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Distinct Responses to Menin Inhibition and Synergy with DOT1L Inhibition in KMT2A -Rearranged Acute Lymphoblastic and Myeloid Leukemia

International journal of molecular sciences, 2024-06, Vol.25 (11), p.6020

2024

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CRISPR-Cas9 Library Screening Identifies Novel Molecular Vulnerabilities in KMT2A-Rearranged Acute Lymphoblastic Leukemia

International journal of molecular sciences, 2023-09, Vol.24 (17), p.13207

2023

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Techno-economic study of a zero-emission methanol based energy storage system

Energy conversion and management, 2019-02, Vol.182, p.530-545

2019

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Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

Haematologica (Roma), 2011-10, Vol.96 (10), p.1478-1487

2011

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Low frequency of DNMT3A mutations in pediatric AML, and the identification of the OCI-AML3 cell line as an in vitro model

Leukemia, 2012-02, Vol.26 (2), p.371-373

2012

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Fate of thiamethoxam from treated seeds in mesocosms and response of aquatic invertebrate communities

Ecotoxicology (London), 2022-03, Vol.31 (2), p.341-356

2022

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Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia

Blood, 2009-06, Vol.113 (23), p.5951-5960

2009

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High-Throughput Drug Library Screening in Primary KMT2A -Rearranged Infant ALL Cells Favors the Identification of Drug Candidates That Activate P53 Signaling

Biomedicines, 2022-03, Vol.10 (3), p.638

2022

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EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

Leukemia, 2010-05, Vol.24 (5), p.942-949

2010

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Selective inhibition of HDAC class IIA as therapeutic intervention for KMT2A-rearranged acute lymphoblastic leukemia

Communications biology, 2024-10, Vol.7 (1), p.1257-11, Article 1257

2024

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Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML

Leukemia, 2009-02, Vol.23 (2), p.262-270

2009

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Facilitators, Barriers, and Best Practices for In-Person and Telehealth Lactation Support During the COVID-19 Pandemic

Nursing for women's health, 2022-12, Vol.26 (6), p.420-428

2022

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NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern

Leukemia, 2013-12, Vol.27 (12), p.2280-2288

2013

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NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

Blood, 2011-09, Vol.118 (13), p.3645-3656

2011

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High BRE expression in pediatric MLL-rearranged AML is associated with favorable outcome

Leukemia, 2010-12, Vol.24 (12), p.2048-2055

2010

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Green certificate trading in the Netherlands in the prospect of the European electricity market

Energy policy, 2003-06, Vol.31 (7), p.609-620

2003

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Green electricity in the market place: the policy challenge

Energy policy, 2002-05, Vol.30 (6), p.525-538

2002

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CBL mutations do not frequently occur in paediatric acute myeloid leukaemia

British journal of haematology, 2012-12, Vol.159 (5), p.577-584

2012

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BCOR and BCORL1 mutations in pediatric acute myeloid leukemia

Haematologica (Roma), 2015-05, Vol.100 (5), p.e194-e195

2015

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The clinical relevance of BAALC and ERG expression levels in pediatric AML

Leukemia, 2013-03, Vol.27 (3), p.735-737

2013

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Preclinical efficacy of gemcitabine in MLL-rearranged infant acute lymphoblastic leukemia

Leukemia, 2020-11, Vol.34 (11), p.2898-2902

2020

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Unique BHLHB3 overexpression in pediatric acute myeloid leukemia with t(6;11)(q27;q23)

Leukemia, 2014-07, Vol.28 (7), p.1564-1568

2014

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Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutation

Journal of medical genetics, 2017-12, Vol.54 (12), p.805-808

2017

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MN1 overexpression is driven by loss of DNMT3B methylation activity in inv(16) pediatric AML

Oncogene, 2018-01, Vol.37 (1), p.107-115

2018

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Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias

International journal of hematology, 2015-07, Vol.102 (1), p.140-143

2015

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Distinct Responses to Menin Inhibition and Synergy with DOT1L Inhibition in KMT2A -Rearranged Acute Lymphoblastic and Myeloid Leukemia

CRISPR-Cas9 Library Screening Identifies Novel Molecular Vulnerabilities in KMT2A-Rearranged Acute Lymphoblastic Leukemia

Techno-economic study of a zero-emission methanol based energy storage system

Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

Low frequency of DNMT3A mutations in pediatric AML, and the identification of the OCI-AML3 cell line as an in vitro model

Fate of thiamethoxam from treated seeds in mesocosms and response of aquatic invertebrate communities

Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia

High-Throughput Drug Library Screening in Primary KMT2A -Rearranged Infant ALL Cells Favors the Identification of Drug Candidates That Activate P53 Signaling

EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

Selective inhibition of HDAC class IIA as therapeutic intervention for KMT2A-rearranged acute lymphoblastic leukemia

Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML

Facilitators, Barriers, and Best Practices for In-Person and Telehealth Lactation Support During the COVID-19 Pandemic

NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

High BRE expression in pediatric MLL-rearranged AML is associated with favorable outcome

Green certificate trading in the Netherlands in the prospect of the European electricity market

Green electricity in the market place: the policy challenge

CBL mutations do not frequently occur in paediatric acute myeloid leukaemia

BCOR and BCORL1 mutations in pediatric acute myeloid leukemia

The clinical relevance of BAALC and ERG expression levels in pediatric AML

Preclinical efficacy of gemcitabine in MLL-rearranged infant acute lymphoblastic leukemia

Unique BHLHB3 overexpression in pediatric acute myeloid leukemia with t(6;11)(q27;q23)

Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutation

MN1 overexpression is driven by loss of DNMT3B methylation activity in inv(16) pediatric AML

Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias

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