Zobrazeno 1 - 7
of 7
pro vyhledávání: '"A. Z. Spitz"'
Autor:
Adam Z. Spitz, Emmanouil Zacharioudakis, Denis E. Reyna, Thomas P. Garner, Evripidis Gavathiotis
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
The BCL-2 family protein BAX functions to regulate mitochondria-driven cell death. Here the authors show that the drug Eltrombopag inhibits BAX and prevents apoptosis induced by cytotoxic stimuli.
Externí odkaz:
https://doaj.org/article/31bab891d7f643189094349969145575
Autor:
Evripidis Gavathiotis, Adam Z. Spitz
Publikováno v:
Trends Pharmacol Sci
Bcl-2-associated X protein (BAX) is a critical executioner of mitochondrial regulated cell death through its lethal activity of permeabilizing the mitochondrial outer membrane (MOM). While the physiological function of BAX ensures tissue homeostasis,
Autor:
Thomas P. Garner, Denis E. Reyna, Evripidis Gavathiotis, Emmanouil Zacharioudakis, Adam Z. Spitz
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications
Nature Communications
The BCL-2 family protein BAX has essential activity in mitochondrial regulation of cell death. While BAX activity ensures tissue homeostasis, when dysregulated it contributes to aberrant cell death in several diseases. During cellular stress BAX is t
Publikováno v:
Current Opinion in Chemical Biology. 39:133-142
The network of protein-protein interactions among the BCL-2 protein family plays a critical role in regulating cellular commitment to mitochondrial apoptosis. Anti-apoptotic BCL-2 proteins are considered promising targets for drug discovery and excit
Autor:
Ross S. Firestone, Scott A. Cameron, Adam Z. Spitz, Peter C. Tyler, Vern L. Schramm, Rodrigo G. Ducati
Publikováno v:
Analytical chemistry. 88(23)
5′-Methylthioadenosine phosphorylase (MTAP) and 5′-methylthioadenosine nucleosidase (MTAN) catalyze the phosphorolysis and hydrolysis of 5′-methylthioadenosine (MTA), respectively. Both enzymes have low KM values for their substrates. Kinetic a
Publikováno v:
ChemInform. 47
A method for the [2 + 2] cycloaddition of aryl ketenes and alkenes is presented. The process involves the in situ generation of a ketene in the presence of a Lewis acid. The utility of products is demonstrated towards the synthesis of a common scaffo
A method for the [2 + 2] cycloaddition of aryl ketenes and alkenes is presented. The process involves the in situ generation of a ketene in the presence of a Lewis acid. The utility of products is demonstrated towards the synthesis of a common scaffo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d155074da8fc3d072f8d53b74cad354c
https://europepmc.org/articles/PMC4814371/
https://europepmc.org/articles/PMC4814371/