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Journal Abstract Search


176 related items for PubMed ID: 10191119

  • 1. A murine model for juvenile NCL: gene targeting of mouse Cln3.
    Greene ND, Bernard DL, Taschner PE, Lake BD, de Vos N, Breuning MH, Gardiner RM, Mole SE, Nussbaum RL, Mitchison HM.
    Mol Genet Metab; 1999 Apr; 66(4):309-13. PubMed ID: 10191119
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  • 2. 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; 19(4):515-27. PubMed ID: 11988019
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  • 3. Altered gene expression in the eye of a mouse model for batten disease.
    Chattopadhyay S, Kingsley E, Serour A, Curran TM, Brooks AI, Pearce DA.
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):2893-905. PubMed ID: 15326100
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  • 4. Developmental impairments of select neurotransmitter systems in brains of Cln3(Deltaex7/8) knock-in mice, an animal model of juvenile neuronal ceroid lipofuscinosis.
    Herrmann P, Druckrey-Fiskaaen C, Kouznetsova E, Heinitz K, Bigl M, Cotman SL, Schliebs R.
    J Neurosci Res; 2008 Jun; 86(8):1857-70. PubMed ID: 18265413
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  • 5. Moving towards therapies for juvenile Batten disease?
    Cooper JD.
    Exp Neurol; 2008 Jun; 211(2):329-31. PubMed ID: 18400221
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  • 9. Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin-Na+, K+ ATPase complex.
    Uusi-Rauva K, Luiro K, Tanhuanpää K, Kopra O, Martín-Vasallo P, Kyttälä A, Jalanko A.
    Exp Cell Res; 2008 Sep 10; 314(15):2895-905. PubMed ID: 18621045
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  • 10. Altered arginine metabolism in the central nervous system (CNS) of the Cln3-/- mouse model of juvenile Batten disease.
    Chan CH, Ramirez-Montealegre D, Pearce DA.
    Neuropathol Appl Neurobiol; 2009 Apr 10; 35(2):189-207. PubMed ID: 19284480
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  • 13. Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.
    Mitchison HM, Taschner PE, Kremmidiotis G, Callen DF, Doggett NA, Lerner TJ, Janes RB, Wallace BA, Munroe PB, O'Rawe AM, Gardiner RM, Mole SE.
    Neuropediatrics; 1997 Feb 10; 28(1):12-4. PubMed ID: 9151311
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  • 15. Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models.
    Chan CH, Mitchison HM, Pearce DA.
    Hum Mol Genet; 2008 Nov 01; 17(21):3332-9. PubMed ID: 18678598
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  • 16. A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease).
    Katz ML, Shibuya H, Liu PC, Kaur S, Gao CL, Johnson GS.
    J Neurosci Res; 1999 Aug 15; 57(4):551-6. PubMed ID: 10440905
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  • 17. Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze.
    Wendt KD, Lei B, Schachtman TR, Tullis GE, Ibe ME, Katz ML.
    Behav Brain Res; 2005 Jun 20; 161(2):175-82. PubMed ID: 15885820
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  • 20. Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X).
    Sarpong A, Schottmann G, Rüther K, Stoltenburg G, Kohlschütter A, Hübner C, Schuelke M.
    Clin Genet; 2009 Jul 20; 76(1):38-45. PubMed ID: 19489875
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