about
RAS mutations in early age leukaemia modulated by NQO1 rs1800566 (C609T) are associated with second-hand smoking exposures.The MLL recombinome of acute leukemias in 2013.ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia.Polymorphisms in CYP1B1, CYP3A5, GSTT1, and SULT1A1 Are Associated with Early Age Acute LeukemiaEvaluation of multiplex ligation dependent probe amplification (MLPA) for identification of acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21 (iAMP21) in a Brazilian population.Distinctive genotypes in infants with T-cell acute lymphoblastic leukaemia.Acute leukemia in early childhood.Development and perspective of current Brazilian studies on the epidemiology of childhood leukemia.COBL is a novel hotspot for IKZF1 deletions in childhood acute lymphoblastic leukemia.Osteopontin and their roles in hematological malignancies: Splice variants on the new avenues.The MLL recombinome of acute leukemias in 2017.Maternal Alcohol Consumption during Pregnancy and Early Age Leukemia Risk in Brazil.Prognostic value of rare IKZF1 deletion in childhood B-cell precursor acute lymphoblastic leukemia: an international collaborative study.N-acetyltransferase 2 polymorphisms and susceptibility to infant leukemia with maternal exposure to dipyrone during pregnancy.Clinical and molecular epidemiology of neonatal leukemia in Brazil.The distribution of MLL breakpoints correlates with outcome in infant acute leukaemia.MTHFR 677C-->T and 1298A-->C polymorphisms in children with Down syndrome and acute myeloid leukemia in Brazil.The role of methylenetetrahydrofolate reductase in acute lymphoblastic leukemia in a Brazilian mixed population.The role of RAS mutations in MLL-rearranged leukaemia: A path to intervention?IKZF1 Gene in Childhood B-cell Precursor Acute Lymphoblastic Leukemia: Interplay between Genetic Susceptibility and Somatic Abnormalities.Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.Cytosine arabinoside-metabolizing enzyme genes are underexpressed in children with MLL gene-rearranged acute lymphoblastic leukemia.Frequency of copy number abnormalities in common genes associated with B-cell precursor acute lymphoblastic leukemia cytogenetic subtypes in Brazilian children.NQO1 rs1800566 (C609T), PON1 rs662 (Q192R), and PON1 rs854560 (L55M) polymorphisms segregate the risk of childhood acute leukemias according to age range distribution.Functional analysis of the two reciprocal fusion genes MLL-NEBL and NEBL-MLL reveal their oncogenic potential.Backtracking to birth of the NUP98-HOXD13 gene fusion in an infant acute myeloid leukemia.Impact of mutations in FLT3, PTPN11 and RAS genes on the overall survival of pediatric B cell precursor acute lymphoblastic leukemia in Brazil.Molecular cytogenetic findings of acute leukemia included in the Brazilian Collaborative Study Group of Infant acute leukemia.Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.Subclonality and prenatal origin ofRASmutations inKMT2A (MLL)-rearranged infant acute lymphoblastic leukaemiaConcordant B-cell precursor acute lymphoblastic leukemia in non-twinned siblingsGenetic variability inN-acetyltransferase 2gene determines susceptibility to childhood lymphoid or myeloid leukemia in BrazilChallenges in the use of NG2 antigen as a marker to predict MLL rearrangements in multi-center studiesOccurrence of identical NOTCH1 mutation in non-twinned sisters with T-cell acute lymphoblastic leukemiaT-cell lymphoblastic leukemia in early childhood presents NOTCH1 mutations and MLL rearrangementsETV6–RUNX1 fusion gene and additional genetic changes in infant leukemia: a genome-wide analysisA novel PAX5 rearrangement in TCF3-PBX1 acute lymphoblastic leukemia: a case reportValidation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALLMolecular studies reveal a MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotypeGATA1 mutations in acute leukemia in children with Down syndrome
P50
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P50
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հետազոտող
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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M Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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Mariana Emerenciano
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P1053
I-2813-2014
P106
P21
P31
P3829
P496
0000-0003-2337-8420