Detalhe da pesquisa
1.
Antiapoptotic PON2 expression and its clinical implications in locally advanced oral squamous cell carcinoma.
Cancer Sci
; 115(6): 2012-2022, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38602182
2.
A Mechanistic Review of Methotrexate and Celecoxib as a Potential Metronomic Chemotherapy for Oral Squamous Cell Carcinoma.
Cancer Invest
; 41(2): 144-154, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36269850
3.
Circulating cell-free DNA as a diagnostic and prognostic marker for cervical cancer.
Int J Gynecol Cancer
; 2023 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37949487
4.
Measuring nonhomologous end-joining, homologous recombination and alternative end-joining simultaneously at an endogenous locus in any transfectable human cell.
Nucleic Acids Res
; 49(13): e74, 2021 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33877327
5.
Human papillomavirus 16 promotes microhomology-mediated end-joining.
Proc Natl Acad Sci U S A
; 116(43): 21573-21579, 2019 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31591214
6.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Nature
; 521(7553): 520-4, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25807483
7.
Liquid biopsy approaches for pleural effusion in lung cancer patients.
Mol Biol Rep
; 47(10): 8179-8187, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33029702
8.
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.
PLoS Genet
; 12(2): e1005821, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26918822
9.
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Hum Mol Genet
; 24(14): 3994-4005, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25877302
10.
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry.
Am J Hum Genet
; 93(2): 357-67, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23849778
11.
Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.
Birth Defects Res C Embryo Today
; 102(2): 115-25, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24975753
12.
Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.
Mamm Genome
; 25(3-4): 120-8, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24306492
13.
Expression of PTGS2 along with genes regulating VEGF signalling pathway and association with high-risk factors in locally advanced oral squamous cell carcinoma.
Cancer Med
; 13(3): e6986, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38426619
14.
Prostaglandin-endoperoxide synthase 2 (PTGS2) gene expression and its association with genes regulating the VEGF signaling pathway in head and neck squamous cell carcinoma.
J Oral Biol Craniofac Res
; 13(5): 567-574, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37559688
15.
Increased Gene Expression of C1orf74 Is Associated with Poor Prognosis in Cervical Cancer.
Cells
; 12(21)2023 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37947608
16.
Precision Radiotherapy: Reduction in Radiation for Oropharyngeal Cancer in the 30 ROC Trial.
J Natl Cancer Inst
; 113(6): 742-751, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33429428
17.
Detection of Early Human Papillomavirus-Associated Cancers by Liquid Biopsy.
JCO Precis Oncol
; 32019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31485558
18.
Coincident myelomeningocele and gastroschisis: report of 2 cases.
J Neurosurg Pediatr
; 21(6): 574-577, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29521606
19.
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Biol Open
; 5(3): 323-35, 2016 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26883626
20.
Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences.
Cell Cycle
; 11(16): 3036-44, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22871734