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Items: 23


Identification of a cytogenetic and molecular subgroup of acute myeloid leukemias showing sensitivity to L-Asparaginase.

Bertuccio SN, Serravalle S, Astolfi A, Lonetti A, Indio V, Leszl A, Pession A, Melchionda F.

Oncotarget. 2017 Jun 19;8(66):109915-109923. doi: 10.18632/oncotarget.18565. eCollection 2017 Dec 15.


Identification of SRF-E2F1 fusion transcript in EWSR-negative myoepithelioma of the soft tissue.

Urbini M, Astolfi A, Indio V, Tarantino G, Serravalle S, Saponara M, Nannini M, Gronchi A, Fiore M, Maestro R, Brenca M, Dei Tos AP, Dagrada GP, Negri T, Pilotti S, Casali PG, Biasco G, Pession A, Stacchiotti S, Pantaleo MA.

Oncotarget. 2017 May 17;8(36):60036-60045. doi: 10.18632/oncotarget.17958. eCollection 2017 Sep 1.


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.

Genes Chromosomes Cancer. 2017 Jul;56(7):582-586. doi: 10.1002/gcc.22462. Epub 2017 May 4.


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.

J Hematol Oncol. 2017 Jan 21;10(1):26. doi: 10.1186/s13045-017-0396-0.


Synergistic Cytotoxic Effect of L-Asparaginase Combined with Decitabine as a Demethylating Agent in Pediatric T-ALL, with Specific Epigenetic Signature.

Serravalle S, Bertuccio SN, Astolfi A, Melchionda F, Pession A.

Biomed Res Int. 2016;2016:1985750. doi: 10.1155/2016/1985750. Epub 2016 Nov 27.


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.

Oncotarget. 2016 Nov 15;7(46):74797-74806. doi: 10.18632/oncotarget.11501.


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.

Oncotarget. 2016 Aug 30;7(35):56746-56757. doi: 10.18632/oncotarget.10778.


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.

J Hematol Oncol. 2015 Jun 12;8:69. doi: 10.1186/s13045-015-0167-8.


Transient abnormal myelopoiesis in a phenotypically normal newborn with polyclonal trisomy 21.

Corazza F, Astolfi A, Libri V, Franzoni M, Serravalle S, Alessandroni R, Melchionda F, Pession A.

Int J Hematol. 2014 Jun;99(6):794-7. doi: 10.1007/s12185-014-1584-0. Epub 2014 Apr 26.


MYCN is a novel oncogenic target in pediatric T-cell acute lymphoblastic leukemia.

Astolfi A, Vendemini F, Urbini M, Melchionda F, Masetti R, Franzoni M, Libri V, Serravalle S, Togni M, Paone G, Montemurro L, Bressanin D, Chiarini F, Martelli AM, Tonelli R, Pession A.

Oncotarget. 2014 Jan 15;5(1):120-30.


Antitumor activity of sustained N-myc reduction in rhabdomyosarcomas and transcriptional block by antigene therapy.

Tonelli R, McIntyre A, Camerin C, Walters ZS, Di Leo K, Selfe J, Purgato S, Missiaglia E, Tortori A, Renshaw J, Astolfi A, Taylor KR, Serravalle S, Bishop R, Nanni C, Valentijn LJ, Faccini A, Leuschner I, Formica S, Reis-Filho JS, Ambrosini V, Thway K, Franzoni M, Summersgill B, Marchelli R, Hrelia P, Cantelli-Forti G, Fanti S, Corradini R, Pession A, Shipley J.

Clin Cancer Res. 2012 Feb 1;18(3):796-807. doi: 10.1158/1078-0432.CCR-11-1981. Epub 2011 Nov 7.


The role of HDACs inhibitors in childhood and adolescence acute leukemias.

Masetti R, Serravalle S, Biagi C, Pession A.

J Biomed Biotechnol. 2011;2011:148046. doi: 10.1155/2011/148046. Epub 2011 Jan 13. Review.


A novel specific signature of pediatric MOZ-CBP acute myeloid leukemia.

Serravalle S, Melchionda F, Astolfi A, Libri V, Masetti R, Pession A.

Leuk Res. 2010 Nov;34(11):e292-3. doi: 10.1016/j.leukres.2010.05.026. Epub 2010 Jul 13. No abstract available.


Pediatric early T-cell precursor leukemia with NF1 deletion and high-sensitivity in vitro to tipifarnib.

Biagi C, Astolfi A, Masetti R, Serravalle S, Franzoni M, Chiarini F, Melchionda F, Pession A.

Leukemia. 2010 Jun;24(6):1230-3. doi: 10.1038/leu.2010.81. Epub 2010 Apr 29. No abstract available.


Trisomy 11 with MLL-PTD in a case of infant AML M0.

Serravalle S, Purgato S, Melchionda F, Astolfi A, Tonelli R, Pession A.

Br J Haematol. 2007 Sep;138(6):817-9. Epub 2007 Jul 26. No abstract available.


ArgBP2, encoding a negative regulator of ABL, is fused to MLL in a case of infant M5 acute myeloid leukemia involving 4q35 and 11q23.

Pession A, Lo Nigro L, Montemurro L, Serravalle S, Fazzina R, Izzi G, Nucifora G, Slany R, Tonelli R.

Leukemia. 2006 Jul;20(7):1310-3. Epub 2006 Apr 20. No abstract available.


X-linked megalocornea: close linkage to DXS87 and DXS94.

Chen JD, Mackey D, Fuller H, Serravalle S, Olsson J, Denton MJ.

Hum Genet. 1989 Oct;83(3):292-4.


A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus.

Chen JD, Hejtmancik JF, Romeo G, Lindlof M, Boehm C, Caskey CT, Kress W, Fischbeck KH, Dreier M, Serravalle S, et al.

Genomics. 1989 Jan;4(1):105-9.


Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.

Chen JD, Denton MJ, Serravalle S, Morgan G.

Aust Paediatr J. 1988 Dec;24(6):351-3.


Localization of the X-linked retinitis pigmentosa locus between DXS7 and DXS84 in a family showing tapetal reflex in heterozygotes.

Chen JD, Halliday F, Serravalle S, Denton M.

Ophthalmic Paediatr Genet. 1988 Nov;9(3):143-7.


Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7.

Denton MJ, Chen JD, Serravalle S, Colley P, Halliday FB, Donald J.

Hum Genet. 1988 Jan;78(1):60-4.


Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.

Morgan G, Donald JA, Chen J, Serravalle S, Colley P, Denton MJ.

Aust Paediatr J. 1988;24 Suppl 1:98-9.


Recombination between Duchenne muscular dystrophy and DNA marker DXS164 (pERT87)

Donald JA, Morgan G, Chen JD, Serravalle S, Colley P, Denton MJ.

Lancet. 1987 Jan 3;1(8523):39-40. No abstract available.


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