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Journal Abstract Search

270 related items for PubMed ID: 15193292

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  • 2. AAV2-mediated ocular gene therapy for infantile neuronal ceroid lipofuscinosis.
    Griffey M, Macauley SL, Ogilvie JM, Sands MS.
    Mol Ther; 2005 Sep; 12(3):413-21. PubMed ID: 15979943
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  • 4. Synergistic effects of treating the spinal cord and brain in CLN1 disease.
    Shyng C, Nelvagal HR, Dearborn JT, Tyynelä J, Schmidt RE, Sands MS, Cooper JD.
    Proc Natl Acad Sci U S A; 2017 Jul 18; 114(29):E5920-E5929. PubMed ID: 28673981
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  • 6. Cln3-mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl-protein thioesterases-1 (Ppt1)-protein and Ppt1-enzyme activity in the lysosome.
    Appu AP, Bagh MB, Sadhukhan T, Mondal A, Casey S, Mukherjee AB.
    J Inherit Metab Dis; 2019 Sep 18; 42(5):944-954. PubMed ID: 31025705
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  • 8. Progressively reduced synaptic vesicle pool size in cultured neurons derived from neuronal ceroid lipofuscinosis-1 knockout mice.
    Virmani T, Gupta P, Liu X, Kavalali ET, Hofmann SL.
    Neurobiol Dis; 2005 Nov 18; 20(2):314-23. PubMed ID: 16242638
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  • 10. Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons.
    Jalanko A, Vesa J, Manninen T, von Schantz C, Minye H, Fabritius AL, Salonen T, Rapola J, Gentile M, Kopra O, Peltonen L.
    Neurobiol Dis; 2005 Feb 18; 18(1):226-41. PubMed ID: 15649713
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  • 11. Synergistic effects of central nervous system-directed gene therapy and bone marrow transplantation in the murine model of infantile neuronal ceroid lipofuscinosis.
    Macauley SL, Roberts MS, Wong AM, McSloy F, Reddy AS, Cooper JD, Sands MS.
    Ann Neurol; 2012 Jun 18; 71(6):797-804. PubMed ID: 22368049
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  • 12. Viral-mediated delivery of the late-infantile neuronal ceroid lipofuscinosis gene, TPP-I to the mouse central nervous system.
    Haskell RE, Hughes SM, Chiorini JA, Alisky JM, Davidson BL.
    Gene Ther; 2003 Jan 18; 10(1):34-42. PubMed ID: 12525835
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  • 13. Neuroprotection of host cells by human central nervous system stem cells in a mouse model of infantile neuronal ceroid lipofuscinosis.
    Tamaki SJ, Jacobs Y, Dohse M, Capela A, Cooper JD, Reitsma M, He D, Tushinski R, Belichenko PV, Salehi A, Mobley W, Gage FH, Huhn S, Tsukamoto AS, Weissman IL, Uchida N.
    Cell Stem Cell; 2009 Sep 04; 5(3):310-9. PubMed ID: 19733542
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  • 19. Cln1-mutations suppress Rab7-RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosis.
    Sarkar C, Sadhukhan T, Bagh MB, Appu AP, Chandra G, Mondal A, Saha A, Mukherjee AB.
    J Inherit Metab Dis; 2020 Sep 04; 43(5):1082-1101. PubMed ID: 32279353
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  • 20. Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disorders.
    Chandra G, Bagh MB, Peng S, Saha A, Sarkar C, Moralle M, Zhang Z, Mukherjee AB.
    Hum Mol Genet; 2015 Oct 01; 24(19):5416-32. PubMed ID: 26160911
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