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Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P lociGenome-wide association study identifies a new melanoma susceptibility locus at 1q21.3A variant in FTO shows association with melanoma risk not due to BMIGenetic testing for melanoma.The effect on melanoma risk of genes previously associated with telomere length.A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindredsFine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsHistologic features of melanoma associated with CDKN2A genotype.Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterationsHeterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry.An upstream negative regulatory element in human granulocyte-macrophage colony-stimulating factor promoter is recognised by AP1 family members.CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer.c-Rel and p65 subunits bind to an upstream NF-kappaB site in human granulocyte macrophage-colony stimulating factor promoter involved in phorbol ester response in 5637 cells.Effect of endothelial cell conditioned medium on the growth of human bone marrow fibroblasts.H and L ferritin gene expression in U937 cells induced to macrophage differentiation.Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.Electrophoretic pattern of NADPH-dependent oxidoreductive activities in K 562 and HL 60 leukemic cell lines.Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.Novel MC1R variants in Ligurian melanoma patients and controls.CDKN2A and MC1R analysis in amelanotic and pigmented melanoma.Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.Molecular characterization of an Italian series of sporadic GISTs.Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations.CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMELCutaneous phenotype andMC1R variants as modifying factors for the development of melanoma inCDKN2A G101W mutation carriers from 4 countriesPredicting the Risk of Pancreatic Cancer: OnCDKN2AMutations in the Melanoma-Pancreatic Cancer Syndrome in ItalyMC1Rvariation and melanoma risk in relation to host/clinical and environmental factors inCDKN2Apositive and negative melanoma patientsClinical genetic testing for familial melanoma in Italy: A cooperative studyEarly onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patientsHigh prevalence of the G101W germline mutation in theCDKN2A(P16ink4a) gene in 62 Italian malignant melanoma familiesNo Evidence for Linkage with Melanoma in Italian Melanoma-Prone FamiliesLactoferrin binding sites and nuclear localization in K562(S) cellsCharacterization, localization, and biosynthesis of acetylcholinesterase in K 562 cellsUnusual Ph translocations in CML: four new cases
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P50
description
hulumtuese
@sq
researcher
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researcher
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wetenschapper
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հետազոտող
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name
Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
@es
Giovanna Bianchi Scarrà
@nl
Giovanna Bianchi Scarrà
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type
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
@es
Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi-Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
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Giovanna Bianchi Scarrà
@en-gb
Giovanna Bianchi Scarrà
@es
Giovanna Bianchi Scarrà
@nl
Giovanna Bianchi Scarrà
@sl
P1053
G-8933-2014
P106
P21
P31
P496
0000-0002-6127-1192