M. Biasi

发表

CYP19A1 polymorphisms and clinical outcomes in postmenopausal women with hormone receptor-positive breast cancer in the BIG 1–98 trial

P. Neven, H. Ditzel, B. Leyland-Jones, 2015, Breast Cancer Research and Treatment.

ESR1 and ESR2 polymorphisms in the BIG 1-98 trial comparing adjuvant letrozole versus tamoxifen or their sequence for early breast cancer

P. Neven, R. Gelber, B. Leyland-Jones, 2015, Breast Cancer Research and Treatment.

CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the breast international group 1-98 trial.

P. Neven, R. Gelber, H. Ditzel, 2012, Journal of the National Cancer Institute.

Chromosome 7 q Allelic Losses in Pancreatic Carcinoma 1

A. Scarpa, G. Zamboni, P. Pederzoli, 2006 .

Chromosome 7q allelic losses in pancreatic carcinoma.

A. Scarpa, G. Zamboni, P. Pederzoli, 1996, Cancer research.

Comparative Evaluation of an Extensive Histopathologic Examination and a Real-Time Reverse-Transcription-Polymerase Chain Reaction Assay for Mammaglobin and Cytokeratin 19 on Axillary Sentinel Lymph Nodes of Breast Carcinoma Patients

G. Viale, P. Maisonneuve, G. Green, 2008, Annals of surgery.

Immunoreactivity for latent membrane protein 1 of Epstein–Barr virus in nevi and melanomas is not related to the viral infection

G. Viale, G. Bertalot, M. Gramegna, 2000, Virchows Archiv.

Cancers of the papilla of vater: mutator phenotype is associated with good prognosis.

G. Capellá, A. Scarpa, G. Zamboni, 1997, Clinical cancer research : an official journal of the American Association for Cancer Research.

Identifying oncogenic drivers associated with increased risk of late distant recurrence in post-menopausal, estrogen receptor-positive, HER2-negative early breast cancer: results from the BIG 1-98 study.

S. Loi, P. Savas, S. Luen, 2020, Annals of oncology : official journal of the European Society for Medical Oncology.

Chromosome 7q Allelic Losses in Pancreatic Carcinoma1

A. Scarpa, P. Pederzoli, A. Magalini, 2006 .

The transactivating isoforms of p63 are overexpressed in high‐grade follicular lymphomas independent of the occurrence of p63 gene amplification

G. Pruneri, G. Viale, A. Neri, 2005, The Journal of pathology.

A novel missense mutation in exon 3 of the COL4A5 gene associated with late‐onset Alport syndrome

P. Pignatti, G. Rizzoni, S. Rossetti, 1995, Clinical genetics.

APC gene mutations and allelic losses in sporadic ampullary tumours: Evidence of genetic difference from tumours associated with familial adenomatous polyposis

A. Scarpa, N. Lemoine, G. Zamboni, 1996, International journal of cancer.

Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes.

P. Pignatti, S. Rossetti, M. Biasi, 1995, Molecular and cellular probes.