Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Susan L. Wang"'
Publikováno v:
Journal of Hematotherapy. 4:389-394
The heterodimer-forming leucine zippers Fos and Jun can efficiently mediate the formation of bispecific F(ab')2 when they are fused separately to two different Fab' fragments. This recombinant method can be used in conjunction with the humanization p
Autor:
Jun R. Huh, R. M. Renny Feldman, Bruce A. Hay, Israel Muro, H.-Arno J. Müller, Hong Yu, Lijuan Wang, Soon Ji Yoo, Rollie J. Clem, Susan L. Wang
Publikováno v:
Nature cell biology. 4(6)
Inhibitor of apoptosis (IAP) proteins suppress apoptosis and inhibit caspases. Several IAPs also function as ubiquitin-protein ligases. Regulators of IAP auto-ubiquitination, and thus IAP levels, have yet to be identified. Here we show that Head invo
Autor:
Stephanie Y. Vernooy, Soon Ji Yoo, Bruce A. Hay, Susan L. Wang, Erin P. Peterson, Christine J. Hawkins
Publikováno v:
Journal of Biological Chemistry.
The caspase family of cysteine proteases plays important roles in bringing about apoptotic cell death. All caspases studied to date cleave substrates COOH-terminal to an aspartate. Here we show that the Drosophila caspase DRONC cleaves COOH-terminal
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03b205c213437b9db03d0102432724b6
https://doi.org/10.1016/s0076-6879(00)22016-8
https://doi.org/10.1016/s0076-6879(00)22016-8
Publikováno v:
ResearcherID
Site-specific proteases play critical roles in regulating many cellular processes. To identify novel site-specific proteases, their regulators, and substrates, we have designed a general reporter system in Saccharomyces cerevisiae in which a transcri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d338565f2d137d8ee35f1ecdba17fcc5
https://resolver.caltech.edu/CaltechAUTHORS:20141125-135327646
https://resolver.caltech.edu/CaltechAUTHORS:20141125-135327646
Publikováno v:
ResearcherID
>Drosophila Reaper (RPR), Head Involution Defective (HID), and GRIM induce caspase-dependent cell death and physically interact with the cell death inhibitor DIAP1. Here we show that HID blocks DIAP1's ability to inhibit caspase activity and provide