Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Hiroshi Tanahashi"'
Autor:
Hiroshi Tanahashi, Tatsuo Suzuki
Publikováno v:
Biochemical and Biophysical Research Communications. 506:478-484
Microphthalmia is a malformation that reduces the size of the ocular globe. The etiologies of this anomaly are various, but the genetic background appears to have a predominant influence on its development through mutations of genes controlling ocula
Autor:
Hiroshi Tanahashi, Katsuji Yoshioka
Publikováno v:
Neuroscience Letters. 439(3):293-297
金沢大学医薬保健研究域医学系
In a previous study, we reported that Alzheimer's disease-associated presenilin-2 interacts with a LIM-domain protein, namely, DRAL/FHL2/SLIM3. In this study, we investigated whether DRAL modifies the m
In a previous study, we reported that Alzheimer's disease-associated presenilin-2 interacts with a LIM-domain protein, namely, DRAL/FHL2/SLIM3. In this study, we investigated whether DRAL modifies the m
Publikováno v:
NeuroReport. 15:175-179
Neurofibrillary tangles, containing hyperphosphorylated microtubule-associated protein tau, are one of the major pathological hallmarks of Alzheimer's disease. To investigate a possible association between tau genotypes and the risk of Alzheimer's di
Autor:
Hiroshi Tanahashi, Takeshi Tabira
Publikováno v:
Neuroscience Letters. 307:9-12
Three novel alternatively spliced transcripts of the beta-site amyloid precursor protein cleaving enzyme (BACE) were cloned from human brain. Alternative splicing of the RNA occurs at an internal donor in exon 3 and/or an internal acceptor in exon 4.
Autor:
Toru Wakatsuki, Mikio Yamamoto, Akio Suzumura, Haruhisa Inoue, Hiroshi Tanahashi, Takeshi Tabira, Keiko Nakagaki, Akiyuki Hada, Makoto Sawada, Keikichi Takahashi, Nobuo Kondoh, Akihide Ryo
Publikováno v:
Glia. 28:265-271
We used the serial analysis of gene expression (SAGE) method to systematically analyze transcripts present in a microglial cell line. Over 10,000 SAGE tags were sequenced, and shown to represent 6,013 unique transcripts. Among the diverse transcripts
Autor:
Hiroshi Tanahashi, Takeshi Tabira
Publikováno v:
Biochemical and Biophysical Research Communications. 258:385-389
Recently we cloned the cDNA encoding human Fe65L2, which interacts with Alzheimer's beta-amyloid precursor protein (APP). The protein has one WW domain and two PID elements (Neurosci. Lett. (1999) 261, 143-146.). Here, we report the entire genome str
Autor:
Takeshi Tabira, Hiroshi Tanahashi
Publikováno v:
NeuroReport. 10:563-568
We screened proteins for interaction with presenilin (PS) 1, and cloned the full-length cDNA of human delta-catenin, which encoded 1225 amino acids. Yeast two-hybrid assay, GST binding assay and immunoprecipitation demonstrated that delta-catenin int
Autor:
Takeshi Tabira, Hiroshi Tanahashi
Publikováno v:
Neuroscience Letters. 261:143-146
We report the cDNA sequence of human Fe65L2. The human Fe65L2 encoded 486 amino acids; the deduced amino acid sequence was shorter by 18 amino acids than the rat protein and had 86% identity to the rat protein Three protein-protein interaction domain
Autor:
Hideki Yamanaka, Kohei Kamimura, Keikichi Takahashi, Takashi Asada, Hiroshi Tanahashi, Takeshi Tabira
Publikováno v:
Journal of the Neurological Sciences. 160:76-81
More than 40 missense mutations and a splice-site mutation in the presenilin 1 (PS-1) gene, two missense mutations of presenilin 2 (PS-2), and more than three missense mutations of amyloid precursor protein (APP) cosegregate with early onset familial
Autor:
Keikichi Takahashi, Kazuharu Ozawa, Keiro Shirotani, Haruhiko Akiyama, Tatsuhide Kunishita, Dehua Chui, Takao Makifuchi, Hiroshi Tanahashi, Takeshi Tabira
Publikováno v:
Journal of Neuroscience Research. 53:99-106
Presenilin 1 (PS1) is a causative gene for chromosome 14-linked familial Alzheimer's disease. The gene product is known to be cleaved into N-terminal fragments (PS1-N) and C-terminal fragments (PS1-C). To understand the pathophysiological role of PS1