Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jason E. Boehm"'
Autor:
Joseph J. Wakshlag, Richard A. Cerione, Jaclyn M. Jansen, Allison M. Miller, Jason E. Boehm, Marc A. Antonyak, Cheryl E. Balkman, Rodney L. Page
Publikováno v:
Journal of Biological Chemistry. 279:41461-41467
Tissue transglutaminase (TGase) exhibits both a GTP binding/hydrolytic capability and an enzymatic transamidation activity. Increases in TGase expression and activation often occur in response to stimuli that promote cellular differentiation and apop
Publikováno v:
Journal of Biological Chemistry. 277:14712-14716
Tissue transglutaminase (TGase) is a dual function enzyme that couples an ability to bind GTP with transamidation activity. Retinoic acid (RA) consistently induces TGase expression and activation, and it was recently shown that increased TGase expres
Publikováno v:
Journal of Biological Chemistry. 274:28632-28636
Mutations in the cytoplasmic domain of the insulin receptor that block the ability of the receptor to stimulate glucose uptake do not block the receptor's ability to inhibit apoptosis (Boehm, J. E., Chaika, O. V., and Lewis, R. E. (1998) J. Biol. Che
Publikováno v:
Journal of Biological Chemistry. 273:7169-7176
The intracellular mechanisms used by insulin and insulin-like growth factors to block programmed cell death are unknown. To identify receptor structures and signaling pathways essential for anti-apoptotic effects on cells, we have created a chimeric
Autor:
Joseph J. Wakshlag, Jason E. Boehm, Cheryl E. Balkman, Richard A. Cerione, C.J. McNeill, R. Fuji, Rodney L. Page, Marsha M. Zgola, Marc A. Antonyak
Publikováno v:
Journal of comparative pathology. 134(2-3)
Tissue transglutaminase II (TGase II) is a dual function protein with both transamidating and guanidine triphosphate (GTP)-binding capabilities. Previous studies have implicated TGase as a pro-apoptotic molecule; however, our recent findings indicate
Publikováno v:
The Journal of biological chemistry. 278(18)
Retinoic acid (RA) is a potent activator of tissue transglutaminase (TGase) expression, and it was recently shown that phosphoinositide 3-kinase (PI3K) activity was required for RA to increase TGase protein levels. To better understand how RA-mediate
Autor:
Marc A. Antonyak, Ugra S. Singh, David A. Lee, Richard A. Cerione, Marsha M. Zgola, Carolyn Combs, Rodney L. Page, Jason E. Boehm
Publikováno v:
The Journal of biological chemistry. 276(36)
Retinoic acid (RA) and its various synthetic analogs affect mammalian cell growth, differentiation, and apoptosis. Whereas treatment of the human leukemia cell line HL60 with RA results in cellular differentiation, addition of the synthetic retinoid,