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1Report
Relation: 科学通报; http://ir.psych.ac.cn/handle/311026/35827
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2Report
Relation: 科学通报; http://ir.psych.ac.cn/handle/311026/27042
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3Academic Journal
المساهمون: 100044,北京大学人民医院眼科视觉损伤与修复教育部重点实验室 视网膜脉络膜疾病诊治北京市重点实验室
المصدر: CSCD ; 万方 ; http://d.g.wanfangdata.com.cn/Periodical_ykyj201610012.aspx
مصطلحات موضوعية: 线粒体疾病, DNA突变分析, 基因学, 遗传性视神经萎缩, 聚合酶链反应, Leber遗传性视神经病变, 视力, Mitochondrial disease, DNA mutational analysis, Genetics, Optic atrophies,genetic, Polymerase chain reaction, Leber hereditary optic neuropathy, Vision
Relation: 中华实验眼科杂志.2016,34(10),920-924.; 1514597; http://hdl.handle.net/20.500.11897/457679
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4Conference
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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5Academic Journal
المساهمون: 100034,北京大学第一医院神经内科, 100034,北京大学第一医院耳鼻喉科
مصطلحات موضوعية: 张力失调 智力障碍 视神经萎缩 聋盲障碍 膜转运蛋白质类 突变 Dystonia Intellectual disability Optic atrophy Deaf-blind disorders Membrane transport proteins Mutation
Relation: 中华神经科杂志.2013,46,(4),243-246.; 1147005; http://hdl.handle.net/20.500.11897/269607
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6Academic Journal
المساهمون: 100034,北京大学第一医院神经内科
مصطلحات موضوعية: 遗传性运动感觉性神经病, 膜蛋白质类, 线粒体蛋白质类, 视神经萎缩, Hereditary motor sensory neuropathies, Membrane proteins, Mitochondrial proteins, Optic atrophy
Relation: 中华神经科杂志.2011,44,(10),702-705.; 1231998; http://hdl.handle.net/20.500.11897/123911
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7Dissertation/ Thesis
المؤلفون: 周鳳寒, Chou, Feng-Han
المساهمون: 醫學檢驗暨生物技術學系所, 高淑慧
مصطلحات موضوعية: 體染色體顯性遺傳視神經萎縮症, 第一型視神經萎縮蛋白, 正常型 OPA1 基因轉染, autosomal dominant optic atrophy, OPA1, wild-type OPA1 transfection
وصف الملف: 99 bytes; text/html
Relation: http://libir.tmu.edu.tw/handle/987654321/58824; http://libir.tmu.edu.tw/bitstream/987654321/58824/2/index.html
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8Dissertation/ Thesis
المؤلفون: 陳怡秀, Chen, Yi-Hsiu
مصطلحات موضوعية: 顯性遺傳視神經萎縮症, 第一型視神經萎縮蛋白, 粒線體網路, 8-羥基去氧鳥糞嘌呤, 粒線體DNA斷損突變, 粒線體核仁, autosomal dominant optic atrophy, OPA1, mitochondrial network, 8-hydroxy-deoxyguanosine, mtDNA deletion, mitochondrial nucleoids
وصف الملف: 140 bytes; text/html
Relation: http://libir.tmu.edu.tw/handle/987654321/58390; http://libir.tmu.edu.tw/bitstream/987654321/58390/2/index.html
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9Dissertation/ Thesis
المؤلفون: 方信元, Fang, Hsin-Yuan
المساهمون: 臺灣大學: 臨床醫學研究所, 柯文哲, 楊偉勛, 林清淵
مصطلحات موضوعية: 肺癌, 肺腺癌, 細胞凋亡, 粒腺體, 腺嘌呤核?三磷酸?家族AAA區域包含3A蛋白, 第一型視神經萎縮蛋白, 半胱氨酸蛋白?14, Lung cancer, Lung adenocarcinoma, Apoptosis, Mitochondria, ATAD3A, OPA1, Caspase-14
وصف الملف: 6123680 bytes; application/pdf
Relation: http://ntur.lib.ntu.edu.tw/handle/246246/253473; http://ntur.lib.ntu.edu.tw/bitstream/246246/253473/1/ntu-100-D93421104-1.pdf
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10Dissertation/ Thesis視神經萎縮蛋白1在肺癌之表現與其生物意義 ; The expression and biological significance of optic atrophy 1 in lung cancer.
المؤلفون: 王俞婷, Wang, Yu-Ting
المساهمون: 周寬基, Kuan-Chih Chow, 中興大學, 方信元, Hsin-Yuan Fang, 邱繡河, Shiow-Her Chiou
مصطلحات موضوعية: optic atrophy 1, 視神經萎縮蛋白1
Relation: http://www.airitilibrary.com/Publication/alDetailedMesh1?DocID=U0005-0102201015225300; U0005-0102201015225300; http://hdl.handle.net/11455/20122
الاتاحة: http://hdl.handle.net/11455/20122
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11
المؤلفون: 徐韻涵, Yun-Han Hsu
المساهمون: 高茂傑, Mou-Chieh Kao
مصطلحات موضوعية: 粒線體, ND4L基因, 雷伯氏遺傳性視神經萎縮症, 同素異位法, 粒線體標的序列, mitochondria, ND4L gene, Leber Hereditary Optic Neuropathy, allotopic expression, mitochondrial targeting sequence
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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المؤلفون: 徐韻涵, Yun-Han Hsu
المساهمون: 高茂傑, Mou-Chieh Kao
مصطلحات موضوعية: 粒線體, ND4L基因, 雷伯氏遺傳性視神經萎縮症, 同素異位法, 粒線體標的序列, mitochondria, ND4L gene, Leber Hereditary Optic Neuropathy, allotopic expression, mitochondrial targeting sequence
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