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Gain of Chromosome 21 or Amplification of Chromosome Arm 21q Is One Mechanism for Increased ERG Expression in Acute Myeloid Leukemia.
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- Genes, Chromosomes & Cancer, 2016, v. 55, n. 2, p. 148, doi. 10.1002/gcc.22321
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- Article
Genetic Characterization of T-PLL Reveals Two Major Biologic Subgroups and JAK3 Mutations as Prognostic Marker.
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- Genes, Chromosomes & Cancer, 2016, v. 55, n. 1, p. 82, doi. 10.1002/gcc.22313
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- Article
Fusion of PDGFRB to MPRIP, CPSF6, and GOLGB1 in three patients with eosinophilia-associated myeloproliferative neoplasms.
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- Genes, Chromosomes & Cancer, 2015, v. 54, n. 12, p. 762, doi. 10.1002/gcc.22287
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- Article
Analysis for loss of heterozygosity on chromosome arm 13q by STR analysis or SNP sequencing can replace analysis of FLT3-ITD to detect patients with prognostically adverse AML.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 12, p. 1008, doi. 10.1002/gcc.22210
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- Article
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 524, doi. 10.1002/gcc.22163
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- Article
Association of the type of 5q loss with complex karyotype, clonal evolution, TP53 mutation status, and prognosis in acute myeloid leukemia and myelodysplastic syndrome.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 5, p. 402, doi. 10.1002/gcc.22151
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- Article
The molecular profile of adult T-cell acute lymphoblastic leukemia: Mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 4, p. 410, doi. 10.1002/gcc.22039
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- Article
Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 12, p. 1079, doi. 10.1002/gcc.21992
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- Article
Diversity of the juxtamembrane and TKD1 mutations (Exons 13-15) in the FLT3 gene with regards to mutant load, sequence, length, localization, and correlation with biological data.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 10, p. 910, doi. 10.1002/gcc.21975
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- Article
ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 4, p. 328, doi. 10.1002/gcc.21918
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- Article
Gene expression of BAALC, CDKN1B, ERG, and MN1 adds independent prognostic information to cytogenetics and molecular mutations in adult acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 3, p. 257, doi. 10.1002/gcc.20950
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- Article
Several lymphoma-specific genetic events in parallel can be found in mature B-cell neoplasms.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 1, p. 43, doi. 10.1002/gcc.20831
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- Article
Associations between imatinib resistance conferring mutations and Philadelphia positive clonal cytogenetic evolution in CML.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 10, p. 910, doi. 10.1002/gcc.20801
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- Article
Toward a comprehensive prognostic scoring system in chronic lymphocytic leukemia based on a combination of genetic parameters.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 9, p. 851, doi. 10.1002/gcc.20794
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- Article
Atypical mRNA fusions in PML-RARA positive, RARA-PML negative acute promyelocytic leukemia.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 5, p. 471, doi. 10.1002/gcc.20757
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- Article
Impact of trisomy 8 on expression of genes located on chromosome 8 in different AML subgroups.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 12, p. 1164, doi. 10.1002/gcc.20380
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- Article
Transient response to imatinib in a chronic eosinophilic leukemia associated with ins(9;4)(q33;q12q25) and a CDK5RAP2‐PDGFRA fusion gene.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 10, p. 950, doi. 10.1002/gcc.20359
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- Article
KIT D 816 V and JAK 2 V 617 F mutations are seen recurrently in hypereosinophilia of unknown significance.
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- American Journal of Hematology, 2015, v. 90, n. 9, p. 774, doi. 10.1002/ajh.24075
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- Article
Impact of Integrating Clinical and Genetic Information.
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- In Silico Biology, 2002, v. 2, n. 3, p. 383
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- Article
Multiparameter flow cytometry provides independent prognostic information in patients with suspected myelodysplastic syndromes: A study on 804 patients.
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- Cytometry. Part B, 2015, v. 88, n. 3, p. 154, doi. 10.1002/cyto.b.21224
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- Article
Multiparameter flow cytometry reveals myelodysplasia-related aberrant antigen expression in myelodysplastic/myeloproliferative neoplasms.
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- Cytometry. Part B, 2013, v. 84B, n. 3, p. 194, doi. 10.1002/cyto.b.21068
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- Article
Evaluation of flow cytometric assessment of myeloid nuclear differentiation antigen expression as a diagnostic marker for myelodysplastic syndromes in a series of 269 patients.
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- Cytometry. Part B, 2012, v. 82B, n. 5, p. 295, doi. 10.1002/cyto.b.21026
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- Article
Frequency and prognostic impact of the aberrant CD8 expression in 5,523 patients with chronic lymphocytic leukemia.
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- Cytometry. Part B, 2012, v. 82B, n. 3, p. 145, doi. 10.1002/cyto.b.21002
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- Article
Frontline therapy of acute promyelocytic leukemia: Randomized comparison of ATRA and intensified chemotherapy versus ATRA and anthracyclines.
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- European Journal of Haematology, 2018, v. 100, n. 2, p. 154, doi. 10.1111/ejh.12994
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- Article
Monitoring of minimal residual disease in acute myeloid leukemia.
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- Journal of Laboratory Medicine / Laboratoriums Medizin, 2005, v. 29, n. 5, p. 343, doi. 10.1515/JLM.2005.048
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- Article
FISH-Diagnostik bei hämatologischen Neoplasien.
