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Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms.
Rumi E, Pietra D, Guglielmelli P, Bordoni R, Casetti I, Milanesi C, Sant'Antonio E, Ferretti V, Pancrazzi A, Rotunno G, Severgnini M, Pietrelli A, Astori C, Fugazza E, Pascutto C, Boveri E, Passamonti F, De Bellis G, Vannucchi A, Cazzola M; Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative. Rumi E, et al. Among authors: de bellis g. Blood. 2013 May 23;121(21):4388-95. doi: 10.1182/blood-2013-02-486050. Epub 2013 Apr 10. Blood. 2013. PMID: 23575445 Free PMC article.
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia.
Rossi D, Gigli L, Gamberucci A, Bordoni R, Pietrelli A, Lorenzini S, Pierantozzi E, Peretto G, De Bellis G, Della Bella P, Ferrari M, Sorrentino V, Benedetti S, Sala S, Di Resta C. Rossi D, et al. Among authors: de bellis g. Heart Rhythm. 2020 Feb;17(2):296-304. doi: 10.1016/j.hrthm.2019.08.018. Epub 2019 Aug 19. Heart Rhythm. 2020. PMID: 31437535
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns.
Cifola I, Lionetti M, Pinatel E, Todoerti K, Mangano E, Pietrelli A, Fabris S, Mosca L, Simeon V, Petrucci MT, Morabito F, Offidani M, Di Raimondo F, Falcone A, Caravita T, Battaglia C, De Bellis G, Palumbo A, Musto P, Neri A. Cifola I, et al. Among authors: de bellis g. Oncotarget. 2015 Jul 10;6(19):17543-58. doi: 10.18632/oncotarget.4028. Oncotarget. 2015. PMID: 26046463 Free PMC article. Clinical Trial.
174 results