논문상세정보
Alteration of the SETBP1 Gene and Splicing Pathway Genes SF3B1, U2AF1, and SRSF2 in Childhood Acute Myeloid Leukemia
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Alteration of the SETBP1 Gene and Splicing Pathway Genes SF3B1, U2AF1, and SRSF2 in Childhood Acute Myeloid Leukemia' 의 주제별 논문영향력
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| 동일주제 총논문수 | 논문피인용 총횟수 | 주제별 논문영향력의 평균 |
| 7,576 | 0 |
0.0% |
주제별 논문영향력
' Alteration of the SETBP1 Gene and Splicing Pathway Genes SF3B1, U2AF1, and SRSF2 in Childhood Acute Myeloid Leukemia' 의 참고문헌
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WT1synonymous single nucleotide polymorphism rs16754 correlates with higher mRNA expression and predicts significantly improved outcome in favorable-risk pediatric acute myeloid leukemia: a report from the children’s oncology group
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WT1 synonymous single nucleotide polymorphism rs16754 correlates with higher mRNA expression and predicts significantly improved outcome in favorable-riskpediatric acute myeloid leukemia: a report from the children’s oncology group
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U.S. National Library of Medicine, SNP database
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Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia
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Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia
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Spectra of Chromosomal Aberrations in 325 Leukemia Patients and Implications for the Development of New Molecular Detection Systems
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Spectra of Chromosomal Aberrations in 325 Leukemia Patients and Implications for the Development of New Molecular Detection Systems
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Single nucleotide polymorphism in the mutational hotspot of WT1predicts a favorable outcome in patients with cytogenetically normal acute myeloid leukemia
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Single nucleotide polymorphism in the mutational hotspot of WT1 predicts a favorable outcome in patients with cytogenetically normal acute myeloid leukemia
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Silent (synonymous) SNPs: should we care about them?
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Silent (synonymous) SNPs: should we care about them?
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SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia
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SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia
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SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia
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SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia
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SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid leukemias
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SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid leukemias
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SETBP1 mutation analysis in 944 patients with MDS and AML
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SETBP1 mutation analysis in 944 patients with MDS and AML
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
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Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children’s Oncology Group and SWOG
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Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children’s Oncology Group and SWOG
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Myeloid malignancies: mutations, models and management
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Myeloid malignancies: mutations, models and management
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Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
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Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
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Mutational analysis of splicing machinery genes SF3B1, U2AF1 and SRSF2 in myelodysplasia and other common tumors
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Mutational analysis of splicing machinery genes SF3B1, U2AF1 and SRSF2 in myelodysplasia and other common tumors
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Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET
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Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET
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Hearing silence: non-neutral evolution at synonymous sites in mammals
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Hearing silence: non-neutral evolution at synonymous sites in mammals
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Frequent pathway mutations of splicing machinery in myelodysplasia
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Frequent pathway mutations of splicing machinery in myelodysplasia
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Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel
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Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel
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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
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Cooperating gene mutations in childhood acute myeloid leukemia with special reference on mutations of ASXL1, TET2, IDH1, IDH2, and DNMT3A
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Cooperating gene mutations in childhood acute myeloid leukemia with special reference on mutations of ASXL1, TET2, IDH1, IDH2, and DNMT3A