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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment. 2014 Minervini GMONTAGNA, MARCOD'ANDREA, EMMAMENIN, CHIARATOSATTO, SILVIO + HUMAN MUTATION - -
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. 2013 D'ANDREA, EMMA + PLOS GENETICS - -
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. 2012 D'ANDREA, EMMA + JAMA - -
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). 2012 D'ANDREA, EMMA + CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION - -
Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy 2011 QUAGGIO, MONICAALAIBAC, MAURO SALVATORE ALESSANDROD'ANDREA, EMMA + PIGMENT CELL & MELANOMA RESEARCH - -
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 2011 D'ANDREA, EMMA + BREAST CANCER RESEARCH - -
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers 2011 D'ANDREA, EMMA + HUMAN GENETICS - -
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer 2010 D'ANDREA, EMMA + PLOS GENETICS - -
Ovarian cancer at the BRCA era: Tube or ovary?Results of tubal sampling protocol applied to all routine cases. III Seminario CientificoCancer: Actualidad, Perspectiva y continuidadCHEMSA Clinica Hospital de Especialidades Medicas Panama (Panama) 2010 CHIARELLI, SILVIAPADOAN, ILARIAD'ANDREA, EMMA - - -
Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation. 2009 ALAIBAC, MAURO SALVATORE ALESSANDROD'ANDREA, EMMA + MUTATION RESEARCH - -
Pathologic findings in 200 consecutive fallopian tube specimens 2009 CHIARELLI, SILVIAD'ANDREA, EMMA + HUMAN PATHOLOGY - -
Rediscovering the Fallopian tube at the time of BRCAmut. Three years experience on tubal sampling protocol applied to all routine cases. 2009 CHIARELLI, SILVIAPADOAN, ILARIAD'ANDREA, EMMA - - -
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations 2008 SCAINI, MARIACHIARAD'ANDREA, EMMA + MELANOMA RESEARCH - -
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from northeast Italy 2008 SCAINI, MARIACHIARAD'ANDREA, EMMA + JOURNAL OF CLINICAL ONCOLOGY - -
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis 2008 D'ANDREA, EMMA + ANNALS OF HUMAN GENETICS - -
TUMORI DELLA SALPINGE: NON SONO POI COSI' RARI. PROTOCOLLO DI PRELIEVI NELLA ROUTINE 2007 PADOAN, ILARIACHIARELLI, SILVIAPARENTI, ANNA ROSITAD'ANDREA, EMMANINFO, VITO - - Pathologica
Methyl group metabolism gene polymorphisms as modifier of breast cancer risk in Italian BRCA1/2 carriers 2007 D'ANDREA, EMMA + BREAST CANCER RESEARCH AND TREATMENT - -
Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status 2006 NITTI, DONATOD'ANDREA, EMMAAMADORI, ALBERTO + JOURNAL OF THE NATIONAL CANCER INSTITUTE - -
Prevalence of BRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectable BRCA1 and BRCA2 point mutations 2006 D'ANDREA, EMMA + GENES, CHROMOSOMES & CANCER - -
Establishment and characterization of xenografts and cancer cell cultures derived from BRCA1 -/- epithelial ovarian cancers 2006 INDRACCOLO SMOSERLE, LIDIAPERSANO LSCAINI, MARIACHIARAFASSINA, AMBROGIOPLEBANI, MARIOAMADORI, ALBERTOD'ANDREA, EMMA + EUROPEAN JOURNAL OF CANCER - -
Mostrati risultati da 1 a 20 di 76
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