Neuroinflammatory correlates of motor neuron dysfunction in the G93A-SOD1 mutant mouse model of familial amyotrophic lateral sclerosis

被引：0
|
作者：
Hensley, K [1 ]
Mou, SY [1 ]
Pye, Q [1 ]
Stewart, C [1 ]
West, M [1 ]
Williamson, K [1 ]
机构：
[1] Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
来源：
FREE RADICAL BIOLOGY AND MEDICINE | 2001年 / 31卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
121
引用
收藏
页码：S46 / S46
页数：1
相关论文
共 50 条
  • [21] Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1 G93A mouse model of amyotrophic lateral sclerosis
    Peters, Owen M.
    Lewis, Elizabeth A.
    Osterloh, Jeannette M.
    Weiss, Alexandra
    Salameh, Johnny S.
    Metterville, Jake
    Brown, Robert H.
    Freeman, Marc R.
    HUMAN MOLECULAR GENETICS, 2018, 27 (21) : 3761 - 3771
  • [22] Complement upregulation and activation on motor neurons and neuromuscular junction in the SOD1 G93A mouse model of familial amyotrophic lateral sclerosis
    Heurich, Bianca
    el Idrissi, Nawal Bahia
    Donev, Rossen M.
    Petri, Susanne
    Claus, Peter
    Neal, James
    Morgan, B. Paul
    Ramaglia, Valeria
    JOURNAL OF NEUROIMMUNOLOGY, 2011, 235 (1-2) : 104 - 109
  • [23] Highlight Commentary on "Redox proteomics analysis of oxidatively modified proteins in G93A-SOD1 transgenic mice - A model of familial amyotrophic lateral sclerosis"
    Calabrese, Vittorio
    FREE RADICAL BIOLOGY AND MEDICINE, 2007, 43 (02) : 160 - 162
  • [24] Neuropathology of familial amyotrophic lateral sclerosis with mutant SOD1 in light of transgenic mouse model
    Uyama, E
    Hirano, A
    AMYOTROPHIC LATERAL SCLEROSIS: PROGRESS AND PERSPECTIVES IN BASIC RESEARCH AND CLINICAL APPLICATION, 1996, 1104 : 109 - 116
  • [25] MPO/HOCl Facilitates Apoptosis and Ferroptosis in the SOD1G93A Motor Neuron of Amyotrophic Lateral Sclerosis
    Peng, Jialing
    Pan, Jingrui
    Mo, Jingjing
    Peng, Ying
    OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2022, 2022
  • [26] A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosis
    Marcuzzo, Stefania
    Bonanno, Silvia
    Figini, Matteo
    Scotti, Alessandro
    Zucca, Ileana
    Minati, Ludovico
    Riva, Nilo
    Domi, Teuta
    Fossaghi, Andrea
    Quattrini, Angelo
    Galbardi, Barbara
    D'Alessandro, Sara
    Grazia Bruzzone, Maria
    Manuel Garcia-Verdugo, Jose
    Moreno-Manzano, Victoria
    Mantegazza, Renato
    Bernasconi, Pia
    EXPERIMENTAL NEUROLOGY, 2017, 293 : 43 - 52
  • [27] Neuroprotective effect of bexarotene in the SOD1G93A mouse model of amyotrophic lateral sclerosis
    Riancho, Javier
    Ruiz-Soto, Maria
    Berciano, Maria T.
    Berciano, Jose
    Lafarga, Miguel
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2015, 9
  • [28] RETRACTED: Resveratrol Ameliorates Motor Neuron Degeneration and Improves Survival in SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (Retracted Article)
    Song, Lin
    Chen, Liang
    Zhang, Xiaojie
    Li, Jia
    Le, Weidong
    BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [29] Retinal glial changes in SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis
    Ramirez, A. I.
    Salobrar-Garcia, E.
    Matamoros, J. A.
    Rojas, P.
    Fernandez Albarral, J. A.
    Lopez-Cuenca, I.
    Sanchez-Puebla, L.
    Elvira-Hurtado, L.
    Santos-Garcia, I.
    de lago, E.
    Ramirez, J. M.
    de Hoz, R.
    Salazar, J. J.
    GLIA, 2023, 71 : E443 - E444
  • [30] Repurposing carbamazepine for the treatment of amyotrophic lateral sclerosis in SOD1-G93A mouse model
    Zhang, Jing-Jing
    Zhou, Qin-Ming
    Chen, Sheng
    Le, Wei-Dong
    CNS NEUROSCIENCE & THERAPEUTICS, 2018, 24 (12) : 1163 - 1174
12345