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Bioorganic & Medicinal Chemistry Letters
|
May 2, 2025
Discovery of TNG-6132, a potent, selective, and orally bioavailable USP1 inhibitor
Scott Throner, Tianshu Feng, Jannik N Andersen, et al.
Molecular Cancer Therapeutics
|
May 6, 2025
CRISPR screens identify POLB as a synthetic lethal enhancer of PARP inhibition exclusively in BRCA-mutated tumors
Katherine Lazarides, Justin L Engel, Michele Meseonznik, et al.
Molecular Cancer Therapeutics
|
January 31, 2025
Characterization of TNG348: A Selective, Allosteric USP1 Inhibitor That Synergizes with PARP Inhibitors in Tumors with Homologous Recombination Deficiency
Antoine Simoneau, Charlotte B Pratt, Hsin-Jung Wu, et al.
Molecular Cancer Therapeutics
|
January 27, 2025
LIG1 Is a Synthetic Lethal Target in BRCA1 Mutant Cancers
Lauren Catherine M Martires, Leanne G Ahronian, Charlotte B Pratt, et al.
Molecular Cell
|
February 4, 2014
Optimal translational termination requires C4 lysyl hydroxylation of eRF1
Tianshu Feng, Atsushi Yamamoto, Sarah E Wilkins, et al.
Molecular Cancer Therapeutics
|
October 13, 2022
Ubiquitinated PCNA Drives USP1 Synthetic Lethality in Cancer
Antoine Simoneau, Justin L Engel, Madhavi Bandi, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
April 3, 2022
Associations of Maternal Prenatal Stress and Depressive Symptoms With Childhood Neurobehavioral Outcomes in the ECHO Cohort of the NICHD Fetal Growth Studies: Fetal Growth Velocity as a Potential Mediator
Vanessa Babineau, Yaneve N Fonge, Emily S Miller, et al.
Nature Chemical Biology
|
October 30, 2012
Oxygenase-catalyzed ribosome hydroxylation occurs in prokaryotes and humans
Wei Ge, Alexander Wolf, Tianshu Feng, et al.
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Search research articles
Search
Showing results (91-100 of 98) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 98 results.
Bioorganic & Medicinal Chemistry Letters
|
May 2, 2025
Discovery of TNG-6132, a potent, selective, and orally bioavailable USP1 inhibitor
Scott Throner, Tianshu Feng, Jannik N Andersen, et al.
Molecular Cancer Therapeutics
|
May 6, 2025
CRISPR screens identify POLB as a synthetic lethal enhancer of PARP inhibition exclusively in BRCA-mutated tumors
Katherine Lazarides, Justin L Engel, Michele Meseonznik, et al.
Molecular Cancer Therapeutics
|
January 31, 2025
Characterization of TNG348: A Selective, Allosteric USP1 Inhibitor That Synergizes with PARP Inhibitors in Tumors with Homologous Recombination Deficiency
Antoine Simoneau, Charlotte B Pratt, Hsin-Jung Wu, et al.
Molecular Cancer Therapeutics
|
January 27, 2025
LIG1 Is a Synthetic Lethal Target in BRCA1 Mutant Cancers
Lauren Catherine M Martires, Leanne G Ahronian, Charlotte B Pratt, et al.
Molecular Cell
|
February 4, 2014
Optimal translational termination requires C4 lysyl hydroxylation of eRF1
Tianshu Feng, Atsushi Yamamoto, Sarah E Wilkins, et al.
Molecular Cancer Therapeutics
|
October 13, 2022
Ubiquitinated PCNA Drives USP1 Synthetic Lethality in Cancer
Antoine Simoneau, Justin L Engel, Madhavi Bandi, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
April 3, 2022
Associations of Maternal Prenatal Stress and Depressive Symptoms With Childhood Neurobehavioral Outcomes in the ECHO Cohort of the NICHD Fetal Growth Studies: Fetal Growth Velocity as a Potential Mediator
Vanessa Babineau, Yaneve N Fonge, Emily S Miller, et al.
Nature Chemical Biology
|
October 30, 2012
Oxygenase-catalyzed ribosome hydroxylation occurs in prokaryotes and humans
Wei Ge, Alexander Wolf, Tianshu Feng, et al.
Page
of 10