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O Komure

Showing results (11-20 of 24) with videos related to

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Neuroscience Letters|August 24, 1999
Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's diseaseM Mogi, A Togari, T Kondo, et al.
Human Molecular Genetics|April 1, 1995
Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA)S Ueno, K Kondoh, Y Kotani, et al.
Human Genetics|June 1, 1994
Anticipation in hereditary dentatorubral-pallidoluysian atrophyA Sano, N Yamauchi, Y Kakimoto, et al.
Neurology|January 1, 1995
DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipationO Komure, A Sano, N Nishino, et al.
Brain Research|June 25, 1993
Increase in [3H]cAMP binding sites and decrease in Gi alpha and Go alpha immunoreactivities in left temporal cortices from patients with schizophreniaN Nishino, N Kitamura, T Hashimoto, et al.
Annals of Neurology|April 13, 2000
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's diseaseH Morino, T Kawarai, Y Izumi, et al.
Human Molecular Genetics|August 1, 1997
Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)Z Matsuyama, H Kawakami, H Maruyama, et al.
Acta Neurologica Scandinavica|May 4, 1999
Spinocerebellar ataxia type 6 in relation to CAG repeat lengthY Kaseda, H Kawakami, Z Matsuyama, et al.
Neurology|September 17, 1999
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degenerationM Yasuda, T Kawamata, O Komure, et al.
Biological Psychiatry|March 26, 1998
Asymmetrical changes in the fodrin alpha subunit in the superior temporal cortices in schizophreniaN Kitamura, N Nishino, T Hashimoto, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Neuroscience Letters|August 24, 1999
Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's diseaseM Mogi, A Togari, T Kondo, et al.
Human Molecular Genetics|April 1, 1995
Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA)S Ueno, K Kondoh, Y Kotani, et al.
Human Genetics|June 1, 1994
Anticipation in hereditary dentatorubral-pallidoluysian atrophyA Sano, N Yamauchi, Y Kakimoto, et al.
Neurology|January 1, 1995
DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipationO Komure, A Sano, N Nishino, et al.
Brain Research|June 25, 1993
Increase in [3H]cAMP binding sites and decrease in Gi alpha and Go alpha immunoreactivities in left temporal cortices from patients with schizophreniaN Nishino, N Kitamura, T Hashimoto, et al.
Annals of Neurology|April 13, 2000
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's diseaseH Morino, T Kawarai, Y Izumi, et al.
Human Molecular Genetics|August 1, 1997
Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)Z Matsuyama, H Kawakami, H Maruyama, et al.
Acta Neurologica Scandinavica|May 4, 1999
Spinocerebellar ataxia type 6 in relation to CAG repeat lengthY Kaseda, H Kawakami, Z Matsuyama, et al.
Neurology|September 17, 1999
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degenerationM Yasuda, T Kawamata, O Komure, et al.
Biological Psychiatry|March 26, 1998
Asymmetrical changes in the fodrin alpha subunit in the superior temporal cortices in schizophreniaN Kitamura, N Nishino, T Hashimoto, et al.
Pageof 3