about
Key roles for MYC, KIT and RET signaling in secondary angiosarcomasMolecular subtyping of serous ovarian tumors reveals multiple connections to intrinsic breast cancer subtypesDistinct gene expression profiles in ovarian cancer linked to Lynch syndromeDistinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.Frequent mismatch-repair defects link prostate cancer to Lynch syndromeMLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.Mutation spectrum in South American Lynch syndrome familiesFamilial colorectal cancer type X: genetic profiles and phenotypic features.Lynch syndrome in South America: past, present and future.Update on Hereditary Colorectal Cancer.Identification of a Natural Killer Cell Receptor Allele That Prolongs Survival of Cytomegalovirus-Positive Glioblastoma Patients.Increased infiltration and tolerised antigen-specific CD8+ TEM cells in tumor but not peripheral blood have no impact on survival of HCMV+ glioblastoma patients.Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations.A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair proteinGain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.Identification of genetic variants for clinical management of familial colorectal tumors.[Molecular characterization of hereditary colorectal cancer in Peru].From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin AmericaTwo new MLH1 germline mutations in Brazilian lynch syndrome familiesLack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportCauses for Frequent Pathogenic Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic DriftSurvival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportResponse to Tolva et alResults of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testingCancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseA snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registriesMLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicingSpectrum and Frequency of Tumors, Cancer Risk and Survival in Chilean Families with Lynch Syndrome: Experience of the Implementation of a Registry
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P50
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onderzoeker
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հետազոտող
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Mev Dominguez-Valentin
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Mev Dominguez-Valentin
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Mev Dominguez-Valentin
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Mev Dominguez-Valentin
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Mev Dominguez-Valentin
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Mev Dominguez-Valentin
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P106
P2798
P31
P496
0000-0001-7856-0057