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Journal Abstract Search

377 related items for PubMed ID: 18265413

  • 21. Neurodevelopmental delay in the Cln3Deltaex7/8 mouse model for Batten disease.
    Osório NS, Sampaio-Marques B, Chan CH, Oliveira P, Pearce DA, Sousa N, Rodrigues F.
    Genes Brain Behav; 2009 Apr; 8(3):337-45. PubMed ID: 19243453
    [Abstract] [Full Text] [Related]

  • 22. 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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  • 23. A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosis.
    Drack AV, Miller JN, Pearce DA.
    J Child Neurol; 2013 Sep 20; 28(9):1112-6. PubMed ID: 23877479
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  • 25. Finding the most appropriate mouse model of juvenile CLN3 (Batten) disease for therapeutic studies: the importance of genetic background and gender.
    Kovács AD, Pearce DA.
    Dis Model Mech; 2015 Apr 20; 8(4):351-61. PubMed ID: 26035843
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  • 26. Moving towards therapies for juvenile Batten disease?
    Cooper JD.
    Exp Neurol; 2008 Jun 20; 211(2):329-31. PubMed ID: 18400221
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  • 28. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.
    Mantel I, Brantley MA, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.
    Klin Monbl Augenheilkd; 2004 May 20; 221(5):427-30. PubMed ID: 15162299
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  • 30. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E, Dyken PR, Phillips P, Brodsky M, Bates S, Glasier C, Mrak RE.
    J Child Neurol; 2004 Jan 20; 19(1):42-6. PubMed ID: 15032383
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  • 32. Astrocytes in juvenile neuronal ceroid lipofuscinosis (CLN3) display metabolic and calcium signaling abnormalities.
    Bosch ME, Kielian T.
    J Neurochem; 2019 Mar 20; 148(5):612-624. PubMed ID: 29964296
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  • 33. Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Leman AR, Pearce DA, Rothberg PG.
    Hum Genet; 2005 May 20; 116(6):544. PubMed ID: 15991331
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  • 34. 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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  • 37. Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis.
    Cao Y, Espinola JA, Fossale E, Massey AC, Cuervo AM, MacDonald ME, Cotman SL.
    J Biol Chem; 2006 Jul 21; 281(29):20483-93. PubMed ID: 16714284
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  • 38. Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Leman AR, Pearce DA, Rothberg PG.
    Hum Genet; 2005 Feb 21; 116(3):236. PubMed ID: 15818814
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  • 40. Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected].
    Mitchison HM, Bernard DJ, Greene ND, Cooper JD, Junaid MA, Pullarkat RK, de Vos N, Breuning MH, Owens JW, Mobley WC, Gardiner RM, Lake BD, Taschner PE, Nussbaum RL.
    Neurobiol Dis; 1999 Oct 21; 6(5):321-34. PubMed ID: 10527801
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