Search Results - "Hervé, Mylène"

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    Proteasome inhibitors to alleviate aberrant IKBKAP mRNA splicing and low IKAP/hELP1 synthesis in familial dysautonomia by Hervé, Mylène, Ibrahim, El Chérif

    Published in Neurobiology of disease (01-07-2017)
    “…Abstract FD is a rare neurodegenerative disorder caused by a mutation of the IKBKAP gene, which induces low expression levels of the Elongator subunit…”
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    Journal Article
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    MicroRNA screening identifies a link between NOVA1 expression and a low level of IKAP in familial dysautonomia by Hervé, Mylène, Ibrahim, El Chérif

    Published in Disease models & mechanisms (01-08-2016)
    “…Familial dysautonomia (FD) is a rare neurodegenerative disease caused by a mutation in intron 20 of the IKBKAP gene (c.2204+6T>C), leading to tissue-specific…”
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    Journal Article
  4. 4

    MicroRNA screening identifies a link between NOVA1 expression and low level of IKAP/ELP1 in Familial dysautonomia by Hervé, Mylène, Ibrahim, El Chérif

    Published in Disease models & mechanisms (01-01-2016)
    “…Familial dysautonomia (FD) is a rare neurodegenerative disease caused by a mutation in intron 20 of the IKBKAP gene (c.2204+6T>C), leading to tissue-specific…”
    Get full text
    Journal Article
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