Detalhe da pesquisa
1.
Clonally expanded PD-1-expressing T cells are enriched in synovial fluid of juvenile idiopathic arthritis patients.
Eur J Immunol
; 53(7): e2250162, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37086046
2.
Digital droplet PCR versus quantitative PCR for lipoprotein (a) kringle IV type 2 repeat polymorphism genetic characterization.
J Clin Lab Anal
; 38(5): e24998, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38444303
3.
Polyploid tubular cells initiate a TGF-ß1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury.
Am J Physiol Cell Physiol
; 325(4): C849-C861, 2023 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37642236
4.
Molecular Profiling of Lymphatic Endothelial Cell Activation In Vitro.
Int J Mol Sci
; 24(23)2023 Nov 22.
Artigo
Inglês
| MEDLINE | ID: mdl-38068914
5.
Effect of space flight on the behavior of human retinal pigment epithelial ARPE-19 cells and evaluation of coenzyme Q10 treatment.
Cell Mol Life Sci
; 78(23): 7795-7812, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-34714361
6.
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients.
Mol Cancer
; 20(1): 32, 2021 02 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33579306
7.
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing.
Bioinformatics
; 36(4): 1267-1269, 2020 02 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31589307
8.
Nanopore sequencing data analysis: state of the art, applications and challenges.
Brief Bioinform
; 19(6): 1256-1272, 2018 11 27.
Artigo
Inglês
| MEDLINE | ID: mdl-28637243
9.
PyPore: a python toolbox for nanopore sequencing data handling.
Bioinformatics
; 35(21): 4445-4447, 2019 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30993318
10.
Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data.
Bioinformatics
; 35(21): 4213-4221, 2019 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30949684
11.
RNA sequencing reveals PNN and KCNQ1OT1 as predictive biomarkers of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy.
Int J Cancer
; 145(9): 2580-2593, 2019 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30973654
12.
Characterization of MinION nanopore data for resequencing analyses.
Brief Bioinform
; 18(6): 940-953, 2017 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27559152
13.
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2.
Nucleic Acids Res
; 44(20): e154, 2016 Nov 16.
Artigo
Inglês
| MEDLINE | ID: mdl-27507884
14.
SLMSuite: a suite of algorithms for segmenting genomic profiles.
BMC Bioinformatics
; 18(1): 321, 2017 Jun 28.
Artigo
Inglês
| MEDLINE | ID: mdl-28659129
15.
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments.
BMC Genomics
; 18(1): 747, 2017 Sep 21.
Artigo
Inglês
| MEDLINE | ID: mdl-28934930
16.
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman.
J Hum Genet
; 62(2): 259-264, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-27734841
17.
Characterization and identification of hidden rare variants in the human genome.
BMC Genomics
; 16: 340, 2015 Apr 24.
Artigo
Inglês
| MEDLINE | ID: mdl-25903059
18.
H3M2: detection of runs of homozygosity from whole-exome sequencing data.
Bioinformatics
; 30(20): 2852-9, 2014 Oct 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24966365
19.
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies.
Hum Hered
; 77(1-4): 63-72, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25060270
20.
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing.
Clin Chem
; 65(12): 1605-1608, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31645339