Mitochondrial disease phenotype in Friedreich's ataxia patient iPSC-derived sensory neurons

被引：0
|
作者：
Eigentler, A. [1 ]
Knaus, L. [1 ]
Dechant, G. [1 ]
Nat, R. [1 ]
机构：
[1] Med Univ Innsbruck, Inst Neurosci, Innsbruck, Austria
来源：
HUMAN GENE THERAPY | 2016年 / 27卷 / 11期
关键词：
D O I：
暂无
中图分类号：
Q81 [生物工程学（生物技术）]; Q93 [微生物学];
学科分类号：
071005 ; 0836 ; 090102 ; 100705 ;
摘要：
OR14
引用
收藏
页码：A29 / A30
页数：2
相关论文
共 50 条
  • [31] Human Huntington's disease iPSC-derived striatal-like neurons display altered maturation and mitochondrial dynamics
    Beatriz, M.
    Vilaca, R.
    Rodrigues, R.
    Schlaeger, T.
    Daley, G.
    Rego, A. C.
    Lopes, C.
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2020, 50 : 89 - 89
  • [32] Mitochondrial Phenotypes in Parkinson's Diseases-A Focus on Human iPSC-Derived Dopaminergic Neurons
    Heger, Leonie M.
    Wise, Rachel M.
    Hees, J. Tabitha
    Harbauer, Angelika B.
    Burbulla, Lena F.
    CELLS, 2021, 10 (12)
  • [33] Biochemistry of cardiomyopathy in the mitochondrial disease Friedreich's ataxia
    Lane, Darius J. R.
    Huang, Michael Li-Hsuan
    Ting, Samantha
    Sivagurunathan, Sutharshani
    Richardson, Des R.
    BIOCHEMICAL JOURNAL, 2013, 453 : 321 - 336
  • [34] Patient-derived iPSC models of Friedreich ataxia: a new frontier for understanding disease mechanisms and therapeutic application
    Maheshwari, Saumya
    Vilema-Enriquez, Gabriela
    Wade-Martins, Richard
    TRANSLATIONAL NEURODEGENERATION, 2023, 12 (01)
  • [35] DNA damage and transcriptional regulation in iPSC-derived neurons from Ataxia Telangiectasia patients
    Alessandro Corti
    Raina Sota
    Matteo Dugo
    Raffaele A. Calogero
    Benedetta Terragni
    Massimo Mantegazza
    Silvana Franceschetti
    Michela Restelli
    Patrizia Gasparini
    Daniele Lecis
    Krystyna H. Chrzanowska
    Domenico Delia
    Scientific Reports, 9
  • [36] DNA damage and transcriptional regulation in iPSC-derived neurons from Ataxia Telangiectasia patients
    Corti, Alessandro
    Sota, Raina
    Dugo, Matteo
    Calogero, Raffaele A.
    Terragni, Benedetta
    Mantegazza, Massimo
    Franceschetti, Silvana
    Restelli, Michela
    Gasparini, Patrizia
    Lecis, Daniele
    Chrzanowska, Krystyna H.
    Delia, Domenico
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [37] Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC-neurons and cardiomyocytes
    Angulo, Mariana B.
    Bertalovitz, Alexander
    Argenziano, Mariana A.
    Yang, Jiajia
    Patel, Aarti
    Zesiewicz, Theresa
    McDonald, Thomas, V
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2023, 11 (01):
  • [38] Friedreich's ataxia: A frataxin mediated mitochondrial disease?
    Gallagher, CL
    Waclawik, AJ
    Salamat, SM
    Lotz, BP
    Fadic, R
    Harding, CO
    Johns, DR
    Beinlich, BR
    NEUROLOGY, 1998, 50 (04) : A414 - A415
  • [39] Patient-derived iPSC models of Friedreich ataxia: a new frontier for understanding disease mechanisms and therapeutic application
    Saumya Maheshwari
    Gabriela Vilema-Enríquez
    Richard Wade-Martins
    Translational Neurodegeneration, 12
  • [40] ALTERED IPSC-DERIVED NEURONS' SODIUM CHANNEL PROPERTIES IN SUBJECTS WITH MONGE'S DISEASE
    Zhao, H. W.
    Gu, X. Q.
    Chailangkarn, T.
    Perkins, G.
    Callacondo, D.
    Appenzeller, O.
    Poulsen, O.
    Zhou, D.
    Muotri, A. R.
    Haddad, G. G.
    NEUROSCIENCE, 2015, 288 : 187 - 199
12345