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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 25233404

  • 1. Astrocytosis in infantile neuronal ceroid lipofuscinosis: friend or foe?
    Shyng C, Sands MS.
    Biochem Soc Trans; 2014 Oct; 42(5):1282-5. PubMed ID: 25233404
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  • 4. An anti-neuroinflammatory that targets dysregulated glia enhances the efficacy of CNS-directed gene therapy in murine infantile neuronal ceroid lipofuscinosis.
    Macauley SL, Wong AM, Shyng C, Augner DP, Dearborn JT, Pearse Y, Roberts MS, Fowler SC, Cooper JD, Watterson DM, Sands MS.
    J Neurosci; 2014 Sep 24; 34(39):13077-82. PubMed ID: 25253854
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  • 7. Human INCL fibroblasts display abnormal mitochondrial and lysosomal networks and heightened susceptibility to ROS-induced cell death.
    Balouch B, Nagorsky H, Pham T, LaGraff JT, Chu-LaGraff Q.
    PLoS One; 2021 Sep 24; 16(2):e0239689. PubMed ID: 33561134
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  • 10. Pathogenesis and therapies for infantile neuronal ceroid lipofuscinosis (infantile CLN1 disease).
    Hawkins-Salsbury JA, Cooper JD, Sands MS.
    Biochim Biophys Acta; 2013 Nov 24; 1832(11):1906-9. PubMed ID: 23747979
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  • 12. Ppt1-deficiency dysregulates lysosomal Ca++ homeostasis contributing to pathogenesis in a mouse model of CLN1 disease.
    Mondal A, Appu AP, Sadhukhan T, Bagh MB, Previde RM, Sadhukhan S, Stojilkovic S, Liu A, Mukherjee AB.
    J Inherit Metab Dis; 2022 May 24; 45(3):635-656. PubMed ID: 35150145
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  • 13. Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis.
    Lange J, Haslett LJ, Lloyd-Evans E, Pocock JM, Sands MS, Williams BP, Cooper JD.
    Acta Neuropathol Commun; 2018 Aug 08; 6(1):74. PubMed ID: 30089511
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  • 14. Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis.
    Kielar C, Maddox L, Bible E, Pontikis CC, Macauley SL, Griffey MA, Wong M, Sands MS, Cooper JD.
    Neurobiol Dis; 2007 Jan 08; 25(1):150-62. PubMed ID: 17046272
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  • 15. In a model of Batten disease, palmitoyl protein thioesterase-1 deficiency is associated with brown adipose tissue and thermoregulation abnormalities.
    Khaibullina A, Kenyon N, Guptill V, Quezado MM, Wang L, Koziol D, Wesley R, Moya PR, Zhang Z, Saha A, Mukherjee AB, Quezado ZM.
    PLoS One; 2012 Jan 08; 7(11):e48733. PubMed ID: 23139814
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  • 16. Histochemical localization of palmitoyl protein thioesterase-1 activity.
    Dearborn JT, Ramachandran S, Shyng C, Lu JY, Thornton J, Hofmann SL, Sands MS.
    Mol Genet Metab; 2016 Feb 08; 117(2):210-6. PubMed ID: 26597320
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  • 17. Disruption of adaptive energy metabolism and elevated ribosomal p-S6K1 levels contribute to INCL pathogenesis: partial rescue by resveratrol.
    Wei H, Zhang Z, Saha A, Peng S, Chandra G, Quezado Z, Mukherjee AB.
    Hum Mol Genet; 2011 Mar 15; 20(6):1111-21. PubMed ID: 21224254
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  • 18. Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis.
    Bible E, Gupta P, Hofmann SL, Cooper JD.
    Neurobiol Dis; 2004 Jul 15; 16(2):346-59. PubMed ID: 15193291
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