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Original Article

A method comparison in monitoring disease progression of G93A mouse model of ALS

, , , , &
Pages 366-372 | Received 26 Mar 2007, Accepted 18 Jun 2007, Published online: 10 Jul 2009

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Chen Zhang, Chen Zhang, Chang Zhou, Chen Zhang, Chang Zhou, Ji-Jun Teng, Ren-Liang Zhao & Yu-Qiang Song. (2009) Multiple administrations of human marrow stromal cells through cerebrospinal fluid prolong survival in a transgenic mouse model of amyotrophic lateral sclerosis. Cytotherapy 11:3, pages 299-306.
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Articles from other publishers (13)

Janice A. Nagy, Carson Semple, PuiChi Lo & Seward B. Rutkove. (2022) Assessing the therapeutic impact of resveratrol in ALS SOD1-G93A mice with electrical impedance myography. Frontiers in Neurology 13.
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Christopher G. Wier, Alexander E. Crum, Anthony B. Reynolds, Chitra C. Iyer, Deepti Chugh, Marilly S. Palettas, Patrick L. Heilman, David M. Kline, W. David Arnold & Stephen J. Kolb. (2019) Muscle contractility dysfunction precedes loss of motor unit connectivity in SOD1(G93A) mice. Muscle & Nerve 59:2, pages 254-262.
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Elizabeth B. Moloney, Barbara Hobo, Fred De Winter & Joost Verhaagen. (2017) Expression of a Mutant SEMA3A Protein with Diminished Signalling Capacity Does Not Alter ALS-Related Motor Decline, or Confer Changes in NMJ Plasticity after BotoxA-Induced Paralysis of Male Gastrocnemic Muscle. PLOS ONE 12:1, pages e0170314.
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Ji-Yoen Kim, Ava Jang, Rohit Reddy, Wan Hee Yoon & Joanna L. Jankowsky. (2016) Neuronal overexpression of human VAPB slows motor impairment and neuromuscular denervation in a mouse model of ALS. Human Molecular Genetics, pages ddw294.
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Jae Chul LeeSoo Young ChoeChoong Ik Cha. (2014) Region-specific changes in the immunoreactivity of Atg9A in the central nervous system of SOD1(G93A) transgenic mice. Anatomy & Cell Biology 47:2, pages 101.
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John D Lee, Nur A Kamaruzaman, Jenny NT Fung, Stephen M Taylor, Bradley J Turner, Julie D Atkin, Trent M Woodruff & Peter G Noakes. (2013) Dysregulation of the complement cascade in the hSOD1G93Atransgenic mouse model of amyotrophic lateral sclerosis. Journal of Neuroinflammation 10:1.
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Lien-Szu Wu, Wei-Cheng Cheng & C.-K. James Shen. (2012) Targeted Depletion of TDP-43 Expression in the Spinal Cord Motor Neurons Leads to the Development of Amyotrophic Lateral Sclerosis-like Phenotypes in Mice. Journal of Biological Chemistry 287:33, pages 27335-27344.
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Gioacchino Tedeschi, Francesca Trojsi, Alessandro Tessitore, Daniele Corbo, Anna Sagnelli, Antonella Paccone, Alessandro D'Ambrosio, Giovanni Piccirillo, Mario Cirillo, Sossio Cirillo, Maria Rosaria Monsurrò & Fabrizio Esposito. (2012) Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis. Neurobiology of Aging 33:5, pages 886-898.
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Nizar Souayah, K. M. Coakley, R. Chen, Norman Ende & Joseph J. McArdle. (2011) Defective Neuromuscular Transmission in the SOD1G93A Transgenic Mouse Improves After Administration of Human Umbilical Cord Blood Cells. Stem Cell Reviews and Reports 8:1, pages 224-228.
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Francisco Javier Miana-Mena, Cristina González-Mingot, Pilar Larrodé, María Jesús Muñoz, Sara Oliván, Lorena Fuentes-Broto, Enrique Martínez-Ballarín, Russel J. Reiter, Rosario Osta & Joaquín José García. (2010) Monitoring systemic oxidative stress in an animal model of amyotrophic lateral sclerosis. Journal of Neurology 258:5, pages 762-769.
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Marco Milanese, Simona Zappettini, Franco Onofri, Laura Musazzi, Daniela Tardito, Tiziana Bonifacino, Mirko Messa, Giorgio Racagni, Cesare Usai, Fabio Benfenati, Maurizio Popoli & Giambattista Bonanno. (2011) Abnormal exocytotic release of glutamate in a mouse model of amyotrophic lateral sclerosis. Journal of Neurochemistry 116:6, pages 1028-1042.
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E.L. Tudor, C.M. Galtrey, M.S. Perkinton, K.-F. Lau, K.J. De Vos, J.C. Mitchell, S. Ackerley, T. Hortobágyi, E. Vámos, P.N. Leigh, C. Klasen, D.M. McLoughlin, C.E. Shaw & C.C.J. Miller. (2010) Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology. Neuroscience 167:3, pages 774-785.
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J. Hegedus, C. T. Putman & T. Gordon. (2009) Progressive motor unit loss in the G93A mouse model of amyotrophic lateral sclerosis is unaffected by gender. Muscle & Nerve 39:3, pages 318-327.
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