Detalhe da pesquisa
1.
CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesin.
Nucleic Acids Res
; 51(18): 9594-9609, 2023 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37702151
2.
Correlation of gene expression with magnetic resonance imaging features of retinoblastoma: a multi-center radiogenomics validation study.
Eur Radiol
; 34(2): 863-872, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37615761
3.
Fanconi anemia-isogenic head and neck cancer cell line pairs: A basic and translational science resource.
Int J Cancer
; 153(1): 183-196, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36912284
4.
MRI Features for Identifying MYCN-amplified RB1 Wild-type Retinoblastoma.
Radiology
; 307(5): e222264, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37191489
5.
HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair.
Nucleic Acids Res
; 48(5): 2442-2456, 2020 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31960047
6.
MR Imaging Features of Retinoblastoma: Association with Gene Expression Profiles.
Radiology
; 288(2): 506-515, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29714679
7.
Genomic landscape of retinoblastoma in Rb-/- p130-/- mice resembles human retinoblastoma.
Genes Chromosomes Cancer
; 56(3): 231-242, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27750399
8.
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
Nat Genet
; 39(2): 159-61, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17200672
9.
Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.
Hum Mutat
; 36(5): 562-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25754594
10.
RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients.
J Med Genet
; 51(6): 366-74, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24688104
11.
High resolution SNP array profiling identifies variability in retinoblastoma genome stability.
Genes Chromosomes Cancer
; 53(1): 1-14, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24249257
12.
Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies.
Lancet Oncol
; 14(4): 327-34, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23498719
13.
Genome-wide siRNA screens identify RBBP9 function as a potential target in Fanconi anaemia-deficient head-and-neck squamous cell carcinoma.
Commun Biol
; 6(1): 37, 2023 01 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36639418
14.
High-Level MYCN-Amplified RB1-Proficient Retinoblastoma Tumors Retain Distinct Molecular Signatures.
Ophthalmol Sci
; 2(3): 100188, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36245757
15.
Detection of cytogenetic changes and chromosomal aneuploidy with fluorescent in situ hybridization in cytological specimens of oral cancers in Fanconi anemia-Proof of concept.
Clin Exp Dent Res
; 8(1): 108-116, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34854575
16.
BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.
Sci Rep
; 12(1): 45, 2022 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34997070
17.
ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation.
Nat Cell Biol
; 23(6): 595-607, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34108663
18.
v-Raf murine sarcoma viral oncogene mutation status in serous borderline ovarian tumors and the effect on clinical behavior.
Int J Gynecol Cancer
; 19(9): 1560-3, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19955937
19.
Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair.
Sci Rep
; 9(1): 768, 2019 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30683899
20.
Mutant huntingtin activates Nrf2-responsive genes and impairs dopamine synthesis in a PC12 model of Huntington's disease.
BMC Mol Biol
; 9: 84, 2008 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-18844975