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- W1556934672 abstract "Publisher Summary This chapter focuses on molecules and mechanisms that are at considerably earlier stages of development, are novel approaches to neuroprotection, and may become the next generation of drugs for the treatment of acute ischemic and hemorrhagic strokes. Neuroprotection by caspase inhibitors and poly [adenosine diphosphate (ADP)-ribose] polymerase inhibitors is described. Caspases are a family of cysteine proteases that are expressed as inactive zymogens and undergo proteolytic maturation in a sequential manner. Poly (ADP-ribose) polymerase-1 (PARP-1) is a chromatin-bound nuclear enzyme involved in a variety of physiological functions related to genomic repair, including deoxyribonucleic acid (DNA) replication and repair, cellular proliferation and differentiation, and apoptosis. Peroxisome proliferator-activated receptors (PPARs) are orphan receptors belonging to the steroids/thyroid/retinoid receptor super family of ligand-activated transcription factors. There are three peroxisome-proliferator-activated receptor (PPAR) isoforms (PPAR-α, -β, -γ), each of which is differentially expressed and displays a distinct pattern of ligand specificity. Src-family protein tyrosine kinases (SFKs) are important signaling enzymes controlling cell growth, proliferation, and migration." @default.
- W1556934672 created "2016-06-24" @default.
- W1556934672 creator A5037517823 @default.
- W1556934672 creator A5068471141 @default.
- W1556934672 date "2006-01-01" @default.
- W1556934672 modified "2023-10-03" @default.
- W1556934672 title "Neuroprotective Agents for the Treatment of Ischemic and Hemorrhagic Stroke" @default.
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- W1556934672 doi "https://doi.org/10.1016/s0065-7743(06)41003-4" @default.
- W1556934672 hasPublicationYear "2006" @default.
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