Gautam, D. K., Nakano, Y., Tada, K.
Experimental results of a new method for the double diffusion into GaAs in an open tube have been presented. New techniques developed for the low concentration Zn diffusion at relatively higher...
Measurement of Neutrino Oscillation with KamLAND: Evidence of Spectral Distortion (2005)
Araki, T., Eguchi, K., Enomoto, S., Furuno, K., Ichimura, K., Ikeda, H., ...
We present results of a study of neutrino oscillation based on a 766 ton/year exposure of KamLAND to reactor antineutrinos. We observe 258 [overline nu ]e candidate events with energies above 3.4 MeV...
Measurement of Neutrino Oscillation with KamLAND: Evidence of Spectral Distortion (2005)
Araki, T., Eguchi, K., Enomoto, S., Furuno, K., Ichimura, K., Ikeda, H., ...
We present results of a study of neutrino oscillation based on a 766 ton/year exposure of KamLAND to reactor antineutrinos. We observe 258 [overline nu ]e candidate events with energies above 3.4 MeV...
Measurement of neutrino oscillation with Kamland: Evidence of spectral distortion (2004)
Araki, T., Eguchi, K., Enomoto, S., Furuno, K., Ichimura, K., Ikeda, H., ...
Online monitoring system and data management for KamLAND (2004)
Motoki, M., Suekane, F., Tada, K., Tsuda, Y.
In January 22, 2002, KamLAND started the data-taking. The KamLAND detector is a complicated system which consists of liquid scintillator, buffer oil, spherical balloon and so on. In order to maintain...
Long-term reduction of serum bilrubin levels in gunn rats by retroviral gene transfer in vivo (1998)
Tada, K., Chowdhury, N.R., Neufeld, D., Bosma, P.J., Heard, M., Prasad, V.R., ...
Analysis, fabrication, and characterization of tunable DFB lasers with chirped gratings. (1997)
CHEN, N, NAKANO, Y, OKAMOTO, K, TADA, K, Morthier, Geert, Baets, Roel
Enhanced tunability in chirped grating DFB lasers (1994)
CHEN, N, NAKANO, Y, TADA, K, OKAMOTO, K, MORTHIER, G, Baets, Roel
Aikawa, J, Chen, W W, Kelley, R I, Tada, K, Moser, H W, Chen, G L
By both histological and biochemical criteria, peroxisomes in patients with Zellweger syndrome appear to be absent or severely deficient. By using 15-30% (wt/vol) Nycodenz/sucrose gradients to study...
DNA gyrase mutations in quinolone-resistant clinical isolates of Neisseria gonorrhoeae.
Deguchi, T, Yasuda, M, Asano, M, Tada, K, Iwata, H, Komeda, H, ...
Eight quinolone-resistant clinical isolates of Neisseria gonorrhoeae were shown to carry mutations in their GyrA proteins. Six isolates had a single amino acid change of serine to phenylalanine at...
Moffatt, S, Tanaka, N, Tada, K, Nose, M, Nakamura, M, Muraoka, O, ...
We examined the biological function of a nonstructural regulatory protein, NS1, of human parvovirus B19. Because of the cytotoxic activity of NS1, human hematopoietic cell lines, K562, Raji, and...
Deguchi, T, Yasuda, M, Uno, M, Tada, K, Iwata, H, Komeda, H, ...
We evaluated the performances of a ligase chain reaction (LCR)-based assay and two enzyme immunoassays (Chlamydiazyme and IDEIA) in the detection of Chlamydia trachomatis in urine specimens. We...
Kondo, Y, Abe, K, Igarashi, Y, Kudo, K, Tada, K, Yoshinaga, K
The mechanisms of Na+ transport across cell membranes were investigated in the in vitro microperfused hamster ascending thin limb (ATL) of Henle's loop using a fluorescent Na+ indicator...
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.
Kure, S, Takayanagi, M, Narisawa, K, Tada, K, Leisti, J
Nonketotic hyperglycinemia (NKH) is an autosomal recessive metabolic disorder caused by the defects in the glycine cleavage system (GCS; EC 2.1.2.10), a multienzyme system that consists of four...
Seppen, J, Tada, K, Hellwig, S, Bakker, C T, Prasad, V R, Roy Chowdhury, N, ...
Crigler-Najjar (CN) disease is an inherited disorder of bilirubin metabolism. The disease is caused by a deficiency of the hepatic enzyme bilirubin UDP-glucuronosyltransferase (B-UGT). Patients with...
The spatial spread of the extracellular antidromic action potentials was measured in eighty-three neurones in the ventromedial nucleus region of the female rat hypothalamus following electrical...
Aikawa, J, Chen, W W, Kelley, R I, Tada, K, Moser, H W, Chen, G L
By both histological and biochemical criteria, peroxisomes in patients with Zellweger syndrome appear to be absent or severely deficient. By using 15-30% (wt/vol) Nycodenz/sucrose gradients to study...
DNA gyrase mutations in quinolone-resistant clinical isolates of Neisseria gonorrhoeae.
Deguchi, T, Yasuda, M, Asano, M, Tada, K, Iwata, H, Komeda, H, ...
