Indio V - Search Results

1

Neuronopathic Gaucher disease models reveal defects in cell growth promoted by Hippo pathway activation.

Messelodi D, Strocchi S, Bertuccio SN, Baden P, Indio V, Giorgi FM, Taddia A, Serravalle S, Valente S, di Fonzo A, Frattini E, Bernardoni R, Pession A, Grifoni D, Deleidi M, Astolfi A, Pession A. Messelodi D, et al. Among authors: indio v. Commun Biol. 2023 Apr 19;6(1):431. doi: 10.1038/s42003-023-04813-2. Commun Biol. 2023. PMID: 37076591 Free PMC article.

2

CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtype.

Masetti R, Pigazzi M, Togni M, Astolfi A, Indio V, Manara E, Casadio R, Pession A, Basso G, Locatelli F. Masetti R, et al. Among authors: indio v. Blood. 2013 Apr 25;121(17):3469-72. doi: 10.1182/blood-2012-11-469825. Epub 2013 Feb 13. Blood. 2013. PMID: 23407549 Free article.

3

DHH-RHEBL1 fusion transcript: a novel recurrent feature in the new landscape of pediatric CBFA2T3-GLIS2-positive acute myeloid leukemia.

Masetti R, Togni M, Astolfi A, Pigazzi M, Manara E, Indio V, Rizzari C, Rutella S, Basso G, Pession A, Locatelli F. Masetti R, et al. Among authors: indio v. Oncotarget. 2013 Oct;4(10):1712-20. doi: 10.18632/oncotarget.1280. Oncotarget. 2013. PMID: 24127550 Free PMC article.

4

Whole transcriptome sequencing of a paediatric case of de novo acute myeloid leukaemia with del(5q) reveals RUNX1-USP42 and PRDM16-SKI fusion transcripts.

Masetti R, Togni M, Astolfi A, Pigazzi M, Indio V, Rivalta B, Manara E, Rutella S, Basso G, Pession A, Locatelli F. Masetti R, et al. Among authors: indio v. Br J Haematol. 2014 Aug;166(3):449-52. doi: 10.1111/bjh.12855. Epub 2014 Mar 27. Br J Haematol. 2014. PMID: 24673627 Free article. Review. No abstract available.

5

Identification of the NUP98-PHF23 fusion gene in pediatric cytogenetically normal acute myeloid leukemia by whole-transcriptome sequencing.

Togni M, Masetti R, Pigazzi M, Astolfi A, Zama D, Indio V, Serravalle S, Manara E, Bisio V, Rizzari C, Basso G, Pession A, Locatelli F. Togni M, et al. Among authors: indio v. J Hematol Oncol. 2015 Jun 12;8:69. doi: 10.1186/s13045-015-0167-8. J Hematol Oncol. 2015. PMID: 26066811 Free PMC article.

6

Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney.

Astolfi A, Melchionda F, Perotti D, Fois M, Indio V, Urbini M, Genovese CG, Collini P, Salfi N, Nantron M, D'Angelo P, Spreafico F, Pession A. Astolfi A, et al. Among authors: indio v. Oncotarget. 2015 Dec 1;6(38):40934-9. doi: 10.18632/oncotarget.5882. Oncotarget. 2015. PMID: 26516930 Free PMC article.

7

Genomic complexity and dynamics of clonal evolution in childhood acute myeloid leukemia studied with whole-exome sequencing.

Masetti R, Castelli I, Astolfi A, Bertuccio SN, Indio V, Togni M, Belotti T, Serravalle S, Tarantino G, Zecca M, Pigazzi M, Basso G, Pession A, Locatelli F. Masetti R, et al. Among authors: indio v. Oncotarget. 2016 Aug 30;7(35):56746-56757. doi: 10.18632/oncotarget.10778. Oncotarget. 2016. PMID: 27462774 Free PMC article.

8

Copy number gain of chromosome 3q is a recurrent event in patients with intraductal papillary mucinous neoplasm (IPMN) associated with disease progression.

Durante S, Vecchiarelli S, Astolfi A, Grassi E, Casadei R, Santini D, Panzacchi R, Ricci C, Serravalle S, Tarantino G, Falconi M, Teti G, Indio V, Pession A, Minni F, Biasco G, Di Marco M. Durante S, et al. Among authors: indio v. Oncotarget. 2016 Nov 15;7(46):74797-74806. doi: 10.18632/oncotarget.11501. Oncotarget. 2016. PMID: 27566563 Free PMC article.

9

Hh/Gli antagonist in acute myeloid leukemia with CBFA2T3-GLIS2 fusion gene.

Masetti R, Bertuccio SN, Astolfi A, Chiarini F, Lonetti A, Indio V, De Luca M, Bandini J, Serravalle S, Franzoni M, Pigazzi M, Martelli AM, Basso G, Locatelli F, Pession A. Masetti R, et al. Among authors: indio v. J Hematol Oncol. 2017 Jan 21;10(1):26. doi: 10.1186/s13045-017-0396-0. J Hematol Oncol. 2017. PMID: 28109323 Free PMC article.

10

HSPA8 as a novel fusion partner of NR4A3 in extraskeletal myxoid chondrosarcoma.

Urbini M, Astolfi A, Pantaleo MA, Serravalle S, Dei Tos AP, Picci P, Indio V, Sbaraglia M, Benini S, Righi A, Gambarotti M, Gronchi A, Colombo C, Dagrada GP, Pilotti S, Maestro R, Polano M, Saponara M, Tarantino G, Pession A, Biasco G, Casali PG, Stacchiotti S. Urbini M, et al. Among authors: indio v. Genes Chromosomes Cancer. 2017 Jul;56(7):582-586. doi: 10.1002/gcc.22462. Epub 2017 May 4. Genes Chromosomes Cancer. 2017. PMID: 28383167

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