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Published in Proceedings of the National Academy of Sciences - PNAS (11.01.2011)
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Published in Neurobiology of disease (01.08.2022)
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A Single Dopamine Pathway Underlies Progressive Locomotor Deficits in a Drosophila Model of Parkinson Disease
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Published in Cell reports (Cambridge) (27.11.2013)
Published in Cell reports (Cambridge) (27.11.2013)
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Published in Human molecular genetics (01.06.2019)
Published in Human molecular genetics (01.06.2019)
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Cerebral Semaphorin3D is a novel risk factor for age-associated cognitive impairment
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Published in Cell communication and signaling (14.06.2023)
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Amyloid Precursor Proteins Are Dynamically Trafficked and Processed during Neuronal Development
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Published in Frontiers in molecular neuroscience (25.11.2016)
Published in Frontiers in molecular neuroscience (25.11.2016)
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A dopamine receptor contributes to paraquat-induced neurotoxicity in Drosophila
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Published in Human molecular genetics (01.01.2015)
Published in Human molecular genetics (01.01.2015)
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A dopamine receptor contributes to paraquat-induced neurotoxicity in Drosophila
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Published in Human molecular genetics (01.01.2015)
Published in Human molecular genetics (01.01.2015)
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PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways
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Published in medRxiv : the preprint server for health sciences (20.06.2024)
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Published in medRxiv : the preprint server for health sciences (20.06.2024)
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Reinhardt, Anita, Feuillette, Sébastien, Cassar, Marlène, Callens, Céline, Thomassin, Hélène, Birman, Serge, Lecourtois, Magalie, Antoniewski, Christophe, Tricoire, Hervé
Published in Frontiers in genetics (2012)
Published in Frontiers in genetics (2012)
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Journal Article
Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models
Reinhardt, Anita, Feuillette, Sébastien, Cassar, Marlène, Callens, Céline, Thomassin, Hélène, Birman, Serge, Lecourtois, Magalie, Antoniewski, Christophe, Tricoire, Hérvé
Published in Frontiers in genetics (2012)
Published in Frontiers in genetics (2012)
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