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Patrick C. Fagan
Observed names:
P Fagan,
P. Fagan,
Patrick Fagan
Observed institutions:
Memorial Sloan Kettering Cancer Center,
Cornell University,
Mercy Hospital,
Ignyta (United States),
University of Nebraska Medical Center
OpenAlex ID:
A5021827432
A novel, orally active LPA 1 receptor antagonist inhibits lung fibrosis in the mouse bleomycin model
2010
·
JS Swaney
, C Chapman
, et al.
·
British Journal of Pharmacology
·
268
PDF
Immuno-oncological Efficacy of RXDX-106, a Novel TAM (TYRO3, AXL, MER) Family Small-Molecule Kinase Inhibitor
2019
·
Yumi Yokoyama
, Erin D. Lew
, et al.
·
Cancer Research
·
89
Synthesis of AZT 5‘-Triphosphate Mimics and Their Inhibitory Effects on HIV-1 Reverse Transcriptase
2004
·
Guangyi Wang
, Nicholas Boyle
, et al.
·
Journal of Medicinal Chemistry
·
60
Pharmacological Blockade of the DP2 Receptor Inhibits Cigarette Smoke-Induced Inflammation, Mucus Cell Metaplasia, and Epithelial Hyperplasia in the Mouse Lung
2009
·
Karin J. Stebbins
, Alex R. Broadhead
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
49
Novel tricyclic antagonists of the prostaglandin D2 receptor DP2 with efficacy in a murine model of allergic rhinitis
2009
·
Brian A. Stearns
, Christopher Baccei
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
46
ALK Fusions in Renal Cell Carcinoma: Response to Entrectinib
2018
·
Jessica J. Tao
, Ge Wei
, et al.
·
JCO Precision Oncology
·
43
Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3 –Positive Acute Myeloid Leukemia
2017
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
·
Molecular Cancer Therapeutics
·
42
Synthesis of 2‘,3‘-Dideoxynucleoside 5‘-α-P-Borano-β,γ-(difluoromethylene)triphosphates and Their Inhibition of HIV-1 Reverse Transcriptase
2005
·
Nicholas A. Boyle
, Vivek K. Rajwanshi
, et al.
·
Journal of Medicinal Chemistry
·
29
Synthesis of Azole Nucleoside 5′‐Monophosphate Mimics (P1Ms) and Their Inhibitory Properties of IMP Dehydrogenases
2004
·
Guangyi Wang
, Kandasamy Sakthivel
, et al.
·
Nucleosides Nucleotides & Nucleic Acids
·
18
2′,3′-Dideoxynucleoside 5′-β,γ-(Difluoromethylene) Triphosphates With α-P-Thio or α-P-Seleno Modifications: Synthesis and Their Inhibition of HIV-1 Reverse Transcriptase
2005
·
Nicholas A. Boyle
, Patrick Fagan
, et al.
·
Nucleosides Nucleotides & Nucleic Acids
·
13
Synthesis of 5'-Triphosphate Mimics (P3Ms) of 3'-Azido-3',5'-Dideoxythymidine and 3',5'-Dideoxy-5'-Difluoromethylenethymidine as HIV-1 Reverse Transcriptase Inhibitors
2005
·
Vivek Rajwanshi
, Marija Prhavc
, et al.
·
Nucleosides Nucleotides & Nucleic Acids
·
6
Entrectinib, a highly potent pan-Trk, ROS1, and ALK inhibitor, has broad-spectrum, histology-agnostic anti-tumor activity in molecularly defined cancers
2016
·
G. Wei
, R. Patel
, et al.
·
European Journal of Cancer
·
4
Discovery and optimization of a biphenylacetic acid series of prostaglandin D2 receptor DP2 antagonists with efficacy in a murine model of allergic rhinitis
2011
·
Jill M. Scott
, Christopher Baccei
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
3
Abstract 5158: Anti-tumor activity of entrectinib, a highly potent pan-TRK, ROS1 and ALK inhibitor, in molecularly defined acute myeloid leukemia
2017
·
Patrick Fagan
, Maria Barrera
, et al.
·
Cancer Research
·
2
Data from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 3 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
PDF
Supplemental Figure 6 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 5 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
PDF
Supplemental Figure 4 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 1 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
PDF
Supplemental Figure 2 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 1 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 5 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 3 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
Supplemental Figure 2 from Antitumor Activity of Entrectinib, a Pan-TRK, ROS1, and ALK Inhibitor, in ETV6-NTRK3–Positive Acute Myeloid Leukemia
2023
·
Kristen M. Smith
, Patrick C. Fagan
, et al.
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Works count:
34
Citation count:
672
H-index:
10
I10-index:
10
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