Search Results - "Hervé, Mylène"
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Proteasome inhibitors to alleviate aberrant IKBKAP mRNA splicing and low IKAP/hELP1 synthesis in familial dysautonomia
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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CX3CR1 is dysregulated in blood and brain from schizophrenia patients
Published in Schizophrenia research (01-10-2015)“…Abstract The molecular mechanisms underlying schizophrenia remain largely unknown. Although schizophrenia is a mental disorder, there is increasing evidence to…”
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MicroRNA screening identifies a link between NOVA1 expression and a low level of IKAP in familial dysautonomia
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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MicroRNA screening identifies a link between NOVA1 expression and low level of IKAP/ELP1 in Familial dysautonomia
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…”
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Translational Identification of Transcriptional Signatures of Major Depression and Antidepressant Response
Published in Frontiers in molecular neuroscience (01-08-2017)“…Major depressive disorder (MDD) is a highly prevalent mental illness whose therapy management remains uncertain, with more than 20% of patients who do not…”
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Translational Identification of Transcriptional Signatures of Major Depression and Antidepressant Response
Published in Frontiers in molecular neuroscience (08-08-2017)“…Major depressive disorder (MDD) is a highly prevalent mental illness whose therapy management remains uncertain, with more than 20% of patients who do not…”
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