Detalhe da pesquisa
1.
Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
Cell
; 144(1): 27-40, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21215367
2.
HER2 amplification by next-generation sequencing to identify HER2-positive invasive breast cancer with negative HER2 immunohistochemistry.
Cancer Cell Int
; 22(1): 350, 2022 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36376842
3.
NGS Analysis Confirms Common TP53 and RB1 Mutations, and Suggests MYC Amplification in Ocular Adnexal Sebaceous Carcinomas.
Int J Mol Sci
; 22(16)2021 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34445161
4.
Association of acute myeloid leukemia's most immature phenotype with risk groups and outcomes.
Haematologica
; 101(5): 607-16, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26819054
5.
The patterns and dynamics of genomic instability in metastatic pancreatic cancer.
Nature
; 467(7319): 1109-13, 2010 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-20981101
6.
Transflip mutations produce deletions in pancreatic cancer.
Genes Chromosomes Cancer
; 54(8): 472-481, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26031834
7.
A clinically relevant population of leukemic CD34(+)CD38(-) cells in acute myeloid leukemia.
Blood
; 119(15): 3571-7, 2012 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-22262762
8.
An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia.
Biomedicines
; 12(3)2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38540211
9.
Targeted pathologic evaluation of bone marrow donors identifies previously undiagnosed marrow abnormalities.
Biol Blood Marrow Transplant
; 19(8): 1254-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23769818
10.
Isogenic Cell Lines Derived from Specific Organ Metastases Exhibit Divergent Cytogenomic Aberrations.
Cancers (Basel)
; 15(5)2023 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36900209
11.
Ring Chromosomes in Hematological Malignancies Are Associated with TP53 Gene Mutations and Characteristic Copy Number Variants.
Cancers (Basel)
; 15(22)2023 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38001699
12.
Mechanism of delayed cell death following simultaneous CRISPR-Cas9 targeting in pancreatic cancers.
bioRxiv
; 2023 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37066222
13.
Complex/cryptic EWSR1::FLI1/ERG Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas.
Genes (Basel)
; 14(6)2023 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37372318
14.
CD34+ cell of origin for immunoglobulin heavy chain variable region unmutated, but not mutated, chronic lymphocytic leukemia.
Leuk Lymphoma
; 63(7): 1617-1623, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35343368
15.
Twin/Multiple Gestations With a Hydatidiform Mole: Clinicopathologic Analysis of 21 Cases With Emphasis on Molecular Genotyping and Parental Contribution.
Am J Surg Pathol
; 46(9): 1180-1195, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35796652
16.
Utility of targeted next-generation sequencing assay to detect 1p/19q co-deletion in formalin-fixed paraffin-embedded glioma specimens.
Hum Pathol
; 126: 63-76, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35561840
17.
Diagnostic Utility of Gene Fusion Panel to Detect Gene Fusions in Fresh and Formalin-Fixed, Paraffin-Embedded Cancer Specimens.
J Mol Diagn
; 23(10): 1343-1358, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34358677
18.
Concomitance of a novel RMDN2-ALK fusion and an EML4-ALK fusion in a lung adenocarcinoma.
Cancer Genet
; 258-259: 18-22, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233240
19.
Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies.
J Mol Diagn
; 23(4): 467-483, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33577993
20.
A comprehensive approach to evaluate genetic abnormalities in multiple myeloma using optical genome mapping.
Blood Cancer J
; 14(1): 78, 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38702349