يعرض 1 - 12 نتائج من 12 نتيجة بحث عن '"神经萎缩"', وقت الاستعلام: 0.47s تنقيح النتائج
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    Academic Journal
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    Conference

    المؤلفون: 吴玲玲

    المساهمون: 北京大学眼科中心

    المصدر: 知网

    Relation: 中华医学会第十二届全国眼科学术大会.; 827032; http://hdl.handle.net/20.500.11897/175028

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    Dissertation/ Thesis
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    المؤلفون: 徐韻涵, Yun-Han Hsu

    المساهمون: 高茂傑, Mou-Chieh Kao

    Time: 37

    وصف الملف: 155 bytes; text/html

    Relation: Abu-Amero, K. K. and T. M. Bosley (2006). "Mitochondrial abnormalities in patients with LHON-like optic neuropathies." Invest. Ophthalmol. Vis. Sci. 47(10): 4211-4220. Bonnefoy, N. and T. Fox (2002). "Genetic transformation of Saccharomyces cerevisiae mitochondria." Methods in enzymology 350: 97-111. Bonnet, C., V. Kaltimbacher, et al. (2007). "Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting Complex I or V subunits." Rejuvenation Research 10(2): 127-144. Chan, D. C. (2006). "Mitochondria: dynamic organelles in disease, aging, and development." Cell 125: 1241-1252. Chatterjee, A., E. Mambo, et al. (2006). "Targeting of mutant hogg1 in mammalian mitochondria and nucleus: effect on cellular survival upon oxidative stress." BMC Cancer 6(1): 235. Chen, L. (1989). "Fluorescent labeling of mitochondria." Methods in cell biology 29: 103-123. Corral-Debrinski, M., N. Belgareh, et al. (1999). "Overexpression of yeast karyopherin Pse1p/Kap121p stimulates the mitochondrial import of hydrophobic proteins in vivo." Molecular Microbiology 31(5): 1499-1511. DiMauro, S. and E. A. Schon (2003). "Mitochondrial respiratory-chain diseases." N Engl J Med 348(26): 2656-2668. Gratzer, S., T. Beilharz, et al. (2000). "The mitochondrial protein targeting suppressor (mts1) mutation maps to the mRNA-binding domain of Npl3p and affects translation on cytoplasmic polysomes." Molecular Microbiology 35(6): 1277-1285. Grey, A. D. N. J. d. (2000). "Mitochondrial gene therapy: an arena for the biomedical use of inteins." Trends in Biotechnology 18(9): 394-399. Henze, K. and W. Martin (2003). "Evolutionary biology: Essence of mitochondria." Nature 426: 127-128. Hirst, J., J. Carroll, et al. (2003). "The nuclear encoded subunits of complex I from bovine heart mitochondria " Biochimica et Biophysica Acta (BBA) - Bioenergetics 1604: 135-150 Jan Smeithink, L. v. d. Heuvel, et al. (2001). "The genetics and pathology of oxidative phosphorylation." Nature Reviews Genetics 2: 342-352. John Guy, X. Q. F. P. E. A. S. G. M. V. C. A. M. W. W. H. A. S. L. (2002). "Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy." Annals of Neurology 52(5): 534-542. Kaltimbacher, V., C. Bonnet, et al. (2006). "mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein." RNA 12(7): 1408-1417. Kao, M.-C., E. Nakamaru-Ogiso, et al. (2005). "Characterization of the membrane domain subunit NuoK (ND4L) of the NADH-quinone oxidoreductase from Escherichia coli." Biochemistry 44: 9545 -9554. Kao, M. C., S. Di Bernardo, et al. (2002). "Characterization of the membrane domain Nqo11 subunit of the proton-translocating NADH-quinone oxidoreductase of Paracoccus denitrificans." Biochemistry 41(13): 4377-4384. Manfredi, G., J. Fu, et al. (2002). "Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus." Nat Genet 30(4): 394-399. Margeot, A., C. Blugeon, et al. (2002). "In Saccharomyces cerevisiae, ATP2 mRNA sorting to the vicinity of mitochondria is essential for respiratory function." The EMBO journal 21: 6893–6904. McBride, H. M., M. Neuspiel, et al. (2006). "Mitochondria: More than just a powerhouse " Current Biology 16: R551 - R560. Oca-Cossio, J., L. Kenyon, et al. (2003). "Limitations of allotopic expression of mitochondrial genes in mammalian cells." Genetics 165(2): 707-720. Shoffner, J. M., M. T. Lott, et al. (1990). "Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation." Cell 61: 931-937. Smith, P. M., G. F. Ross, et al. (2004). "Strategies for treating disorders of the mitochondrial genome " Biochimica et Biophysica Acta 1659: 232-239. Taylor, R. W. and D. M. Turnbull (2005). "Mitochondrial DNA mutations in human disease." Nature Reviews Genetics 6: 389-402. Tsukihara, T., K. Shimokata, et al. (2003). "The low-spin heme of cytochrome c oxidase as the driving element of the proton-pumping process." Proceedings of the National Academy of Sciences 100(26): 15304-15309. Wallace, D. C. (2005). "The mitochondrial genome in human adaptive radiation and disease: On the road to therapeutics and performance enhancement " Gene 354(18): 169-180. Wallace, D. C. (2007). "Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine." Annual Review of Biochemistry 76(1): 781-821. Woese, C. R. (1977). "Endosymbionts and mitochondrial origins." Journal of Molecular Evolution 10(2): 93-96.; http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/35596

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