Lhfpl5-flox 基因敲除小鼠

1. Kalay, Ersan, Li, Yun, Uzumcu, Abdullah, Kremer, Hannie, Wollnik, Bernd. . Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. In Human mutation, 27, 633-9. doi:. https://pubmed.ncbi.nlm.nih.gov/16752389/

2. György, Bence, Sage, Cyrille, Indzhykulian, Artur A, Corey, David P, Maguire, Casey A. 2017. Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV. In Molecular therapy : the journal of the American Society of Gene Therapy, 25, 379-391. doi:10.1016/j.ymthe.2016.12.010. https://pubmed.ncbi.nlm.nih.gov/28082074/

3. Erickson, Timothy, Pacentine, Itallia V, Venuto, Alexandra, Clemens, Rachel, Nicolson, Teresa. 2020. The lhfpl5 Ohnologs lhfpl5a and lhfpl5b Are Required for Mechanotransduction in Distinct Populations of Sensory Hair Cells in Zebrafish. In Frontiers in molecular neuroscience, 12, 320. doi:10.3389/fnmol.2019.00320. https://pubmed.ncbi.nlm.nih.gov/32009898/