Marion Delenclos

Affiliations: 
Aarhus University, Aarhus, Denmark 
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"Marion Delenclos"
Mean distance: 16.49 (cluster 32)
 
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Publications

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Lim MJ, Boschen SL, Kurti A, et al. (2023) Investigating the Pathogenic Interplay of Alpha-Synuclein, Tau, and Amyloid Beta in Lewy Body Dementia: Insights from Viral-Mediated Overexpression in Transgenic Mouse Models. Biomedicines. 11
Fagen SJ, Burgess JD, Lim MJ, et al. (2023) Honokiol decreases alpha-synuclein mRNA levels and reveals novel targets for modulating alpha-synuclein expression. Frontiers in Aging Neuroscience. 15: 1179086
Hou X, Chen TH, Koga S, et al. (2023) Alpha-synuclein-associated changes in PINK1-PRKN-mediated mitophagy are disease context dependent. Brain Pathology (Zurich, Switzerland). e13175
Delenclos M, Burgess JD, Lamprokostopoulou A, et al. (2019) Cellular models of alpha-synuclein toxicity and aggregation. Journal of Neurochemistry
Delenclos M, Faroqi AH, Yue M, et al. (2017) Neonatal AAV delivery of alpha-synuclein induces pathology in the adult mouse brain. Acta Neuropathologica Communications. 5: 51
Delenclos M, Trendafilova T, Jones DR, et al. (2015) A Rapid, Semi-Quantitative Assay to Screen for Modulators of Alpha-Synuclein Oligomerization Ex vivo. Frontiers in Neuroscience. 9: 511
Delenclos M, Carrascal L, Jensen K, et al. (2015) Corrigendum to “Immunolocalization of human alpha-synuclein in the Thy1-aSyn (“Line 61”) transgenic mouse line” [Neuroscience 277 (2014) 647–664] Neuroscience. 285: 356
Delenclos M, Carrascal L, Jensen K, et al. (2014) Immunolocalization of human alpha-synuclein in the Thy1-aSyn ("Line 61") transgenic mouse line. Neuroscience. 277: 647-64
Drasbek KR, Holm MM, Delenclos M, et al. (2008) Mapping of the spontaneous deletion in the Ap3d1 gene of mocha mice: fast and reliable genotyping. Bmc Research Notes. 1: 119
Drasbek KR, Vardya I, Delenclos M, et al. (2008) SSADH deficiency leads to elevated extracellular GABA levels and increased GABAergic neurotransmission in the mouse cerebral cortex. Journal of Inherited Metabolic Disease. 31: 662-8
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