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Mrityunjay Tyagi

Showing results (11-20 of 20) with videos related to

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Chemistry (Weinheim an Der Bergstrasse, Germany)|November 29, 2013
Rational design of boradiazaindacene (BODIPY)-based functional moleculesMonika Gupta, Soumyaditya Mula, Mrityunjay Tyagi, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 28, 2018
Resveratrol analogue, trans-4,4'-dihydroxystilbene (DHS), inhibits melanoma tumor growth and suppresses its metastatic colonization in lungsBhaskar Saha, Ganesh B Pai, Mahesh Subramanian, et al.
Biomacromolecules|June 10, 2025
Robust Hydrogen-Bonded Organic Framework for pH-Responsive Drug DeliverySucheta Chatterjee, Mrityunjay Tyagi, Ayan Ghosh, et al.
Nature Structural & Molecular Biology|December 19, 2022
Polλ promotes microhomology-mediated end-joiningGurushankar Chandramouly, Joonas Jamsen, Nikita Borisonnik, et al.
Nature Communications|July 10, 2024
PARG is essential for Polθ-mediated DNA end-joining by removing repressive poly-ADP-ribose marksUmeshkumar Vekariya, Leonid Minakhin, Gurushankar Chandramouly, et al.
Nature Communications|August 14, 2024
Structural basis for a Polθ helicase small-molecule inhibitor revealed by cryo-EMFumiaki Ito, Ziyuan Li, Leonid Minakhin, et al.
Scientific Reports|December 22, 2021
Carbon nano-dot for cancer studies as dual nano-sensor for imaging intracellular temperature or pH variationTrilochan Gadly, Goutam Chakraborty, Mrityunjay Tyagi, et al.
Journal of Medicinal Chemistry|October 22, 2025
RTx-303, an Orally Bioavailable Polθ Polymerase Inhibitor That Potentiates PARP Inhibitors in BRCA Mutant TumorsGurushankar Chandramouly, William Fried, John Gordon, et al.
Nature Communications|April 5, 2024
Discovery of a small-molecule inhibitor that traps Polθ on DNA and synergizes with PARP inhibitorsWilliam Fried, Mrityunjay Tyagi, Leonid Minakhin, et al.
Molecular Cancer Therapeutics|December 8, 2023
4'-Ethynyl-2'-Deoxycytidine (EdC) Preferentially Targets Lymphoma and Leukemia Subtypes by Inducing Replicative StressMarissa L Calbert, Gurushankar Chandramouly, Clare M Adams, et al.
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Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 29, 2013
Rational design of boradiazaindacene (BODIPY)-based functional moleculesMonika Gupta, Soumyaditya Mula, Mrityunjay Tyagi, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 28, 2018
Resveratrol analogue, trans-4,4'-dihydroxystilbene (DHS), inhibits melanoma tumor growth and suppresses its metastatic colonization in lungsBhaskar Saha, Ganesh B Pai, Mahesh Subramanian, et al.
Biomacromolecules|June 10, 2025
Robust Hydrogen-Bonded Organic Framework for pH-Responsive Drug DeliverySucheta Chatterjee, Mrityunjay Tyagi, Ayan Ghosh, et al.
Nature Structural & Molecular Biology|December 19, 2022
Polλ promotes microhomology-mediated end-joiningGurushankar Chandramouly, Joonas Jamsen, Nikita Borisonnik, et al.
Nature Communications|July 10, 2024
PARG is essential for Polθ-mediated DNA end-joining by removing repressive poly-ADP-ribose marksUmeshkumar Vekariya, Leonid Minakhin, Gurushankar Chandramouly, et al.
Nature Communications|August 14, 2024
Structural basis for a Polθ helicase small-molecule inhibitor revealed by cryo-EMFumiaki Ito, Ziyuan Li, Leonid Minakhin, et al.
Scientific Reports|December 22, 2021
Carbon nano-dot for cancer studies as dual nano-sensor for imaging intracellular temperature or pH variationTrilochan Gadly, Goutam Chakraborty, Mrityunjay Tyagi, et al.
Journal of Medicinal Chemistry|October 22, 2025
RTx-303, an Orally Bioavailable Polθ Polymerase Inhibitor That Potentiates PARP Inhibitors in BRCA Mutant TumorsGurushankar Chandramouly, William Fried, John Gordon, et al.
Nature Communications|April 5, 2024
Discovery of a small-molecule inhibitor that traps Polθ on DNA and synergizes with PARP inhibitorsWilliam Fried, Mrityunjay Tyagi, Leonid Minakhin, et al.
Molecular Cancer Therapeutics|December 8, 2023
4'-Ethynyl-2'-Deoxycytidine (EdC) Preferentially Targets Lymphoma and Leukemia Subtypes by Inducing Replicative StressMarissa L Calbert, Gurushankar Chandramouly, Clare M Adams, et al.
Pageof 2