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T Kitamoto

Showing results (141-150 of 183) with videos related to

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Neurology|July 25, 2007
Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob diseaseM Noguchi-Shinohara, T Hamaguchi, T Kitamoto, et al.
Neuroradiology|October 1, 1995
Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180S Ishida, M Sugino, N Koizumi, et al.
The American Journal of Pathology|June 1, 1992
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob diseaseT Kitamoto, R W Shin, K Doh-ura, et al.
Neuroscience Letters|July 13, 2000
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219GluT Muramoto, T Tanaka, N Kitamoto, et al.
Acta Neuropathologica|December 14, 1999
Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tanglesM Yamazaki, K Oyanagi, O Mori, et al.
Journal of Human Genetics|April 27, 2001
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genesA Iida, A Sekine, S Saito, et al.
Revue Neurologique|January 1, 1991
[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]C Tranchant, K Doh-Ura, G Steinmetz, et al.
The Journal of Biological Chemistry|April 5, 2000
p300 mediates functional synergism between AF-1 and AF-2 of estrogen receptor alpha and beta by interacting directly with the N-terminal A/B domainsY Kobayashi, T Kitamoto, Y Masuhiro, et al.
Archives of Neurology|December 1, 1986
Nonfamilial prealbumin-type amyloid polyneuropathyJ Ochiai, S Tobimatsu, T Kobayashi, et al.
Biochemical and Biophysical Research Communications|May 24, 1996
Humanized prion protein knock-in by Cre-induced site-specific recombination in the mouseT Kitamoto, K Nakamura, K Nakao, et al.
Pageof 19

Showing results (141-150 of 183) with videos related to

Sort By:
Pageof 19
Neurology|July 25, 2007
Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob diseaseM Noguchi-Shinohara, T Hamaguchi, T Kitamoto, et al.
Neuroradiology|October 1, 1995
Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180S Ishida, M Sugino, N Koizumi, et al.
The American Journal of Pathology|June 1, 1992
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob diseaseT Kitamoto, R W Shin, K Doh-ura, et al.
Neuroscience Letters|July 13, 2000
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219GluT Muramoto, T Tanaka, N Kitamoto, et al.
Acta Neuropathologica|December 14, 1999
Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tanglesM Yamazaki, K Oyanagi, O Mori, et al.
Journal of Human Genetics|April 27, 2001
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genesA Iida, A Sekine, S Saito, et al.
Revue Neurologique|January 1, 1991
[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]C Tranchant, K Doh-Ura, G Steinmetz, et al.
The Journal of Biological Chemistry|April 5, 2000
p300 mediates functional synergism between AF-1 and AF-2 of estrogen receptor alpha and beta by interacting directly with the N-terminal A/B domainsY Kobayashi, T Kitamoto, Y Masuhiro, et al.
Archives of Neurology|December 1, 1986
Nonfamilial prealbumin-type amyloid polyneuropathyJ Ochiai, S Tobimatsu, T Kobayashi, et al.
Biochemical and Biophysical Research Communications|May 24, 1996
Humanized prion protein knock-in by Cre-induced site-specific recombination in the mouseT Kitamoto, K Nakamura, K Nakao, et al.
Pageof 19