Detalhe da pesquisa
1.
Bone morphogenetic protein and Notch signalling crosstalk in poor-prognosis, mesenchymal-subtype colorectal cancer.
J Pathol;
242(2): 178-192, 2017 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28299802
2.
Investigation of the atypical FBXW7 mutation spectrum in human tumours by conditional expression of a heterozygous propellor tip missense allele in the mouse intestines.
Gut;
63(5): 792-9, 2014 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23676439
3.
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
PLoS Genet;
7(6): e1002105, 2011 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21655089
4.
A basal gradient of Wnt and stem-cell number influences regional tumour distribution in human and mouse intestinal tracts.
Gut;
62(1): 83-93, 2013 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22287596
5.
The C-terminus of Apc does not influence intestinal adenoma development or progression.
J Pathol;
226(1): 73-83, 2012 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22009253
6.
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.
Nat Genet;
36(12): 1291-5, 2004 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15516931
7.
Therapeutic Potential of Protein Tyrosine Kinase 6 in Colorectal Cancer.
Cancers (Basel);
15(14)2023 Jul 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37509364
8.
Functional analysis reveals driver cooperativity and novel mechanisms in endometrial carcinogenesis.
EMBO Mol Med;
15(10): e17094, 2023 Oct 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37589076
9.
FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development.
J Pathol;
224(2): 180-9, 2011 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21503901
10.
Alterations to Genome Organisation in Stem Cells, Their Differentiation and Associated Diseases.
Results Probl Cell Differ;
70: 71-102, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36348105
11.
Severe polyposis in Apc(1322T) mice is associated with submaximal Wnt signalling and increased expression of the stem cell marker Lgr5.
Gut;
59(12): 1680-6, 2010 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20926645
12.
NRF2 Mediates Therapeutic Resistance to Chemoradiation in Colorectal Cancer through a Metabolic Switch.
Antioxidants (Basel);
10(9)2021 Aug 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34573012
13.
The Apc 1322T mouse develops severe polyposis associated with submaximal nuclear beta-catenin expression.
Gastroenterology;
136(7): 2204-2213.e1-13, 2009 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19248780
14.
NRF2 metagene signature is a novel prognostic biomarker in colorectal cancer.
Cancer Genet;
248-249: 1-10, 2020 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32871287
15.
The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability.
Clin Epigenetics;
12(1): 102, 2020 07 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32641106
16.
CRISPR-Cas9 Causes Chromosomal Instability and Rearrangements in Cancer Cell Lines, Detectable by Cytogenetic Methods.
CRISPR J;
2(6): 406-416, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31742432
17.
The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression.
Sci Rep;
9(1): 13463, 2019 09 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31530880
18.
Genetic imprinting: conflict at the Callipyge locus.
Curr Biol;
15(8): R291-4, 2005 Apr 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15854893
19.
Genomic imprinting: CTCF protects the boundaries.
Curr Biol;
14(7): R284-6, 2004 Apr 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15062124
20.
Tandem repeat hypothesis in imprinting: deletion of a conserved direct repeat element upstream of H19 has no effect on imprinting in the Igf2-H19 region.
Mol Cell Biol;
24(13): 5650-6, 2004 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15199123