Detalhe da pesquisa
1.
Rhabdoid tumors in patients conceived following ART: is there an association?
Hum Reprod
; 38(10): 2028-2038, 2023 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37553222
2.
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
em Inglês
| MEDLINE | ID: mdl-37450044
3.
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
em Inglês
| MEDLINE | ID: mdl-35522148
4.
T-cell prolymphocytic leukemia is associated with deregulation of oncogenic microRNAs on transcriptional and epigenetic level.
Genes Chromosomes Cancer
; 61(7): 432-436, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35218115
5.
Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC.
Neuropathol Appl Neurobiol
; 48(4): e12797, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35152461
6.
ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance.
Acta Neuropathol
; 143(6): 697-711, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501487
7.
Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor.
Genes Chromosomes Cancer
; 60(8): 586-590, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33896072
8.
The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma.
Blood
; 133(9): 962-966, 2019 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30567752
9.
CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D1- mantle cell lymphoma.
Blood
; 133(9): 940-951, 2019 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30538135
10.
Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors.
Acta Neuropathol
; 142(2): 361-374, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34003336
11.
Reconstruction of rearranged T-cell receptor loci by whole genome and transcriptome sequencing gives insights into the initial steps of T-cell prolymphocytic leukemia.
Genes Chromosomes Cancer
; 59(4): 261-267, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31677197
12.
Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults.
Acta Neuropathol
; 139(2): 277-286, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31732806
13.
Spinal cord atypical teratoid/rhabdoid tumors in children: Clinical, genetic, and outcome characteristics in a representative European cohort.
Pediatr Blood Cancer
; 67(1): e28022, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31571386
14.
Non-leukemic pediatric mixed phenotype acute leukemia/lymphoma: Genomic characterization and clinical outcome in a prospective trial for pediatric lymphoblastic lymphoma.
Genes Chromosomes Cancer
; 58(6): 365-372, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30578714
15.
Multiple DICER1-related tumors in a child with a large interstitial 14q32 deletion.
Genes Chromosomes Cancer
; 57(5): 223-230, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29315962
16.
The extraordinary challenge of treating patients with congenital rhabdoid tumors-a collaborative European effort.
Pediatr Blood Cancer
; 65(6): e26999, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29418059
17.
MYC expression and translocation analyses in low-grade and transformed follicular lymphoma.
Histopathology
; 71(6): 960-971, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28730642
18.
Atypical teratoid/rhabdoid tumor arising in a malignant glioma.
Pediatr Blood Cancer
; 64(1): 96-99, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27472468
19.
Molecular characterization of acute lymphoblastic leukemia with high CRLF2 gene expression in childhood.
Pediatr Blood Cancer
; 64(10)2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28371317
20.
Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
Genes Chromosomes Cancer
; 55(9): 677-87, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27121553