Detalhe da pesquisa
1.
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.
Am J Med Genet A
; 194(5): e63542, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38234180
2.
Truncated ERG Oncoproteins from TMPRSS2-ERG Fusions Are Resistant to SPOP-Mediated Proteasome Degradation.
Mol Cell
; 59(6): 904-16, 2015 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26344096
3.
FGFR2-IIIb Expression by Immunohistochemistry Has High Specificity in Cholangiocarcinoma with FGFR2 Genomic Alterations.
Dig Dis Sci
; 67(8): 3797-3805, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34773565
4.
Identification of EWSR1 rearrangements in patients with immature hematopoietic neoplasms: A case series and review of literature.
Ann Diagn Pathol
; 58: 151942, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35344861
5.
Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia.
Genes Chromosomes Cancer
; 60(2): 108-111, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33078871
6.
Theragnostic chromosomal rearrangements in treatment-naive pancreatic ductal adenocarcinomas obtained via endoscopic ultrasound.
J Cell Mol Med
; 25(8): 4110-4123, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704908
7.
Clinical utility of next generation sequencing to detect IGH/IL3 rearrangements [t(5;14)(q31.1;q32.1)] in B-lymphoblastic leukemia/lymphoma.
Ann Diagn Pathol
; 53: 151761, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33991782
8.
Optimizing clinical cytology touch preparations for next generation sequencing.
Genomics
; 112(6): 5313-5323, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33144219
9.
Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
Genes Chromosomes Cancer
; 59(7): 422-427, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32196814
10.
UCH-L1 bypasses mTOR to promote protein biosynthesis and is required for MYC-driven lymphomagenesis in mice.
Blood
; 132(24): 2564-2574, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30257881
11.
Detection of cryptic CCND1 rearrangements in mantle cell lymphoma by next generation sequencing.
Ann Diagn Pathol
; 46: 151533, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32408254
12.
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratory.
Genes Chromosomes Cancer
; 58(8): 567-577, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30707474
13.
Genome U-Plot: a whole genome visualization.
Bioinformatics
; 34(10): 1629-1634, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29281001
14.
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
Eur J Haematol
; 102(1): 87-96, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30270457
15.
Copy number variant analysis using genome-wide mate-pair sequencing.
Genes Chromosomes Cancer
; 57(9): 459-470, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29726617
16.
Integrated mate-pair and RNA sequencing identifies novel, targetable gene fusions in peripheral T-cell lymphoma.
Blood
; 128(9): 1234-45, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27297792
17.
Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2+ breast cancer samples.
BMC Cancer
; 18(1): 738, 2018 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30005627
18.
Identification of a pyruvate-to-lactate signature in pancreatic intraductal papillary mucinous neoplasms.
Pancreatology
; 18(1): 46-53, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29170050
19.
Novel targeted therapy strategies for biliary tract cancers and hepatocellular carcinoma.
Future Oncol
; 14(6): 553-566, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29460642
20.
Common fragile sites (CFS) and extremely large CFS genes are targets for human papillomavirus integrations and chromosome rearrangements in oropharyngeal squamous cell carcinoma.
Genes Chromosomes Cancer
; 56(1): 59-74, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636103