Eight quinolone-resistant clinical isolates of Neisseria gonorrhoeae were shown to carry mutations in their GyrA proteins. Six isolates had a single amino acid change of serine to phenylalanine at...
Moffatt, S, Tanaka, N, Tada, K, Nose, M, Nakamura, M, Muraoka, O, ...
We examined the biological function of a nonstructural regulatory protein, NS1, of human parvovirus B19. Because of the cytotoxic activity of NS1, human hematopoietic cell lines, K562, Raji, and...
Deguchi, T, Yasuda, M, Uno, M, Tada, K, Iwata, H, Komeda, H, ...
We evaluated the performances of a ligase chain reaction (LCR)-based assay and two enzyme immunoassays (Chlamydiazyme and IDEIA) in the detection of Chlamydia trachomatis in urine specimens. We...
Kondo, Y, Abe, K, Igarashi, Y, Kudo, K, Tada, K, Yoshinaga, K
The mechanisms of Na+ transport across cell membranes were investigated in the in vitro microperfused hamster ascending thin limb (ATL) of Henle's loop using a fluorescent Na+ indicator...
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.
Kure, S, Takayanagi, M, Narisawa, K, Tada, K, Leisti, J
Nonketotic hyperglycinemia (NKH) is an autosomal recessive metabolic disorder caused by the defects in the glycine cleavage system (GCS; EC 2.1.2.10), a multienzyme system that consists of four...
The spatial spread of the extracellular antidromic action potentials was measured in eighty-three neurones in the ventromedial nucleus region of the female rat hypothalamus following electrical...
Seppen, J, Tada, K, Hellwig, S, Bakker, C T, Prasad, V R, Roy Chowdhury, N, ...
Crigler-Najjar (CN) disease is an inherited disorder of bilirubin metabolism. The disease is caused by a deficiency of the hepatic enzyme bilirubin UDP-glucuronosyltransferase (B-UGT). Patients with...
Endo, H, Hasegawa, K, Narisawa, K, Tada, K, Kagawa, Y, Ohta, S
A patient with lactic acidosis showed a lowered pyruvate dehydrogenase E1 activity and fatigued on slight exercise. The cDNA encoding the pyruvate dehydrogenase E1 alpha-subunit from his lymphocytes,...
Gyrate atrophy with hyperornithinaemia: different types of responsiveness to vitamin B6.
Hayasaka, S, Saito, T, Nakajima, H, Takaku, Y, Shiono, T, Mizuno, K, ...
Three cases of Japanese patients with gyrate atrophy of the choroid and retina with hyperornithinaemia were studied clinically and biochemically. The types of disease differed in responsiveness to...
Hayasaka, S., Saito, T., Nakajima, H., Takahashi, O., Mizuno, K., Tada, K.
Five patients with gyrate atrophy of the choroid and retina were examined ophthalmologically, especially ophthalmoscopically, to evaluate trials of vitamin B6 (pyridoxine) or supplementary proline....
Gotoh, Y I, Minegishi, M, Yamaguchi, Y, Konno, T, Tada, K
The possibility that the peanut agglutinin (PNA) receptor and/or its co-ordinate structures on the surface of leukaemia cells might be recognized by lectin free crude interleukin-2 (IL-2) activated...
Gotoh, Y I, Yamaguchi, Y, Minegishi, M, Konno, T, Tada, K
Two severe combined-immunodeficiency patients successfully transplanted with fetal thymus and liver or haploidentical lectin-treated marrow cells lacked NK activity, with a normal number of HNK1+...
Assessment of the capacity of cerebral collateral circulation using ultrasonic Doppler technique.
Tada, K, Nukada, T, Yoneda, S, Kuriyama, Y, Abe, H
A new non-invasive method for the assessment of cerebral collateral circulation via the circle of Willis using an ultrasonic directional Doppler flowmeter is described. The technique was found useful...
Ring chromosome 10 and its clinical features.
Nakai, H, Adachi, M, Katsushima, N, Yamazaki, N, Sakamoto, M, Tada, K
A 2-year-old boy with mental and growth retardation is presented; he has a 46,XY,r(10)(p15q26) chromosome complement. Five previously reported cases of ring chromosome 10 were reviewed and compared...
Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.
Corbeel, L, Tada, K, Colombo, J P, Eeckels, R, Eggermont, E, Jaeken, J, ...
The clinical and metabolic data of 2 cases of methylmalonic acidaemia with propionic acidaemia are reported together with those of 3 other patients with nonketotic hyperglycinaemia. Liver enzymatic...
Biliary lipid compositions in cholestatic diseases of infancy.
Tazawa, Y, Yamada, M, Nakagawa, M, Konno, T, Tada, K
Biliary lipid compositions in infants with cholestasis were analysed. Bile acid and phospholipid values were appreciably lower in infants with idiopathic neonatal hepatitis syndrome or corrected...
Parameter extraction from subthreshold spectra in cleaved gain- and index-coupled DFB LDs.
Morthier, Geert, SATO, K, Baets, Roel, SUDOH, TK, NAKANO, Y, TADA, K