Magnani I - Search Results

1

A stable marker chromosome with a cryptic centromere: evidence for centromeric sequences associated with an inverted duplication.

Sacchi N, Magnani I, Fuhrman-Conti AM, Monard SP, Darfler M. Sacchi N, et al. Among authors: magnani i. Cytogenet Cell Genet. 1996;73(1-2):123-9. doi: 10.1159/000134322. Cytogenet Cell Genet. 1996. PMID: 8646879

2

Identification of the chromosome 14 origin of a C-negative marker associated with a 14q32 deletion by chromosome painting.

Magnani I, Sacchi N, Darfler M, Nisson PE, Tornaghi R, Fuhrman-Conti AM. Magnani I, et al. Clin Genet. 1993 Apr;43(4):180-5. doi: 10.1111/j.1399-0004.1993.tb04444.x. Clin Genet. 1993. PMID: 7687207 Review.

3

Interphase cytogenetics of the t(8;21)(q22;q22) associated with acute myelogenous leukemia by two-color fluorescence in situ hybridization.

Sacchi N, Magnani I, Kearney L, Wijsman J, Hagemeijer A, Darfler M. Sacchi N, et al. Among authors: magnani i. Cancer Genet Cytogenet. 1995 Feb;79(2):97-103. doi: 10.1016/0165-4608(94)00266-e. Cancer Genet Cytogenet. 1995. PMID: 7889521

4

Functional marker chromosomes lacking detectable alpha satellite DNA: a tool for centromere study.

Magnani I, Meneveri R, Marozzi A, Ginelli E, Fuhrman-Conti AM, Darfler M, Monard SP, Sacchi N. Magnani I, et al. Chromosome Res. 1998 Jan;6(1):69-71. Chromosome Res. 1998. PMID: 9510515 No abstract available.

5

Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20.

Bassi C, Magnani I, Sacchi N, Saccone S, Ventura A, Rocchi M, Marozzi A, Ginelli E, Meneveri R. Bassi C, et al. Among authors: magnani i. Gene. 2000 Oct 3;256(1-2):43-50. doi: 10.1016/s0378-1119(00)00354-1. Gene. 2000. PMID: 11054534

6

Detection and subcellular localization of an AML1 chimeric protein in the t(8;21) positive acute myeloid leukemia.

Sacchi N, Schiaffonati L, Magnani I, Pappalardo C, Hughes AJ Jr, Darfler M, Hoogeveen AT. Sacchi N, et al. Among authors: magnani i. Oncogene. 1996 Jan 18;12(2):437-44. Oncogene. 1996. PMID: 8570222

7

The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines.

Beghini A, Magnani I, Roversi G, Piepoli T, Di Terlizzi S, Moroni RF, Pollo B, Fuhrman Conti AM, Cowell JK, Finocchiaro G, Larizza L. Beghini A, et al. Among authors: magnani i. Oncogene. 2003 May 1;22(17):2581-91. doi: 10.1038/sj.onc.1206336. Oncogene. 2003. PMID: 12735302

8

Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses.

Magnani I, Moroni RF, Roversi G, Beghini A, Pfundt R, Schoenmakers EF, Larizza L. Magnani I, et al. Cancer Genet Cytogenet. 2005 Sep;161(2):140-5. doi: 10.1016/j.cancergencyto.2005.02.010. Cancer Genet Cytogenet. 2005. PMID: 16102584

9

Malformation syndrome with t(2;22) in a cancer family with chromosome instability.

Magnani I, Larizza L, Doneda L, Weitnauer L, Rizzi R, Di Lernia R. Magnani I, et al. Cancer Genet Cytogenet. 1989 Apr;38(2):223-7. doi: 10.1016/0165-4608(89)90663-8. Cancer Genet Cytogenet. 1989. PMID: 2720635

10

A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines.

Magnani I, Chiariello E, Conti AM, Finocchiaro G. Magnani I, et al. Cancer Genet Cytogenet. 1999 Apr 15;110(2):82-6. doi: 10.1016/s0165-4608(98)00190-3. Cancer Genet Cytogenet. 1999. PMID: 10214354

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