Settlement of Three Buildings on Piled Foundations (9999)
Results of settlement observation are presented for 3 storied reinforced concrete buildings. The buildings are supported on friction group piles in a sand stratum overlying a nearby 40 m thick...
Regulation of STAT3-mediated signaling by LMW-DSP2. (2006)
Sekine, Y., Tsuji, S., Ikeda, O., Sato, N., Aoki, N., Aoyama, K., ...
Signal transducer and activator of transcription 3 (STAT3), which mediates biological actions in many physiological processes, is activated by cytokines and growth factors, and has been reported to...
Regulation of STAT3-mediated signaling by LMW-DSP2. (2006)
Sekine, Y., Tsuji, S., Ikeda, O., Sato, N., Aoki, N., Aoyama, K., ...
Signal transducer and activator of transcription 3 (STAT3), which mediates biological actions in many physiological processes, is activated by cytokines and growth factors, and has been reported to...
横山, 幸男, Yokoyama, Yukio, Tsuji, S., Sato, H.
A simple and versatile cation-exchange chromatography technique for the simultaneous determination of urinary creatinine (Cre), creatine (Cm), methionine (Met), tyrosine (Tyr), phenylalanine (Phe),...
Structures of glycoprotein Ibα and its complex with von Willebrand Factor A1 domain (2002)
Huizinga, E.G., Tsuji, S., Romijn, R.A.P., Schiphorst, M.E., Groot, P.G. De, Sixma, J.J., ...
Nagawa, M, Ichikawa, M, Koyama, T, Shirai, H, Taniguchi, Y, Hongo, A, ...
Ikehara, Y, Kojima, N, Kurosawa, N, Kudo, T, Kono, M, Nishihara, S, ...
Aglietta, M, Alpat, B, Alyea, E D, Antonioli, P, Badino, G, Bari, G, ...
An energy signature for very deep underground muons observed by the LVD experiment (1998)
Aglietta, M, Alpat, B, Alyea, E D, Antonioli, P, Badino, G, Bari, G, ...
Upper limit on the prompt muon flux derived from the LVD data (1998)
Aglietta, M, Alpat, B, Alyea, E D, Antonioli, P, Badino, G, Bari, G, ...
Search for point sources with muons observed by LVD (1998)
Aglietta, M, Alpat, B, Alyea, E D, Antonioli, P, Badino, G, Bari, G, ...
Takiyama, Y, Sakoe, K, Soutome, M, Namekawa, M, Ogawa, T, Nakano, I, ...
Ishikawa, K., Mizusawa, H., Saito, M., Tanaka, H., Nakajima, N., Kondo, N., ...
We carried out linkage analysis and clinical assessment on 41 patients with autosomal dominant pure cerebellar ataxia (ADCA) type III from eight Japanese families. The presenting symptom was gait...
Tamagawa, Y, Kitamura, K, Ishida, T, Ishikawa, K, Tanaka, H, Tsuji, S, ...
Takiyama, Y., Igasrashi, S., Rogaeva, E.A., Endo, K., Rogaev, E.I., Tanaka, H., ...
The size of the (CAG)n repeat array in the 3′ end of the MJDI gene and the haplotype at a series of microsateilite markers surrounding the MJD1 gene were examined in a large cohort of Japanese and...
Genetic Similarity Using DNA Fingerprinting in Cattle to Determine Relationship Coefficient (1993)
Mannen, H., Tsuji, S., Mukai, F., Goto, N., Ohtagaki, S.
The relation between relationship coefficient and genetic similarity was evaluated using DNA fingerprinting in Japanese Black cattle. We proposed a new method for evaluating heterozygous and...
BamHI polymorphism at N-acetyl-alpha-galactosaminidase locus (NAGA) (1991)
Yamauchi, T, Tanaka, H, Hiraiwa, M, Uda, Y, Miyatake, T, Tsuji, S
A new RFLP locus D8S163 maps to human chromosome 8pter-8p22 (1991)
Kaneko, K., Wagner, M. J., Wells, D. E., Tanaka, H., Miyataka, T., Tsuji, S.
Tsuji, S, Qureshi, M A, Hou, E W, Fitch, W M, Li, S S
The nucleotide sequences of the cDNAs encoding LDH (EC 1.1.1.27) subunits LDH-A (muscle), LDH-B (liver), and LDH-C (oocyte) from Xenopus laevis, LDH-A (muscle) and LDH-B (heart) from pig, and LDH-B...
Tsuji, S, Martin, B M, Barranger, J A, Stubblefield, B K, LaMarca, M E, Ginns, E I
Nucleotide sequence analysis of a genomic clone from an Ashkenazic Jewish patient with type 1 Gaucher disease revealed a single-base mutation (adenosine to guanosine transition) in exon 9 of the...
A new RFLP locus D8S163 maps to human chromosome 8pter-8p22
Kaneko, K., Wagner, M.J., Wells, D.E., Tanaka, H., Miyatake, T., Tsuji, S.
