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Daniel Magoon
Institution:
Maine Molecular Quality Controls (United States)
Observed institutions:
Harvard University,
Johns Hopkins University,
Johns Hopkins Medicine,
Maine Molecular Quality Controls (United States),
Johns Hopkins Hospital,
Sidney Kimmel Comprehensive Cancer Center
show all 6
OpenAlex ID:
A5011067274
RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia
2011
·
Johannes Zuber
, Junwei Shi
, et al.
·
Nature
·
1,870
A phase 1 dosing study of ruxolitinib in children with relapsed or refractory solid tumors, leukemias, or myeloproliferative neoplasms: A Children's Oncology Group phase 1 consortium study (ADVL1011)
2015
·
Mignon L. Loh
, Sarah K. Tasian
, et al.
·
Pediatric Blood & Cancer
·
132
Dynamic Chemotherapy-Induced Upregulation of CXCR4 Expression: A Mechanism of Therapeutic Resistance in Pediatric AML
2013
·
Edward Allan R. Sison
, Emily McIntyre
, et al.
·
Molecular Cancer Research
·
107
A phase 1 study of the CXCR4 antagonist plerixafor in combination with high‐dose cytarabine and etoposide in children with relapsed or refractory acute leukemias or myelodysplastic syndrome: A Pediatric Oncology Experimental Therapeutics Investigators’ Consortium study (POE 10‐03)
2017
·
Todd M. Cooper
, Edward Allan Racela Sison
, et al.
·
Pediatric Blood & Cancer
·
79
A Phase I Study of Quizartinib Combined with Chemotherapy in Relapsed Childhood Leukemia: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2016
·
Todd M. Cooper
, Jeannette Cassar
, et al.
·
Clinical Cancer Research
·
75
Plerixafor as a chemosensitizing agent in pediatric acute lymphoblastic leukemia: efficacy and potential mechanisms of resistance to CXCR4 inhibition
2014
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Oncotarget
·
65
PDF
POL5551, a novel and potent CXCR4 antagonist, enhances sensitivity to chemotherapy in pediatric ALL
2015
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Oncotarget
·
38
PDF
NPMc+ cooperates with Flt3/ITD mutations to cause acute leukemia recapitulating human disease
2013
·
Rachel Rau
, Daniel Magoon
, et al.
·
Experimental Hematology
·
35
PDF
Knock-in of the Wt1 R394W mutation causes MDS and cooperates with Flt3/ITD to drive aggressive myeloid neoplasms in mice
2018
·
Colleen E. Annesley
, Cara Rabik
, et al.
·
Oncotarget
·
8
PDF
A Phase I Study Of AC220 (Quizartinib) In Combination With Cytarabine and Etoposide In Relapsed/Refractory Childhood ALL and AML: A Therapeutic Advances In Childhood Leukemia & Lymphoma (TACL) Study
2013
·
Todd Michael Cooper
, Jemily Malvar
, et al.
·
Blood
·
7
A Phase I Study of AC220 in Combination with Cytarabine and Etoposide in Relapsed/Refractory Childhood ALL and AML: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2012
·
Todd Cooper
, Richard Sposto
, et al.
·
Blood
·
7
Chemosensitization and Mobilization Of AML/ALL/MDS With Plerixafor (AMD 3100), a CXCR4 Antagonist: A Phase I Study Of Plerixafor + Cytarabine and Etoposide In Pediatric Patients With Acute Leukemia and MDS
2013
·
Todd Michael Cooper
, Sharyn D. Baker
, et al.
·
Blood
·
5
Safety and biological activity of the FLT3 inhibitor lestaurtinib in infant MLL-rearranged (MLL-r) ALL: Children's Oncology Group protocol AALL0631.
2012
·
Di Sun
, Allison Kaeding
, et al.
·
Journal of Clinical Oncology
·
3
A Wilms Tumor 1 (WT1) Mutation Causes Myelodysplastic Syndrome in a Knock-in Mouse Model, and a Mixed Myelodysplastic/Myeloproliferative Neoplam in Double Knock-in Mice with WT1 and FLT3/ITD Mutations
2015
·
Colleen E. Annesley
, Amy S. Duffield
, et al.
·
Blood
·
1
POL5551, a Novel and Potent CXCR4 Antagonist, Enhances Sensitivity to Chemotherapy in an in Vivo Model of High-Risk (HR) Pediatric Acute Lymphoblastic Leukemia (ALL)
2014
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Blood
·
1
Extended Exposure To The CXCR4 Inhibitor Plerixafor May Lead To Enhanced Microenvironment Interactions in Acute Lymphoblastic Leukemia (ALL)
2013
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Blood
·
1
The Novel CXCR4 Antagonist POL5551 Decreases Surface CXCR4 (s-CXCR4) Expression, Inhibits Chemotaxis, and Enhances Chemosensitivity in Acute Lymphoblastic Leukemia (ALL)
2012
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Blood
·
1
Chemotherapy-Induced CXCR4 Modulation Predicts the In Vivo Efficacy of Plerixafor As a Chemosensitizer in Acute Leukemia
2011
·
Edward Allan R. Sison
, Daniel Magoon
, et al.
·
Blood
·
1
Upregulation of Surface CXCR4 In Response to Chemotherapy Confers a Stromal-Mediated Survival Advantage In Acute Leukemia
2010
·
Edward Allan R. Sison
, Emily McIntyre
, et al.
·
Blood
·
1
Cytoplasmic Nucleophosmin (NPMc+) Mutations and FMS-Like Tyrosine Kinase 3 (Flt3) Internal Tandem Duplication (ITD) Mutations Cooperate to Cause Leukemia In a Mouse Model
2010
·
Rachel E. Rau
, Daniel Magoon
, et al.
·
Blood
·
1
A-109 Validation of a Multiplexed External Control Panel to Monitor the Performance of the Roche cobas® eplex respiratory pathogen panel 3
2026
·
Nithya Sivaji
, Jack Aldana Proulx
, et al.
·
Clinical Chemistry
Supplemental Figures and Tables from A Phase I Study of Quizartinib Combined with Chemotherapy in Relapsed Childhood Leukemia: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2023
·
Todd M. Cooper
, Jeannette Cassar
, et al.
Supplemental Table and Figure Legends from A Phase I Study of Quizartinib Combined with Chemotherapy in Relapsed Childhood Leukemia: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2023
·
Todd M. Cooper
, Jeannette Cassar
, et al.
Data from A Phase I Study of Quizartinib Combined with Chemotherapy in Relapsed Childhood Leukemia: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2023
·
Todd M. Cooper
, Jeannette Cassar
, et al.
Data from A Phase I Study of Quizartinib Combined with Chemotherapy in Relapsed Childhood Leukemia: A Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study
2023
·
Todd M. Cooper
, Jeannette Cassar
, et al.
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Works count:
35
Citation count:
2,438
H-index:
8
I10-index:
8
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