Search Results - "Rideout, Hardy"

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    Pathological roles of α-synuclein in neurological disorders by Vekrellis, Kostas, PhD, Xilouri, Maria, PhD, Emmanouilidou, Evangelia, PhD, Rideout, Hardy J, PhD, Stefanis, Leonidas, Dr

    Published in Lancet neurology (01-11-2011)
    “…Summary Substantial genetic, neuropathological, and biochemical evidence implicates the presynaptic neuronal protein α-synuclein in Parkinson's disease and…”
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    Journal Article
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    Neuronal death signaling pathways triggered by mutant LRRK2 by Rideout, Hardy J

    Published in Biochemical Society transactions (08-02-2017)
    “…Autosomal dominantly inherited mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson's disease…”
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    The Neurobiology of LRRK2 and its Role in the Pathogenesis of Parkinson’s Disease by Rideout, Hardy J., Stefanis, Leonidas

    Published in Neurochemical research (01-03-2014)
    “…Leucine-rich repeat kinase 2 (LRRK2) is a large, widely expressed protein of largely unknown function. Mutations in the gene encoding LRRK2 have been linked to…”
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    LRRK2 Parkinson disease mutations enhance its microtubule association by Kett, Lauren R., Boassa, Daniela, Ho, Cherry Cheng-Ying, Rideout, Hardy J., Hu, Junru, Terada, Masako, Ellisman, Mark, Dauer, William T.

    Published in Human molecular genetics (15-02-2012)
    “…Dominant missense mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic causes of Parkinson disease (PD) and genome-wide association…”
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    Activation of FADD-Dependent Neuronal Death Pathways as a Predictor of Pathogenicity for LRRK2 Mutations by Melachroinou, Katerina, Leandrou, Emmanouela, Valkimadi, Polytimi-Eleni, Memou, Anna, Hadjigeorgiou, Georgios, Stefanis, Leonidas, Rideout, Hardy J

    Published in PloS one (10-11-2016)
    “…Despite the plethora of sequence variants in LRRK2, only a few clearly segregate with PD. Even within this group of pathogenic mutations, the phenotypic…”
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    Defining (and blocking) neuronal death in Parkinson’s disease: Does it matter what we call it? by Memou, Anna, Dimitrakopoulos, Lampros, Kedariti, Maria, Kentros, Michalis, Lamprou, Andriana, Petropoulou-Vathi, Lilian, Valkimadi, Polytimi-Eleni, Rideout, Hardy J.

    Published in Brain research (15-11-2021)
    “…•Neuronal loss in Parkinson’s disease can take multiple forms.•Evidence of apoptotic, necroptotic, and pyroptotic signaling exists in PD.•The role of the…”
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    The WD40 domain is required for LRRK2 neurotoxicity by Jorgensen, Nathan D, Peng, Yong, Ho, Cherry C-Y, Rideout, Hardy J, Petrey, Donald, Liu, Peng, Dauer, William T

    Published in PloS one (24-12-2009)
    “…Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson disease (PD). LRRK2 contains an "enzymatic core" composed of…”
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    Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications? by Simone, Chiara, Ramirez, Agnese, Bucchia, Monica, Rinchetti, Paola, Rideout, Hardy, Papadimitriou, Dimitra, Re, Diane B, Corti, Stefania

    “…Spinal muscular atrophy (SMA) is a genetic neurological disease that causes infant mortality; no effective therapies are currently available. SMA is due to…”
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    The Parkinson Disease Protein Leucine-Rich Repeat Kinase 2 Transduces Death Signals via Fas-Associated Protein with Death Domain and Caspase-8 in a Cellular Model of Neurodegeneration by Ho, Cherry Cheng-Ying, Rideout, Hardy J, Ribe, Elena, Troy, Carol M, Dauer, William T

    Published in The Journal of neuroscience (28-01-2009)
    “…Neurodegenerative illnesses such as Parkinson and Alzheimer disease are an increasingly prevalent problem in aging societies, yet no therapies exist that…”
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    A motif within the armadillo repeat of Parkinson’s-linked LRRK2 interacts with FADD to hijack the extrinsic death pathway by Antoniou, Nasia, Vlachakis, Dimitrios, Memou, Anna, Leandrou, Emmanouela, Valkimadi, Polytimi-Eleni, Melachroinou, Katerina, Re, Diane B., Przedborski, Serge, Dauer, William T., Stefanis, Leonidas, Rideout, Hardy J.

    Published in Scientific reports (22-02-2018)
    “…In experimental models, both in vivo and cellular, over-expression of Parkinson’s linked mutant leucine-rich repeat kinase 2 (LRRK2) is sufficient to induce…”
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    The Current State-of-the Art of LRRK2-Based Biomarker Assay Development in Parkinson’s Disease by Rideout, Hardy J., Chartier-Harlin, Marie-Christine, Fell, Matthew J., Hirst, Warren D., Huntwork-Rodriguez, Sarah, Leyns, Cheryl E. G., Mabrouk, Omar S., Taymans, Jean-Marc

    Published in Frontiers in neuroscience (18-08-2020)
    “…Evidence is mounting that LRRK2 activity, particularly its kinase activity, is elevated in multiple forms of Parkinson’s disease, both idiopathic as well as…”
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    The Future of Targeted Gene-Based Treatment Strategies and Biomarkers in Parkinson's Disease by Polissidis, Alexia, Petropoulou-Vathi, Lilian, Nakos-Bimpos, Modestos, Rideout, Hardy J

    Published in Biomolecules (Basel, Switzerland) (16-06-2020)
    “…Biomarkers and disease-modifying therapies are both urgent unmet medical needs in the treatment of Parkinson's disease (PD) and must be developed concurrently…”
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    Editorial: LRRK2-Fifteen Years From Cloning to the Clinic by Rideout, Hardy, Greggio, Elisa, Kortholt, Arjan, Nichols, R Jeremy

    Published in Frontiers in neuroscience (11-04-2022)
    “…Along these lines, Cabezudo et al. discuss how mutant LRRK2-driven inflammation may trigger PD starting from peripheral organs such as the gut and immune…”
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    Perspective on the current state of the LRRK2 field by Taymans, Jean-Marc, Fell, Matt, Greenamyre, Tim, Hirst, Warren D., Mamais, Adamantios, Padmanabhan, Shalini, Peter, Inga, Rideout, Hardy, Thaler, Avner

    Published in NPJ Parkinson's Disease (01-07-2023)
    “…Almost 2 decades after linking LRRK2 to Parkinson’s disease, a vibrant research field has developed around the study of this gene and its protein product…”
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    Involvement of macroautophagy in the dissolution of neuronal inclusions by Rideout, Hardy J., Lang-Rollin, Isabelle, Stefanis, Leonidas

    “…Ubiquitinated inclusions are a common feature of many neurodegenerative conditions. We have proposed that, at least in part, such inclusions may be formed due…”
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