Humanin improves bioenergetic state of cells harboring A3243G mitochondrial DNA mutation

被引：0
|
作者：
Kariya, S
Hirano, M
Furiya, Y
Nishiwaki, T
Ueno, S
机构：
来源：
ANNALS OF NEUROLOGY | 2003年 / 54卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：S46 / S46
页数：1
相关论文
共 50 条
  • [21] The mitochondrial A3243G mutation presenting as severe cardiomyopathy
    Vilarinho, L
    Santorelli, FM
    Rosas, MJ
    Tavares, C
    MeloPires, M
    DiMauro, S
    JOURNAL OF MEDICAL GENETICS, 1997, 34 (07) : 607 - 609
  • [22] Clinical spectrum in 75 patients with the MELAS A3243G mitochondrial DNA mutation
    Shanske, S
    Hirano, M
    Santorelli, FM
    Kulikova, R
    Xia, W
    DeVivo, DC
    DiMauro, S
    NEUROLOGY, 1996, 46 (02) : 3012 - 3012
  • [23] Clinical features of A3243G mitochondrial tRNA mutation
    Chae, JH
    Hwang, H
    Lim, BC
    Cheong, HI
    Hwang, YS
    Kim, KJ
    BRAIN & DEVELOPMENT, 2004, 26 (07): : 459 - 462
  • [24] Quantification of heteroplasmic A3243G mutation of mitochondrial DNA by realtime PCR.
    Bai, R
    Wong, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 499 - 499
  • [25] Endothelial Corneal Dystrophy Associated with A3243G Mitochondrial DNA Point Mutation
    Bakhoum, Mathieu F.
    White, Eugenia C.
    Wu, Wei-Pu
    Sengillo, Jesse D.
    Kramer, Gregory D.
    Perry, Henry D.
    Tsang, Stephen H.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [26] The study of mitochondrial A3243G mutation in different samples
    Ma, Yinan
    Fang, Fang
    Yang, Yanling
    Zou, Liping
    Zhang, Ying
    Wang, Songtao
    Xu, Yufeng
    Pei, Pei
    Qi, Yu
    MITOCHONDRION, 2009, 9 (02) : 139 - 143
  • [27] Detection and quantification of the A3243G mutation of mitochondrial DNA by ligation detection reaction
    Nigou, M
    Parfait, B
    Clauser, E
    Olivier, JL
    MOLECULAR AND CELLULAR PROBES, 1998, 12 (05) : 273 - 282
  • [28] Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation
    Deschauer, M
    Müller, T
    Wieser, T
    Schulte-Mattler, W
    Kornhuber, M
    Zierz, S
    ARCHIVES OF NEUROLOGY, 2001, 58 (11) : 1885 - 1888
  • [29] Mitochondrial DNA point mutation A3243G in NIDDM persons (The Pilot Study)
    Pape-Medvidovic, E
    Martin-Kleiner, I
    Pavlic-Renar, I
    Metelko, Z
    Kusec, R
    Boranic, M
    DIABETES, 2003, 52 : A503 - A503
  • [30] GENOTYPE TO PHENOTYPE CORRELATIONS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES ASSOCIATED WITH THE A3243G MUTATION OF MITOCHONDRIAL-DNA
    MARIOTTI, C
    SAVARESE, N
    SUOMALAINEN, A
    RIMOLDI, M
    COMI, G
    PRELLE, A
    ANTOZZI, C
    SERVIDEI, S
    JARRE, L
    DIDONATO, S
    ZEVIANI, M
    JOURNAL OF NEUROLOGY, 1995, 242 (05) : 304 - 312
12345