Resultados de búsqueda - Gentilini, Davide

NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis por Gentilini, Davide, Oliveri, Antonino, Fazia, Teresa, Pini, Alessandro, Marelli, Susan, Bernardinelli, Luisa, Di Blasio, Anna Maria

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Soluble EMMPRIN levels discriminate aortic ectasia in Marfan syndrome patients por Rurali, Erica, Perrucci, Gianluca L., Gaetano, Raffaella, Pini, Alessandro, Moschetta, Donato, Gentilini, Davide, Nigro, Patrizia, Pompilio, Giulio

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Differences in Visceral Fat and Fat Bacterial Colonization between Ulcerative Colitis and Crohn’s Disease. An In Vivo and In Vitro Study por Zulian, Alessandra, Cancello, Raffaella, Ruocco, Chiara, Gentilini, Davide, Di Blasio, Anna Maria, Danelli, Piergiorgio, Micheletto, Giancarlo, Cesana, Elisabetta, Invitti, Cecilia

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Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset por Rossetti, Raffaella, Moleri, Silvia, Guizzardi, Fabiana, Gentilini, Davide, Libera, Laura, Marozzi, Anna, Moretti, Costanzo, Brancati, Francesco, Bonomi, Marco, Persani, Luca

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Is the Pain Just Physical? The Role of Psychological Distress, Quality of Life, and Autistic Traits in Ehlers–Danlos Syndrome, an Internet-Based Survey in Italy por Rocchetti, Matteo, Bassotti, Alessandra, Corradi, Jacopo, Damiani, Stefano, Pasta, Gianluigi, Annunziata, Salvatore, Guerrieri, Viviana, Mosconi, Mario, Gentilini, Davide, Brondino, Natascia

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Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females por Gentilini, Davide, Garagnani, Paolo, Pisoni, Serena, Bacalini, Maria Giulia, Calzari, Luciano, Mari, Daniela, Vitale, Giovanni, Franceschi, Claudio, Di Blasio, Anna Maria

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A Pan-Cancer Approach to Predict Responsiveness to Immune Checkpoint Inhibitors by Machine Learning por Polano, Maurizio, Chierici, Marco, Dal Bo, Michele, Gentilini, Davide, Di Cintio, Federica, Baboci, Lorena, Gibbs, David L., Furlanello, Cesare, Toffoli, Giuseppe

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Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles por Cassarino, Maria Francesca, Ambrogio, Alberto G., Cassarino, Andrea, Terreni, Maria Rosa, Gentilini, Davide, Sesta, Antonella, Cavagnini, Francesco, Losa, Marco, Pecori Giraldi, Francesca

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Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth por Spada, Elena, Calzari, Luciano, Corsaro, Luigi, Fazia, Teresa, Mencarelli, Monica, Di Blasio, Anna Maria, Bernardinelli, Luisa, Zangheri, Giulia, Vignali, Michele, Gentilini, Davide

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Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families por Fazia, Teresa, Marzanati, Daria, Carotenuto, Anna Laura, Beecham, Ashley, Hadjixenofontos, Athena, McCauley, Jacob L., Saddi, Valeria, Piras, Marialuisa, Bernardinelli, Luisa, Gentilini, Davide

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Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny por Tannorella, Pierpaola, Calzari, Luciano, Daolio, Cecilia, Mainini, Ester, Vimercati, Alessandro, Gentilini, Davide, Soli, Fiorenza, Pedrolli, Annalisa, Bonati, Maria Teresa, Larizza, Lidia, Russo, Silvia

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Responders and non-responders to influenza vaccination: a DNA methylation approach on blood cells por Gensous, Noémie, Franceschi, Claudio, Blomberg, Bonnie B., Pirazzini, Chiara, Ravaioli, Francesco, Gentilini, Davide, Di Blasio, Anna Maria, Garagnani, Paolo, Frasca, Daniela, Bacalini, Maria Giulia

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Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach por Fazia, Teresa, Nova, Andrea, Gentilini, Davide, Beecham, Ashley, Piras, Marialuisa, Saddi, Valeria, Ticca, Anna, Bitti, Pierpaolo, McCauley, Jacob L., Berzuini, Carlo, Bernardinelli, Luisa

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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations por Colombo, Elisa Adele, Mutlu-Albayrak, Hatice, Shafeghati, Yousef, Balasar, Mine, Piard, Juliette, Gentilini, Davide, Di Blasio, Anna Maria, Gervasini, Cristina, Van Maldergem, Lionel, Larizza, Lidia

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Accelerated epigenetic aging in Down syndrome por Horvath, Steve, Garagnani, Paolo, Bacalini, Maria Giulia, Pirazzini, Chiara, Salvioli, Stefano, Gentilini, Davide, Di Blasio, Anna Maria, Giuliani, Cristina, Tung, Spencer, Vinters, Harry V, Franceschi, Claudio

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A New Epigenetic Model to Stratify Glioma Patients According to Their Immunosuppressive State por Polano, Maurizio, Fabbiani, Emanuele, Adreuzzi, Eva, Cintio, Federica Di, Bedon, Luca, Gentilini, Davide, Mongiat, Maurizio, Ius, Tamara, Arcicasa, Mauro, Skrap, Miran, Dal Bo, Michele, Toffoli, Giuseppe

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Analysis of BMP15-Induced Transcriptome in Human Granulosa Cells for the Identification of Novel Candidate Genes for Primary Ovarian Insufficiency por Rossetti, Raffaella, Fornili, Marco, Moleri, Silvia, Ferrari, Ilaria, Gentilini, Davide, Paffoni, Alessio, Somigliana, Edgardo, Biganzoli, Elia, Marozzi, Anna, Brancati, Francesco, Moretti, Costanzo G, Giuliani, Cristina, Persani, Luca

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Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas por Antonelli, Manila, Fadda, Antonio, Loi, Eleonora, Moi, Loredana, Zavattari, Cesare, Sulas, Pia, Gentilini, Davide, Cameli, Cinzia, Bacchelli, Elena, Badiali, Manuela, Arcella, Antonella, Morra, Isabella, Giangaspero, Felice, Zavattari, Patrizia

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Acid sensing ion channel 2: A new potential player in the pathophysiology of multiple sclerosis por Fazia, Teresa, Pastorino, Roberta, Notartomaso, Serena, Busceti, Carla, Imbriglio, Tiziana, Cannella, Milena, Gentilini, Davide, Morani, Gabriele, Ticca, Anna, Bitti, Pierpaolo, Berzuini, Carlo, Dalmay, Tamas, Battaglia, Giuseppe, Bernardinelli, Luisa

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Altered modulation of lamin A/C‐HDAC2 interaction and p21 expression during oxidative stress response in HGPS por Mattioli, Elisabetta, Andrenacci, Davide, Garofalo, Cecilia, Prencipe, Sabino, Scotlandi, Katia, Remondini, Daniel, Gentilini, Davide, Di Blasio, Anna Maria, Valente, Sergio, Scarano, Emanuela, Cicchilitti, Lucia, Piaggio, Giulia, Mai, Antonello, Lattanzi, Giovanna

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