Surace C - Search Results

1

Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes.

Marzella R, Viggiano L, Miolla V, Storlazzi CT, Ricco A, Gentile E, Roberto R, Surace C, Fratello A, Mancini M, Archidiacono N, Rocchi M. Marzella R, et al. Among authors: surace c. Genomics. 2000 Feb 1;63(3):307-13. doi: 10.1006/geno.1999.6092. Genomics. 2000. PMID: 10704278

2

Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia.

Storlazzi CT, Anelli L, Surace C, Rocchi M, Albano F, Pastore D, Liso V, Specchia G. Storlazzi CT, et al. Among authors: surace c. Cancer Genet Cytogenet. 2002 Apr 15;134(2):109-13. doi: 10.1016/s0165-4608(01)00625-2. Cancer Genet Cytogenet. 2002. PMID: 12034521

3

Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia.

Storlazzi CT, Anelli L, Surace C, Lonoce A, Zagaria A, Nanni M, Curzi P, Rocchi M. Storlazzi CT, et al. Among authors: surace c. Cancer Genet Cytogenet. 2002 Jul 15;136(2):141-5. doi: 10.1016/s0165-4608(02)00530-7. Cancer Genet Cytogenet. 2002. PMID: 12237239

4

Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case.

Specchia G, Storlazzi CT, Cuneo A, Surace C, Mestice A, Pannunzio A, Rocchi M, Liso V. Specchia G, et al. Among authors: surace c. Ann Hematol. 2001 Apr;80(4):246-50. doi: 10.1007/s002770000273. Ann Hematol. 2001. PMID: 11401094

5

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation.

Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G, Zagaria A, Jimenez Velasco A, Heiniger A, Scaravaglio P, Torres Gomez A, Roman Gomez J, Archidiacono N, Banfi S, Rocchi M. Saglio G, et al. Among authors: surace c. Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9882-7. doi: 10.1073/pnas.152171299. Epub 2002 Jul 11. Proc Natl Acad Sci U S A. 2002. PMID: 12114534 Free PMC article.

6

Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.

Surace C, Storlazzi CT, Engellau J, Domanski HA, Gustafson P, Panagopoulos I, D'Addabbo P, Rocchi M, Mandahl N, Mertens F. Surace C, et al. Virchows Arch. 2005 Nov;447(5):869-74. doi: 10.1007/s00428-005-0041-0. Epub 2005 Aug 26. Virchows Arch. 2005. PMID: 16133367

7

Episomal amplification of MYCN in a case of medulloblastoma.

Surace C, Pedeutour F, Trombetta D, Burel-Vandenbos F, Rocchi M, Storlazzi CT. Surace C, et al. Virchows Arch. 2008 May;452(5):491-7. doi: 10.1007/s00428-008-0592-y. Virchows Arch. 2008. PMID: 18286303

8

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.

Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strömbeck B, D'Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Mühlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Solè F, Van Roy N, Johansson B, Rocchi M. Storlazzi CT, et al. Among authors: surace c. Hum Mol Genet. 2006 Mar 15;15(6):933-42. doi: 10.1093/hmg/ddl010. Epub 2006 Feb 1. Hum Mol Genet. 2006. PMID: 16452126

9

Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma.

Sainati L, Leszl A, Surace C, Perilongo G, Rocchi M, Basso G. Sainati L, et al. Among authors: surace c. Cancer Genet Cytogenet. 2002 Apr 1;134(1):18-20. doi: 10.1016/s0165-4608(01)00586-6. Cancer Genet Cytogenet. 2002. PMID: 11996790

10

Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype.

Surace C, Leszl A, Perilongo G, Rocchi M, Basso G, Sainati L. Surace C, et al. Med Pediatr Oncol. 2002 Nov;39(5):536-9. doi: 10.1002/mpo.10181. Med Pediatr Oncol. 2002. PMID: 12228913

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