Detalhe da pesquisa
1.
The RAS-signaling-pathway-mutation-related prognosis in B-cell acute lymphoblastic leukemia: A report from South China children's leukemia group.
Hematol Oncol
; 42(3): e3265, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38564328
2.
New insights into the clinical characteristics of SETD2-mutated acute myeloid leukaemia.
Br J Haematol
; 202(1): 111-115, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37038274
3.
Spectrum and clinical features of gene mutations in Chinese pediatric acute lymphoblastic leukemia.
BMC Pediatr
; 23(1): 62, 2023 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739388
4.
MN1::ETV6-positive de novo T-cell acute lymphoblastic leukaemia is sensitive to venetoclax: A case report.
Br J Haematol
; 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38685592
5.
Posttransplant cyclophosphamide for haploidentical stem cell transplantation in children with Wiskott-Aldrich syndrome.
Pediatr Blood Cancer
; 65(8): e27092, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29745014
6.
Structural Basis of the Interaction between Tuberous Sclerosis Complex 1 (TSC1) and Tre2-Bub2-Cdc16 Domain Family Member 7 (TBC1D7).
J Biol Chem
; 291(16): 8591-601, 2016 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26893383
7.
Using circulating tumor DNA to monitor myelodysplastic syndromes status.
Hematol Oncol
; 37(4): 531-533, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31291480
8.
Sequential haplo-identical conditioning transplant regimen for pediatric patients with relapsed or refractory hemophagocytic lymphohistiocytosis.
Bone Marrow Transplant
; 59(4): 513-517, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287082
9.
DNA damage response alterations in clear cell renal cell carcinoma: clinical, molecular, and prognostic implications.
Eur J Med Res
; 29(1): 107, 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38326910
10.
Analysis of the Genetic Characteristics and Metastatic Pathways of G1 and G2 Colorectal Neuroendocrine Neoplasms.
J Endocr Soc
; 8(2): bvad168, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38205165
11.
First reported case of splenic diffuse red pulp small B-cell lymphoma with novel mutations in CXCR4 and TRAF3 genes.
Int J Hematol
; 118(3): 394-399, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36935465
12.
Case report: Targeted sequencing facilitates the diagnosis and management of rare multifocal pure ground-glass opacities with intrapulmonary metastasis.
Front Oncol
; 13: 1276095, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38322291
13.
Eosinophilia in a patient with aggressive systemic mastocytosis harboring a KIT D816V mutation: A case report.
SAGE Open Med Case Rep
; 11: 2050313X231197322, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37663152
14.
The influence of methotrexate-related transporter and metabolizing enzyme gene polymorphisms on peri-engraftment syndrome and graft-versus-host disease after haplo-hematopoietic stem cell transplantation in pediatric patients with malignant hematological diseases.
Front Immunol
; 14: 1229266, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37731501
15.
The mutational pattern of homologous recombination repair genes in urothelial carcinoma and its correlation with immunotherapeutic response.
Cancer Med
; 12(24): 22370-22380, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37986697
16.
Next-generation sequencing revealed factors associated with cumulative incidence of relapse and leukemia-free survival in patients with newly diagnosed acute myeloid leukemia.
Cancer Pathog Ther
; 1(1): 25-32, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38328603
17.
The clinical impact of IKZF1 mutation in acute myeloid leukemia.
Exp Hematol Oncol
; 12(1): 33, 2023 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36997950
18.
Case Report: Pathogenesis With a Rare RHOA A161E Mutation in a Patient With Angioimmunoblastic T-Cell Lymphoma.
Front Genet
; 13: 948744, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35910204
19.
Clinical and Genetic Characteristics of IKZF1 Mutation in Chinese Children With B-Cell Acute Lymphoblastic Leukemia.
Front Genet
; 13: 822832, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35419036
20.
A Novel Prognostic Scoring Model for Myelodysplastic Syndrome Patients With SF3B1 Mutation.
Front Oncol
; 12: 905490, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35832562