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Journal Abstract Search

180 related items for PubMed ID: 33368303

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  • 2. 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; 8(11):e78694. PubMed ID: 24223841
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  • 6. 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; 8(10):e75963. PubMed ID: 24124525
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  • 7. 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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  • 8. Disruption of the autophagy-lysosome pathway is involved in neuropathology of the nclf mouse model of neuronal ceroid lipofuscinosis.
    Thelen M, Damme M, Schweizer M, Hagel C, Wong AM, Cooper JD, Braulke T, Galliciotti G.
    PLoS One; 2012 Oct 23; 7(4):e35493. PubMed ID: 22536393
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  • 9. Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.
    Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR.
    Am J Med Genet; 1998 May 26; 77(4):289-97. PubMed ID: 9600738
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  • 10. Neuronal Ceroid Lipofuscinosis Type 6 (CLN6) clinical findings and molecular diagnosis: Costa Rica's experience.
    Badilla-Porras R, Echeverri-McCandless A, Weimer JM, Ulate-Campos A, Soto-Rodríguez A, Gutiérrez-Mata A, Hernández-Con L, Bogantes-Ledezma S, Balmaceda-Meza A, Brudvig J, Sanabria-Castro A.
    Orphanet J Rare Dis; 2022 Jan 10; 17(1):13. PubMed ID: 35012600
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  • 11. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease.
    Kleine Holthaus SM, Herranz-Martin S, Massaro G, Aristorena M, Hoke J, Hughes MP, Maswood R, Semenyuk O, Basche M, Shah AZ, Klaska IP, Smith AJ, Mole SE, Rahim AA, Ali RR.
    Hum Mol Genet; 2019 Dec 01; 28(23):3867-3879. PubMed ID: 31807779
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  • 18. A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case report.
    Sun G, Yao F, Tian Z, Ma T, Yang Z.
    BMC Med Genet; 2018 Oct 01; 19(1):177. PubMed ID: 30285654
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