Current Environment: Production

Scott Armstrong | Education

Medical School

University of Texas Southwestern Medical School

1996, Dallas, TX

Internship

Boston Combined Residency Program (BCRP)

1998, Boston, MA

Residency

Boston Combined Residency Program (BCRP)

1998, Boston, MA

Fellowship

Dana-Farber/Boston Children's Cancer and Blood Disorders Center

2001, Boston, MA

Scott Armstrong | Professional History

Scott A. Armstrong, MD, PhD, became the President of Dana-Farber/Boston Children’s Cancer and Blood Disorders Center in 2019 and has been Chairman of the Department of Pediatric Oncology at Dana-Farber Cancer Institute since 2016. He also serves as Associate Chief of the Division of Hematology/Oncology at Boston Children’s Hospital. He was previously the Director of the Center for Epigenetics Research at Memorial Sloan Kettering Cancer Center and Professor of Pediatrics at the Weill Cornell Medical College. Dr. Armstrong earned his medical degree and his PhD from University of Texas Southwestern Medical School in 1996. After internship and residency training with the Boston Combined Residency Program (BCRP) at Boston Medical Center and Boston Children’s Hospital, he completed a hematology/oncology fellowship at Dana-Farber/Boston Children’s Cancer and Blood Disorders Center.

The major focus of his career has been on delineating the biology of childhood cancers and the development of new therapeutic approaches for children with cancer. His research program has focused on the mechanisms of leukemia development and the relationship between leukemia and normal hematopoietic stem cells. He continues to direct a vigorous research program that focuses on development of new therapeutics that target chromatin based mechanisms, and he is actively involved in the development and translation of a number of new small molecule approaches that likely will be tested in clinical trials in the near future.

Scott Armstrong | Publications

  1. The Prolonged Half-Life of the p53 Missense Variant R248Q Promotes Accumulation and Heterotetramer Formation with Wildtype p53 to Exert the Dominant-Negative Effect. Cancer Res. 2025 Mar 31. View The Prolonged Half-Life of the p53 Missense Variant R248Q Promotes Accumulation and Heterotetramer Formation with Wildtype p53 to Exert the Dominant-Negative Effect. Abstract

  2. Targeting the Menin-KMT2A interaction in leukemia: Lessons learned and future directions. Int J Cancer. 2025 Jan 30. View Targeting the Menin-KMT2A interaction in leukemia: Lessons learned and future directions. Abstract

  3. Epigenetic Therapies. Cold Spring Harb Perspect Med. 2024 Dec 18. View Epigenetic Therapies. Abstract

  4. Catalytic inhibition of KAT6/KAT7 enhances the efficacy and overcomes primary and acquired resistance to Menin inhibitors in MLL leukaemia. bioRxiv. 2024 Dec 12. View Catalytic inhibition of KAT6/KAT7 enhances the efficacy and overcomes primary and acquired resistance to Menin inhibitors in MLL leukaemia. Abstract

  5. Revumenib Revises the Treatment Landscape for KMT2A-r Leukemia. J Clin Oncol. 2025 Jan; 43(1):85-88. View Revumenib Revises the Treatment Landscape for KMT2A-r Leukemia. Abstract

  6. NUP98 fusion proteins and KMT2A-MENIN antagonize PRC1.1 to drive gene expression in AML. Cell Rep. 2024 11 26; 43(11):114901. View NUP98 fusion proteins and KMT2A-MENIN antagonize PRC1.1 to drive gene expression in AML. Abstract

  7. CRISPR Dependency Screens in Primary Hematopoietic Stem Cells Identify KDM3B as a Genotype-specific Vulnerability in IDH2- and TET2-mutant Cells. Cancer Discov. 2024 Oct 04; 14(10):1860-1878. View CRISPR Dependency Screens in Primary Hematopoietic Stem Cells Identify KDM3B as a Genotype-specific Vulnerability in IDH2- and TET2-mutant Cells. Abstract

  8. Preclinical efficacy of the potent, selective menin-KMT2A inhibitor JNJ-75276617 (bleximenib) in KMT2A- and NPM1-altered leukemias. Blood. 2024 09 12; 144(11):1206-1220. View Preclinical efficacy of the potent, selective menin-KMT2A inhibitor JNJ-75276617 (bleximenib) in KMT2A- and NPM1-altered leukemias. Abstract

