Radice P - Search Results

1

Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome.

Uccini S, Perotti D, Colarossi C, Stoppacciaro A, Sardella M, Mannarino O, Collini P, Casieri P, Cozzi D, Amoroso L, Spreafico F, Radice P, Dominici C. Uccini S, et al. Among authors: radice p. Pediatr Blood Cancer. 2008 Sep;51(3):344-8. doi: 10.1002/pbc.21507. Pediatr Blood Cancer. 2008. PMID: 18293378

2

Allelotyping in Wilms tumors identifies a putative third tumor suppressor gene on chromosome 11.

Radice P, Perotti D, De Benedetti V, Mondini P, Radice MT, Pilotti S, Luksch R, Fossati Bellani F, Pierotti MA. Radice P, et al. Among authors: radice mt. Genomics. 1995 Jun 10;27(3):497-501. doi: 10.1006/geno.1995.1082. Genomics. 1995. PMID: 7558032

3

Genetic evidence for an independent origin of multiple preneoplastic and neoplastic lung lesions.

Sozzi G, Miozzo M, Pastorino U, Pilotti S, Donghi R, Giarola M, De Gregorio L, Manenti G, Radice P, Minoletti F, et al. Sozzi G, et al. Among authors: radice p. Cancer Res. 1995 Jan 1;55(1):135-40. Cancer Res. 1995. PMID: 7805023

4

Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors.

Miozzo M, Perotti D, Minoletti F, Mondini P, Pilotti S, Luksch R, Fossati-Bellani F, Pierotti MA, Sozzi G, Radice P. Miozzo M, et al. Among authors: radice p. Genomics. 1996 Nov 1;37(3):310-5. doi: 10.1006/geno.1996.0565. Genomics. 1996. PMID: 8938443

5

No evidence of WT1 involvement in a Burkitt's lymphoma in a patient with Denys-Drash syndrome.

Perotti D, Mondini P, Giardini R, Ferrari A, Massimino M, Gambirasio F, Pierotti MA, Fossati-Bellani F, Radice P. Perotti D, et al. Among authors: radice p. Ann Oncol. 1998 Jun;9(6):627-31. doi: 10.1023/a:1008248905766. Ann Oncol. 1998. PMID: 9681076 Free article.

6

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: radice p. Genes Chromosomes Cancer. 2001 May;31(1):42-7. doi: 10.1002/gcc.1116. Genes Chromosomes Cancer. 2001. PMID: 11284034

7

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: radice p. Hum Mutat. 2004 Nov;24(5):400-7. doi: 10.1002/humu.20096. Hum Mutat. 2004. PMID: 15459955

8

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: radice p. 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

9

WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities.

Perotti D, Mondini P, Terenziani M, Spreafico F, Collini P, Fossati-Bellani F, Radice P. Perotti D, et al. Among authors: radice p. J Pediatr Hematol Oncol. 2005 Apr;27(4):197-201. doi: 10.1097/01.mph.0000161270.22313.2f. J Pediatr Hematol Oncol. 2005. PMID: 15838390

10

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: radice p. 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

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