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- W2770793072 endingPage "21" @default.
- W2770793072 startingPage "8" @default.
- W2770793072 abstract "The ideal biomarker for central nervous system (CNS) trauma in patients would be a molecular marker specific for injured nervous tissue that would provide a consistent and reliable assessment of the presence and severity of injury and the prognosis for recovery. One candidate biomarker is the protein tau, a microtubule-associated protein abundant in the axonal compartment of CNS neurons. Following axonal injury, tau becomes modified primarily by hyperphosphorylation of its various amino acid residues and cleavage into smaller fragments. These posttrauma products can leak into the cerebrospinal fluid or bloodstream and become candidate biomarkers of CNS injury. This review examines the primary molecular changes that tau undergoes following traumatic brain injury and spinal cord injury, and reviews the current literature in traumatic CNS biomarker research with a focus on the potential for hyperphosphorylated and cleaved tau as sensitive biomarkers of injury." @default.
- W2770793072 created "2017-12-04" @default.
- W2770793072 creator A5002661666 @default.
- W2770793072 creator A5053657905 @default.
- W2770793072 creator A5082748723 @default.
- W2770793072 date "2017-11-22" @default.
- W2770793072 modified "2023-09-27" @default.
- W2770793072 title "CNS Injury: Posttranslational Modification of the Tau Protein as a Biomarker" @default.
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- W2770793072 doi "https://doi.org/10.1177/1073858417742125" @default.
- W2770793072 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29283022" @default.
- W2770793072 hasPublicationYear "2017" @default.