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Esther H Q Ong

Showing results (1-10 of 7) with videos related to

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BMC Genomics|July 20, 2022
Deep learning for de-convolution of Smad2 versus Smad3 binding sitesJeremy W K Ng, Esther H Q Ong, Lisa Tucker-Kellogg, et al.
Bioorganic & Medicinal Chemistry|December 3, 2014
Design, synthesis and biological evaluation of FLT3 covalent inhibitors with a resorcylic acid coreJin Xu, Esther H Q Ong, Jeffrey Hill, et al.
Chemmedchem|August 10, 2013
Rational design of resorcylic acid lactone analogues as covalent MNK1/2 kinase inhibitors by tuning the reactivity of an enamide Michael acceptorJin Xu, Anqi Chen, Joma Joy, et al.
Chemical Biology & Drug Design|March 23, 2021
Designing a leucine-rich antibacterial nonapeptide with potent activity against mupirocin-resistant MRSA via a structure-activity relationship studyQi An Ang, Giovinna Arfan, Chu Yang Fann Ong, et al.
Antibiotics (Basel, Switzerland)|March 31, 2016
An FDA-Drug Library Screen for Compounds with Bioactivities against Meticillin-Resistant Staphylococcus aureus (MRSA)Qiu Ying Lau, Yoke Yan Fion Tan, Vanessa Chai Yin Goh, et al.
Chemmedchem|October 17, 2014
3-Deazaneplanocin A and neplanocin A analogues and their effects on apoptotic cell deathEric K W Tam, Tuan Minh Nguyen, Cheryl Z H Lim, et al.
Journal of Medicinal Chemistry|March 25, 2016
Structure-Activity Relationship Studies of Mitogen Activated Protein Kinase Interacting Kinase (MNK) 1 and 2 and BCR-ABL1 Inhibitors Targeting Chronic Myeloid Leukemic CellsJoseph Cherian, Kassoum Nacro, Zhi Ying Poh, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
BMC Genomics|July 20, 2022
Deep learning for de-convolution of Smad2 versus Smad3 binding sitesJeremy W K Ng, Esther H Q Ong, Lisa Tucker-Kellogg, et al.
Bioorganic & Medicinal Chemistry|December 3, 2014
Design, synthesis and biological evaluation of FLT3 covalent inhibitors with a resorcylic acid coreJin Xu, Esther H Q Ong, Jeffrey Hill, et al.
Chemmedchem|August 10, 2013
Rational design of resorcylic acid lactone analogues as covalent MNK1/2 kinase inhibitors by tuning the reactivity of an enamide Michael acceptorJin Xu, Anqi Chen, Joma Joy, et al.
Chemical Biology & Drug Design|March 23, 2021
Designing a leucine-rich antibacterial nonapeptide with potent activity against mupirocin-resistant MRSA via a structure-activity relationship studyQi An Ang, Giovinna Arfan, Chu Yang Fann Ong, et al.
Antibiotics (Basel, Switzerland)|March 31, 2016
An FDA-Drug Library Screen for Compounds with Bioactivities against Meticillin-Resistant Staphylococcus aureus (MRSA)Qiu Ying Lau, Yoke Yan Fion Tan, Vanessa Chai Yin Goh, et al.
Chemmedchem|October 17, 2014
3-Deazaneplanocin A and neplanocin A analogues and their effects on apoptotic cell deathEric K W Tam, Tuan Minh Nguyen, Cheryl Z H Lim, et al.
Journal of Medicinal Chemistry|March 25, 2016
Structure-Activity Relationship Studies of Mitogen Activated Protein Kinase Interacting Kinase (MNK) 1 and 2 and BCR-ABL1 Inhibitors Targeting Chronic Myeloid Leukemic CellsJoseph Cherian, Kassoum Nacro, Zhi Ying Poh, et al.
Pageof 1