  9. A MOZ-TIF2 leukemia mouse model displays KAT6-dependent H3K23 propionylation and overexpression of a set of active developmental genes. Proc Natl Acad Sci U S A. 2024 Jun 25; 121(26):e2405905121. View A MOZ-TIF2 leukemia mouse model displays KAT6-dependent H3K23 propionylation and overexpression of a set of active developmental genes. Abstract

  10. PI3K? maintains the self-renewal of acute myeloid leukemia stem cells by regulating the pentose phosphate pathway. Blood. 2024 05 09; 143(19):1965-1979. View PI3K? maintains the self-renewal of acute myeloid leukemia stem cells by regulating the pentose phosphate pathway. Abstract

  11. Mezigdomide is effective alone and in combination with menin inhibition in preclinical models of KMT2A-r and NPM1c AML. Blood. 2024 04 11; 143(15):1513-1527. View Mezigdomide is effective alone and in combination with menin inhibition in preclinical models of KMT2A-r and NPM1c AML. Abstract

  12. Therapeutic targeting Tudor domains in leukemia via CRISPR-Scan Assisted Drug Discovery. Sci Adv. 2024 Feb 23; 10(8):eadk3127. View Therapeutic targeting Tudor domains in leukemia via CRISPR-Scan Assisted Drug Discovery. Abstract

  13. Inherited blood cancer predisposition through altered transcription elongation. Cell. 2024 Feb 01; 187(3):642-658.e19. View Inherited blood cancer predisposition through altered transcription elongation. Abstract

  14. Immunoproteasome function maintains oncogenic gene expression in KMT2A-complex driven leukemia. Mol Cancer. 2023 12 04; 22(1):196. View Immunoproteasome function maintains oncogenic gene expression in KMT2A-complex driven leukemia. Abstract

  15. The future of HOXA- expressing leukemias: Menin inhibitor response and resistance. Curr Opin Hematol. 2024 03 01; 31(2):64-70. View The future of HOXA- expressing leukemias: Menin inhibitor response and resistance. Abstract

  16. Epitope editing enables targeted immunotherapy of acute myeloid leukaemia. Nature. 2023 Sep; 621(7978):404-414. View Epitope editing enables targeted immunotherapy of acute myeloid leukaemia. Abstract

  17. KDM6A epigenetically regulates subtype plasticity in small cell lung cancer. Nat Cell Biol. 2023 09; 25(9):1346-1358. View KDM6A epigenetically regulates subtype plasticity in small cell lung cancer. Abstract

  18. UBR5 forms ligand-dependent complexes on chromatin to regulate nuclear hormone receptor stability. Mol Cell. 2023 08 03; 83(15):2753-2767.e10. View UBR5 forms ligand-dependent complexes on chromatin to regulate nuclear hormone receptor stability. Abstract

  19. MLL3 regulates the CDKN2A tumor suppressor locus in liver cancer. Elife. 2023 06 01; 12. View MLL3 regulates the CDKN2A tumor suppressor locus in liver cancer. Abstract

  20. MEN1 mutations mediate clinical resistance to menin inhibition. Nature. 2023 03; 615(7954):913-919. View MEN1 mutations mediate clinical resistance to menin inhibition. Abstract

  21. The menin inhibitor revumenib in KMT2A-rearranged or NPM1-mutant leukaemia. Nature. 2023 03; 615(7954):920-924. View The menin inhibitor revumenib in KMT2A-rearranged or NPM1-mutant leukaemia. Abstract

  22. Mutant NPM1 Directly Regulates Oncogenic Transcription in Acute Myeloid Leukemia. Cancer Discov. 2023 03 01; 13(3):746-765. View Mutant NPM1 Directly Regulates Oncogenic Transcription in Acute Myeloid Leukemia. Abstract

  23. A Molecular Switch between Mammalian MLL Complexes Dictates Response to Menin-MLL Inhibition. Cancer Discov. 2023 01 09; 13(1):146-169. View A Molecular Switch between Mammalian MLL Complexes Dictates Response to Menin-MLL Inhibition. Abstract

