Bianca De Nicolo, Erica Cataldi-Stagetti, Chiara Diquigiovanni, Elena Bonora, Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies, «ANTIOXIDANTS», 2023, 12, pp. 353 - 371 [articolo]
Bianca De Nicolo, Erica Cataldi-Stagetti, Chiara Diquigiovanni, Elena Bonora, Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and PathologiesCalcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies, «ANTIOXIDANTS», 2023, 12, Article number: 353, pp. 1 - 19 [articolo]Open Access
Diquigiovanni C.; Rizzardi N.; Kampmeier A.; Liparulo I.; Bianco F.; De Nicolo B.; Cataldi-Stagetti E.; Cuna E.; Severi G.; Seri M.; Bertrand M.; Haack T.B.; Marina A.D.; Braun F.; Fato R.; Kuechler A.; Bergamini C.; Bonora E., Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q, «OPEN BIOLOGY», 2023, 13, Article number: 230040, pp. 230040 - .230052 [articolo]Open Access
Orsini, Arianna; Diquigiovanni, Chiara; Bonora, Elena, Omics Technologies Improving Breast Cancer Research and Diagnostics, «INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES», 2023, 24, pp. 12690 - 12714 [articolo]Open Access
Bonora, Elena; Chakrabarty, Sanjiban; Kellaris, Georgios; Tsutsumi, Makiko; Bianco, Francesca; Bergamini, Christian; Ullah, Farid; Isidori, Federica; Liparulo, Irene; Diquigiovanni, Chiara; Masin, Luca; Rizzardi, Nicola; Cratere, Mariapia Giuditta; Boschetti, Elisa; Papa, Valentina; Maresca, Alessandra; Cenacchi, Giovanna; Casadio, Rita; Martelli, Pierluigi; Matera, Ivana; Ceccherini, Isabella; Fato, Romana; Raiola, Giuseppe; Arrigo, Serena; Signa, Sara; Sementa, Angela Rita; Severino, Mariasavina; Striano, Pasquale; Fiorillo, Chiara; Goto, Tsuyoshi; Uchino, Shumpei; Oyazato, Yoshinobu; Nakamura, Hisayoshi; Mishra, Sushil K; Yeh, Yu-Sheng; Kato, Takema; Nozu, Kandai; Tanboon, Jantima; Morioka, Ichiro; Nishino, Ichizo; Toda, Tatsushi; Goto, Yu-Ichi; Ohtake, Akira; Kosaki, Kenjiro; Yamaguchi, Yoshiki; Nonaka, Ikuya; Iijima, Kazumoto; Mimaki, Masakazu; Kurahashi, Hiroki; Raams, Anja; MacInnes, Alyson; Alders, Mariel; Engelen, Marc; Linthorst, Gabor; de Koning, Tom; den Dunnen, Wilfred; Dijkstra, Gerard; van Spaendonck, Karin; van Gent, Dik C; Aronica, Eleonora M; Picco, Paolo; Carelli, Valerio; Seri, Marco; Katsanis, Nicholas; Duijkers, Floor A M; Taniguchi-Ikeda, Mariko; De Giorgio, Roberto, Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy, «BRAIN», 2021, 144, pp. 1451 - 1466 [articolo]
Diquigiovanni C.; Bonora E., Genetics of familial non-medullary thyroid carcinoma (FNMTC), «CANCERS», 2021, 13, Article number: 2178, pp. 2178 - 2193 [articolo]Open Access
Bianco F.; Lattanzio G.; Lorenzini L.; Diquigiovanni C.; Mazzoni M.; Clavenzani P.; Calza L.; Giardino L.; Sternini C.; Bonora E.; De Giorgio R., Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility, «EUROPEAN JOURNAL OF HISTOCHEMISTRY», 2021, 65, pp. 3289 - 3296 [articolo]Open Access
Srivastava, Aayushi; Giangiobbe, Sara; Skopelitou, Diamanto; Miao, Beiping; Paramasivam, Nagarajan; Diquigiovanni, Chiara; Bonora, Elena; Hemminki, Kari; Försti, Asta; Bandapalli, Obul Reddy, Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer, «FRONTIERS IN ENDOCRINOLOGY», 2021, 12, Article number: 600682, pp. 1 - 10 [articolo]Open Access
Acquaviva G.; de Biase D.; Diquigiovanni C.; Argento C.M.; De Leo A.; Bonora E.; Rhoden K.J.; Pession A.; Tallini G., BRAF exon 15 mutations in papillary carcinoma and adjacent thyroid parenchyma: A search for the early molecular events associated with tumor development, «CANCERS», 2020, 12, Article number: 430, pp. 1 - 15 [articolo]Open Access
Diquigiovanni C.; Bergamini C.; Diaz R.; Liparulo I.; Bianco F.; Masin L.; Baldassarro V.A.; Rizzardi N.; Tranchina A.; Buscherini F.; Wischmeijer A.; Pippucci T.; Scarano E.; Cordelli D.M.; Fato R.; Seri M.; Paracchini S.; Bonora E., A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism, «FASEB JOURNAL», 2019, 33, pp. 11284 - 11302 [articolo]
Kumar, Abhishek*; Bandapalli, Obul Reddy; Paramasivam, Nagarajan; Giangiobbe, Sara; Diquigiovanni, Chiara; Bonora, Elena; Eils, Roland; Schlesner, Matthias; Hemminki, Kari; Försti, Asta, Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family, «SCIENTIFIC REPORTS», 2018, 8, Article number: 11635, pp. 1 - 12 [articolo]Open Access
Diquigiovanni, Chiara; Bergamini, Christian; Evangelisti, Cecilia; Isidori, Federica; Vettori, Andrea; Tiso, Natascia; Argenton, Francesco; Costanzini, Anna; Iommarini, Luisa; Anbunathan, Hima; Pagotto, Uberto; Repaci, Andrea; Babbi, Giulia; Casadio, Rita; Lenaz, Giorgio; Rhoden, Kerry J.; Porcelli, Anna Maria; Fato, Romana; Bowcock, Anne; Seri, Marco; Romeo, Giovanni; Bonora, Elena, Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer, «INTERNATIONAL JOURNAL OF CANCER», 2018, 143, pp. 1706 - 1719 [articolo]Open Access
Bonora, Elena; Bianco, Francesca; Stanzani, Agnese; Diquigiovanni, Chiara; Rinaldi, Rita; D'Angelo, Roberto; Cogliandro, ROSANNA FRANCESCA; Smith, Joshua D.; Nickerson, Deborah; Bamshad, Mike; Assadi, Ghazaleh; Clavenzani, Paolo; Lindberg, Greger; D'Amato, Mauro; Graziano, Claudio; Stanghellini, Vincenzo; Seri, Marco; DE GIORGIO, Roberto, Novel Mutations in Neurogenic Chronic Intestinal Pseudo-Obstruction Identified by High-Throughput Sequencing, «GASTROENTEROLOGY», 2017, 152, pp. S129 - S129 [abstract]
Graziano, C; Wischmeijer, A; Pippucci, T; Fusco, C; Diquigiovanni, C; Nõukas, M; Sauk, M; Kurg, A; Rivieri, F; Blau, N; Hoffmann, Gf; Chaubey, A; Schwartz, Ce; Romeo, G; Bonora, E; Garavelli, L; Seri, M., Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant., «GENE», 2015, 559, pp. 144 - 148 [articolo]
Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC, Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients., «EMBO MOLECULAR MEDICINE», 2014, 6, pp. 795 - 809 [articolo]Open Access
