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Journal of Medicinal Chemistry
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August 12, 2024
Discovery of CW-3308 as a Potent, Selective, and Orally Efficacious PROTAC Degrader of BRD9
Changwei Wang, Mi Wang, Yu Wang, et al.
ACS Medicinal Chemistry Letters
|
June 18, 2021
SD-91 as A Potent and Selective STAT3 Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression
Haibin Zhou, Longchuan Bai, Renqi Xu, et al.
Emerging Infectious Diseases
|
December 3, 2008
Antibodies to Nipah or Nipah-like viruses in bats, China
Yan Li, Jianmin Wang, Andrew C Hickey, et al.
Journal of the American Chemical Society
|
May 7, 2013
Diastereomeric spirooxindoles as highly potent and efficacious MDM2 inhibitors
Yujun Zhao, Liu Liu, Wei Sun, et al.
Molecular Cancer Therapeutics
|
June 21, 2008
Reactivation of p53 by a specific MDM2 antagonist (MI-43) leads to p21-mediated cell cycle arrest and selective cell death in colon cancer
Sanjeev Shangary, Ke Ding, Su Qiu, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
January 26, 2016
Electronic cigarette inhalation alters innate immunity and airway cytokines while increasing the virulence of colonizing bacteria
John H Hwang, Matthew Lyes, Katherine Sladewski, et al.
Healthcare (Basel, Switzerland)
|
July 29, 2023
Protocol Report on the Transcranial Photobiomodulation for Alzheimer's Disease (TRAP-AD) Study
Dan V Iosifescu, Xiaotong Song, Maia B Gersten, et al.
Cardiology in the Young
|
September 1, 2025
Relationship between anaesthesia strategy and intracardiac hemodynamics during paediatric cardiac catheterisation
Andrew H Smith, Steven J Healan, Genevieve E Staudt, et al.
Cancer Research
|
November 18, 2008
SM-164: a novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP
Jianfeng Lu, Longchuan Bai, Haiying Sun, et al.
Angewandte Chemie (International Ed. in English)
|
December 29, 2017
Design of the First-in-Class, Highly Potent Irreversible Inhibitor Targeting the Menin-MLL Protein-Protein Interaction
Shilin Xu, Angelo Aguilar, Tianfeng Xu, et al.
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of 50
Search research articles
Search
Showing results (401-410 of 494) with videos related to
Sort By:
Page
of 50
Journal of Medicinal Chemistry
|
August 12, 2024
Discovery of CW-3308 as a Potent, Selective, and Orally Efficacious PROTAC Degrader of BRD9
Changwei Wang, Mi Wang, Yu Wang, et al.
ACS Medicinal Chemistry Letters
|
June 18, 2021
SD-91 as A Potent and Selective STAT3 Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression
Haibin Zhou, Longchuan Bai, Renqi Xu, et al.
Emerging Infectious Diseases
|
December 3, 2008
Antibodies to Nipah or Nipah-like viruses in bats, China
Yan Li, Jianmin Wang, Andrew C Hickey, et al.
Journal of the American Chemical Society
|
May 7, 2013
Diastereomeric spirooxindoles as highly potent and efficacious MDM2 inhibitors
Yujun Zhao, Liu Liu, Wei Sun, et al.
Molecular Cancer Therapeutics
|
June 21, 2008
Reactivation of p53 by a specific MDM2 antagonist (MI-43) leads to p21-mediated cell cycle arrest and selective cell death in colon cancer
Sanjeev Shangary, Ke Ding, Su Qiu, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
January 26, 2016
Electronic cigarette inhalation alters innate immunity and airway cytokines while increasing the virulence of colonizing bacteria
John H Hwang, Matthew Lyes, Katherine Sladewski, et al.
Healthcare (Basel, Switzerland)
|
July 29, 2023
Protocol Report on the Transcranial Photobiomodulation for Alzheimer's Disease (TRAP-AD) Study
Dan V Iosifescu, Xiaotong Song, Maia B Gersten, et al.
Cardiology in the Young
|
September 1, 2025
Relationship between anaesthesia strategy and intracardiac hemodynamics during paediatric cardiac catheterisation
Andrew H Smith, Steven J Healan, Genevieve E Staudt, et al.
Cancer Research
|
November 18, 2008
SM-164: a novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP
Jianfeng Lu, Longchuan Bai, Haiying Sun, et al.
Angewandte Chemie (International Ed. in English)
|
December 29, 2017
Design of the First-in-Class, Highly Potent Irreversible Inhibitor Targeting the Menin-MLL Protein-Protein Interaction
Shilin Xu, Angelo Aguilar, Tianfeng Xu, et al.
Page
of 50