  24. SETD2 Haploinsufficiency Enhances Germinal Center-Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis. Cancer Discov. 2022 07 06; 12(7):1782-1803. View SETD2 Haploinsufficiency Enhances Germinal Center-Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis. Abstract

  25. MOZ and Menin-MLL Complexes Are Complementary Regulators of Chromatin Association and Transcriptional Output in Gastrointestinal Stromal Tumor. Cancer Discov. 2022 07 06; 12(7):1804-1823. View MOZ and Menin-MLL Complexes Are Complementary Regulators of Chromatin Association and Transcriptional Output in Gastrointestinal Stromal Tumor. Abstract

  26. IKAROS and MENIN coordinate therapeutically actionable leukemogenic gene expression in MLL-r acute myeloid leukemia. Nat Cancer. 2022 05; 3(5):595-613. View IKAROS and MENIN coordinate therapeutically actionable leukemogenic gene expression in MLL-r acute myeloid leukemia. Abstract

  27. Antigen presentation safeguards the integrity of the hematopoietic stem cell pool. Cell Stem Cell. 2022 05 05; 29(5):760-775.e10. View Antigen presentation safeguards the integrity of the hematopoietic stem cell pool. Abstract

  28. Bone Marrow Surveillance of Pediatric Cancer Survivors Identifies Clones that Predict Therapy-Related Leukemia. Clin Cancer Res. 2022 04 14; 28(8):1614-1627. View Bone Marrow Surveillance of Pediatric Cancer Survivors Identifies Clones that Predict Therapy-Related Leukemia. Abstract

  29. MLL::AF9 degradation induces rapid changes in transcriptional elongation and subsequent loss of an active chromatin landscape. Mol Cell. 2022 03 17; 82(6):1140-1155.e11. View MLL::AF9 degradation induces rapid changes in transcriptional elongation and subsequent loss of an active chromatin landscape. Abstract

  30. The menin-MLL1 interaction is a molecular dependency in NUP98-rearranged AML. Blood. 2022 02 10; 139(6):894-906. View The menin-MLL1 interaction is a molecular dependency in NUP98-rearranged AML. Abstract

  31. Menin Inhibitors in Acute Myeloid Leukemia-What Does the Future Hold? Cancer J. 2022 Jan-Feb 01; 28(1):62-66. View Menin Inhibitors in Acute Myeloid Leukemia-What Does the Future Hold? Abstract

  32. YBX1 mediates translation of oncogenic transcripts to control cell competition in AML. Leukemia. 2022 02; 36(2):426-437. View YBX1 mediates translation of oncogenic transcripts to control cell competition in AML. Abstract

  33. Evaluation of the Efficacy of Doxycycline, Ciprofloxacin, Levofloxacin, and Co-trimoxazole Using In Vitro and In Vivo Models of Q Fever. Antimicrob Agents Chemother. 2021 10 18; 65(11):e0067321. View Evaluation of the Efficacy of Doxycycline, Ciprofloxacin, Levofloxacin, and Co-trimoxazole Using In Vitro and In Vivo Models of Q Fever. Abstract

  34. Taspase1 orchestrates fetal liver hematopoietic stem cell and vertebrae fates by cleaving TFIIA. JCI Insight. 2021 08 09; 6(15). View Taspase1 orchestrates fetal liver hematopoietic stem cell and vertebrae fates by cleaving TFIIA. Abstract

  35. High-resolution characterization of gene function using single-cell CRISPR tiling screen. Nat Commun. 2021 07 01; 12(1):4063. View High-resolution characterization of gene function using single-cell CRISPR tiling screen. Abstract

  36. A JAK/STAT-mediated inflammatory signaling cascade drives oncogenesis in AF10-rearranged AML. Blood. 2021 06 17; 137(24):3403-3415. View A JAK/STAT-mediated inflammatory signaling cascade drives oncogenesis in AF10-rearranged AML. Abstract

  37. Histone PTM Crosstalk Stimulates Dot1 Methyltransferase Activity. Trends Biochem Sci. 2021 07; 46(7):522-524. View Histone PTM Crosstalk Stimulates Dot1 Methyltransferase Activity. Abstract

