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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

Sci Rep. 2017; 
GengRuishuang,OmarAkil,GopalSuhasini R,ChenDaniel H-C,StepanyanRuben,BaschMartin L,DinculescuAstra,FurnessDavid N,SapersteinDavid,HauswirthWilliam,LustigLawrence R,AlagramamKum
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Gene Synthesis A construct containing only the above 5′ and 3′ UTR sequences and a unique NotI site between them was synthesized by GenScript (Piscataway, NJ). Get A Quote

摘要

Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by mutations in the clarin-1 gene (CLRN1). Clrn1 knockout (KO) mice develop hair cell defects by postnatal day 2 (P2) and are deaf by P21-P25. Early onset profound hearing loss in KO mice and lack of information about the cochlear cell type that requires Clrn1 expression pose challenges to therapeutic investigation. We generated KO mice harboring a transgene, TgAC1, consisting of Clrn1-UTR (Clrn1 cDNA including its 5' and 3' UTR) under the control of regulatory elements (Atoh1 3' enhancer/β-globin basal promoter) to direct expression of Clrn1 in hair cells during development and down regulate it postnatally. Th... More

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