O. Komure

发表

Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's disease

H. Ichinose, Y. Mizuno, T. Kondo, 1999, Neuroscience Letters.

The effect of tau genotype on clinical features in FTDP-17.

R. Petersen, M. Farrer, D. Neary, 2005, Parkinsonism & related disorders.

Neuroleptic Malignant Syndrome Associated with Withdrawal of Antiparkinsonian Drugs

S. Kuno, H. Nishitani, E. Mizuta, 1990 .

Phenotypic heterogeneity within a new family with the MAPT p301s mutation

H. Kaneyuki, K. Maeda, T. Kawamata, 2005, Annals of neurology.

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.

M. Oda, H. Kawakami, H. Morino, 2003, American journal of human genetics.

Spinocerebellar ataxia type 6 in relation to CAG repeat length

H. Kawakami, M. Nishimura, Z. Matsuyama, 1999, Acta neurologica Scandinavica.

Pallidonigroluysian degeneration with iron deposition: a study of three autopsy cases

M. Sasahara, F. Hazama, S. Kuno, 2004, Acta Neuropathologica.

Caspase activities and tumor necrosis factor receptor R1 (p55) level are elevated in the substantia nigra from Parkinsonian brain

H. Ichinose, Y. Mizuno, T. Kondo, 2000, Journal of Neural Transmission.

A novel missense mutant inactivates GTP cyclohydrolase I in dopa-responsive dystonia

S. Ueno, M. Hirano, O. Komure, 1999, Neuroscience Letters.

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

B. Ghetti, K. Arima, R. Uitti, 2002, Neurology.

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

G. Schellenberg, S. Tanimukai, P. Poorkaj, 1999, Neurology.

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

M. Oda, H. Kawakami, H. Morino, 2004, Archives of neurology.

Mutations of optineurin in amyotrophic lateral

Takeo Kato, T. Takumi, S. Matsuura, 2010 .

Mutations of optineurin in amyotrophic lateral sclerosis

Takeo Kato, T. Takumi, S. Matsuura, 2010, Nature.

Tau mutations altering splicing of tau exon 10 in japanese frontotemporal dementia

G. Schellenberg, M. Goedert, M. Hasegawa, 2001 .

Contribution of the interleukin‐1β gene polymorphism in multiple system atrophy

R. Kaji, H. Kawakami, H. Morino, 2002 .

Increase in [3H]cAMP binding sites and decrease in Gi alpha and Go alpha immunoreactivities in left temporal cortices from patients with schizophrenia.

O. Shirakawa, T. Mita, N. Nishino, 1993, Brain research.

[A case of myeloradiculitis as a complication of visceral larva migrans due to Ascaris suum].

T. Oeda, Y. Nawa, T. Saida, 2004, Rinsho shinkeigaku = Clinical neurology.

Effects of l-threo-DOPS, a noradrenaline precursor, on the long-term potentiation in the rat hippocampal mossy fiber-CA3 region

M. Sasa, S. Takaori, N. Sakai, 1991, Brain Research.

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8

H. Kawakami, H. Morino, T. Kurashige, 2019, Journal of the Neurological Sciences.

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

A. Sano, K. Umino, I. Kanazawa, 1994, Nature Genetics.

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

I. Kanazawa, G. Sobue, T. Shimohata, 1999, Human molecular genetics.

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA).

F. Hazama, A. Sano, S. Ueno, 1995, Human molecular genetics.

A unique origin and multistep process for the generation of expanded DRPLA triplet repeats.

I. Kanazawa, T. Miyashita, Koichiro Nakamura, 1996, Human molecular genetics.

Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia

O. Shirakawa, T. Kawamata, M. Yanagi, 2008, Schizophrenia Research.

Asymmetrical changes in the fodrin α subunit in the superior temporal cortices in schizophrenia

O. Shirakawa, T. Mita, N. Nishino, 1998, Biological Psychiatry.

Increase in [3H]cAMP binding sites and decrease in Giα and Goα immunoreactivities in left temporal cortices from patients with schizophrenia

O. Shirakawa, T. Mita, N. Nishino, 1993, Brain Research.

Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies

G. Sobue, H. Ichijo, K. Takeda, 1999, Genes to cells : devoted to molecular & cellular mechanisms.

Anticipation in hereditary dentatorubral-pallidoluysian atrophy

I. Kondo, F. Hazama, A. Sano, 1994, Human Genetics.

The loss of βII-protein kinase C in the striatum from patients with Huntington's disease

C. Tanaka, N. Saito, N. Nishino, 1992, Brain Research.

Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation

R. Takahashi, R. Kaji, H. Kusaka, 2011, Acta Neuropathologica.

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Y. Goto, S. Niwa, A. Sano, 2020, Journal of Human Genetics.

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy

I. Kanazawa, M. Yamada, I. Kondo, 1995, Neurology.

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations

R. Takahashi, H. Kusaka, H. Kawakami, 2018, Journal of neuropathology and experimental neurology.

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

H. Kawakami, M. Nishimura, Z. Matsuyama, 1997, Human molecular genetics.

The loss of beta II-protein kinase C in the striatum from patients with Huntington's disease.

C. Tanaka, N. Saito, N. Nishino, 1992, Brain research.

No association between apolipoprotein E alleles and olivopontocerebellar atrophy

T. Kawarai, H. Kawakami, Shigenobu Nakamura, 1998, Journal of the Neurological Sciences.

Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.

R. Kaji, H. Kawakami, H. Morino, 2002, Movement disorders : official journal of the Movement Disorder Society.

A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease

T. Kawarai, H. Kawakami, H. Morino, 2000, Annals of neurology.

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Y. Goto, S. Niwa, A. Sano, 2020, Journal of human genetics.

Asymmetrical changes in the fodrin alpha subunit in the superior temporal cortices in schizophrenia.

O. Shirakawa, T. Mita, N. Nishino, 1998, Biological psychiatry.