FMRP

  • hnRNP Q Regulates Internal Ribosome Entry Site-Mediated <em>fmr1</em> Translation in Neurons
    Research Article | Spotlight
    hnRNP Q Regulates Internal Ribosome Entry Site-Mediated fmr1 Translation in Neurons

    Fragile X syndrome (FXS) caused by loss of fragile X mental retardation protein (FMRP), is the most common cause of inherited intellectual disability. Numerous studies show that FMRP is an RNA binding protein that regulates translation of its binding targets and plays key roles in neuronal functions.

    Jung-Hyun Choi, Sung-Hoon Kim, Young-Hun Jeong, Sung Wook Kim, Kyung-Tai Min, Kyong-Tai Kim
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