  38. Pathological angiogenesis in retinopathy engages cellular senescence and is amenable to therapeutic elimination via BCL-xL inhibition. Cell Metab. 2021 04 06; 33(4):818-832.e7. View Pathological angiogenesis in retinopathy engages cellular senescence and is amenable to therapeutic elimination via BCL-xL inhibition. Abstract

  39. HAND1 and BARX1 Act as Transcriptional and Anatomic Determinants of Malignancy in Gastrointestinal Stromal Tumor. Clin Cancer Res. 2021 03 15; 27(6):1706-1719. View HAND1 and BARX1 Act as Transcriptional and Anatomic Determinants of Malignancy in Gastrointestinal Stromal Tumor. Abstract

  40. Targeting Chromatin Complexes in Myeloid Malignancies and Beyond: From Basic Mechanisms to Clinical Innovation. Cells. 2020 12 21; 9(12). View Targeting Chromatin Complexes in Myeloid Malignancies and Beyond: From Basic Mechanisms to Clinical Innovation. Abstract

  41. Synergistic targeting of FLT3 mutations in AML via combined menin-MLL and FLT3 inhibition. Blood. 2020 11 19; 136(21):2442-2456. View Synergistic targeting of FLT3 mutations in AML via combined menin-MLL and FLT3 inhibition. Abstract

  42. Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors. Nat Genet. 2020 Nov; 52(11):1265. View Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors. Abstract

  43. Novel inhibitors of the histone methyltransferase DOT1L show potent antileukemic activity in patient-derived xenografts. Blood. 2020 10 22; 136(17):1983-1988. View Novel inhibitors of the histone methyltransferase DOT1L show potent antileukemic activity in patient-derived xenografts. Abstract

  44. Paediatric Strategy Forum for medicinal product development of epigenetic modifiers for children: ACCELERATE in collaboration with the European Medicines Agency with participation of the Food and Drug Administration. Eur J Cancer. 2020 11; 139:135-148. View Paediatric Strategy Forum for medicinal product development of epigenetic modifiers for children: ACCELERATE in collaboration with the European Medicines Agency with participation of the Food and Drug Administration. Abstract

  45. Leukemia Cell of Origin Influences Apoptotic Priming and Sensitivity to LSD1 Inhibition. Cancer Discov. 2020 10; 10(10):1500-1513. View Leukemia Cell of Origin Influences Apoptotic Priming and Sensitivity to LSD1 Inhibition. Abstract

  46. It's Not What You Say But How You Say It: Targeting RNA Methylation in AML. Mol Cell. 2020 06 18; 78(6):996-998. View It's Not What You Say But How You Say It: Targeting RNA Methylation in AML. Abstract

  47. Chromatin Complexes Maintain Self-Renewal of Myeloid Progenitors in AML: Opportunities for Therapeutic Intervention. Stem Cell Reports. 2020 07 14; 15(1):6-12. View Chromatin Complexes Maintain Self-Renewal of Myeloid Progenitors in AML: Opportunities for Therapeutic Intervention. Abstract

  48. Oncogenic Gene-Expression Programs in Leiomyosarcoma and Characterization of Conventional, Inflammatory, and Uterogenic Subtypes. Mol Cancer Res. 2020 09; 18(9):1302-1314. View Oncogenic Gene-Expression Programs in Leiomyosarcoma and Characterization of Conventional, Inflammatory, and Uterogenic Subtypes. Abstract

  49. Higher-Order Linearization and Regularity in Nonlinear Homogenization. Arch Ration Mech Anal. 2020; 237(2):631-741. View Higher-Order Linearization and Regularity in Nonlinear Homogenization. Abstract

  50. Loss of H3K36 Methyltransferase SETD2 Impairs V(D)J Recombination during Lymphoid Development. iScience. 2020 Mar 27; 23(3):100941. View Loss of H3K36 Methyltransferase SETD2 Impairs V(D)J Recombination during Lymphoid Development. Abstract

  51. Therapeutic targeting of preleukemia cells in a mouse model of NPM1 mutant acute myeloid leukemia. Science. 2020 01 31; 367(6477):586-590. View Therapeutic targeting of preleukemia cells in a mouse model of NPM1 mutant acute myeloid leukemia. Abstract