Ginns, E I, Choudary, P V, Tsuji, S, Martin, B, Stubblefield, B, Sawyer, J, ...
Analysis of immunologic cross-reacting material in Chinese hamster-human somatic cell hybrids allowed assignment of the structural gene for glucocerebrosidase (glucosylceramidase;...
McInnes, B, Potier, M, Wakamatsu, N, Melancon, S B, Klavins, M H, Tsuji, S, ...
Sandhoff disease is caused by mutations affecting the beta subunit of lysosomal beta-hexosaminidase (EC 3.2.1.52) and displays a wide spectrum of clinical phenotypes. We report a 57-year-old patient...
Tsuji, S, Kobayashi, H, Uchida, Y, Ihara, Y, Miyatake, T
In previous studies, we discovered a growth inhibitory factor (GIF) that was abundant in normal human brain, but greatly reduced in Alzheimer's disease (AD) brain. Molecular cloning of a full-length...
Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study
Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., ...
Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder originally described in families of Portuguese-Azorean ancestry. The cloning of the MJD1 gene allowed identification...
Ishikawa, K, Tanaka, H, Saito, M, Ohkoshi, N, Fujita, T, Yoshizawa, K, ...
Autosomal dominant cerebellar ataxia is a group of clinically and genetically heterogeneous disorders. We carried out genomewide linkage analysis in 15 families with autosomal dominant pure...
Takano, H, Cancel, G, Ikeuchi, T, Lorenzetti, D, Mawad, R, Stevanin, G, ...
To test the hypothesis that the frequencies of normal alleles (ANs) with a relatively large number of CAG repeats (large ANs) are related to the prevalences of the dominant spinocerebellar ataxias...
Mitochondrial DNA variation and evolution of Japanese black cattle (Bos taurus).
Mannen, H, Tsuji, S, Loftus, R T, Bradley, D G
This article describes complete mitochondrial DNA displacement loop sequences from 32 Japanese Black cattle and the analysis of these data in conjunction with previously published sequences from...
Kondo, R, Wakamatsu, N, Yoshino, H, Fukuhara, N, Miyatake, T, Tsuji, S
To analyze the genetic abnormality in a Japanese patient with adult-type metachromatic leukodystrophy (MLD), we first elucidated the genomic organization of the human arylsulfatase A (ASA) gene and...
Tsuji, S, Qureshi, M A, Hou, E W, Fitch, W M, Li, S S
The nucleotide sequences of the cDNAs encoding LDH (EC 1.1.1.27) subunits LDH-A (muscle), LDH-B (liver), and LDH-C (oocyte) from Xenopus laevis, LDH-A (muscle) and LDH-B (heart) from pig, and LDH-B...
Tsuji, S, Martin, B M, Barranger, J A, Stubblefield, B K, LaMarca, M E, Ginns, E I
Nucleotide sequence analysis of a genomic clone from an Ashkenazic Jewish patient with type 1 Gaucher disease revealed a single-base mutation (adenosine to guanosine transition) in exon 9 of the...
A new RFLP locus D8S163 maps to human chromosome 8pter-8p22
Kaneko, K., Wagner, M.J., Wells, D.E., Tanaka, H., Miyatake, T., Tsuji, S.
Ginns, E I, Choudary, P V, Tsuji, S, Martin, B, Stubblefield, B, Sawyer, J, ...
Analysis of immunologic cross-reacting material in Chinese hamster-human somatic cell hybrids allowed assignment of the structural gene for glucocerebrosidase (glucosylceramidase;...
McInnes, B, Potier, M, Wakamatsu, N, Melancon, S B, Klavins, M H, Tsuji, S, ...
Sandhoff disease is caused by mutations affecting the beta subunit of lysosomal beta-hexosaminidase (EC 3.2.1.52) and displays a wide spectrum of clinical phenotypes. We report a 57-year-old patient...
Tsuji, S, Kobayashi, H, Uchida, Y, Ihara, Y, Miyatake, T
In previous studies, we discovered a growth inhibitory factor (GIF) that was abundant in normal human brain, but greatly reduced in Alzheimer's disease (AD) brain. Molecular cloning of a full-length...
Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study
Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., ...
Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder originally described in families of Portuguese-Azorean ancestry. The cloning of the MJD1 gene allowed identification...
Takano, H, Cancel, G, Ikeuchi, T, Lorenzetti, D, Mawad, R, Stevanin, G, ...
To test the hypothesis that the frequencies of normal alleles (ANs) with a relatively large number of CAG repeats (large ANs) are related to the prevalences of the dominant spinocerebellar ataxias...
Mitochondrial DNA variation and evolution of Japanese black cattle (Bos taurus).
Mannen, H, Tsuji, S, Loftus, R T, Bradley, D G
This article describes complete mitochondrial DNA displacement loop sequences from 32 Japanese Black cattle and the analysis of these data in conjunction with previously published sequences from...
Kondo, R, Wakamatsu, N, Yoshino, H, Fukuhara, N, Miyatake, T, Tsuji, S
To analyze the genetic abnormality in a Japanese patient with adult-type metachromatic leukodystrophy (MLD), we first elucidated the genomic organization of the human arylsulfatase A (ASA) gene and...
