Detalhe da pesquisa
1.
Hypermutation of the inactive X chromosome is a frequent event in cancer.
Cell
; 155(3): 567-81, 2013 Oct 24.
Artigo
Inglês
| MEDLINE | ID: mdl-24139898
2.
SOX11 expression is restricted to EBV-negative Burkitt lymphoma and associates with molecular genetic features.
Blood
; 2024 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38620074
3.
Genomic basis for RNA alterations in cancer.
Nature
; 578(7793): 129-136, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32025019
4.
The fifth edition of the WHO classification of mature B-cell neoplasms: open questions for research.
J Pathol
; 262(3): 255-270, 2024 03.
Artigo
Inglês
| MEDLINE | ID: mdl-38180354
5.
Variant ALK-fusion positive anaplastic large cell lymphoma (ALCL): A population-based paediatric study of the NHL-BFM study group.
Br J Haematol
; 204(5): 1894-1898, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38279625
6.
AMD3100-Mediated CXCR4 Inhibition Impairs Development of Primary Lymphoma of the Central Nervous System.
Am J Pathol
; 193(8): 1101-1115, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37196929
7.
DNA methylation-associated allelic inactivation regulates Keratin 19 gene expression during pancreatic development and carcinogenesis.
J Pathol
; 261(2): 139-155, 2023 10.
Artigo
Inglês
| MEDLINE | ID: mdl-37555362
8.
Author Correction: Genomic basis for RNA alterations in cancer.
Nature
; 614(7948): E37, 2023 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-36697831
9.
Author Correction: The landscape of genomic alterations across childhood cancers.
Nature
; 559(7714): E10, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29875405
10.
The landscape of genomic alterations across childhood cancers.
Nature
; 555(7696): 321-327, 2018 03 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29489754
11.
Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex.
J Med Genet
; 60(1): 48-56, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34740919
12.
Human activation-induced deaminase lacks strong replicative strand bias or preference for cytosines in hairpin loops.
Nucleic Acids Res
; 50(9): 5145-5157, 2022 05 20.
Artigo
Inglês
| MEDLINE | ID: mdl-35524550
13.
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(7): e1009679, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34324492
14.
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(9): e1009809, 2021 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-34547032
15.
Proteogenomic Profiling of High-Grade B-Cell Lymphoma With 11q Aberrations and Burkitt Lymphoma Reveals Lymphoid Enhancer Binding Factor 1 as a Novel Biomarker.
Mod Pathol
; 36(7): 100170, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36997001
16.
Rhabdoid tumors in patients conceived following ART: is there an association?
Hum Reprod
; 38(10): 2028-2038, 2023 Oct 03.
Artigo
Inglês
| MEDLINE | ID: mdl-37553222
17.
Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics.
Acta Neuropathol
; 146(3): 527-541, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37450044
18.
Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome.
Haematologica
; 108(1): 181-195, 2023 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35708139
19.
Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas.
Haematologica
; 108(2): 543-554, 2023 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35522148
20.
The B-cell receptor controls fitness of MYC-driven lymphoma cells via GSK3ß inhibition.
Nature
; 546(7657): 302-306, 2017 06 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28562582