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K Doh-ura

Showing results (1-10 of 53) with videos related to

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Uirusu|April 30, 2002
[Current topics of prion disease]H Furukawa, K Doh-ura
No to Shinkei = Brain and Nerve|August 1, 1997
[Gene mutation and pathology in human prion disease]H Tashiro, K Doh-ura
Rinsho Shinkeigaku = Clinical Neurology|December 1, 1996
[Prion diseases and a new variant of Creutzfeldt-Jakob disease]K Doh-ura, T Kitamoto
Journal of Virology|April 25, 2000
Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulationK Doh-Ura, T Iwaki, B Caughey
Pathology International|July 27, 1999
Argyrophilic grains in late-onset Creutzfeldt-Jakob diseased brainT Kawashima, K Doh-ura, T Iwaki
Rinsho Shinkeigaku = Clinical Neurology|February 1, 1989
[Recurrent unilateral painful oculomotor nerve palsy with an ipsilateral posterior ethmoidal mucocele]K Doh-ura, J Kira, Y Itoyama, et al.
Microbial Pathogenesis|January 1, 1995
Identification of differentially expressed genes in scrapie-infected mouse neuroblastoma cellsK Doh-ura, S Perryman, R Race, et al.
Neurology|February 1, 1991
A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndromeT Kitamoto, K Yamaguchi, K Doh-ura, et al.
Acta Neuropathologica|June 23, 1999
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsyH Kikuchi, K Doh-ura, J Kira, et al.
Acta Neuropathologica|November 9, 2001
Cognitive dysfunction in patients with amyotrophic lateral sclerosis is associated with spherical or crescent-shaped ubiquitinated intraneuronal inclusions in the parahippocampal gyrus and amygdala, but not in the neostriatumT Kawashima, K Doh-ura, H Kikuchi, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Uirusu|April 30, 2002
[Current topics of prion disease]H Furukawa, K Doh-ura
No to Shinkei = Brain and Nerve|August 1, 1997
[Gene mutation and pathology in human prion disease]H Tashiro, K Doh-ura
Rinsho Shinkeigaku = Clinical Neurology|December 1, 1996
[Prion diseases and a new variant of Creutzfeldt-Jakob disease]K Doh-ura, T Kitamoto
Journal of Virology|April 25, 2000
Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulationK Doh-Ura, T Iwaki, B Caughey
Pathology International|July 27, 1999
Argyrophilic grains in late-onset Creutzfeldt-Jakob diseased brainT Kawashima, K Doh-ura, T Iwaki
Rinsho Shinkeigaku = Clinical Neurology|February 1, 1989
[Recurrent unilateral painful oculomotor nerve palsy with an ipsilateral posterior ethmoidal mucocele]K Doh-ura, J Kira, Y Itoyama, et al.
Microbial Pathogenesis|January 1, 1995
Identification of differentially expressed genes in scrapie-infected mouse neuroblastoma cellsK Doh-ura, S Perryman, R Race, et al.
Neurology|February 1, 1991
A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndromeT Kitamoto, K Yamaguchi, K Doh-ura, et al.
Acta Neuropathologica|June 23, 1999
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsyH Kikuchi, K Doh-ura, J Kira, et al.
Acta Neuropathologica|November 9, 2001
Cognitive dysfunction in patients with amyotrophic lateral sclerosis is associated with spherical or crescent-shaped ubiquitinated intraneuronal inclusions in the parahippocampal gyrus and amygdala, but not in the neostriatumT Kawashima, K Doh-ura, H Kikuchi, et al.
Pageof 6