Detalhe da pesquisa
1.
A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Carcinogenesis
; 37(1): 10-17, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26498247
2.
Lynch syndrome associated with two MLH1 promoter variants and allelic imbalance of MLH1 expression.
Hum Mutat
; 36(6): 622-30, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25762362
3.
A reinvestigation of somatic hypermethylation at the PTEN CpG island in cancer cell lines.
Biol Proced Online
; 14(1): 5, 2012 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22490388
4.
De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one.
Int J Cancer
; 128(4): 869-78, 2011 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20473912
5.
Epigenetic inactivation of a cluster of genes flanking MLH1 in microsatellite-unstable colorectal cancer.
Cancer Res
; 67(19): 9107-16, 2007 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17909015
6.
Scarcity of Recurrent Regulatory Driver Mutations in Colorectal Cancer Revealed by Targeted Deep Sequencing.
JNCI Cancer Spectr
; 3(2): pkz012, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31360895
7.
Disruption of a -35 kb Enhancer Impairs CTCF Binding and MLH1 Expression in Colorectal Cells.
Clin Cancer Res
; 24(18): 4602-4611, 2018 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29898989
8.
Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients.
Cancer Genet
; 209(11): 497-500, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27886675
9.
Integrated Genetic, Epigenetic, and Transcriptional Profiling Identifies Molecular Pathways in the Development of Laterally Spreading Tumors.
Mol Cancer Res
; 14(12): 1217-1228, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27671336
10.
Arrested Hematopoiesis and Vascular Relaxation Defects in Mice with a Mutation in Dhfr.
Mol Cell Biol
; 36(8): 1222-36, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26830229
11.
Mosaic Epigenetic Inheritance as a Cause of Early-Onset Colorectal Cancer.
JAMA Oncol
; 1(7): 953-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26181641
12.
Implementation of novel pyrosequencing assays to screen for common mutations of BRAF and KRAS in a cohort of sporadic colorectal cancers.
Diagn Mol Pathol
; 18(2): 62-71, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19430299
13.
Routine testing for mismatch repair deficiency in sporadic colorectal cancer is justified.
J Pathol
; 207(4): 377-84, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16175654
14.
MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer.
Gastroenterology
; 129(5): 1392-9, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16285940