Controlling programmed cell death with a cyclophilincyclosporin-based chemical inducer of dimerization
Open Access
- 1 September 1996
- journal article
- Published by Elsevier in Chemistry & Biology
- Vol. 3 (9), 731-738
- https://doi.org/10.1016/s1074-5521(96)90249-5
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Dimeric ligands define a role for transcriptional activation domains in reinitiationNature, 1996
- Functional analysis of Fas signaling in vivo using synthetic inducers of dimerizationCurrent Biology, 1996
- FLICE, A Novel FADD-Homologous ICE/CED-3–like Protease, Is Recruited to the CD95 (Fas/APO-1) Death-Inducing Signaling ComplexCell, 1996
- Involvement of MACH, a Novel MORT1/FADD-Interacting Protease, in Fas/APO-1- and TNF Receptor–Induced Cell DeathCell, 1996
- A License to KillCell, 1996
- Rational Design of Orthogonal Receptor–Ligand CombinationsAngewandte Chemie International Edition in English, 1995
- Mechanistic studies of a signaling pathway activated by the organic dimerizer FK1012Chemistry & Biology, 1994
- Synthesis of the main metabolite (OL-17) of cyclosporin AThe Journal of Organic Chemistry, 1992
- Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexesCell, 1991
- Lpr and gld: Single Gene Models of Systemic Autoimmunity and Lymphoproliferative DiseaseAnnual Review of Immunology, 1991