  52. A Menin-MLL Inhibitor Induces Specific Chromatin Changes and Eradicates Disease in Models of MLL-Rearranged Leukemia. Cancer Cell. 2019 12 09; 36(6):660-673.e11. View A Menin-MLL Inhibitor Induces Specific Chromatin Changes and Eradicates Disease in Models of MLL-Rearranged Leukemia. Abstract

  53. Resistance Mechanisms to SYK Inhibition in Acute Myeloid Leukemia. Cancer Discov. 2020 02; 10(2):214-231. View Resistance Mechanisms to SYK Inhibition in Acute Myeloid Leukemia. Abstract

  54. A dominant-negative effect drives selection of TP53 missense mutations in myeloid malignancies. Science. 2019 08 09; 365(6453):599-604. View A dominant-negative effect drives selection of TP53 missense mutations in myeloid malignancies. Abstract

  55. Rationale for targeting BCL6 in MLL-rearranged acute lymphoblastic leukemia. Genes Dev. 2019 09 01; 33(17-18):1265-1279. View Rationale for targeting BCL6 in MLL-rearranged acute lymphoblastic leukemia. Abstract

  56. Acute myeloid leukemia driven by the CALM-AF10 fusion gene is dependent on BMI1. Exp Hematol. 2019 06; 74:42-51.e3. View Acute myeloid leukemia driven by the CALM-AF10 fusion gene is dependent on BMI1. Abstract

  57. Targeting chromatin complexes in fusion protein-driven malignancies. Nat Rev Cancer. 2019 05; 19(5):255-269. View Targeting chromatin complexes in fusion protein-driven malignancies. Abstract

  58. Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and Are Targetable by BET Bromodomain Inhibition. Cancer Res. 2019 03 01; 79(5):994-1009. View Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and Are Targetable by BET Bromodomain Inhibition. Abstract

  59. IKZF2 Drives Leukemia Stem Cell Self-Renewal and Inhibits Myeloid Differentiation. Cell Stem Cell. 2019 01 03; 24(1):153-165.e7. View IKZF2 Drives Leukemia Stem Cell Self-Renewal and Inhibits Myeloid Differentiation. Abstract

  60. Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma. Elife. 2018 11 15; 7. View Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma. Abstract

  61. Inhibition of MEK and ATR is effective in a B-cell acute lymphoblastic leukemia model driven by Mll-Af4 and activated Ras. Blood Adv. 2018 10 09; 2(19):2478-2490. View Inhibition of MEK and ATR is effective in a B-cell acute lymphoblastic leukemia model driven by Mll-Af4 and activated Ras. Abstract

  62. Improved potency and reduced toxicity of the antifungal peptoid AEC5 through submonomer modification. Bioorg Med Chem Lett. 2018 12 01; 28(22):3514-3519. View Improved potency and reduced toxicity of the antifungal peptoid AEC5 through submonomer modification. Abstract

  63. HOXA9 Reprograms the Enhancer Landscape to Promote Leukemogenesis. Cancer Cell. 2018 10 08; 34(4):643-658.e5. View HOXA9 Reprograms the Enhancer Landscape to Promote Leukemogenesis. Abstract

  64. Location, Location, Location: Mutant NPM1c Cytoplasmic Localization Is Required to Maintain Stem Cell Genes in AML. Cancer Cell. 2018 09 10; 34(3):355-357. View Location, Location, Location: Mutant NPM1c Cytoplasmic Localization Is Required to Maintain Stem Cell Genes in AML. Abstract

  65. Gastrointestinal stromal tumor enhancers support a transcription factor network predictive of clinical outcome. Proc Natl Acad Sci U S A. 2018 06 19; 115(25):E5746-E5755. View Gastrointestinal stromal tumor enhancers support a transcription factor network predictive of clinical outcome. Abstract

  66. The DOT1L inhibitor pinometostat reduces H3K79 methylation and has modest clinical activity in adult acute leukemia. Blood. 2018 06 14; 131(24):2661-2669. View The DOT1L inhibitor pinometostat reduces H3K79 methylation and has modest clinical activity in adult acute leukemia. Abstract

