{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,7,16]],"date-time":"2026-07-16T20:57:27Z","timestamp":1784235447642,"version":"3.55.0"},"posted":{"date-parts":[[2024,1,26]]},"group-title":"Pathology","reference-count":82,"publisher":"openRxiv","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2024,1,26]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                <jats:p>\n                  Pendrin and prestin are evolutionary conserved membrane proteins that are essential for normal hearing. Pendrin is an anion transporter required for normal development and maintenance of ion homeostasis in the inner ear, while prestin is a voltage-dependent motor responsible for cochlear amplification essential for high sensitivity and frequency selectivity of mammalian hearing. Dysfunction of these proteins result in hearing loss in humans, and numerous deafness-associated pendrin and prestin variants have been identified in patients. However, the pathogenic impacts of many of these variants are ambiguous. Here we report results from our ongoing efforts in experimentally characterizing pendrin and prestin variants using\n                  <jats:italic>in vitro<\/jats:italic>\n                  functional assays, providing invaluable information regarding their pathogenicity.\n                <\/jats:p>","DOI":"10.1101\/2024.01.23.576877","type":"posted-content","created":{"date-parts":[[2024,1,26]],"date-time":"2024-01-26T21:45:10Z","timestamp":1706305510000},"source":"Crossref","is-referenced-by-count":2,"title":["Functional studies of deafness-associated pendrin and prestin 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