Detalhe da pesquisa
1.
Fluorescence in-situ hybridisation for TP63 rearrangements in T cell lymphomas: single-site experience of 470 patients and implications for clinical testing.
Histopathology
; 76(3): 481-485, 2020 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-31557339
2.
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
Inglês
| MEDLINE | ID: mdl-27297792
3.
Gastroblastoma harbors a recurrent somatic MALAT1-GLI1 fusion gene.
Mod Pathol
; 30(10): 1443-1452, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28731043
4.
The oncogenic transcription factor IRF4 is regulated by a novel CD30/NF-κB positive feedback loop in peripheral T-cell lymphoma.
Blood
; 125(20): 3118-27, 2015 May 14.
Artigo
Inglês
| MEDLINE | ID: mdl-25833963
5.
ALK-negative anaplastic large cell lymphoma is a genetically heterogeneous disease with widely disparate clinical outcomes.
Blood
; 124(9): 1473-80, 2014 Aug 28.
Artigo
Inglês
| MEDLINE | ID: mdl-24894770
6.
Chromosomal rearrangements and copy number abnormalities of TP63 correlate with p63 protein expression in lung adenocarcinoma.
Mod Pathol
; 28(3): 359-66, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25189640
7.
Clinical utility of fluorescence in situ hybridization-based diagnosis of BCR-ABL1 like (Philadelphia chromosome like) B-acute lymphoblastic leukemia.
Am J Hematol
; 95(3): E68-E72, 2020 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31919873
8.
Prognostic irrelevance of ring sideroblast percentage in World Health Organization-defined myelodysplastic syndromes without excess blasts.
Blood
; 119(24): 5674-7, 2012 Jun 14.
Artigo
Inglês
| MEDLINE | ID: mdl-22538853
9.
SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value.
Blood
; 119(2): 569-72, 2012 Jan 12.
Artigo
Inglês
| MEDLINE | ID: mdl-22096241
10.
Trisomies in multiple myeloma: impact on survival in patients with high-risk cytogenetics.
Blood
; 119(9): 2100-5, 2012 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22234687
11.
Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas.
Blood
; 120(11): 2280-9, 2012 Sep 13.
Artigo
Inglês
| MEDLINE | ID: mdl-22855598
12.
Differences in the distribution of cytogenetic subtypes between multiple myeloma patients with and without a family history of monoclonal gammopathy and multiple myeloma.
Eur J Haematol
; 91(3): 193-195, 2013 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-23647020
13.
Spliceosome mutations involving SRSF2, SF3B1, and U2AF35 in chronic myelomonocytic leukemia: prevalence, clinical correlates, and prognostic relevance.
Am J Hematol
; 88(3): 201-6, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23335386
14.
Evaluation of revised IPSS cytogenetic risk stratification and prognostic impact of monosomal karyotype in 783 patients with primary myelodysplastic syndromes.
Am J Hematol
; 88(8): 690-3, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23686868
15.
Cutaneous extramedullary plasmacytoma: clinical, prognostic, and interphase cytogenetic analysis.
Am J Dermatopathol
; 35(3): 357-63, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23000906
16.
The B cell antigen receptor in atypical chronic lymphocytic leukemia with t(14;19)(q32;q13) demonstrates remarkable stereotypy.
Int J Cancer
; 128(11): 2759-64, 2011 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20715110
17.
Isolated del(5q) in myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients.
Am J Hematol
; 86(5): 393-8, 2011 May.
Artigo
Inglês
| MEDLINE | ID: mdl-21523797
18.
Biologic and genetic characterization of the novel amyloidogenic lambda light chain-secreting human cell lines, ALMC-1 and ALMC-2.
Blood
; 112(5): 1931-41, 2008 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-18567838
19.
Secondary cutaneous involvement by systemic anaplastic lymphoma kinase-negative anaplastic large-cell lymphoma with 6p25.3 rearrangement.
Histopathology
; 67(6): 932-5, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-25930107
20.
Chromosome 1 abnormalities in myeloid malignancies: a literature survey and karyotype-phenotype associations.
Eur J Haematol
; 84(3): 191-200, 2010 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-20002154