about
Update in genetic susceptibility in melanomaTERT promoter mutation status as an independent prognostic factor in cutaneous melanoma.Genomic analysis and clinical management of adolescent cutaneous melanoma.Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling.Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.Role of CPI-17 in restoring skin homoeostasis in cutaneous field of cancerization: effects of topical application of a film-forming medical device containing photolyase and UV filters.Association Between Confocal Morphologic Classification and Clinical Phenotypes of Multiple Primary and Familial Melanomas.Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations.Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF.Inherited functional variants of the lymphocyte receptor CD5 influence melanoma survival.The MC1R melanoma risk variant p.R160W is associated with Parkinson disease.Melanocortin 1 receptor (MC1R) polymorphisms' influence on size and dermoscopic features of nevi.A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk.IRF4 rs12203592 functional variant and melanoma survival.The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients.Time and tumor type (primary or metastatic) do not influence the detection of BRAF/NRAS mutations in formalin fixed paraffin embedded samples from melanomas.Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline mutationsGenome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11qReplyAssociation of the POT1 Germline Missense Variant p.I78T With Familial MelanomaInherited MC1R variants in patients with melanoma are associated with better survival in womenComprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families WorldwideLack of Mutations in POT1 Gene in Selected Families with Familial Non-Medullary Thyroid CancerDetection of cell-free circulating BRAFV 600E by droplet digital polymerase chain reaction in patients with and without melanoma under dermatological surveillanceMC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohortPOT1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma familiesGenome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibilitySex as a predictor of response to cancer immunotherapy
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Miriam Potrony
@ast
Miriam Potrony
@en
Miriam Potrony
@es
Miriam Potrony
@nl
Miriam Potrony
@sl
type
label
Miriam Potrony
@ast
Miriam Potrony
@en
Miriam Potrony
@es
Miriam Potrony
@nl
Miriam Potrony
@sl
prefLabel
Miriam Potrony
@ast
Miriam Potrony
@en
Miriam Potrony
@es
Miriam Potrony
@nl
Miriam Potrony
@sl
P108
P106
P108
P21
P31
P496
0000-0003-2766-0765