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Future Medicinal Chemistry
|
August 11, 2017
A novel series of N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amines as highly potent CDK4/6 inhibitors
Solomon Tadesse, Ge Zhu, Laychiluh B Mekonnen, et al.
The Journal of Nursing Research : JNR
|
December 5, 2022
Disaster Preparedness Among Nurses in China: A Cross-Sectional Study
Ying Wang, Yu Liu, Mingfeng Yu, et al.
Chemistryopen
|
February 20, 2014
Incorporation of Bulky and Cationic Cyclam-Triazole Moieties into Marimastat Can Generate Potent MMP Inhibitory Activity without Inducing Cytotoxicity
Mingfeng Yu, Ngee H Lim, Samantha Ellis, et al.
Future Medicinal Chemistry
|
October 28, 2017
CDK5 in oncology: recent advances and future prospects
Jimma Likisa Lenjisa, Solomon Tadesse, Nishat Zareen Khair, et al.
Plos One
|
July 2, 2014
Incorporating a piperidinyl group in the fluorophore extends the fluorescence lifetime of click-derived cyclam-naphthalimide conjugates
Mingfeng Yu, Sandra Ast, Qun Yu, et al.
European Journal of Medicinal Chemistry
|
March 25, 2015
Discovery of 4-(dihydropyridinon-3-yl)amino-5-methylthieno[2,3-d]pyrimidine derivatives as potent Mnk inhibitors: synthesis, structure-activity relationship analysis and biological evaluation
Mingfeng Yu, Peng Li, Sunita K C Basnet, et al.
Future Medicinal Chemistry
|
January 14, 2015
Targeting Pim kinases for cancer treatment: opportunities and challenges
Bich Thuy Le, Malika Kumarasiri, Julian R J Adams, et al.
Molecular Pharmacology
|
June 6, 2015
Pharmacologic Inhibition of MNKs in Acute Myeloid Leukemia
Theodosia Teo, Frankie Lam, Mingfeng Yu, et al.
Metallomics : Integrated Biometal Science
|
August 19, 2014
Neuroprotective peptide-macrocycle conjugates reveal complex structure-activity relationships in their interactions with amyloid β
Mingfeng Yu, Timothy M Ryan, Samantha Ellis, et al.
Endocrine-Related Cancer
|
September 2, 2016
Targeting CDK9: a promising therapeutic opportunity in prostate cancer
Muhammed H Rahaman, Malika Kumarasiri, Laychiluh B Mekonnen, et al.
Page
of 6
Search research articles
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Showing results (21-30 of 60) with videos related to
Sort By:
Page
of 6
Future Medicinal Chemistry
|
August 11, 2017
A novel series of N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amines as highly potent CDK4/6 inhibitors
Solomon Tadesse, Ge Zhu, Laychiluh B Mekonnen, et al.
The Journal of Nursing Research : JNR
|
December 5, 2022
Disaster Preparedness Among Nurses in China: A Cross-Sectional Study
Ying Wang, Yu Liu, Mingfeng Yu, et al.
Chemistryopen
|
February 20, 2014
Incorporation of Bulky and Cationic Cyclam-Triazole Moieties into Marimastat Can Generate Potent MMP Inhibitory Activity without Inducing Cytotoxicity
Mingfeng Yu, Ngee H Lim, Samantha Ellis, et al.
Future Medicinal Chemistry
|
October 28, 2017
CDK5 in oncology: recent advances and future prospects
Jimma Likisa Lenjisa, Solomon Tadesse, Nishat Zareen Khair, et al.
Plos One
|
July 2, 2014
Incorporating a piperidinyl group in the fluorophore extends the fluorescence lifetime of click-derived cyclam-naphthalimide conjugates
Mingfeng Yu, Sandra Ast, Qun Yu, et al.
European Journal of Medicinal Chemistry
|
March 25, 2015
Discovery of 4-(dihydropyridinon-3-yl)amino-5-methylthieno[2,3-d]pyrimidine derivatives as potent Mnk inhibitors: synthesis, structure-activity relationship analysis and biological evaluation
Mingfeng Yu, Peng Li, Sunita K C Basnet, et al.
Future Medicinal Chemistry
|
January 14, 2015
Targeting Pim kinases for cancer treatment: opportunities and challenges
Bich Thuy Le, Malika Kumarasiri, Julian R J Adams, et al.
Molecular Pharmacology
|
June 6, 2015
Pharmacologic Inhibition of MNKs in Acute Myeloid Leukemia
Theodosia Teo, Frankie Lam, Mingfeng Yu, et al.
Metallomics : Integrated Biometal Science
|
August 19, 2014
Neuroprotective peptide-macrocycle conjugates reveal complex structure-activity relationships in their interactions with amyloid β
Mingfeng Yu, Timothy M Ryan, Samantha Ellis, et al.
Endocrine-Related Cancer
|
September 2, 2016
Targeting CDK9: a promising therapeutic opportunity in prostate cancer
Muhammed H Rahaman, Malika Kumarasiri, Laychiluh B Mekonnen, et al.
Page
of 6