Detalhe da pesquisa
1.
Author Correction: TP53 loss creates therapeutic vulnerability in colorectal cancer.
Nature
; 597(7875): E6, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34433970
2.
TP53 loss creates therapeutic vulnerability in colorectal cancer.
Nature
; 520(7549): 697-701, 2015 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25901683
3.
Pediatric myeloid sarcoma: a single institution clinicopathologic and molecular analysis.
Pediatr Hematol Oncol
; 37(1): 76-89, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31682773
4.
Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcoma.
Genes Chromosomes Cancer
; 54(12): 796-808, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26355645
5.
Amplification and over-expression of MAP3K3 gene in human breast cancer promotes formation and survival of breast cancer cells.
J Pathol
; 232(1): 75-86, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24122835
6.
Detailed genome-wide SNP analysis of major salivary carcinomas localizes subtype-specific chromosome sites and oncogenes of potential clinical significance.
Am J Pathol
; 182(6): 2048-57, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23583282
7.
Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency.
Nature
; 456(7224): 971-5, 2008 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-19011615
8.
Genomic segmental polymorphisms in inbred mouse strains.
Nat Genet
; 36(9): 952-4, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15322544
9.
LncRNA PVT-1 promotes osteosarcoma cancer stem-like properties through direct interaction with TRIM28 and TSC2 ubiquitination.
Oncogene
; 41(50): 5373-5384, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36348010
10.
Overexpression of Separase induces aneuploidy and mammary tumorigenesis.
Proc Natl Acad Sci U S A
; 105(35): 13033-8, 2008 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-18728194
11.
Oncogenic Orphan Nuclear Receptor NR4A3 Interacts and Cooperates with MYB in Acinic Cell Carcinoma.
Cancers (Basel)
; 12(9)2020 Aug 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32867110
12.
Cell cycle regulator gene CDC5L, a potential target for 6p12-p21 amplicon in osteosarcoma.
Mol Cancer Res
; 6(6): 937-46, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18567798
13.
Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
Anticancer Res
; 29(4): 1255-62, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19414372
14.
Deletion of 1p32-p36 is the most frequent genetic change and poor prognostic marker in adenoid cystic carcinoma of the salivary glands.
Clin Cancer Res
; 14(16): 5181-7, 2008 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18698036
15.
Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia.
Pediatr Blood Cancer
; 51(2): 171-7, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18253961
16.
Genetic abnormalities associated with chemoradiation resistance of head and neck squamous cell carcinoma.
Clin Cancer Res
; 13(15 Pt 1): 4386-91, 2007 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17671120
17.
Generation of an induced pluripotent stem cell line from an individual with a heterozygous RECQL4 mutation.
Stem Cell Res
; 33: 36-40, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30312871
18.
A homozygous p53 R282W mutant human embryonic stem cell line generated using TALEN-mediated precise gene editing.
Stem Cell Res
; 27: 131-135, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29414603
19.
Frequent detection of CBFA2T3::GLIS2 fusion and RAM-phenotype in pediatric non-Down syndrome acute megakaryoblastic leukemia: a possible novel relationship with aberrant cytoplasmic CD3 expression.
Leuk Lymphoma
; 64(2): 462-467, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36346368
20.
Establishment of a human embryonic stem cell line with homozygous TP53 R248W mutant by TALEN mediated gene editing.
Stem Cell Res
; 29: 215-219, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29730572