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PUBMED FOR HANDHELDS

Journal Abstract Search


241 related items for PubMed ID: 32940364

  • 1. Microglial phagocytosis dysfunction in the dentate gyrus is related to local neuronal activity in a genetic model of epilepsy.
    Sierra-Torre V, Plaza-Zabala A, Bonifazi P, Abiega O, Díaz-Aparicio I, Tegelberg S, Lehesjoki AE, Valero J, Sierra A.
    Epilepsia; 2020 Nov; 61(11):2593-2608. PubMed ID: 32940364
    [Abstract] [Full Text] [Related]

  • 2. Early microglial activation precedes neuronal loss in the brain of the Cstb-/- mouse model of progressive myoclonus epilepsy, EPM1.
    Tegelberg S, Kopra O, Joensuu T, Cooper JD, Lehesjoki AE.
    J Neuropathol Exp Neurol; 2012 Jan; 71(1):40-53. PubMed ID: 22157618
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  • 3. Abnormal microglial activation in the Cstb(-/-) mouse, a model for progressive myoclonus epilepsy, EPM1.
    Okuneva O, Körber I, Li Z, Tian L, Joensuu T, Kopra O, Lehesjoki AE.
    Glia; 2015 Mar; 63(3):400-11. PubMed ID: 25327891
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  • 4. Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- Microglia.
    Körber I, Katayama S, Einarsdottir E, Krjutškov K, Hakala P, Kere J, Lehesjoki AE, Joensuu T.
    PLoS One; 2016 Mar; 11(6):e0158195. PubMed ID: 27355630
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  • 6. A pathogenetic hypothesis of Unverricht-Lundborg disease onset and progression.
    Franceschetti S, Sancini G, Buzzi A, Zucchini S, Paradiso B, Magnaghi G, Frassoni C, Chikhladze M, Avanzini G, Simonato M.
    Neurobiol Dis; 2007 Mar; 25(3):675-85. PubMed ID: 17188503
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  • 7. Neuronal Hyperactivity Disturbs ATP Microgradients, Impairs Microglial Motility, and Reduces Phagocytic Receptor Expression Triggering Apoptosis/Microglial Phagocytosis Uncoupling.
    Abiega O, Beccari S, Diaz-Aparicio I, Nadjar A, Layé S, Leyrolle Q, Gómez-Nicola D, Domercq M, Pérez-Samartín A, Sánchez-Zafra V, Paris I, Valero J, Savage JC, Hui CW, Tremblay MÈ, Deudero JJ, Brewster AL, Anderson AE, Zaldumbide L, Galbarriatu L, Marinas A, Vivanco Md, Matute C, Maletic-Savatic M, Encinas JM, Sierra A.
    PLoS Biol; 2016 May; 14(5):e1002466. PubMed ID: 27228556
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  • 9. Seizures induce widespread upregulation of cystatin B, the gene mutated in progressive myoclonus epilepsy, in rat forebrain neurons.
    D'Amato E, Kokaia Z, Nanobashvili A, Reeben M, Lehesjoki AE, Saarma M, Lindvall O.
    Eur J Neurosci; 2000 May; 12(5):1687-95. PubMed ID: 10792446
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  • 11. Unverricht-Lundborg disease.
    Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A.
    Epileptic Disord; 2016 Sep 01; 18(S2):28-37. PubMed ID: 27582036
    [Abstract] [Full Text] [Related]

  • 12. Gene expression alterations in the cerebellum and granule neurons of Cstb(-/-) mouse are associated with early synaptic changes and inflammation.
    Joensuu T, Tegelberg S, Reinmaa E, Segerstråle M, Hakala P, Pehkonen H, Korpi ER, Tyynelä J, Taira T, Hovatta I, Kopra O, Lehesjoki AE.
    PLoS One; 2014 Sep 01; 9(2):e89321. PubMed ID: 24586687
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  • 15. Increased Microglial Activity, Impaired Adult Hippocampal Neurogenesis, and Depressive-like Behavior in Microglial VPS35-Depleted Mice.
    Appel JR, Ye S, Tang F, Sun D, Zhang H, Mei L, Xiong WC.
    J Neurosci; 2018 Jun 27; 38(26):5949-5968. PubMed ID: 29853629
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  • 16. Neuropathological changes in a mouse model of progressive myoclonus epilepsy: cystatin B deficiency and Unverricht-Lundborg disease.
    Shannon P, Pennacchio LA, Houseweart MK, Minassian BA, Myers RM.
    J Neuropathol Exp Neurol; 2002 Dec 27; 61(12):1085-91. PubMed ID: 12484571
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  • 18. Reduced cystatin B activity correlates with enhanced cathepsin activity in progressive myoclonus epilepsy.
    Rinne R, Saukko P, Järvinen M, Lehesjoki AE.
    Ann Med; 2002 Dec 27; 34(5):380-5. PubMed ID: 12452481
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  • 19. Insights into the Genetic Profile of Two Siblings Affected by Unverricht-Lundborg Disease Using Patient-Derived hiPSCs.
    Lucchino V, Scaramuzzino L, Scalise S, Lo Conte M, Zannino C, Benedetto GL, Aguglia U, Ferlazzo E, Cuda G, Parrotta EI.
    Cells; 2022 Nov 04; 11(21):. PubMed ID: 36359887
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  • 20. Molecular background of EPM1-Unverricht-Lundborg disease.
    Joensuu T, Lehesjoki AE, Kopra O.
    Epilepsia; 2008 Apr 04; 49(4):557-63. PubMed ID: 18028412
    [Abstract] [Full Text] [Related]


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