Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Felipe Antonio de Oliveira Garcia"'
Autor:
Felipe Antonio de Oliveira Garcia, Edilene Santos de Andrade, Henrique de Campos Reis Galvão, Cristina da Silva Sábato, Natália Campacci, Andre Escremin de Paula, Adriane Feijó Evangelista, Iara Viana Vidigal Santana, Matias Eliseo Melendez, Rui Manuel Reis, Edenir Inez Palmero
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Familial colorectal cancer type X (FCCTX) is a heterogeneous colorectal cancer predisposition syndrome that, although displays a cancer pattern similar to Lynch syndrome, is mismatch repair proficient and does not exhibit microsatellite inst
Externí odkaz:
https://doaj.org/article/98fb41d67fd1417e81bfd791b569a1b5
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Molecular biology is currently a fast-advancing science. Sequencing techniques are getting cheaper, but the interpretation of genetic variants requires expertise and computational power, therefore is still a challenge. Next-generation sequencing rele
Externí odkaz:
https://doaj.org/article/48578514220f41c7a2a98e86dbc7b601
Autor:
Wellington dos Santos, Edilene Santos de Andrade, Felipe Antonio de Oliveira Garcia, Natália Campacci, Cristina da Silva Sábato, Matias Eliseo Melendez, Rui Manuel Reis, Henrique de Campos Reis Galvão, Edenir Inez Palmero
Publikováno v:
Cancers; Volume 14; Issue 17; Pages: 4233
Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRC) syndrome, characterized by germline pathogenic variants in mismatch repair (MMR)-related genes that lead to microsatellite instability. Patients who meet the clinical criteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8219b807b5af01f6fa028f6ef79ee08
https://doi.org/10.3390/cancers14174233
https://doi.org/10.3390/cancers14174233
Autor:
Daniel Antunes Moreno, Murilo Bonatelli, Augusto Perazzolo Antoniazzi, Flávia Escremim de Paula, Leticia Ferro Leal, Felipe Antônio de Oliveira Garcia, André Escremim de Paula, Gustavo Ramos Teixeira, Iara Viana Vidigal Santana, Fabiano Saggioro, Luciano Neder, Elvis Terci Valera, Carlos Alberto Scrideli, João Stavale, Suzana Maria Fleury Malheiros, Matheus Lima, Glaucia Noeli Maroso Hajj, Hernan Garcia-Rivello, Silvia Christiansen, Susana Nunes, Maria João Gil-da-Costa, Jorge Pinheiro, Flavia Delgado Martins, Carlos Almeida Junior, Bruna Minniti Mançano, Rui Manuel Reis
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
PurposeMedulloblastomas are the most common primary malignant brain tumors in children. They are divided into molecular subgroups: WNT-activated, SHH-Activated, TP53 mutant or wild type, and non-WNT/non-SHH (Groups 3 and 4). WNT-activated medulloblas
Externí odkaz:
https://doaj.org/article/b4ae3852c8ca4836ba46c60e80d0fe85
Autor:
Rebeca Silveira Grasel, Paula Silva Felicio, André Escremim de Paula, Natalia Campacci, Felipe Antônio de Oliveira Garcia, Edilene Santos de Andrade, Adriane Feijó Evangelista, Gabriela Carvalho Fernandes, Cristina da Silva Sabato, Pedro De Marchi, Cristiano de Pádua Souza, Cláudia Alessandra Andrade de Paula, Giovana Tardin Torrezan, Henrique de Campos Reis Galvão, Dirce Maria Carraro, Edenir Inêz Palmero
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
The use of gene panels introduces a new dilemma in the genetics field due to the high frequency of variants of uncertain significance (VUS). The objective of this study was to provide evidence that may help in the classification of these germline var
Externí odkaz:
https://doaj.org/article/9d0b2b6e93ec44d29e8eecba43646e6d