  67. A Non-catalytic Function of SETD1A Regulates Cyclin K and the DNA Damage Response. Cell. 2018 02 22; 172(5):1007-1021.e17. View A Non-catalytic Function of SETD1A Regulates Cyclin K and the DNA Damage Response. Abstract

  68. LSD1 inhibition exerts its antileukemic effect by recommissioning PU.1- and C/EBPa-dependent enhancers in AML. Blood. 2018 04 12; 131(15):1730-1742. View LSD1 inhibition exerts its antileukemic effect by recommissioning PU.1- and C/EBPa-dependent enhancers in AML. Abstract

  69. MEF2C Phosphorylation Is Required for Chemotherapy Resistance in Acute Myeloid Leukemia. Cancer Discov. 2018 04; 8(4):478-497. View MEF2C Phosphorylation Is Required for Chemotherapy Resistance in Acute Myeloid Leukemia. Abstract

  70. Peptidomimetic blockade of MYB in acute myeloid leukemia. Nat Commun. 2018 01 09; 9(1):110. View Peptidomimetic blockade of MYB in acute myeloid leukemia. Abstract

  71. Mixed-Lineage Leukemia Fusions and Chromatin in Leukemia. Cold Spring Harb Perspect Med. 2017 Nov 01; 7(11). View Mixed-Lineage Leukemia Fusions and Chromatin in Leukemia. Abstract

  72. SETD2 alterations impair DNA damage recognition and lead to resistance to chemotherapy in leukemia. Blood. 2017 12 14; 130(24):2631-2641. View SETD2 alterations impair DNA damage recognition and lead to resistance to chemotherapy in leukemia. Abstract

  73. Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors. Nat Genet. 2017 09 27; 49(10):1558. View Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors. Abstract

  74. miR-99 regulates normal and malignant hematopoietic stem cell self-renewal. J Exp Med. 2017 Aug 07; 214(8):2453-2470. View miR-99 regulates normal and malignant hematopoietic stem cell self-renewal. Abstract

  75. A UTX-MLL4-p300 Transcriptional Regulatory Network Coordinately Shapes Active Enhancer Landscapes for Eliciting Transcription. Mol Cell. 2017 Jul 20; 67(2):308-321.e6. View A UTX-MLL4-p300 Transcriptional Regulatory Network Coordinately Shapes Active Enhancer Landscapes for Eliciting Transcription. Abstract

  76. PGBD5 promotes site-specific oncogenic mutations in human tumors. Nat Genet. 2017 Jul; 49(7):1005-1014. View PGBD5 promotes site-specific oncogenic mutations in human tumors. Abstract

  77. Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells. Nat Genet. 2017 Jun; 49(6):866-875. View Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells. Abstract

  78. Degradation of the BAF Complex Factor BRD9 by Heterobifunctional Ligands. Angew Chem Int Ed Engl. 2017 05 15; 56(21):5738-5743. View Degradation of the BAF Complex Factor BRD9 by Heterobifunctional Ligands. Abstract

  79. Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations. EMBO Mol Med. 2017 04; 9(4):498-507. View Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations. Abstract

  80. Myeloid progenitor cluster formation drives emergency and leukaemic myelopoiesis. Nature. 2017 04 06; 544(7648):53-58. View Myeloid progenitor cluster formation drives emergency and leukaemic myelopoiesis. Abstract

  81. PI3K pathway regulates ER-dependent transcription in breast cancer through the epigenetic regulator KMT2D. Science. 2017 03 24; 355(6331):1324-1330. View PI3K pathway regulates ER-dependent transcription in breast cancer through the epigenetic regulator KMT2D. Abstract

  82. ENL links histone acetylation to oncogenic gene expression in acute myeloid leukaemia. Nature. 2017 03 09; 543(7644):265-269. View ENL links histone acetylation to oncogenic gene expression in acute myeloid leukaemia. Abstract

  83. Histone Acetyltransferase Activity of MOF Is Required for MLL-AF9 Leukemogenesis. Cancer Res. 2017 04 01; 77(7):1753-1762. View Histone Acetyltransferase Activity of MOF Is Required for MLL-AF9 Leukemogenesis. Abstract

