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Clinical features and prognostic impact of PRDM16 expression in adult acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 11, p. 800, doi. 10.1002/gcc.22483
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- Article
Prognostic impact of specific molecular profiles in pediatric acute megakaryoblastic leukemia in non-Down syndrome.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 5, p. 394, doi. 10.1002/gcc.22444
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- Article
ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 5, p. 382, doi. 10.1002/gcc.22443
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- Article
NUP98- NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 7, p. 683, doi. 10.1002/gcc.22064
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- Article
Mutation and expression analyses of the MET and CDKN2A genes in rhabdomyosarcoma with emphasis on MET overexpression.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 4, p. 348, doi. 10.1002/gcc.20416
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- Article
Inherited chromosomally integrated human herpesvirus‐6 in a patient with XIAP deficiency.
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- Transplant Infectious Disease, 2020, v. 22, n. 5, p. 1, doi. 10.1111/tid.13331
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- Article
Corrigendum: The landscape of somatic mutations in Down syndrome-related myeloid disorders.
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- Nature Genetics, 2013, v. 45, n. 12, p. 1516, doi. 10.1038/ng1213-1516
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- Article
The landscape of somatic mutations in Down syndrome-related myeloid disorders.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1293, doi. 10.1038/ng.2759
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- Article
Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis.
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- Nephrology Dialysis Transplantation, 2013, v. 28, n. 8, p. 2123, doi. 10.1093/ndt/gft216
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- Article
CBL mutations in infant acute lymphoblastic leukaemia.
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- British Journal of Haematology, 2012, v. 156, n. 5, p. 672, doi. 10.1111/j.1365-2141.2011.08900.x
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- Article
DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.
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- British Journal of Haematology, 2012, v. 156, n. 3, p. 413, doi. 10.1111/j.1365-2141.2011.08879.x
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- Article
Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 476, doi. 10.1111/bjh.14247
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- Article
High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3- ITD, KMT2A- PTD, and NUP98- NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial.
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- British Journal of Haematology, 2016, v. 172, n. 4, p. 581, doi. 10.1111/bjh.13869
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- Article
CSF3R and CALR mutations in paediatric myeloid disorders and the association of CSF3R mutations with translocations, including t(8; 21).
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- British Journal of Haematology, 2015, v. 170, n. 3, p. 391, doi. 10.1111/bjh.13439
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- Article
SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia.
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- British Journal of Haematology, 2014, v. 164, n. 1, p. 156, doi. 10.1111/bjh.12595
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- Article
Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia.
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- British Journal of Haematology, 2014, v. 164, n. 1, p. 142, doi. 10.1111/bjh.12559
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- Article
Clinical features of 35 Down syndrome patients with transient abnormal myelopoiesis at a single institution.
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- International Journal of Hematology, 2021, v. 113, n. 5, p. 662, doi. 10.1007/s12185-020-03066-7
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- Article
WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group.
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- International Journal of Hematology, 2013, v. 98, n. 4, p. 437, doi. 10.1007/s12185-013-1409-6
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- Article
RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group.
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- International Journal of Hematology, 2012, v. 95, n. 5, p. 509, doi. 10.1007/s12185-012-1033-x
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- Article
NOTCH1 mutation in a female with myeloid/NK cell precursor acute leukemia.
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- Pediatric Blood & Cancer, 2010, v. 55, n. 7, p. 1406, doi. 10.1002/pbc.22758
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- Article