Detalhe da pesquisa
1.
p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression.
Int J Mol Sci
; 24(12)2023 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37373225
2.
DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes.
Int J Mol Sci
; 24(16)2023 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37628757
3.
Random forest for spatialization of daily evapotranspiration (ET0) in watersheds in the Atlantic Forest.
Environ Monit Assess
; 194(6): 449, 2022 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35606615
4.
Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes.
Clin Genet
; 100(4): 478-483, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34259353
5.
TAPES: A tool for assessment and prioritisation in exome studies.
PLoS Comput Biol
; 15(10): e1007453, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31613886
6.
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
Clin Genet
; 92(4): 405-414, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28195393
7.
Illustrated identification key to females of the genus Sabethes Robineau-Desvoidy recorded from Brazil (Diptera: Culicidae), in dichotomous and interactive formats, including an updated list of species and new records for the states.
Zootaxa
; 5406(2): 253-287, 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38480153
8.
Alteration of DNA Methylation and Epigenetic Scores Associated With Features of Schizophrenia and Common Variant Genetic Risk.
Biol Psychiatry
; 95(7): 647-661, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37480976
9.
HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS.
Neurol Neuroimmunol Neuroinflamm
; 11(2): e200190, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38150649
10.
Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing.
BMC Med Genomics
; 16(1): 126, 2023 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37296477
11.
Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis.
Clin Epigenetics
; 15(1): 20, 2023 02 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36765422
12.
Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis.
Front Immunol
; 14: 1162796, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37325639
13.
Nutritional and chemical composition of Alpinia zerumbet leaves, a traditional functional food.
Food Res Int
; 173(Pt 2): 113417, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37803755
14.
Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis.
Neurology
; 101(7): e679-e689, 2023 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37541839
15.
Mosquito Fauna and Spatial Distribution in an Atlantic Forest Area in Rio de Janeiro State, Brazil, Reveal a High Risk of Transmission of Yellow Fever and Other Arboviruses.
Trop Med Infect Dis
; 7(12)2022 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36548665
16.
Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity.
Clin Epigenetics
; 14(1): 194, 2022 12 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36585691
17.
Epigenome-wide association studies: current knowledge, strategies and recommendations.
Clin Epigenetics
; 13(1): 214, 2021 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34863305
18.
Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer.
PLoS One
; 15(7): e0235613, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32634176
19.
Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients.
Sci Rep
; 10(1): 22217, 2020 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33335118
20.
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.
Mol Genet Genomic Med
; 7(8): e850, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31297992