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Journal Abstract Search
314 related items for PubMed ID: 16242638
1. 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; 20(2):314-23. PubMed ID: 16242638 [Abstract] [Full Text] [Related]
6. Adeno-associated virus 2-mediated gene therapy decreases autofluorescent storage material and increases brain mass in a murine model of infantile neuronal ceroid lipofuscinosis. Griffey M, Bible E, Vogler C, Levy B, Gupta P, Cooper J, Sands MS. Neurobiol Dis; 2004 Jul; 16(2):360-9. PubMed ID: 15193292 [Abstract] [Full Text] [Related]
7. 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(1):226-41. PubMed ID: 15649713 [Abstract] [Full Text] [Related]
8. Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice. Kim SJ, Zhang Z, Sarkar C, Tsai PC, Lee YC, Dye L, Mukherjee AB. J Clin Invest; 2008 Sep; 118(9):3075-86. PubMed ID: 18704195 [Abstract] [Full Text] [Related]
13. Neuronal trafficking of palmitoyl protein thioesterase provides an excellent model to study the effects of different mutations which cause infantile neuronal ceroid lipofuscinocis. Salonen T, Heinonen-Kopra O, Vesa J, Jalanko A. Mol Cell Neurosci; 2001 Aug; 18(2):131-40. PubMed ID: 11520175 [Abstract] [Full Text] [Related]
14. Intrathecal enzyme replacement therapy improves motor function and survival in a preclinical mouse model of infantile neuronal ceroid lipofuscinosis. Lu JY, Nelvagal HR, Wang L, Birnbaum SG, Cooper JD, Hofmann SL. Mol Genet Metab; 2015 Aug; 116(1-2):98-105. PubMed ID: 25982063 [Abstract] [Full Text] [Related]
15. Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene. Johnson BA, Ikeda S, Pinto LH, Ikeda A. Vis Neurosci; 2006 Aug; 23(6):887-98. PubMed ID: 17266781 [Abstract] [Full Text] [Related]
16. Morphologic and functional correlates of synaptic pathology in the cathepsin D knockout mouse model of congenital neuronal ceroid lipofuscinosis. Koch S, Molchanova SM, Wright AK, Edwards A, Cooper JD, Taira T, Gillingwater TH, Tyynelä J. J Neuropathol Exp Neurol; 2011 Dec; 70(12):1089-96. PubMed ID: 22082660 [Abstract] [Full Text] [Related]