J
JingQi Huang
Researcher at Merck & Co.
Publications - 11
Citations - 906
JingQi Huang is an academic researcher from Merck & Co.. The author has contributed to research in topics: Computer science & Caspase. The author has an hindex of 7, co-authored 7 publications receiving 879 citations.
Papers
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Journal ArticleDOI
Involvement of Caspases in Proteolytic Cleavage of Alzheimer’s Amyloid-β Precursor Protein and Amyloidogenic Aβ Peptide Formation
François G. Gervais,Daigen Xu,George S. Robertson,John P. Vaillancourt,Yanxia Zhu,JingQi Huang,Andréa C. LeBlanc,Smith David W,Michael Rigby,Mark S. Shearman,Earl E. Clarke,Hui Zheng,Leonardus H. T. Van Der Ploeg,Salvatore C. Ruffolo,Nancy A. Thornberry,Steve Xanthoudakis,Robert Zamboni,Sophie Roy,Donald W. Nicholson +18 more
TL;DR: Caspases appear to play a dual role in proteolytic processing of APP and the resulting propensity for Aβ peptide formation, as well as in the ultimate apoptotic death of neurons in Alzheimer's disease.
Journal ArticleDOI
Differential Efficacy of Caspase Inhibitors on Apoptosis Markers during Sepsis in Rats and Implication for Fractional Inhibition Requirements for Therapeutics
Nathalie Méthot,JingQi Huang,Nathalie Coulombe,John P. Vaillancourt,Dita M. Rasper,John Tam,Yongxin Han,John Colucci,Robert Zamboni,Steven Xanthoudakis,Sylvie Toulmond,Donald W. Nicholson,Sophie Roy +12 more
TL;DR: Findings suggest that putative caspase-independent apoptosis may be overestimated in some systems since blockade of spectrin proteolysis and other cell death markers does not accurately reflect the high degrees of casp enzyme-3 inhibition needed to prevent DNA fragmentation.
Journal ArticleDOI
Disruption of largest subunit RNA polymerase II genes in Trypanosoma brucei.
TL;DR: It is concluded that the alpha-amanitin-resistant transcription of protein coding genes in T. brucei is not mediated by a diverged form of the largest subunit of pol II and that the presence of both the pol IIA and pol IIB genes is not essential for trypanosome viability.
Journal ArticleDOI
A Caspase Active Site Probe Reveals High Fractional Inhibition Needed to Block DNA Fragmentation
Nathalie Méthot,John P. Vaillancourt,JingQi Huang,John Colucci,Yongxin Han,Stéphane Ménard,Robert Zamboni,Sylvie Toulmond,Donald W. Nicholson,Sophie Roy +9 more
TL;DR: The use of a novel radiolabeled caspase inhibitor, [125I]M808, and an active site occupancy assay, which measure the fractional inhibition required to block apoptosis-induced DNA fragmentation suggest that a high and persistent fractional inhibited will be required for successful caspases inhibition-based therapies.
Patent
Antibodies that recognize app cleaved by caspases and methods of use
François G. Gervais,Sophie Roy,Donald W. Nicholson,Daigen Xu,George S. Robertson,JingQi Huang +5 more
TL;DR: In this paper, the roles of apoptotic proteases and caspases in cleavage of amyloid-β precursor protein (APP) and biogenesis of AMyloidogenic Aβ peptide species are described.