  84. NUP98 Fusion Proteins Interact with the NSL and MLL1 Complexes to Drive Leukemogenesis. Cancer Cell. 2016 Dec 12; 30(6):863-878. View NUP98 Fusion Proteins Interact with the NSL and MLL1 Complexes to Drive Leukemogenesis. Abstract

  85. DNMT3A mutations promote anthracycline resistance in acute myeloid leukemia via impaired nucleosome remodeling. Nat Med. 2016 12; 22(12):1488-1495. View DNMT3A mutations promote anthracycline resistance in acute myeloid leukemia via impaired nucleosome remodeling. Abstract

  86. Controlled stem cell amplification by HOXB4 depends on its unique proline-rich region near the N terminus. Blood. 2017 01 19; 129(3):319-323. View Controlled stem cell amplification by HOXB4 depends on its unique proline-rich region near the N terminus. Abstract

  87. Histone acetyltransferase activity of MOF is required for adult but not early fetal hematopoiesis in mice. Blood. 2017 01 05; 129(1):48-59. View Histone acetyltransferase activity of MOF is required for adult but not early fetal hematopoiesis in mice. Abstract

  88. Discovery and Characterization of a Peptoid with Antifungal Activity against Cryptococcus neoformans. ACS Med Chem Lett. 2016 Dec 08; 7(12):1139-1144. View Discovery and Characterization of a Peptoid with Antifungal Activity against Cryptococcus neoformans. Abstract

  89. AACR Cancer Progress Report 2016. Clin Cancer Res. 2016 10 01; 22 Suppl 19:S1-S137. View AACR Cancer Progress Report 2016. Abstract

  90. Targeting the kinase activities of ATR and ATM exhibits antitumoral activity in mouse models of MLL-rearranged AML. Sci Signal. 2016 09 13; 9(445):ra91. View Targeting the kinase activities of ATR and ATM exhibits antitumoral activity in mouse models of MLL-rearranged AML. Abstract

  91. Targeting Chromatin Regulators Inhibits Leukemogenic Gene Expression in NPM1 Mutant Leukemia. Cancer Discov. 2016 10; 6(10):1166-1181. View Targeting Chromatin Regulators Inhibits Leukemogenic Gene Expression in NPM1 Mutant Leukemia. Abstract

  92. Forward genetic screen of human transposase genomic rearrangements. BMC Genomics. 2016 Aug 04; 17:548. View Forward genetic screen of human transposase genomic rearrangements. Abstract

  93. The UK Neovascular AMD Database Report 3: inter-centre variation in visual acuity outcomes and establishing real-world measures of care. Eye (Lond). 2016 Nov; 30(11):1462-1468. View The UK Neovascular AMD Database Report 3: inter-centre variation in visual acuity outcomes and establishing real-world measures of care. Abstract

  94. Patient-derived xenotransplants can recapitulate the genetic driver landscape of acute leukemias. Leukemia. 2017 01; 31(1):151-158. View Patient-derived xenotransplants can recapitulate the genetic driver landscape of acute leukemias. Abstract

  95. Reply to "Uveal melanoma cells are resistant to EZH2 inhibition regardless of BAP1 status". Nat Med. 2016 06 07; 22(6):578-9. View Reply to "Uveal melanoma cells are resistant to EZH2 inhibition regardless of BAP1 status". Abstract

  96. Erratum: Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins. Nat Med. 2016 06 07; 22(6):692. View Erratum: Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins. Abstract

  97. The role of DOT1L in the maintenance of leukemia gene expression. Curr Opin Genet Dev. 2016 02; 36:68-72. View The role of DOT1L in the maintenance of leukemia gene expression. Abstract

  98. Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins. Nat Med. 2016 06; 22(6):672-8. View Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins. Abstract

  99. Exploiting the Epigenome to Control Cancer-Promoting Gene-Expression Programs. Cancer Cell. 2016 Apr 11; 29(4):464-476. View Exploiting the Epigenome to Control Cancer-Promoting Gene-Expression Programs. Abstract

  100. Integrated genomic DNA/RNA profiling of hematologic malignancies in the clinical setting. Blood. 2016 06 16; 127(24):3004-14. View Integrated genomic DNA/RNA profiling of hematologic malignancies in the clinical setting. Abstract

