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Journal Abstract Search

321 related items for PubMed ID: 24084090

  • 1. Apoptotic photoreceptor loss and altered expression of lysosomal proteins in the nclf mouse model of neuronal ceroid lipofuscinosis.
    Bartsch U, Galliciotti G, Jofre GF, Jankowiak W, Hagel C, Braulke T.
    Invest Ophthalmol Vis Sci; 2013 Oct 23; 54(10):6952-9. PubMed ID: 24084090
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  • 2. Progressive retinal degeneration and glial activation in the CLN6 (nclf) mouse model of neuronal ceroid lipofuscinosis: a beneficial effect of DHA and curcumin supplementation.
    Mirza M, Volz C, Karlstetter M, Langiu M, Somogyi A, Ruonala MO, Tamm ER, Jägle H, Langmann T.
    PLoS One; 2013 Oct 23; 8(10):e75963. PubMed ID: 24124525
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  • 7. Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease).
    Seigel GM, Lotery A, Kummer A, Bernard DJ, Greene ND, Turmaine M, Derksen T, Nussbaum RL, Davidson B, Wagner J, Mitchison HM.
    Mol Cell Neurosci; 2002 Apr 23; 19(4):515-27. PubMed ID: 11988019
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  • 8. Protein product of CLN6 gene responsible for variant late-onset infantile neuronal ceroid lipofuscinosis interacts with CRMP-2.
    Benedict JW, Getty AL, Wishart TM, Gillingwater TH, Pearce DA.
    J Neurosci Res; 2009 Jul 23; 87(9):2157-66. PubMed ID: 19235893
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  • 9. Rapid and Progressive Loss of Multiple Retinal Cell Types in Cathepsin D-Deficient Mice-An Animal Model of CLN10 Disease.
    Bassal M, Liu J, Jankowiak W, Saftig P, Bartsch U.
    Cells; 2021 Mar 21; 10(3):. PubMed ID: 33800998
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  • 10. Accumulation of bis(monoacylglycero)phosphate and gangliosides in mouse models of neuronal ceroid lipofuscinosis.
    Jabs S, Quitsch A, Käkelä R, Koch B, Tyynelä J, Brade H, Glatzel M, Walkley S, Saftig P, Vanier MT, Braulke T.
    J Neurochem; 2008 Aug 21; 106(3):1415-25. PubMed ID: 18498441
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  • 11. A murine model of variant late infantile ceroid lipofuscinosis recapitulates behavioral and pathological phenotypes of human disease.
    Morgan JP, Magee H, Wong A, Nelson T, Koch B, Cooper JD, Weimer JM.
    PLoS One; 2013 Aug 21; 8(11):e78694. PubMed ID: 24223841
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  • 15. A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging.
    Kopra O, Vesa J, von Schantz C, Manninen T, Minye H, Fabritius AL, Rapola J, van Diggelen OP, Saarela J, Jalanko A, Peltonen L.
    Hum Mol Genet; 2004 Dec 01; 13(23):2893-906. PubMed ID: 15459177
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  • 16. Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis.
    Chang B, Bronson RT, Hawes NL, Roderick TH, Peng C, Hageman GS, Heckenlively JR.
    Invest Ophthalmol Vis Sci; 1994 Mar 01; 35(3):1071-6. PubMed ID: 8125718
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  • 17. Failure of Autophagy-Lysosomal Pathways in Rod Photoreceptors Causes the Early Retinal Degeneration Phenotype Observed in Cln6nclf Mice.
    von Eisenhart-Rothe P, Grubman A, Greferath U, Fothergill LJ, Jobling AI, Phipps JA, White AR, Fletcher EL, Vessey KA.
    Invest Ophthalmol Vis Sci; 2018 Oct 01; 59(12):5082-5097. PubMed ID: 30372735
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  • 18. Analysis of cathepsin B and cathepsin L treatment to clear toxic lysosomal protein aggregates in neuronal ceroid lipofuscinosis.
    Di Spiezio A, Marques ARA, Schmidt L, Thießen N, Gallwitz L, Fogh J, Bartsch U, Saftig P.
    Biochim Biophys Acta Mol Basis Dis; 2021 Oct 01; 1867(10):166205. PubMed ID: 34214607
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  • 20. An altered secretome is an early marker of the pathogenesis of CLN6 Batten disease.
    Best HL, Clare AJ, McDonald KO, Wicky HE, Hughes SM.
    J Neurochem; 2021 May 01; 157(3):764-780. PubMed ID: 33368303
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