K. Takahashi

发表

A distinct familial presenile dementia with a novel missense mutation in the tau gene.

G. Schellenberg, J. Trojanowski, V. Lee, 1999, Neuroreport.

Pro‐apoptotic effect of presenilin 2 (PS2) overexpression is associated with down‐regulation of Bcl‐2 in cultured neurons

T. Tabira, S. Takeda, W. Araki, 2001, Journal of neurochemistry.

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene

K. Arima, T. Iwatsubo, T. Tabira, 2000, Neurology.

Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11‐splice site in the tau gene

T. Tabira, M. Hasegawa, I. Akiguchi, 2001, Annals of neurology.

Apoptotic neurons in Alzheimer's disease frequently show intracellular Abeta42 labeling.

T. Tabira, H. Akiyama, F. Checler, 2001, Journal of Alzheimer's disease : JAD.

Determination of a cleavage site of presenilin 2 protein in stably transfected SH-SY5Y human neuroblastoma cell lines.

T. Tabira, T. Kunishita, K. Ozawa, 1997, Biochemical and biophysical research communications.

Overexpression of Presenilin‐2 Enhances Apoptotic Death of Cultured Cortical Neurons

T. Tabira, S. Takeda, W. Araki, 2000, Annals of the New York Academy of Sciences.

Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.

T. Tabira, M. Uchino, E. Uyama, 2000, Internal medicine.

Developmental and differential expression of beta amyloid protein precursor mRNAs in mouse brain.

T. Tabira, Y. Ohyagi, K. Takahashi, 1990, Biochemical and biophysical research communications.

Genetic Risk Factors in Japanese Alzheimer’s Disease Patients: α1-ACT, VLDLR, and ApoE

T. Tabira, K. Takahashi, H. Tanahashi, 1998, Neurobiology of Aging.

Novel mutation of the Notch3 gene in a Japanese patient with CADASIL

T. Tabira, T. Katayama, A. Ishiko, 2007, European journal of neurology.

Detection of granular osmiophilic material of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy by light microscopy in frozen sections

M. Uchino, H. Hino, E. Uyama, 2009, Neuropathology and applied neurobiology.

Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

T. Tabira, M. Uchino, E. Uyama, 1999, Alzheimer disease and associated disorders.

[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].

T. Tabira, Y. Sunada, K. Takahashi, 2001, Rinsho shinkeigaku = Clinical neurology.