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Showing results (131-140 of 160) with videos related to

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Dementia and Geriatric Cognitive Disorders|October 13, 2001
Genetic analysis in patients with familial and sporadic frontotemporal dementia: two tau mutations in only familial cases and no association with apolipoprotein epsilon4A Kowalska, T Asada, K Arima, et al.
Journal of Neurochemistry|December 26, 2001
Pro-apoptotic effect of presenilin 2 (PS2) overexpression is associated with down-regulation of Bcl-2 in cultured neuronsW Araki, K Yuasa, S Takeda, et al.
Archives of Physical Medicine and Rehabilitation|November 2, 2001
Motoneuron pool excitability of hemiplegic patients: assessing recovery stages by using H-reflex and M responseT Higashi, K Funase, K Kusano, et al.
The Journal of Biological Chemistry|May 25, 1993
Functional erythropoietin receptor of the cells with neural characteristics. Comparison with receptor properties of erythroid cellsS Masuda, M Nagao, K Takahata, et al.
Journal of Neuroscience Research|September 15, 1996
An alpha-chain TCR CDR3 peptide can enhance EAE induced by myelin basic protein or proteolipid proteinT Yamamura, T C Geng, M F Kozovska, et al.
International Immunology|July 1, 1994
Analysis of T cell antigen receptors of myelin basic protein specific T cells in SJL/J mice demonstrates an alpha chain CDR3 motif associated with encephalitogenic T cellsT Yamamura, T Kondo, S Sakanaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1987
Experimental allergic encephalomyelitis mediated by murine encephalitogenic T cell lines specific for myelin proteolipid apoproteinJ Satoh, K Sakai, M Endoh, et al.
Internal Medicine (Tokyo, Japan)|September 2, 2000
Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASILE Uyama, M Tokunaga, A Suenaga, et al.
Annals of Neurology|July 18, 2001
Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau geneK Miyamoto, A Kowalska, M Hasegawa, et al.
Brain & Development|July 14, 1998
Baló's concentric sclerosis in a 4-year-old Japanese infantY Murakami, T Matsuishi, T Shimizu, et al.
Pageof 16

Showing results (131-140 of 160) with videos related to

Sort By:
Pageof 16
Dementia and Geriatric Cognitive Disorders|October 13, 2001
Genetic analysis in patients with familial and sporadic frontotemporal dementia: two tau mutations in only familial cases and no association with apolipoprotein epsilon4A Kowalska, T Asada, K Arima, et al.
Journal of Neurochemistry|December 26, 2001
Pro-apoptotic effect of presenilin 2 (PS2) overexpression is associated with down-regulation of Bcl-2 in cultured neuronsW Araki, K Yuasa, S Takeda, et al.
Archives of Physical Medicine and Rehabilitation|November 2, 2001
Motoneuron pool excitability of hemiplegic patients: assessing recovery stages by using H-reflex and M responseT Higashi, K Funase, K Kusano, et al.
The Journal of Biological Chemistry|May 25, 1993
Functional erythropoietin receptor of the cells with neural characteristics. Comparison with receptor properties of erythroid cellsS Masuda, M Nagao, K Takahata, et al.
Journal of Neuroscience Research|September 15, 1996
An alpha-chain TCR CDR3 peptide can enhance EAE induced by myelin basic protein or proteolipid proteinT Yamamura, T C Geng, M F Kozovska, et al.
International Immunology|July 1, 1994
Analysis of T cell antigen receptors of myelin basic protein specific T cells in SJL/J mice demonstrates an alpha chain CDR3 motif associated with encephalitogenic T cellsT Yamamura, T Kondo, S Sakanaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1987
Experimental allergic encephalomyelitis mediated by murine encephalitogenic T cell lines specific for myelin proteolipid apoproteinJ Satoh, K Sakai, M Endoh, et al.
Internal Medicine (Tokyo, Japan)|September 2, 2000
Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASILE Uyama, M Tokunaga, A Suenaga, et al.
Annals of Neurology|July 18, 2001
Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau geneK Miyamoto, A Kowalska, M Hasegawa, et al.
Brain & Development|July 14, 1998
Baló's concentric sclerosis in a 4-year-old Japanese infantY Murakami, T Matsuishi, T Shimizu, et al.
Pageof 16