{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T21:38:38Z","timestamp":1793482718303,"version":"4.5.0"},"reference-count":42,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T00:00:00Z","timestamp":1649116800000},"content-version":"vor","delay-in-days":94,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["alz-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["A&amp;D Transl Res &amp; Clin Interv"],"published-print":{"date-parts":[[2022,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>The neuronal mechanism driving Alzheimer's disease (AD) is incompletely understood.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Immunohistochemistry, pharmacology, biochemistry, and behavioral testing are employed in two pathological contexts\u2014AD and a transgenic mouse model\u2014to investigate T14, a 14mer peptide, as a key signaling molecule in the neuropathology.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>T14 increases in AD brains as the disease progresses and is conspicuous in 5XFAD mice, where its immunoreactivity corresponds to that seen in AD: neurons immunoreactive for T14 in proximity to T14\u2010immunoreactive plaques. NBP14 is a cyclized version of T14, which dose\u2010dependently displaces binding of its linear counterpart to alpha\u20107 nicotinic receptors in AD brains. In 5XFAD mice, intranasal NBP14 for 14\u00a0weeks decreases brain amyloid and restores novel object recognition to that in wild\u2010types.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>These findings indicate that the T14 system, for which the signaling pathway is described here, contributes to the neuropathological process and that NBP14 warrants consideration for its therapeutic potential.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/trc2.12274","type":"journal-article","created":{"date-parts":[[2022,4,6]],"date-time":"2022-04-06T00:01:10Z","timestamp":1649203270000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["A novel process driving Alzheimer's disease validated in a mouse model: Therapeutic 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