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A case of pediatric acute myeloid leukemia with t(11;16)(q23;q24) leading to a novel KMT2A‐USP10 fusion gene.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 10, p. 522, doi. 10.1002/gcc.22646
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- Publication type:
- Article
Involvement of the MLL gene in adult T-lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2012, v. 51, n. 12, p. 1114, doi. 10.1002/gcc.21996
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- Publication type:
- Article
Acute leukemias with ETV6/ABL1 ( TEL/ABL) fusion: Poor prognosis and prenatal origin.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 10, p. 873, doi. 10.1002/gcc.20796
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- Publication type:
- Article
Covert preleukemia driven by MLL gene fusion.
- Published in:
- Genes, Chromosomes & Cancer, 2009, v. 48, n. 1, p. 98, doi. 10.1002/gcc.20622
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- Publication type:
- Article
Evolution of AF6-RAS association and its implications in mixed-lineage leukemia.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01326-5
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- Publication type:
- Article
Acute Promyelocytic Leukemia with a Rare PML Exon 4/RARA Exon 3 Fusion Transcript Variant.
- Published in:
- Acta Haematologica, 2013, v. 130, n. 3, p. 176, doi. 10.1159/000348551
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- Publication type:
- Article
Molecular Identification of a New Splicing Variant of the MLL-MLLT11 Fusion Transcript in an Adult with Acute Myeloid Leukemia and t(1;11)(q21;q23).
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- Acta Haematologica, 2012, v. 128, n. 3, p. 131, doi. 10.1159/000338258
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- Publication type:
- Article
Submicroscopic Deletion of FGFR1 Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with ZMYM2-FGFR1 Rearrangements: A Case Study.
- Published in:
- Acta Haematologica, 2012, v. 127, n. 2, p. 119, doi. 10.1159/000334707
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- Publication type:
- Article
De novo Acute Myeloid Leukemia Associated with t(11;17)(q23;q25) and MLL-SEPT9 Rearrangement in an Elderly Patient: A Case Study and Review of the Literature.
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- Acta Haematologica, 2011, v. 126, n. 4, p. 195, doi. 10.1159/000329389
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- Publication type:
- Article
Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.
- Published in:
- Acta Neuropathologica, 2011, v. 121, n. 6, p. 763, doi. 10.1007/s00401-011-0817-z
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- Publication type:
- Article
Genetic and clinical characterization of 45 acute leukemia patients with MLL gene rearrangements from a single institution
- Published in:
- Molecular Oncology, 2012, v. 6, n. 5, p. 553, doi. 10.1016/j.molonc.2012.06.004
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- Publication type:
- Article
Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
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- Molecular Oncology, 2011, v. 5, n. 6, p. 555, doi. 10.1016/j.molonc.2011.08.003
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- Publication type:
- Article
The distribution of MLL breakpoints correlates with outcome in infant acute leukaemia.
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- British Journal of Haematology, 2013, v. 161, n. 2, p. 224, doi. 10.1111/bjh.12250
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- Publication type:
- Article
CBL mutations do not frequently occur in paediatric acute myeloid leukaemia.
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- British Journal of Haematology, 2012, v. 159, n. 5, p. 577, doi. 10.1111/bjh.12068
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- Publication type:
- Article
TOP3A, a new partner gene fused to MLL in an adult patient with de novo acute myeloid leukaemia.
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- British Journal of Haematology, 2012, v. 157, n. 1, p. 128, doi. 10.1111/j.1365-2141.2011.08908.x
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- Publication type:
- Article
Acute monocytic leukaemia originating from MLL-MLLT3-positive pre-B cells.
- Published in:
- 2010
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- Publication type:
- Letter
FLNA, a new partner gene fused to MLL in a patient with acute myelomonoblastic leukaemia.
- Published in:
- 2009
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- Publication type:
- Letter
Complex MLL rearrangement in non-infiltrated bone marrow in an infant with stage II precursor B-lymphoblastic lymphoma.
- Published in:
- European Journal of Haematology, 2014, v. 93, n. 4, p. 349, doi. 10.1111/ejh.12314
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- Publication type:
- Article
Genomic DNA of leukemic patients: Target for clinical diagnosis of MLL rearrangements.
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- Biotechnology Journal, 2006, v. 1, n. 6, p. 656, doi. 10.1002/biot.200600037
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- Publication type:
- Article
Prenatal origin of KRAS mutation in a child with an acute myelomonocytic leukaemia bearing the KMT2A/MLL‐AFDN/MLLT4/AF6 fusion transcript.
