T. Tsuda

发表

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

D. Pollen, J. Haines, M. Pericak-Vance, 1995, Nature.

Impaired chemosensitivity to hypoxia is a marker of multiple system atrophy

Y. Itoyama, T. Tsuda, H. Onodera, 2002, Annals of neurology.

Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein response

Y. Itoyama, T. Kudo, P. George-Hyslop, 1999, Nature Cell Biology.

Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2*

P. S. St George-Hyslop, Y. Itoyama, T. Kudo, 2001, The Journal of Biological Chemistry.

Homozygous inheritance of the Machado‐Joseph disease gene

P. S. St George-Hyslop, A. Lang, E. Rogaeva, 1994, Annals of neurology.

Analysis of the c‐FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease

D. Pollen, J. Haines, E. Rogaev, 1993, Neurology.

Impaired chemosensitivity and perception of dyspnoea in Parkinson's disease

Y. Itoyama, T. Tsuda, H. Onodera, 2000, The Lancet.

High prevalence of spinocerebellar ataxia type 1 (SCA1) in an isolated region of Japan

Y. Itoyama, K. Abe, H. Kato, 2000, Journal of the Neurological Sciences.

A presenilin‐1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRI

P. S. St George-Hyslop, Y. Itoyama, M. Shoji, 1997, Neurology.

Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis

P. Fraser, W. Tatton, P. George-Hyslop, 1994, Neuron.

Transcranial magnetic stimulation alleviates truncal ataxia in spinocerebellar degeneration

Y. Itoyama, Y. Shiga, K. Miyazawa, 2002, Journal of neurology, neurosurgery, and psychiatry.

Mutation of the gene for the human lysosomal serine protease cathepsin G is not the cause of aberrant APP processing in familial Alzheimer disease

E. Rogaeva, P. George-Hyslop, Y. Liang, 1993, Neuroscience Letters.

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.

Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases

D. Pollen, R. Sherrington, E. Rogaeva, 1995, Neuroscience Letters.

Possible Involvement of Iron-Dependent Lipid Peroxidation in the Delayed Neuronal Death of Rat Brain after a Transient Ischemia

H. Arai, K. Kogure, T. Tsuda, 1987 .

Roles of Calcium-Activated Enzymic Reactions in Ischemia-Induced Neuronal Injury

K. Kogure, T. Araki, T. Tsuda, 1989 .

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

J. Rommens, R. Sherrington, E. Rogaev, 1995, Nature.

Predictors and underlying causes of medically intractable localization-related epilepsy in childhood.

Katsuhiro Kobayashi, K. Kobayashi, H. Yoshinaga, 2001, Pediatric neurology.

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14

D. Pollen, J. Haines, M. Pericak-Vance, 1992, Nature Genetics.

Ophthalmological findings in patients with spinocerebellar ataxia type 1 are not correlated with neurological anticipation

Y. Itoyama, M. Tamai, T. Abe, 2001, Graefe's Archive for Clinical and Experimental Ophthalmology.

Macular degeneration associated with aberrant expansion of trinucleotide repeat of the SCA7 gene in 2 Japanese families.

M. Tamai, T. Abe, T. Tsuda, 2000, Archives of ophthalmology.

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

J. Weissenbach, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14.

J. Haines, E. Rogaev, P. S. St George-Hyslop, 1994, American journal of human genetics.

A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairment

W. Snow, M. Tierney, J. Szalai, 1996, Neurology.

Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium?

M. Freedman, D. Pollen, J. Haines, 1994, Annals of neurology.

No association between apolipoprotein E genotype and late-onset depression in Alzheimer's disease

M. Cantillon, P. George-Hyslop, W. Barker, 1997, Biological Psychiatry.

Alzheimer's disease and possible gene interaction.

D. Pollen, J. Haines, M. Pericak-Vance, 1994, Science.

Therapeutic efficacy of transcranial magnetic stimulation for hereditary spinocerebellar degeneration.

Y. Itoyama, Y. Shiga, K. Miyazawa, 1999, The Tohoku journal of experimental medicine.

SOD1 missense mutation in an Italian family with ALS

P. S. St George-Hyslop, G. Vaula, L. Pinessi, 1994, Neurology.

Mg2+ Administered up to twenty-four hours following reperfusion prevents ischemic damage of the CA1 neurons in the rat hippocampus

K. Kogure, T. Tsuda, T. Watanabe, 1991, Neuroscience.

Interfamilial and Intrafamilial Phenotypic Heterogeneity in Familial Alzheimer's Disease

P. George-Hyslop, D. Loewenstein, W. Barker, 1997, Journal of geriatric psychiatry and neurology.

Influence of Apolipoprotein E3 on the Production of Paired Helical Filament in Guamanian Parkinsonism‐dementia Complex/Amyotrophic Lateral Sclerosis and Alzheimer's Disease

D. McLachlan, T. Tsuda, D. Mclachlan, 2001 .

Postischemic changes of calcium and endogenous antagonist in the rat hippocampus studied by proton-induced X-ray emission analysis

K. Kogure, T. Tsuda, K. Ishii, 1989, Brain Research.

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

J. Weissenbach, K. Kidd, R. Sherrington, 1995, Human molecular genetics.