Dmd061242 353..357
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چکیده
Cytochrome P450 enzymes from the CYP2C subfamily play a prominent role in the metabolic clearance of many drugs. CYP2C enzymes have also been implicated in the metabolism of arachidonic acid to vasoactive epoxyeicosatrienoic acids. CYP2C8, CYP2C9, and CYP2C19 are expressed in the adult liver at significant levels; however, the expression of CYP2C enzymes in extrahepatic tissues such as the brain is less well characterized. Form-specific antibodies to CYP2C9 and CYP2C19 were prepared by affinity purification of antibodies raised to unique peptides. CYP2C9 and CYP2C19 were located in microsomal fractions of all five human brain regions examined, namely the frontal cortex, hippocampus, basal ganglia, amygdala, and cerebellum. Both CYP2C9 and CYP2C19 were detected predominantly within the neuronal soma but with expression extending down axons and dendrites in certain regions. Finally, a comparison of cortex samples from alcoholics and age-matched controls suggested that CYP2C9 expression was increased in alcoholics.
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Dmd061242 353..357
Cytochrome P450 enzymes from the CYP2C subfamily play a prominent role in the metabolic clearance of many drugs. CYP2C enzymes have also been implicated in the metabolism of arachidonic acid to vasoactive epoxyeicosatrienoic acids. CYP2C8, CYP2C9, and CYP2C19 are expressed in the adult liver at significant levels; however, the expression of CYP2C enzymes in extrahepatic tissues such as the brai...
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abelian [326, 408, 91, 337]. Abstract [117]. Accelerated [512]. Accelerating [398]. Achieve [477]. Acoustic [525]. Adaptive [241, 390, 471]. Adaptively [523, 390]. Adic [130]. Advance [279]. Adversarial [458]. Adversaries [353, 345, 357, 403, 450, 472, 501, 236]. Adversary [173]. AES [373, 474, 346, 459]. AES-192 [474]. AES-256 [474]. AES-like [459]. after [76]. Against [353, 480, 520, 348, 500...
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Presenilin 1 (PS1), a causative molecule of familial Alzheimer's disease (AD), is known to be an unprimed substrate of GSK3 (Twomey et al. 2006) and is phosphorylated at serine 353, 357 residues in its cytoplasmic loop region (Kirschenbaum et al. 2001). In this report, we investigated the effect of PS1 phosphorylation on AD pathophysiology and obtained two important results – PS1 phosphorylati...
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