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Journal Abstract Search

117 related items for PubMed ID: 12071349

  • 21. Identification and in silico characterization of a novel compound heterozygosity associated with hereditary aceruloplasminemia.
    Hofmann WP, Welsch C, Takahashi Y, Miyajima H, Mihm U, Krick C, Zeuzem S, Sarrazin C.
    Scand J Gastroenterol; 2007 Sep; 42(9):1088-94. PubMed ID: 17710675
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  • 22. [Pathological study on central nervous system of patients with hereditary ceruloplasmin deficiency].
    Kawanami T.
    Nihon Naika Gakkai Zasshi; 2004 Aug 10; 93(8):1585-90. PubMed ID: 15384687
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  • 23. Effects of diabetes mellitus on astrocyte GFAP and glutamate transporters in the CNS.
    Coleman E, Judd R, Hoe L, Dennis J, Posner P.
    Glia; 2004 Nov 01; 48(2):166-78. PubMed ID: 15378652
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  • 24. Neuroprotection conferred by astrocytes is insufficient to protect animals from succumbing to Japanese encephalitis.
    Mishra MK, Koli P, Bhowmick S, Basu A.
    Neurochem Int; 2007 Apr 01; 50(5):764-73. PubMed ID: 17353066
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  • 28. Age-dependent expression of hephaestin in the brain of ceruloplasmin-deficient mice.
    Cui R, Duan XL, Anderson GJ, Qiao YT, Yu P, Qian ZM, Yoshida K, Takeda S, Guo P, Yang ZL, Chang YZ.
    J Trace Elem Med Biol; 2009 Apr 01; 23(4):290-9. PubMed ID: 19747625
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  • 29. Implications for oxidative stress and astrocytes following 26S proteasomal depletion in mouse forebrain neurones.
    Elkharaz J, Ugun-Klusek A, Constantin-Teodosiu D, Lawler K, Mayer RJ, Billett E, Lowe J, Bedford L.
    Biochim Biophys Acta; 2013 Dec 01; 1832(12):1930-8. PubMed ID: 23851049
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  • 30. Treatment of symptomatic heterozygous aceruloplasminemia with oral zinc sulphate.
    Kuhn J, Bewermeyer H, Miyajima H, Takahashi Y, Kuhn KF, Hoogenraad TU.
    Brain Dev; 2007 Aug 01; 29(7):450-3. PubMed ID: 17307325
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  • 31. Extensive brain pathology in a patient with aceruloplasminemia with a prolonged duration of illness.
    Kaneko K, Hineno A, Yoshida K, Ohara S, Morita H, Ikeda S.
    Hum Pathol; 2012 Mar 01; 43(3):451-6. PubMed ID: 21889188
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  • 34. Rapid increases in glial fibrillary acidic protein mRNA and protein levels in the copper-deficient, brindled mouse.
    Shafit-Zagardo B, Peterson C, Goldman JE.
    J Neurochem; 1988 Oct 01; 51(4):1258-66. PubMed ID: 3047319
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  • 35. Late onset diabetes mellitus in patients with hereditary aceruloplasminemia.
    Miyajima H, Takahashi Y, Shimizu H, Sakai N, Kamata T, Kaneko E.
    Intern Med; 1996 Aug 01; 35(8):641-5. PubMed ID: 8894739
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  • 36. Increase of glial fibrillary acidic protein fragments in the spinal cord of motor neuron degeneration mutant mouse.
    Fujita K, Yamauchi M, Matsui T, Titani K, Takahashi H, Kato T, Isomura G, Ando M, Nagata Y.
    Brain Res; 1998 Feb 23; 785(1):31-40. PubMed ID: 9526038
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  • 37. A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.
    Yazaki M, Yoshida K, Nakamura A, Furihata K, Yonekawa M, Okabe T, Yamashita N, Ohta M, Ikeda S.
    J Neurol Sci; 1998 Feb 23; 156(1):30-4. PubMed ID: 9559983
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  • 38. Effects of alcohol administration during adulthood on parvalbumin and glial fibrillary acidic protein immunoreactivity in the rat cerebral cortex.
    Udomuksorn W, Mukem S, Kumarnsit E, Vongvatcharanon S, Vongvatcharanon U.
    Acta Histochem; 2011 May 23; 113(3):283-9. PubMed ID: 20056265
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  • 39. Increase of glial fibrillary acidic protein and S-100B in hippocampus and cortex of diabetic rats: effects of vitamin E.
    Baydas G, Nedzvetskii VS, Tuzcu M, Yasar A, Kirichenko SV.
    Eur J Pharmacol; 2003 Feb 21; 462(1-3):67-71. PubMed ID: 12591097
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  • 40. Defective electron transfer in complexes I and IV in patients with aceruloplasminemia.
    Kohno S, Miyajima H, Takahashi Y, Suzuki H, Hishida A.
    J Neurol Sci; 2000 Dec 15; 182(1):57-60. PubMed ID: 11102640
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