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Tu, P. H., Raju, P., Robinson, K. A., Gurney, M. E., Trojanowski, J. Q., Lee, V. M. (1996) Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proceedings of the National Academy of Sciences, 93 (7) 3155-3160 doi:10.1073/pnas.93.7.3155

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Reference TypeJournal (article/letter/editorial)
TitleTransgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
JournalProceedings of the National Academy of Sciences
AuthorsTu, P. H.Author
Raju, P.Author
Robinson, K. A.Author
Gurney, M. E.Author
Trojanowski, J. Q.Author
Lee, V. M.Author
Year1996 (April 2)Volume93
Issue7
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.93.7.3155Search in ResearchGate
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Mindat Ref. ID1586444Long-form Identifiermindat:1:5:1586444:2
GUID0
Full ReferenceTu, P. H., Raju, P., Robinson, K. A., Gurney, M. E., Trojanowski, J. Q., Lee, V. M. (1996) Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proceedings of the National Academy of Sciences, 93 (7) 3155-3160 doi:10.1073/pnas.93.7.3155
Plain TextTu, P. H., Raju, P., Robinson, K. A., Gurney, M. E., Trojanowski, J. Q., Lee, V. M. (1996) Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proceedings of the National Academy of Sciences, 93 (7) 3155-3160 doi:10.1073/pnas.93.7.3155
In(1996, April) Proceedings of the National Academy of Sciences Vol. 93 (7) Proceedings of the National Academy of Sciences

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Urushitani, M., Ezzi, S. A., Julien, J.-P. (2007) Therapeutic effects of immunization with mutant superoxide dismutase in mice models of amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences, 104 (7) 2495-2500 doi:10.1073/pnas.0606201104
Crino, P. B., Trojanowski, J. Q., Dichter, M. A., Eberwine, J. (1996) Embryonic neuronal markers in tuberous sclerosis: Single-cell molecular pathology. Proceedings of the National Academy of Sciences, 93 (24) 14152-14157 doi:10.1073/pnas.93.24.14152
Johnston, J. A., Dalton, M. J., Gurney, M. E., Kopito, R. R. (2000) Formation of high molecular weight complexes of mutant Cu,Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences, 97 (23) 12571-12576 doi:10.1073/pnas.220417997
Ripps, M. E., Huntley, G. W., Hof, P. R., Morrison, J. H., Gordon, J. W. (1995) Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences, 92 (3) 689-693 doi:10.1073/pnas.92.3.689
Lee, J.-p., Palfrey, H. C., Bindokas, V. P., Ghadge, G. D., Ma, L., Miller, R. J., Roos, R. P. (1999) The role of immunophilins in mutant superoxide dismutase-1linked familial amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences, 96 (6) 3251-3256 doi:10.1073/pnas.96.6.3251
Yim, M. B., Kang, J. H., Yim, H. S., Kwak, H. S., Chock, P. B., Stadtman, E. R. (1996) A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide. Proceedings of the National Academy of Sciences, 93 (12) 5709-5714 doi:10.1073/pnas.93.12.5709
Mourelatos, Z., Gonatas, N. K., Stieber, A., Gurney, M. E., Dal Canto, M. C. (1996) The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease. Proceedings of the National Academy of Sciences, 93 (11) 5472-5477 doi:10.1073/pnas.93.11.5472
Rowland, L. P. (1995) Amyotrophic lateral sclerosis: human challenge for neuroscience. Proceedings of the National Academy of Sciences, 92 (5) 1251-1253 doi:10.1073/pnas.92.5.1251
Guareschi, S., Cova, E., Cereda, C., Ceroni, M., Donetti, E., Bosco, D. A., Trotti, D., Pasinelli, P. (2012) An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1. Proceedings of the National Academy of Sciences, 109 (13) 5074-5079 doi:10.1073/pnas.1115402109
Rabizadeh, S., Gralla, E. B., Borchelt, D. R., Gwinn, R., Valentine, J. S., Sisodia, S., Wong, P., Lee, M., Hahn, H., Bredesen, D. E. (1995) Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells. Proceedings of the National Academy of Sciences, 92 (7) 3024-3028 doi:10.1073/pnas.92.7.3024
Stathopulos, P. B., Rumfeldt, J. A. O., Scholz, G. A., Irani, R. A., Frey, H. E., Hallewell, R. A., Lepock, J. R., Meiering, E. M. (2003) Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis show enhanced formation of aggregates in vitro. Proceedings of the National Academy of Sciences, 100 (12) 7021-7026 doi:10.1073/pnas.1237797100
 
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