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- Journal of Laboratory Medicine / Laboratoriums Medizin, 2005, v. 29, n. 5, p. 335, doi. 10.1515/JLM.2005.0472005
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- Article
Molecular diagnostics, targeted therapy, and the indication for allogeneic stem cell transplantation in acute lymphoblastic leukemia.
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- 2011
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- Publication type:
- Journal Article
Molecular Diagnostics, Targeted Therapy, and the Indication for Allogeneic StemCell Transplantation in Acute Lymphoblastic Leukemia.
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- Advances in Hematology, 2011, v. 2011, p. 1, doi. 10.1155/2011/154745
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- Publication type:
- Article
Clinical utility gene card for: Hereditary thrombocythemia.
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- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 1, doi. 10.1038/ejhg.2013.117
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- Article
FLT3 Length Mutations as Marker for Follow-Up Studies in Acute Myeloid Leukaemia.
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- Acta Haematologica, 2004, v. 112, n. 1/2, p. 68, doi. 10.1159/000077561
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- Article
Monitoring of acute myeloid leukemia by flow cytometry.
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- Current Oncology Reports, 2003, v. 5, n. 5, p. 405, doi. 10.1007/s11912-003-0027-5
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- Publication type:
- Article
D324N single‐nucleotide polymorphism in the FLT3 gene is associated with higher risk of myeloid leukemias.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 4, p. 332, doi. 10.1002/gcc.20294
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- Publication type:
- Article
Acute myeloid leukemia with a complex aberrant karyotype is a distinct biological entity characterized by genomic imbalances and a specific gene expression profile.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 3, p. 227, doi. 10.1002/gcc.20193
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- Article
AML M3 and AML M3 variant each have a distinct gene expression signature but also share patterns different from other genetically defined AML subtypes.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 2, p. 113, doi. 10.1002/gcc.20175
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- Article
Pattern robustness of diagnostic gene expression signatures in leukemia.
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- Genes, Chromosomes & Cancer, 2005, v. 42, n. 3, p. 299, doi. 10.1002/gcc.20126
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- Publication type:
- Article
Distinct sequences on 11q13.5 and 11q2324 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.
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- Genes, Chromosomes & Cancer, 2004, v. 39, n. 4, p. 263, doi. 10.1002/gcc.20002
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- Article
Molecular characterization of acute leukemias by use of microarray technology.
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- Genes, Chromosomes & Cancer, 2003, v. 37, n. 4, p. 396, doi. 10.1002/gcc.10225
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- Publication type:
- Article
Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: A detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
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- Genes, Chromosomes & Cancer, 2002, v. 35, n. 1, p. 20, doi. 10.1002/gcc.10088
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- Publication type:
- Article
Balanced chromosome abnormalities inv(16) and t(15;17) in therapy-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop.
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- Genes, Chromosomes & Cancer, 2002, v. 33, n. 4, p. 395, doi. 10.1002/gcc.10043
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- Publication type:
- Article
A case of atypical myelodysplastic syndrome with micromegakaryocytes, normal platelet count, and t(3;12)(q21;p13) with inv(3)(q21q26).
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 3, p. 292, doi. 10.1002/(SICI)1098-2264(199711)20:3<292::AID-GCC10>3.0.CO;2-R
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- Article
dic(9; 20): A new recurrent chromosome abnormality in adult acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 1995, v. 13, n. 1, p. 54, doi. 10.1002/gcc.2870130109
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- Publication type:
- Article
Neue Erkenntnisse in der Diagnostik chronischer myeloproliferativer Syndrome.
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- Medizinische Klinik (Urban & Vogel), 2007, v. 102, n. 9, p. 770
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- Publication type:
- Article
Microarray-Genexpressionsanalysen in der Leukämiediagnostik.
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- Medizinische Klinik (Urban & Vogel), 2006, v. 101, n. 11, p. 908, doi. 10.1007/s00063-006-1124-7
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- Publication type:
- Article
Re: Prognositc Significance of a Short Sequence Insertion of the MCL-1 Promoter in Chronic Lymphocytic Leukemia.
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- 2005
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- Publication type:
- Letter
Distinct gene expression patterns associated with FLT3- and NRAS-activating mutations in acute myeloid leukemia with normal karyotype.
- Published in:
- Oncogene, 2005, v. 24, n. 9, p. 1580, doi. 10.1038/sj.onc.1208344
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- Publication type:
- Article
The fusion protein AML1-ETO in acute myeloid leukemia with translocation t(8;21) induces c-jun protein expression via the proximal AP-1 site of the c-jun promoter in an indirect, JNK-dependent manner.
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- Oncogene, 2003, v. 22, n. 36, p. 5646, doi. 10.1038/sj.onc.1206673
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- Publication type:
- Article
Diagnostic Strategies in the Indication to Allogeneic Hematopoietic Transplantation in AML.
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- European Journal of Clinical & Medical Oncology, 2011, v. 3, n. 1, p. 14
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- Publication type:
- Article
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
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- Nature Genetics, 2013, v. 45, n. 1, p. 18, doi. 10.1038/ng.2495
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- Publication type:
- Article
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis.
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- British Journal of Haematology, 2013, v. 161, n. 5, p. 649, doi. 10.1111/bjh.12297
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- Article
EZH2 mutations and their association with PICALM-MLLT10 positive acute leukaemia.
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- British Journal of Haematology, 2012, v. 157, n. 3, p. 387, doi. 10.1111/j.1365-2141.2011.08986.x
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- Publication type:
- Article