Detalhe da pesquisa
1.
Exploring the frequency of a TP53 polyadenylation signal variant in tumor DNA from patients diagnosed with lung adenocarcinomas, sarcomas and uterine leiomyomas.
Genet Mol Biol
; 46(3 Suppl 1): e20230133, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38252059
2.
BRCA1 and BRCA2 germline mutation analysis from a cohort of 1267 patients at high risk for breast cancer in Brazil.
Breast Cancer Res Treat
; 199(1): 127-136, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36881271
3.
Neoadjuvant carboplatin in triple-negative breast cancer: results from NACATRINE, a randomized phase II clinical trial.
Breast Cancer Res Treat
; 202(1): 57-65, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37578666
4.
miRNA expression profiling of hereditary breast tumors from BRCA1- and BRCA2-germline mutation carriers in Brazil.
BMC Cancer
; 20(1): 143, 2020 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32087690
5.
Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer.
Genet Mol Biol
; 43(2): e20190097, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325485
6.
Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer.
Genet Mol Biol
; 43(2): e20190072, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32453342
7.
From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America.
Int J Cancer
; 145(2): 318-326, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303536
8.
Evaluation of MLH1 variants of unclear significance.
Genes Chromosomes Cancer
; 57(7): 350-358, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29520894
9.
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
Hum Mutat
; 39(5): 593-620, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29446198
10.
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
BMC Cancer
; 17(1): 623, 2017 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28874130
11.
Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil.
Genet Mol Biol
; 39(2): 210-22, 2016 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27223485
12.
BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome.
Genet Mol Biol
; 39(2): 223-31, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27303907
13.
Age at cancer onset in germline TP53 mutation carriers: association with polymorphisms in predicted G-quadruplex structures.
Carcinogenesis
; 35(4): 807-15, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24336192
14.
Unveiling the role of MGMT and DAPK hypermethylation in response to anti-EGFR agents: Molecular insights for advancing HNSCC treatment.
Head Neck
; 46(3): 461-472, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38095042
15.
The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
Front Psychol
; 15: 1306388, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38500651
16.
Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?
Gene
; 898: 148069, 2024 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38070788
17.
The interference of cold ischemia time in the quality of total RNA from frozen tumor samples.
Cell Tissue Bank
; 14(2): 167-73, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22562477
18.
RAD50 Deficient in a Breast Cancer Model Predicts Sensitivity to PARP Inhibitors.
Curr Cancer Drug Targets
; 23(11): 900-909, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37076963
19.
Insights on variant analysis in silico tools for pathogenicity prediction.
Front Genet
; 13: 1010327, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36568376
20.
Cost-Effectiveness of BRCA 1/2 Genetic Test and Preventive Strategies: Using Real-World Data From an Upper-Middle Income Country.
Front Oncol
; 12: 951310, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35898894