M. Watanabe

发表

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

J. Schulz, C. Shaw, L. Schöls, 2004, Nature Genetics.

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

T. Gibson, M. Koenig, Mitsunori Watanabe, 2001, Nature Genetics.

Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan

K. Okamoto, Mitsunori Watanabe, Y. Ikeda, 2000, Neurology.

Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis

Y. Itoyama, M. Shoji, K. Okamoto, 1997, Journal of the Neurological Sciences.

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.

N. Drouot, A. Durr, L. Schöls, 2009, Brain : a journal of neurology.

Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis

A. Monaco, M. Brin, J. Volkmann, 2002, European Journal of Human Genetics.

Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations.

A. Børresen-Dale, L. Chessa, R. Gatti, 1998, American journal of human genetics.

A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report

E. Matsubara, M. Shoji, K. Okamoto, 2010, Journal of the Neurological Sciences.

Bunina bodies in amyotrophic lateral sclerosis immunostained with rabbit anti-cystatin C serum

S. Hirai, K. Okamoto, M. Amari, 1993, Neuroscience Letters.

Histological Evidence of Protein Aggregation in Mutant SOD1 Transgenic Mice and in Amyotrophic Lateral Sclerosis Neural Tissues

D. Price, P. Wong, J. Rothstein, 2001, Neurobiology of Disease.

Genetic analysis of the cystatin C gene in familial and sporadic ALS patients

S. Hirai, K. Okamoto, M. Amari, 2006, Brain Research.

Cerebrospinal fluid tau in dementia disorders: a large scale multicenter study by a Japanese study group

S. Hirai, K. Nakashima, H. Arai, 2002, Neurobiology of Aging.

Combination assay of CSF Tau, Aβ1-40 and Aβ1-42(43) as a biochemical marker of Alzheimer's disease

S. Hirai, E. Matsubara, M. Shoji, 1998, Journal of the Neurological Sciences.

Induction of nitrotyrosine-like immunoreactivity in the lower motor neuron of amyotrophic lateral sclerosis

Y. Itoyama, M. Watanabe, K. Abe, 1995, Neuroscience Letters.

Reuptake of L‐DOPA‐derived extracellular DA in the striatum of a rodent model of Parkinson's disease via norepinephrine transporter

M. Shoji, Mitsunori Watanabe, T. Kawarabayashi, 2008, Synapse.

Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI

Mikio Shoji, Mitsunori Watanabe, Koichi Okamoto, 2000, Journal of the Neurological Sciences.

Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics

Y. Itoyama, M. Shoji, K. Okamoto, 1998, Journal of the Neurological Sciences.

Prevalence of autosomal dominant cerebellar ataxia in Aomori, the northernmost prefecture of Honshu, Japan.

E. Matsubara, M. Shoji, Mitsunori Watanabe, 2010, Internal medicine.

An unusual case of chronic relapsing tetanus associated with mandibular osteomyelitis.

M. Fujimuro, E. Matsubara, M. Shoji, 2009, Internal medicine.

Internal Medicine Vol.47

M. Fujimuro, E. Matsubara, M. Shoji, 2009 .

Loss of β-III Spectrin Leads to Purkinje Cell Dysfunction Recapitulating the Behavior and Neuropathology of Spinocerebellar Ataxia Type 5 in Humans

M. Dutia, J. Rothstein, A. Lyndon, 2010, The Journal of Neuroscience.

Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.

S. Tsuji, V. Wong, A. Dürr, 2007, Archives of neurology.

Generation of Amyloid β Protein from a Presenilin-1 and βAPP Complex☆

P. George-Hyslop, E. Matsubara, M. Shoji, 2002 .

Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1- 2 polymorphism and contribution to founder effect

M. Shoji, K. Okamoto, Mitsunori Watanabe, 1999, Journal of medical genetics.

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses

I. Kanazawa, S. Tsuji, Toshihiro Hayashi, 2014, Journal of Human Genetics.

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses

I. Kanazawa, S. Tsuji, Toshihiro Hayashi, 2014, Journal of Human Genetics.

Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3

A. Lyndon, E. Matsubara, M. Shoji, 2010, Brain Research.

Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls

M. Shoji, K. Okamoto, Mitsunori Watanabe, 1998, Journal of the Neurological Sciences.

Fundamental Morphological Changes in Human Olivary Hypertrophy

S. Hirai, Koichi E. Okamoto, Mitsunori Watanabe, 1992, Acta pathologica japonica.

Factors responsible for neurofibrillary tangles and neuronal cell losses in tauopathy

D. Westaway, E. Matsubara, M. Shoji, 2011, Journal of neuroscience research.

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

I. Kanazawa, S. Tsuji, M. Miwa, 1997, American journal of human genetics.

Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double‐transgenic mouse model

D. Westaway, E. Matsubara, M. Shoji, 2010, Journal of neuroscience research.

Amyloid β protein levels in cerebrospinal fluid are elevated in early‐onset Alzheimer's disease

S. Younkin, L. Younkin, S. Hirai, 1994 .

Interaction of PDZRhoGEF with Microtubule-associated Protein 1 Light Chains

J. Rothstein, Mitsunori Watanabe, M. Jackson, 2006, Journal of Biological Chemistry.

The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

G. Schellenberg, R. Sherrington, T. Bird, 1996, Annals of neurology.

A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea.

Y. Itoyama, T. Kameya, Koji Abe, 1996, Neurological research.

Upregulation of protein-tyrosine nitration in the anterior horn cells of amyotrophic lateral sclerosis.

Y. Itoyama, H. Konno, M. Watanabe, 1997, Neurological research.

A Japanese family with adrenoleukodystrophy with a codon 291 deletion: a clinical, biochemical, pathological, and genetic report

S. Tsuji, M. Shoji, K. Okamoto, 1998, Journal of Neurological Sciences.

Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1- 2 polymorphism and contribution to founder effect

M. Shoji, K. Okamoto, I. Kondo, 1999, Journal of medical genetics.

Oculomotor nuclear pathology in amyotrophic lateral sclerosis

Mitsunori Watanabe, Koichi Okamoto, S. Hirai, 2004, Acta Neuropathologica.

Accumulation of NACP/α-synuclein in Lewy body disease and multiple system atrophy

S. Hirai, E. Matsubara, M. Shoji, 2000, Journal of neurology, neurosurgery, and psychiatry.