Detalhe da pesquisa
1.
Machine learning approaches for the discovery of gene-gene interactions in disease data.
Brief Bioinform
; 14(2): 251-60, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22611119
2.
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Gut
; 62(7): 977-84, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22543157
3.
Epithelial-to-Mesenchymal Transition Supports Ovarian Carcinosarcoma Tumorigenesis and Confers Sensitivity to Microtubule Targeting with Eribulin.
Cancer Res
; 82(23): 4457-4473, 2022 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36206301
4.
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.
Nat Commun
; 13(1): 2306, 2022 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35484142
5.
FAK regulates IL-33 expression by controlling chromatin accessibility at c-Jun motifs.
Sci Rep
; 11(1): 229, 2021 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33420223
6.
Role of PLEXIND1/TGFß Signaling Axis in Pancreatic Ductal Adenocarcinoma Progression Correlates with the Mutational Status of KRAS.
Cancers (Basel)
; 13(16)2021 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34439202
7.
Repression of the Type I Interferon Pathway Underlies MYC- and KRAS-Dependent Evasion of NK and B Cells in Pancreatic Ductal Adenocarcinoma.
Cancer Discov
; 10(6): 872-887, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32200350
8.
Feasibility and clinical utility of endoscopic ultrasound guided biopsy of pancreatic cancer for next-generation molecular profiling.
Chin Clin Oncol
; 8(2): 16, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31070037
9.
Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes.
Sci Rep
; 6: 30457, 2016 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27456059
10.
CXCR2 Inhibition Profoundly Suppresses Metastases and Augments Immunotherapy in Pancreatic Ductal Adenocarcinoma.
Cancer Cell
; 29(6): 832-845, 2016 06 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27265504
11.
Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk.
Mol Genet Genomic Med
; 3(3): 182-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26029704
12.
A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis.
PLoS One
; 9(12): e101488, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25526632
13.
Support Vector Machine classifier for estrogen receptor positive and negative early-onset breast cancer.
PLoS One
; 8(7): e68606, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23894323