Mondini P - Search Results

1

Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility.

Ciceri S, Gamba B, Corbetta P, Mondini P, Terenziani M, Catania S, Nantron M, Bianchi M, D'Angelo P, Torri F, Macciardi F, Collini P, Di Martino M, Melchionda F, Di Cataldo A, Spreafico F, Radice P, Perotti D; AIEOP study group. Ciceri S, et al. Among authors: mondini p. Oncotarget. 2018 Sep 25;9(75):34079-34089. doi: 10.18632/oncotarget.26123. eCollection 2018 Sep 25. Oncotarget. 2018. PMID: 30344923 Free PMC article.

2

SacI identifies an additional RFLP at the D11S12 locus.

Radice P, Borrello MG, De Benedetti V, Mondini P, Pierotti MA, Della Porta G. Radice P, et al. Among authors: mondini p. Nucleic Acids Res. 1991 Apr 11;19(7):1717. doi: 10.1093/nar/19.7.1717-a. Nucleic Acids Res. 1991. PMID: 1674134 Free PMC article.

3

TaqI RFLP of the human tropomyosin gene (TPM3) involved in the generation of the TRK oncogene.

Michieli P, Pierotti MA, De Benedetti V, Donghi R, Mondini P, Radice P, Della Porta G. Michieli P, et al. Among authors: mondini p. Nucleic Acids Res. 1991 Sep 11;19(17):4796. doi: 10.1093/nar/19.17.4796. Nucleic Acids Res. 1991. PMID: 1679928 Free PMC article.

4

Loss of heterozygosity in human germinal tumors.

Radice P, Pierotti MA, Lacerenza S, Mondini P, Radice MT, Pilotti S, Della Porta G. Radice P, et al. Among authors: mondini p. Cytogenet Cell Genet. 1989;52(1-2):72-6. doi: 10.1159/000132843. Cytogenet Cell Genet. 1989. PMID: 2612217

5

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: mondini p. Genomics. 1995 Jun 10;27(3):497-501. doi: 10.1006/geno.1995.1082. Genomics. 1995. PMID: 7558032

6

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: mondini p. Genomics. 1996 Nov 1;37(3):310-5. doi: 10.1006/geno.1996.0565. Genomics. 1996. PMID: 8938443

7

Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes.

Pensotti V, Radice P, Presciuttini S, Calistri D, Gazzoli I, Grimalt Perez A, Mondini P, Buonsanti G, Sala P, Rossetti C, Ranzani GN, Bertario L, Pierotti MA. Pensotti V, et al. Among authors: mondini p. Genes Chromosomes Cancer. 1997 Jul;19(3):135-42. Genes Chromosomes Cancer. 1997. PMID: 9218993

8

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: mondini p. Ann Oncol. 1998 Jun;9(6):627-31. doi: 10.1023/a:1008248905766. Ann Oncol. 1998. PMID: 9681076 Free article.

9

Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.

Giarola M, Wells D, Mondini P, Pilotti S, Sala P, Azzarelli A, Bertario L, Pierotti MA, Delhanty JD, Radice P. Giarola M, et al. Among authors: mondini p. Br J Cancer. 1998 Sep;78(5):582-7. doi: 10.1038/bjc.1998.544. Br J Cancer. 1998. PMID: 9744495 Free PMC article.

10

Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.

Giarola M, Stagi L, Presciuttini S, Mondini P, Radice MT, Sala P, Pierotti MA, Bertario L, Radice P. Giarola M, et al. Among authors: mondini p. Hum Mutat. 1999;13(2):116-23. doi: 10.1002/(SICI)1098-1004(1999)13:2<116::AID-HUMU3>3.0.CO;2-2. Hum Mutat. 1999. PMID: 10094547

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