Detalhe da pesquisa
1.
Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.
Cell
; 148(1-2): 59-71, 2012 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22265402
2.
Acquisition of an immunosuppressive protumorigenic macrophage phenotype depending on c-Jun phosphorylation.
Proc Natl Acad Sci U S A
; 111(49): 17582-7, 2014 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25422452
3.
NF-kappaB functions as a tumour promoter in inflammation-associated cancer.
Nature
; 431(7007): 461-6, 2004 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-15329734
4.
Mutation spectrum in HNPCC in the Israeli population.
Fam Cancer
; 7(4): 309-17, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18389388
5.
[A new oncogenetic service of counseling and diagnosing for hereditary non-polyposis colorectal cancer (HNPCC)].
Harefuah
; 146(7): 510-4, 576, 575, 2007 Jul.
Artigo
em Hebraico
| MEDLINE | ID: mdl-17803162
6.
Specific induction of tie1 promoter by disturbed flow in atherosclerosis-prone vascular niches and flow-obstructing pathologies.
Circ Res
; 94(3): 394-401, 2004 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-14670840
7.
Human and mouse VEGFA-amplified hepatocellular carcinomas are highly sensitive to sorafenib treatment.
Cancer Discov
; 4(6): 730-43, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24687604
8.
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.
Fam Cancer
; 9(2): 141-50, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19851887
9.
Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I.
Fam Cancer
; 8(3): 187-94, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19101824