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Genetic alterations and their clinical implications in older patients with acute myeloid leukemia

Leukemia, 2016-07, Vol.30 (7), p.1485-1492

2016

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The prognostic impact and stability of Isocitrate dehydrogenase 2 mutation in adult patients with acute myeloid leukemia

Leukemia, 2011-02, Vol.25 (2), p.246-253

2011

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Epidemiology of bloodstream infections in patients with haematological malignancies with and without neutropenia

Epidemiology and infection, 2010-07, Vol.138 (7), p.1044-1051

2010

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Prognostic significance of NPM1 mutation-modulated microRNA−mRNA regulation in acute myeloid leukemia

Leukemia, 2016-02, Vol.30 (2), p.274-284

2016

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Overexpression of FLT3-ITD driven by spi-1 results in expanded myelopoiesis with leukemic phenotype in zebrafish

Leukemia, 2016-10, Vol.30 (10), p.2098-2101

2016

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Calreticulin mutation was rarely detected in patients with myelodysplastic syndrome

Leukemia, 2014-07, Vol.28 (7), p.1555-1557

2014

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Persistence of mutant isocitrate dehydrogenase in patients with acute myeloid leukemia in remission

Leukemia, 2012-03, Vol.26 (3), p.527-529

2012

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CEBPA methylation as a prognostic biomarker in patients with de novo acute myeloid leukemia

Leukemia, 2011-01, Vol.25 (1), p.32-40

2011

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P422: OMIPALISIB, A DUAL PI3K/MTOR INHIBITOR, TARGETS MITOCHONDRIA AND IMPAIRS OXIDATIVE PHOSPHORYLATION IN ACUTE MYELOID LEUKEMIA

HemaSphere, 2022-06, Vol.6, p.322-323

2022

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Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patients

Leukemia, 2009-07, Vol.23 (7), p.1303-1310

2009

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A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias

Leukemia, 2006-10, Vol.20 (10), p.1899-1903

2006

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Clinical significance of cytogenetics and interphase fluorescence in situ hybridization analysis in newly diagnosed multiple myeloma in Taiwan

Annals of oncology, 2005-09, Vol.16 (9), p.1530-1538

2005

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Overexpression of SOX4 correlates with poor prognosis of acute myeloid leukemia and is leukemogenic in zebrafish

Blood cancer journal (New York), 2017-08, Vol.7 (8), p.e593-e593

2017

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p210Bcr−Abl desensitizes Cdc42 GTPase signaling for SDF-1α-directed migration in chronic myeloid leukemia cells

Oncogene, 2009-11, Vol.28 (46), p.4105-4115

2009

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KINOME EXPRESSION PROFILING FOR RISK STRATIFICATION OF MYELODYSPLASTIC SYNDROMES

Leukemia research reports, 2024, Vol.21, p.100433, Article 100433

2024

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Reply to ‘Heterogeneity within AML with CEBPA mutations; only CEBPA double mutations, but not single CEBPA mutations are associated with favorable prognosis’

British journal of cancer, 2009-08, Vol.101 (4), p.738-740

2009

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S131: CLINICAL IMPLICATIONS OF SECONDARY‐AML TYPE MUTATIONS IN PATIENTS WITH DE NOVO ACUTE MYELOID LEUKEMIA

HemaSphere, 2022-06, Vol.6 (Suppl), p.32-33

2022

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Acute and chronic arsenic poisoning associated with treatment of acute promyelocytic leukaemia

British journal of haematology, 1998-12, Vol.103 (4), p.1092-1095

1998

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Splenic actinomycotic abscess in a patient with acute myeloid leukemia

Annals of hematology, 2002-09, Vol.81 (9), p.532-534

2002

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Methylation of the p15(INK4B) gene in myelodysplastic syndrome: it can be detected early at diagnosis or during disease progression and is highly associated with leukaemic transformation

British journal of haematology, 2001-01, Vol.112 (1), p.148-154

2001

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Minimally differentiated acute myeloid leukemia in Taiwan: predominantly occurs in children less than 3 years and adults between 51 and 70 years

Leukemia, 1999-10, Vol.13 (10), p.1506-1512

1999

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A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias

Leukemia, 2007-10, Vol.21 (10), p.2236

2007

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329 Similar survival between reduced intensity and myeloablative conditioning in MDS patients receiving allogeneic stem cell transplantation

Leukemia research, 2011, Vol.35, p.S132-S132

2011

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Genetic alterations and their clinical implications in older patients with acute myeloid leukemia

Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia

The prognostic impact and stability of Isocitrate dehydrogenase 2 mutation in adult patients with acute myeloid leukemia

Epidemiology of bloodstream infections in patients with haematological malignancies with and without neutropenia

Prognostic significance of NPM1 mutation-modulated microRNA−mRNA regulation in acute myeloid leukemia

Overexpression of FLT3-ITD driven by spi-1 results in expanded myelopoiesis with leukemic phenotype in zebrafish

Calreticulin mutation was rarely detected in patients with myelodysplastic syndrome

Persistence of mutant isocitrate dehydrogenase in patients with acute myeloid leukemia in remission

CEBPA methylation as a prognostic biomarker in patients with de novo acute myeloid leukemia

P422: OMIPALISIB, A DUAL PI3K/MTOR INHIBITOR, TARGETS MITOCHONDRIA AND IMPAIRS OXIDATIVE PHOSPHORYLATION IN ACUTE MYELOID LEUKEMIA

Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patients

A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias

Clinical significance of cytogenetics and interphase fluorescence in situ hybridization analysis in newly diagnosed multiple myeloma in Taiwan

Overexpression of SOX4 correlates with poor prognosis of acute myeloid leukemia and is leukemogenic in zebrafish

p210Bcr−Abl desensitizes Cdc42 GTPase signaling for SDF-1α-directed migration in chronic myeloid leukemia cells

KINOME EXPRESSION PROFILING FOR RISK STRATIFICATION OF MYELODYSPLASTIC SYNDROMES

Reply to ‘Heterogeneity within AML with CEBPA mutations; only CEBPA double mutations, but not single CEBPA mutations are associated with favorable prognosis’

S131: CLINICAL IMPLICATIONS OF SECONDARY‐AML TYPE MUTATIONS IN PATIENTS WITH DE NOVO ACUTE MYELOID LEUKEMIA

Acute and chronic arsenic poisoning associated with treatment of acute promyelocytic leukaemia

Erratum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia

Splenic actinomycotic abscess in a patient with acute myeloid leukemia

Methylation of the p15(INK4B) gene in myelodysplastic syndrome: it can be detected early at diagnosis or during disease progression and is highly associated with leukaemic transformation

Minimally differentiated acute myeloid leukemia in Taiwan: predominantly occurs in children less than 3 years and adults between 51 and 70 years

A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias

329 Similar survival between reduced intensity and myeloablative conditioning in MDS patients receiving allogeneic stem cell transplantation

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