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  1. Article

    Open Access

    Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment

    KCNQ4 is frequently mutated in autosomal dominant non-syndromic hearing loss (NSHL), a typically late-onset, initially high-frequency loss that progresses over time (DFNA2). Most KCNQ4 mutations linked to hearing...

    **sei Jung, Haiyue Lin, Young Ik Koh, Kunhi Ryu… in Experimental & Molecular Medicine (2019)

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  2. Article

    Open Access

    Enhancement of 5-HT2A receptor function and blockade of Kv1.5 by MK801 and ketamine: implications for PCP derivative-induced disease models

    MK801 and ketamine, which are phencyclidine (PCP) derivative N-methyl-d-aspartate receptor (NMDAr) blockers, reportedly enhance the function of 5-hydroxytryptamine (HT)-2A receptors (5-HT2ARs). Both are believed ...

    Haiyue Lin, Jae Gon Kim, Sang Woong Park, Hyun Ju Noh… in Experimental & Molecular Medicine (2018)

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