Testi MA - Search Results

1

Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.

Perotti D, De Vecchi G, Testi MA, Lualdi E, Modena P, Mondini P, Ravagnani F, Collini P, Di Renzo F, Spreafico F, Terenziani M, Sozzi G, Fossati-Bellani F, Radice P. Perotti D, et al. Among authors: testi ma. Hum Mutat. 2004 Nov;24(5):400-7. doi: 10.1002/humu.20096. Hum Mutat. 2004. PMID: 15459955

2

Advances in cancer cytogenetics.

Sozzi G, Testi MA, Croce CM. Sozzi G, et al. Among authors: testi ma. J Cell Biochem. 1999;Suppl 32-33:173-82. doi: 10.1002/(sici)1097-4644(1999)75:32+<173::aid-jcb21>3.0.co;2-g. J Cell Biochem. 1999. PMID: 10629117 Review.

3

A novel zinc finger gene is fused to EWS in small round cell tumor.

Mastrangelo T, Modena P, Tornielli S, Bullrich F, Testi MA, Mezzelani A, Radice P, Azzarelli A, Pilotti S, Croce CM, Pierotti MA, Sozzi G. Mastrangelo T, et al. Among authors: testi ma. Oncogene. 2000 Aug 3;19(33):3799-804. doi: 10.1038/sj.onc.1203762. Oncogene. 2000. PMID: 10949935

4

Low grade fibromyxoid sarcoma. a further low-grade soft tissue malignancy characterized by a ring chromosome.

Mezzelani A, Sozzi G, Nessling M, Riva C, Della Torre G, Testi MA, Azzarelli A, Pierotti MA, Lichter P, Pilotti S. Mezzelani A, et al. Among authors: testi ma. Cancer Genet Cytogenet. 2000 Oct 15;122(2):144-8. doi: 10.1016/s0165-4608(00)00288-0. Cancer Genet Cytogenet. 2000. PMID: 11106828

5

Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours.

Perotti D, Testi MA, Mondini P, Pilotti S, Green ED, Pession A, Sozzi G, Pierotti MA, Fossati-Bellani F, Radice P. Perotti D, et al. Among authors: testi ma. Genes Chromosomes Cancer. 2001 May;31(1):42-7. doi: 10.1002/gcc.1116. Genes Chromosomes Cancer. 2001. PMID: 11284034

6

UQCRH gene encoding mitochondrial Hinge protein is interrupted by a translocation in a soft-tissue sarcoma and epigenetically inactivated in some cancer cell lines.

Modena P, Testi MA, Facchinetti F, Mezzanzanica D, Radice MT, Pilotti S, Sozzi G. Modena P, et al. Among authors: testi ma. Oncogene. 2003 Jul 17;22(29):4586-93. doi: 10.1038/sj.onc.1206472. Oncogene. 2003. PMID: 12881716

7

Bilateral preaxial polydactyly in a WAGR syndrome patient.

Manoukian S, Crolla JA, Mammoliti PM, Testi MA, Zanini R, Carpanelli ML, Piozzi E, Sozzi G, De Vecchi G, Terenziani M, Spreafico F, Collini P, Radice P, Perotti D. Manoukian S, et al. Among authors: testi ma. Am J Med Genet A. 2005 May 1;134(4):426-9. doi: 10.1002/ajmg.a.30647. Am J Med Genet A. 2005. PMID: 15742368

8

Wilms tumor in monozygous twins: clinical, pathological, cytogenetic and molecular case report.

Perotti D, Vecchi GD, Lualdi E, Testi MA, Sozzi G, Collini P, Spreafico F, Terenziani M, Fossati-Bellani F, Radice P. Perotti D, et al. Among authors: testi ma. J Pediatr Hematol Oncol. 2005 Oct;27(10):521-5. doi: 10.1097/01.mph.0000184309.22583.66. J Pediatr Hematol Oncol. 2005. PMID: 16217254

9

A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor.

Terenziani M, Sardella M, Gamba B, Testi MA, Spreafico F, Ardissino G, Fedeli F, Fossati-Bellani F, Radice P, Perotti D. Terenziani M, et al. Among authors: testi ma. Pediatr Nephrol. 2009 Jul;24(7):1413-7. doi: 10.1007/s00467-008-1056-y. Epub 2008 Dec 2. Pediatr Nephrol. 2009. PMID: 19048299

10

Targeted RNA-sequencing analysis for fusion transcripts detection in tumor diagnostics: assessment of bioinformatic tools reliability in FFPE samples.

Capone I, Bozzi F, Dagrada GP, Verderio P, Conca E, Busico A, Testi MA, Monti V, Duca M, Proto C, Damian S, Piccolo A, Perrone F, Tamborini E, Devecchi A, Collini P, Lorenzini D, Vingiani A, Agnelli L, Pruneri G. Capone I, et al. Among authors: testi ma. Explor Target Antitumor Ther. 2022;3(5):582-597. doi: 10.37349/etat.2022.00102. Epub 2022 Oct 27. Explor Target Antitumor Ther. 2022. PMID: 36338518 Free PMC article.

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