Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Paula D. Nathaniel"'
Autor:
Simon C. Watkins, Csaba Szabó, Larry W. Jenkins, Patrick M. Kochanek, Yi-Chen Lai, Fengli Guo, Robert S. B. Clark, Yaming Chen, Paula D. Nathaniel
Publikováno v:
Journal of Neurochemistry. 104:1700-1711
Poly-ADP-ribosylation is a post-translational modification performed by poly(ADP-ribose) polymerases (PARP), involved in many diverse cellular functions including DNA repair, transcription, and long-term potentiation. Paradoxically, PARP over-activat
Autor:
Csaba Szabó, Larry W. Jenkins, Paula D. Nathaniel, C. Edward Dixon, Robert S. B. Clark, Vincent Vagni
Publikováno v:
Journal of Neurotrauma. 24:1399-1405
Poly(ADP-ribose) polymerase-1 (PARP-1) is an enzyme best known for its role in DNA repair and as a mediator of NAD+ depletion and energy failure-induced cell death. We tested the effect of the potent and selective ideno-isoquinolone PARP-1 inhibitor
Autor:
Jun Chen, Lina Du, Fengli Guo, Steven H. Graham, Paula D. Nathaniel, Patrick M. Kochanek, Simon C. Watkins, Xiaopeng Zhang, Romesh Draviam, Robert S. B. Clark, Csaba Szabó
Publikováno v:
Journal of Neurochemistry. 82:181-191
Programmed cell death occurs after ischemic, excitotoxic, and traumatic brain injury (TBI). Recently, a caspase-independent pathway involving intranuclear translocation of mitochondrial apoptosis-inducing factor (AIF) has been reported in vitro; but
Autor:
Robert S. B. Clark, Neal A. Seidberg, Kunlin Jin, Patrick M. Kochanek, Paula D. Nathaniel, Minzhi Chen, Simon C. Watkins, John A. Melick, Steven H. Graham, J. E. Loeffert, C. E. Dixon
Publikováno v:
Journal of Neurochemistry. 74:740-753
During programmed cell death, activation of caspase-3 leads to proteolysis of DNA repair proteins, cytoskeletal proteins, and the inhibitor of caspase-activated deoxyribonuclease, culminating in morphologic changes and DNA damage defining apoptosis.
Autor:
Yichen, Lai, Yaming, Chen, Simon C, Watkins, Paula D, Nathaniel, Fengli, Guo, Patrick M, Kochanek, Larry W, Jenkins, Csaba, Szabó, Robert S B, Clark
Publikováno v:
Journal of neurochemistry. 104(6)
Poly-ADP-ribosylation is a post-translational modification performed by poly(ADP-ribose) polymerases (PARP), involved in many diverse cellular functions including DNA repair, transcription, and long-term potentiation. Paradoxically, PARP over-activat
Autor:
Simon C. Watkins, Sean Alber, Patrick M. Kochanek, Steven H. Graham, Robert S. B. Clark, C. Edward Dixon, Xiaopeng Zhang, Paula D. Nathaniel, John A. Melick
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 27(2)
The pathobiology of traumatic brain injury (TBI) includes activation of multiple caspases followed by cell death with a spectrum of apoptotic phenotypes. There are initiator (e.g. caspase-2, −8, and −9) and effector (e.g. caspase-3 and −7) casp
Autor:
Patrick M. Kochanek, Milos D. Ikonomovic, Donald W. Marion, Xiaopeng Zhang, Steven T. DeKosky, Robert S. B. Clark, Paula D. Nathaniel, Larry W. Jenkins, Yarning Chen
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 26(7)
Activation of protein kinase B (PKB, also known as Akt) by phosphorylation at serine-473 and threonine-308 promotes cell survival in multiple in vitro and in vivo models where neuronal death is seen, including traumatic brain injury (TBI); however, w
Autor:
Xiaopeng Zhang, Paula D. Nathaniel, Patrick M. Kochanek, Simon C. Watkins, Donald W. Marion, Robert S. B. Clark, Steven H. Graham
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 17(10)
Programmed cell death involves a complex and interrelated cascade of cysteine proteases termed caspases that are synthesized as inactive zymogens, which are proteolytically processed to active enzymes. Caspase-8 is an initiator caspase that becomes a
Autor:
Minzhi Chen, Kunlin Jin, Simon C. Watkins, Donald W. Marion, Steven H. Graham, Romesh Draviam, Robert S. B. Clark, Rodnina Pinto, Patrick M. Kochanek, Paula D. Nathaniel
Publikováno v:
Journal of neurotrauma. 18(7)
DNA damage is a common sequela of traumatic brain injury (TBI). Available techniques for the in situ identification of DNA damage include DNA polymerase I-mediated biotin-dATP nick-translation (PANT), the Klenow fragment of DNA polymerase I-mediated
Publikováno v:
Critical Care Medicine. 33:A16