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Jim Wong

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

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The Journal of Cell Biology|June 14, 2006
HURP controls spindle dynamics to promote proper interkinetochore tension and efficient kinetochore captureJim Wong, Guowei Fang
Methods in Molecular Biology (Clifton, N.J.)|June 10, 2004
A Xenopus cell-free system for analysis of the Chfr ubiquitin ligase involved in control of mitotic entryDongmin Kang, Jim Wong, Guowei Fang
The Journal of Cell Biology|January 25, 2002
The checkpoint protein Chfr is a ligase that ubiquitinates Plk1 and inhibits Cdc2 at the G2 to M transitionDongmin Kang, James Chen, Jim Wong, et al.
Molecular Biology of the Cell|March 7, 2008
Aurora A regulates the activity of HURP by controlling the accessibility of its microtubule-binding domainJim Wong, Robert Lerrigo, Chang-Young Jang, et al.
The Journal of Cell Biology|April 16, 2008
DDA3 recruits microtubule depolymerase Kif2a to spindle poles and controls spindle dynamics and mitotic chromosome movementChang-Young Jang, Jim Wong, Judith A Coppinger, et al.
Critical Care Medicine|September 23, 2009
Gene expression profiling: classification of mice with left ventricle systolic dysfunction using microarray analysisJim Wong, Christine Chang, Rani Agrawal, et al.
The Journal of Experimental Medicine|January 16, 2020
Mutation position is an important determinant for predicting cancer neoantigensAude-Hélène Capietto, Suchit Jhunjhunwala, Samuel B Pollock, et al.
Cancer Discovery|May 1, 2024
A Next-Generation BRAF Inhibitor Overcomes Resistance to BRAF Inhibition in Patients with BRAF-Mutant Cancers Using Pharmacokinetics-Informed Dose EscalationRona Yaeger, Meredith A McKean, Rizwan Haq, et al.
Journal of Medicinal Chemistry|August 1, 2024
Discovery of Pyrazolopyrazines as Selective, Potent, and Mutant-Active MET Inhibitors with Intracranial EfficacyQuinn A Bumpers, Robert W Pipal, Anna M Benz-Weeden, et al.
ACS Medicinal Chemistry Letters|February 19, 2025
Design of Potent Menin-KMT2A Interaction Inhibitors with Improved <i>In Vitro</i> ADME Properties and Reduced hERG AffinityBruno D Chapsal, Jennifer R Kimbrough, Stephanie M Bester, et al.
Pageof 1

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

Sort By:
Pageof 1
The Journal of Cell Biology|June 14, 2006
HURP controls spindle dynamics to promote proper interkinetochore tension and efficient kinetochore captureJim Wong, Guowei Fang
Methods in Molecular Biology (Clifton, N.J.)|June 10, 2004
A Xenopus cell-free system for analysis of the Chfr ubiquitin ligase involved in control of mitotic entryDongmin Kang, Jim Wong, Guowei Fang
The Journal of Cell Biology|January 25, 2002
The checkpoint protein Chfr is a ligase that ubiquitinates Plk1 and inhibits Cdc2 at the G2 to M transitionDongmin Kang, James Chen, Jim Wong, et al.
Molecular Biology of the Cell|March 7, 2008
Aurora A regulates the activity of HURP by controlling the accessibility of its microtubule-binding domainJim Wong, Robert Lerrigo, Chang-Young Jang, et al.
The Journal of Cell Biology|April 16, 2008
DDA3 recruits microtubule depolymerase Kif2a to spindle poles and controls spindle dynamics and mitotic chromosome movementChang-Young Jang, Jim Wong, Judith A Coppinger, et al.
Critical Care Medicine|September 23, 2009
Gene expression profiling: classification of mice with left ventricle systolic dysfunction using microarray analysisJim Wong, Christine Chang, Rani Agrawal, et al.
The Journal of Experimental Medicine|January 16, 2020
Mutation position is an important determinant for predicting cancer neoantigensAude-Hélène Capietto, Suchit Jhunjhunwala, Samuel B Pollock, et al.
Cancer Discovery|May 1, 2024
A Next-Generation BRAF Inhibitor Overcomes Resistance to BRAF Inhibition in Patients with BRAF-Mutant Cancers Using Pharmacokinetics-Informed Dose EscalationRona Yaeger, Meredith A McKean, Rizwan Haq, et al.
Journal of Medicinal Chemistry|August 1, 2024
Discovery of Pyrazolopyrazines as Selective, Potent, and Mutant-Active MET Inhibitors with Intracranial EfficacyQuinn A Bumpers, Robert W Pipal, Anna M Benz-Weeden, et al.
ACS Medicinal Chemistry Letters|February 19, 2025
Design of Potent Menin-KMT2A Interaction Inhibitors with Improved <i>In Vitro</i> ADME Properties and Reduced hERG AffinityBruno D Chapsal, Jennifer R Kimbrough, Stephanie M Bester, et al.
Pageof 1