Tannous, Dina Khader Issa, Sparacino, Davide, D'Aleo, Maria Pia, Monaco, Francesca, Dello Russo, Claudio, Mesoraca, Alvaro, Giorlandino, Claudio

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Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Exam... von Libotte, Francesco, Carpineto, Sonia Lorena, Dello Russo, Claudio, Viola, Antonella, Margiotti, Katia, Restaldi, Fabrizia, Novelli, Antonio, Mesoraca, Alvaro, Giorlandino, Claudio

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Nitric Oxide Modulates Chromatin Folding in Human Endothelial Cells via Protein Phosphatase 2A Activation and Class II Histone Deacetylases Nuclear Shuttling von Illi, Barbara, Russo, Claudio Dello, Colussi, Claudia, Rosati, Jessica, Pallaoro, Michele, Spallotta, Francesco, Rotili, Dante, Valente, Sergio, Ragone, Gianluca, Martelli, Fabio, Biglioli, Paolo, Steinkuhler, Christian, Gallinari, Paola, Mai, Antonello, Capogrossi, Maurizio C, Gaetano, Carlo

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Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre study von Mesoraca, Alvaro, Margiotti, Katia, Dello Russo, Claudio, Cesta, Anthony, Cima, Antonella, Longo, Salvatore Antonio, Barone, Maria Antonietta, Viola, Antonella, Sparacino, Davide, Giorlandino, Claudio

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Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosis von Dello Russo, Claudio, Di Giacomo, Gianluca, Mesoraca, Alvaro, D'Emidio, Laura, Iaconianni, Paola, Minutolo, Elisa, Lippa, Assunta, Giorlandino, Claudio

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Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD) von Giorlandino, Claudio, Mesoraca, Alvaro, Bizzoco, Domenico, Dello Russo, Claudio, Cima, Antonella, Di Giacomo, Gianluca, Cignini, Pietro, Padula, Francesco, Dugo, Nella, D'Emidio, Laura, Brizzi, Cristiana, Raffio, Raffaella, Milite, Vincenzo, Mangiafico, Lucia, Coco, Claudio, Carcioppolo, Ornella, Vigna, Roberto, Mastrandrea, Marialuisa, Mobili, Luisa

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Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal Diagnosis von Dello Russo, Claudio, Cesta, Anthony, Longo, Salvatore, Barone, Maria A, Cima, Antonella, Mesoraca, Alvaro, Sparacino, Davide, Viola, Antonella, Giorlandino, Claudio

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Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA von Dello Russo, Claudio, Cesta, Anthony, Longo, Salvatore, Barone, Maria A., Cima, Antonella, Mesoraca, Alvaro, Sparacino, Davide, Viola, Antonella, Giorlandino, Claudio

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Agnathia-Otocephaly Complex Due to a De Novo Deletion in the IOTX2/I Gene von Fabiani, Marco, Libotte, Francesco, Margiotti, Katia, Tannous, Dina Khader Issa, Sparacino, Davide, D’Aleo, Maria Pia, Monaco, Francesca, Dello Russo, Claudio, Mesoraca, Alvaro, Giorlandino, Claudio

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A new approach for Next Generation Sequencing in prenatal diagnosis applied to a case of Charcot-Marie-Tooth syndrome von Dello Russo, Claudio, Padula, Francesco, Di Giacomo, Gianluca, Mesoraca, Alvaro, Gabrielli, Ivan, Bizzoco, Domenico, Giorlandino, Claudio

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Electrical storm in systemic sclerosis: Inside the electroanatomic substrate von Casella, Michela, Carbucicchio, Corrado, Russo, Eleonora, Pizzamiglio, Francesca, Golia, Paolo, Conti, Sergio, Costa, Fabrizio, Dello Russo, Antonio, Tondo, Claudio

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Método para determinar la probabilidad de riesgo de trastornos cromosómicos y genéticos a partir de ADN libre de origen fetal von MESORACA, Alvaro, DELLO RUSSO, Claudio, GIORLANDINO, Claudio

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METHOD FOR DETERMINING THE PROBABILITY OF THE RISK OF CHROMOSOMAL AND GENETIC DISORDERS FROM FREE DNA OF FETAL ORIGIN von MESORACA, Alvaro, DELLO RUSSO, Claudio, GIORLANDINO, Claudio

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METHOD FOR DETERMINING THE PROBABILITY OF THE RISK OF CHROMOSOMAL AND GENETIC DISORDERS FROM FREE DNA OF FETAL ORIGIN von MESORACA, Alvaro, DELLO RUSSO, Claudio, GIORLANDINO, Claudio

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Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening von Russo, Claudio Dello, Di Giacomo, Gianluca, Cignini, Pietro, Padula, Francesco, Mangiafico, Lucia, Mesoraca, Alvaro, D'Emidio, Laura, McCluskey, Megan R, Paganelli, Arianna, Giorlandino, Claudio

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METHOD FOR THE DIRECT DETERMINATION OF FETAL ANEUPLOIDIES BY NON-INVASIVE ANALYSIS OF THE FETAL DNA FROM MATERNAL BLOOD BY MEANS OF DPCR von MESORACA, Alvaro, DELLO RUSSO, Claudio, GIORLANDINO, Claudio

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