Matsumine, H, Saito, M, Shimoda-Matsubayashi, S, Tanaka, H, Ishikawa, A, Nakagawa-Hattori, Y, ...
An autosomal recessive form of juvenile Parkinsonism (AR-JP) (MIM 600116) is a levodopa-responsive Parkinsonism whose pathological finding is a highly selective degeneration of dopaminergic neurons...
Ishikawa, K, Tanaka, H, Saito, M, Ohkoshi, N, Fujita, T, Yoshizawa, K, ...
Autosomal dominant cerebellar ataxia is a group of clinically and genetically heterogeneous disorders. We carried out genomewide linkage analysis in 15 families with autosomal dominant pure...
Onodera, O, Oyake, M, Takano, H, Ikeuchi, T, Igarashi, S, Tsuji, S
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder characterized by genetic anticipation and variable combinations of symptoms including myoclonus,...
Tomita, Y., Watanabe, H., Kobayashi, H., Nishiyama, T., Tsuji, S., Imai, K., ...
Immunohistochemical examination demonstrated expression of intercellular adhesion molecule-1 (ICAM-1) on 17 of 44 transitional cell cancers (TCCs) but not on normal transitional cells. ICAM-1 was...
Imaizumi, T, Takeshita, A, Ashihara, T, Nakamura, M, Tsuji, S, Shibazaki, H
Since indomethacin may be effective in the treatment of orthostatic hypotension, the ability of this drug to increase reflex vasoconstriction was studied in six patients with orthostatic hypotension...
Kurita, M, Matsumoto, M, Tsuji, S, Kawakami, M, Suzuki, Y, Hayashi, H, ...
Of human malignantly transformed cell lines, xeroderma pigmentosum (XP) cell lines were found to be highly susceptible to homologous complement (C): cells were opsonized by C3 fragments on incubation...
Phenytoin promotes Th2 type immune response in mice
Okada, K, Sugiura, T, Kuroda, E, Tsuji, S, Yamashita, U
The effects of chronic administration of phenytoin, a common anticonvulsive drug, on immune responses were studied in mice. Anti-keyhole limpet haemocyanin (KLH) IgE antibody response after...
Yamamoto, A, Taniuchi, S, Tsuji, S, Hasui, M, Kobayashi, Y
Neutrophils, short-lived leucocytes that die by apoptosis, play an important role in the first stage of defense against bacterial infections. It has been reported that phagocytosis of intact bacteria...
Ikeuchi, T., Igarashi, S., Takiyama, Y., Onodera, O., Oyake, M., Takano, H., ...
Autosomal dominant dentatorubral-pallidoluysian atrophy (DRPLA) and Machado-Joseph disease (MJD) are neurodegenerative disorders caused by CAG trinucleotide repeat expansions. An inverse correlation...
Takano, H., Onodera, O., Takahashi, H., Igarashi, S., Yamada, M., Oyake, M., ...
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disease caused by unstable expansion of a CAG repeat in the DRPLA gene. We performed detailed quantitative...
Cortical deafness in multiple sclerosis
Tabira, T, Tsuji, S, Nagashima, T, Nakajima, T, Kuroiwa, Y
Cortical deafness in a patient with multiple sclerosis is reported. Complete recovery from total deafness was seen following stages of auditory agnosia and pure word deafness. The otological and...
Long term course of change in anti-Yo antibody content in paraneoplastic cerebellar degeneration.
Tanaka, K, Tanaka, M, Igarashi, S, Onodera, O, Nakajima, T, Yamazaki, M, ...
Otsuki, M., Soma, Y., Arai, T., Otsuka, A., Tsuji, S.
A 67 year old Japanese male patient had pure agraphia after a haemorrhage in the left superior parietal lobule. He developed difficulty in letter formation but showed no linguistic errors, consistent...
Focal (segmental) dyshidrosis in syringomyelia
Sudo, K., Fujiki, N., Tsuji, S., Ajiki, M., Higashi, T., Niino, M., ...
The features or mechanisms of dyshidrosis have not been sufficiently clarified. Neither has the difference between hyperhidrosis and hypohidrosis. To clarify the features and mechanisms of...
Wakamatsu, N., Hayashi, M., Kawai, H., Kondo, H., Gotoda, Y., Nishida, Y., ...
OBJECTIVES—Mutational analysis of the sterol 27-hydroxylase (CYP27) gene was performed on three patients from two Japanese families who had cerebrotendinous xanthomatosis (CTX) associated with...
Nocturnal decrease in vasopressin secretion into plasma in patients with multiple system atrophy
Ozawa, T., Tanaka, H., Nakano, R., Sato, M., Inuzuka, T., Soma, Y., ...
To determine whether the nocturnal decrease in arginine vasopressin (AVP) secretion into the plasma, found in a patient with multiple system atrophy (MSA) reported previously, is a usual finding in...