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- British Journal of Haematology, 2019, v. 185, n. 3, p. 563, doi. 10.1111/bjh.15534
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- Publication type:
- Article
Subclonality and prenatal origin of RAS mutations in KMT2A (MLL)-rearranged infant acute lymphoblastic leukaemia.
- Published in:
- British Journal of Haematology, 2015, v. 170, n. 2, p. 268, doi. 10.1111/bjh.13279
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- Publication type:
- Article
Outcomes for Australian children with relapsed/refractory acute lymphoblastic leukaemia treated with blinatumomab.
- Published in:
- 2021
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- Publication type:
- journal article
Secondary acute monocytic leukemia positive for 11q23 rearrangement in Nijmegen breakage syndrome.
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, n. 8, p. 1469, doi. 10.1002/pbc.24994
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- Publication type:
- Article
Distinct pattern of genomic breakpoints in CML and BCR::ABL1-positive ALL: analysis of 971 patients.
- Published in:
- Molecular Cancer, 2024, v. 23, n. 1, p. 1, doi. 10.1186/s12943-024-02053-4
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- Publication type:
- Article
Dietary composition and nutrient content of the New Nordic Diet.
- Published in:
- Public Health Nutrition, 2013, v. 16, n. 5, p. 777, doi. 10.1017/S1368980012004521
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- Publication type:
- Article
Guidelines for the New Nordic Diet.
- Published in:
- 2012
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- Publication type:
- journal article
Novel Diagnostic and Therapeutic Options for KMT2A -Rearranged Acute Leukemias.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.749472
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- Publication type:
- Article
RE: Acute myeloid leukemia associated with FGFR1 abnormalities.
- Published in:
- 2013
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- Publication type:
- Letter
TEL/AML1-positive patients lacking TEL exon 5 resemble canonical TEL/AML1 cases.
- Published in:
- Pediatric Blood & Cancer, 2011, v. 56, n. 2, p. 217, doi. 10.1002/pbc.22686
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- Publication type:
- Article
ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia.
- Published in:
- BMC Cancer, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2407-14-127
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- Publication type:
- Article
ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia.
- Published in:
- 2014
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- Publication type:
- journal article
A novel spliced fusion of MLL with CT45A2 in a pediatric biphenotypic acute leukemia.
- Published in:
- BMC Cancer, 2010, v. 10, p. 518, doi. 10.1186/1471-2407-10-518
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- Publication type:
- Article
Prenatal origin of childhood AML occurs less frequently than in childhood ALL.
- Published in:
- BMC Cancer, 2006, v. 6, p. 100, doi. 10.1186/1471-2407-6-100
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- Publication type:
- Article
Editorial: Categorising Migrants: Standards, complexities, and politics.
- Published in:
- Anti-Trafficking Review, 2018, n. 11, p. 1, doi. 10.14197/atr.201218111
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- Publication type:
- Article
Acute myeloid leukemia with t(10;11)(p11‐12;q23.3): Results of Russian Pediatric AML registration study.
- Published in:
- International Journal of Laboratory Hematology, 2019, v. 41, n. 2, p. 287, doi. 10.1111/ijlh.12969
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- Publication type:
- Article
KMT2A-ARHGEF12, a therapy related fusion with poor prognosis.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 10, p. 7021, doi. 10.1007/s11033-021-06621-5
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- Publication type:
- Article
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
- Published in:
- 2017
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- Publication type:
- journal article
Acute promyelocytic leukemia with trisomy 8 showing normal PML-RARA FISH signal patterns: diagnostic application of long-distance polymerase chain reaction in molecularly discrepant leukemia cases.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Genomic analysis of a four-way t(4;11;22;10) associated with MLL-AF4 in an adult acute lymphoblastic leukemia.
- Published in:
- 2012
- By:
- Publication type:
- Letter
A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques.
- Published in:
- 2009
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- Publication type:
- case study
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
- Published in:
- Cytogenetic & Genome Research, 2019, v. 157, n. 3, p. 213, doi. 10.1159/000499640
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- Publication type:
- Article
Identification of a Cryptic Insertion ins(11;X) (q23;q28q12) Resulting in a KMT2A - FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia.
- Published in:
- Cytogenetic & Genome Research, 2017, v. 150, n. 3/4, p. 281, doi. 10.1159/000458165
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- Publication type:
- Article