  101. MLL1 and DOT1L cooperate with meningioma-1 to induce acute myeloid leukemia. J Clin Invest. 2016 Apr 01; 126(4):1438-50. View MLL1 and DOT1L cooperate with meningioma-1 to induce acute myeloid leukemia. Abstract

  102. Ezh2 Controls an Early Hematopoietic Program and Growth and Survival Signaling in Early T Cell Precursor Acute Lymphoblastic Leukemia. Cell Rep. 2016 Mar 01; 14(8):1953-65. View Ezh2 Controls an Early Hematopoietic Program and Growth and Survival Signaling in Early T Cell Precursor Acute Lymphoblastic Leukemia. Abstract

  103. MLL-AF9- and HOXA9-mediated acute myeloid leukemia stem cell self-renewal requires JMJD1C. J Clin Invest. 2016 Mar 01; 126(3):997-1011. View MLL-AF9- and HOXA9-mediated acute myeloid leukemia stem cell self-renewal requires JMJD1C. Abstract

  104. Editorial overview: Differentiation and disease. Curr Opin Cell Biol. 2015 Dec; 37:v-vi. View Editorial overview: Differentiation and disease. Abstract

  105. Drugging Chromatin in Cancer: Recent Advances and Novel Approaches. Mol Cell. 2015 Nov 19; 60(4):561-70. View Drugging Chromatin in Cancer: Recent Advances and Novel Approaches. Abstract

  106. A chromatin-independent role of Polycomb-like 1 to stabilize p53 and promote cellular quiescence. Genes Dev. 2015 Nov 01; 29(21):2231-43. View A chromatin-independent role of Polycomb-like 1 to stabilize p53 and promote cellular quiescence. Abstract

  107. Impact of FLT3-ITD location on sensitivity to TKI-therapy in vitro and in vivo. Leukemia. 2016 05; 30(5):1220-1225. View Impact of FLT3-ITD location on sensitivity to TKI-therapy in vitro and in vivo. Abstract

  108. JMJD1C is required for the survival of acute myeloid leukemia by functioning as a coactivator for key transcription factors. Genes Dev. 2015 Oct 15; 29(20):2123-39. View JMJD1C is required for the survival of acute myeloid leukemia by functioning as a coactivator for key transcription factors. Abstract

  109. Tumor-specific HSP90 inhibition as a therapeutic approach in JAK-mutant acute lymphoblastic leukemias. Blood. 2015 Nov 26; 126(22):2479-83. View Tumor-specific HSP90 inhibition as a therapeutic approach in JAK-mutant acute lymphoblastic leukemias. Abstract

  110. Loss of BAP1 function leads to EZH2-dependent transformation. Nat Med. 2015 Nov; 21(11):1344-9. View Loss of BAP1 function leads to EZH2-dependent transformation. Abstract

  111. The PZP Domain of AF10 Senses Unmodified H3K27 to Regulate DOT1L-Mediated Methylation of H3K79. Mol Cell. 2015 Oct 15; 60(2):319-27. View The PZP Domain of AF10 Senses Unmodified H3K27 to Regulate DOT1L-Mediated Methylation of H3K79. Abstract

  112. Mediator kinase inhibition further activates super-enhancer-associated genes in AML. Nature. 2015 Oct 08; 526(7572):273-276. View Mediator kinase inhibition further activates super-enhancer-associated genes in AML. Abstract

  113. Hematopoietic Differentiation Is Required for Initiation of Acute Myeloid Leukemia. Cell Stem Cell. 2015 Nov 05; 17(5):611-23. View Hematopoietic Differentiation Is Required for Initiation of Acute Myeloid Leukemia. Abstract

  114. Inactivation of Eed impedes MLL-AF9-mediated leukemogenesis through Cdkn2a-dependent and Cdkn2a-independent mechanisms in a murine model. Exp Hematol. 2015 Nov; 43(11):930-935.e6. View Inactivation of Eed impedes MLL-AF9-mediated leukemogenesis through Cdkn2a-dependent and Cdkn2a-independent mechanisms in a murine model. Abstract

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