Detalhe da pesquisa
1.
Nucleus-Translocated ACSS2 Promotes Gene Transcription for Lysosomal Biogenesis and Autophagy.
Mol Cell
; 66(5): 684-697.e9, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28552616
2.
Recurrent mutations in topoisomerase IIα cause a previously undescribed mutator phenotype in human cancers.
Proc Natl Acad Sci U S A
; 119(4)2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35058360
3.
Characterization of colibactin-associated mutational signature in an Asian oral squamous cell carcinoma and in other mucosal tumor types.
Genome Res
; 30(6): 803-813, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32661091
4.
Genome-scale mutational signatures of aflatoxin in cells, mice, and human tumors.
Genome Res
; 27(9): 1475-1486, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28739859
5.
Regulatory crosstalk between lineage-survival oncogenes KLF5, GATA4 and GATA6 cooperatively promotes gastric cancer development.
Gut
; 64(5): 707-19, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25053715
6.
*K-means and cluster models for cancer signatures.
Biomol Detect Quantif
; 13: 7-31, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29021969
7.
Mutation Clusters from Cancer Exome.
Genes (Basel)
; 8(8)2017 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28809811
8.
Aristolochic acids and their derivatives are widely implicated in liver cancers in Taiwan and throughout Asia.
Sci Transl Med
; 9(412)2017 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29046434
9.
Genomic profiling reveals mutational landscape in parathyroid carcinomas.
JCI Insight
; 2(6): e92061, 2017 03 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28352668
10.
Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.
J Clin Endocrinol Metab
; 100(2): E360-4, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25387265
11.
Mutation signatures implicate aristolochic acid in bladder cancer development.
Genome Med
; 7(1): 38, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26015808
12.
Whole-exome sequencing of breast cancer, malignant peripheral nerve sheath tumor and neurofibroma from a patient with neurofibromatosis type 1.
Cancer Med
; 4(12): 1871-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26432421
13.
Next-generation sequencing of translocation renal cell carcinoma reveals novel RNA splicing partners and frequent mutations of chromatin-remodeling genes.
Clin Cancer Res
; 20(15): 4129-40, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24899691
14.
Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers.
Nat Genet
; 45(12): 1474-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24185513
15.
Genome-wide mutational signatures of aristolochic acid and its application as a screening tool.
Sci Transl Med
; 5(197): 197ra101, 2013 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23926199
16.
Janus kinase 3-activating mutations identified in natural killer/T-cell lymphoma.
Cancer Discov
; 2(7): 591-7, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22705984
17.
Exome sequencing of liver fluke-associated cholangiocarcinoma.
Nat Genet
; 44(6): 690-3, 2012 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22561520
18.
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes.
Nat Genet
; 44(5): 570-4, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22484628
19.
First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum.
Genome Biol
; 12(9): R96, 2011 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-21955916
20.
Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing.
Cancer Res
; 71(1): 29-39, 2011 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21097718