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789 results on '"Sasaki, D."'

206. Idiopathic Megacolon with Neurological Abnormal findings. A Case Report.

Author

Konuma, Y., primary, Saito, H., additional, Uno, R., additional, Sakamoto, J., additional, Higashino, H., additional, Nakajima, H., additional, Munakata, A., additional, Yoshida, Y., additional, Tanaka, M., additional, Tsutsui, M., additional, Kon, M., additional, Morita, T., additional, and Sasaki, D., additional

Published
1994
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212. Changes in intraluminal pressure in rat large intestines with aging and effects of dietary fiber.

Author

Murakami, Hideki, Iwane, Satoru, Munakata, Akihiro, Nakaji, Shigeyuki, Sugawara, Kazuo, Tsuchida, Shigeki, Sasaki, Daisuke, Murakami, H, Iwane, S, Munakata, A, Nakaji, S, Sugawara, K, Tsuchida, S, and Sasaki, D

Subjects
LARGE intestine physiology, AGE distribution, ANIMAL experimentation, DIETARY fiber, GASTROINTESTINAL motility, PRESSURE, RATS, TIME
Abstract

Changes in intraluminal pressure in rat colon with aging and with the effects of dietary fiber were measured. A pressure sensor was inserted into the rat large intestine under endoscopic guidance. The intraluminal pressure curve in the colon was recorded, and the motility index was calculated by this curve. The rats were divided into three groups with a fiber-free diet, a cellulose diet (10% w/w), or a pectin diet (10% w/w). Intraluminal pressure was measured in the proximal, middle, and distal colon at 2, 4, 8, 12, and 16 months after birth. Intraluminal pressure in three sites increased with age and decreased in the latter half of the study. The motility index was lower during the course in the fiber groups, especially the pectin group more than the nonfiber group. This result suggests that long-term ingestion of dietary fiber might have a prophylactic effect on the development of diverticula. [ABSTRACT FROM AUTHOR]

Published
2001
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214. Quantum Magnetic Vortices at Finite Temperature in (3+1)-D.

Author

Marino, E. C. and Sasaki, D. G. G.

Subjects
*QUANTUM theory, *ABELIAN functions, *PHYSICS
Abstract

We study the effect of a finite temperature on the correlation function of quantum magnetic vortex lines in the framework of the (3 + 1)-dimensional Abelian Higgs model. The vortex energy is inferred from the large distance behavior of these correlation functions. For large straight vortices of length L, we obtain that the energy is proportional to TL² differently from the zero temperature result which is proportional to L. The case of closed strings is also analyzed. For T = 0, we evaluate the correlation function and energy of a large ring. Finite closed vortices do not exist as genuine excitations for any temperature. [ABSTRACT FROM AUTHOR]

Published
2000
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216. Functionalization and Applications of Telechelic Oligopropylenes:  Preparation of α,ω-Dihydroxy- and Diaminooligopropylenes

Author

Hagiwara, T., Saitoh, H., Tobe, A., Sasaki, D., Yano, S., and Sawaguchi, T.

Abstract

Difunctional propylene oligomers which may be used for preparing novel block copolymers were synthesized from telechelic oligomers containing two terminal vinylidene double bonds (PP-TVDs). The PP-TVDs were converted to α,ω-dihydroxyoligopropylenes (PP-OHs) in good yield by hydroboration with BH3·THF or 9-BBN, followed by oxidation. Multiple NMR signals from the α-methylene protons and the β-methyl carbons were ascribed to epimers formed during the hydroboration. α,ω-Diaminooligopropylene (PP-NH2) was prepared from PP-OH via tosylate and azide. Copolymerizations of PP-NH2 with terephthalic acid were carried out, and copolymers with molecular weights larger than that of the parent polymer were obtained.

Published
2005

217. Optical and Scanning Probe Analysis of Glycolipid Reorganization upon Concanavalin A Binding to Mannose-Coated Lipid Bilayers

Author

Bondurant, B., Last, J. A., Waggoner, T. A., Slade, A., and Sasaki, D. Y.

Abstract

Molecular level associations between components within the lipid bilayer as proteins complex to the membrane surface are fundamental to the complete understanding of protein−membrane interactions. To characterize these protein-induced membrane-organizational processes, we have prepared a new fluorescently labeled glycolipid (PSMU) that enables monitoring of glycolipid aggregation within the lipid membrane. The glycolipid's mannosamine headgroup was specifically recognized by the lectin concanavalin A (Con A). Fluorescence studies with liposomes composed of 5 mol % PSMU/distearylphosphatidylcholine found that the membrane reorganized in response to Con A adsorption. Initially aggregated structures of glycolipid were dispersed as a consequence of specific affinity with the lectin through steric restrictions imposed by other bound Con A, the distance between mannosyl receptor sites, and possible protein insertion events. The protein binding and membrane reorganizational process was slow (ca. days). An association constant for Con A with the glycolipid membrane was estimated to be 3 × 106 M-1, around 2 orders of magnitude higher than that for methyl-d-α-mannopyranoside. Nanoscale imaging with the atomic force microscope found that the glycolipid formed 10 nm wide dendrite structures throughout the membrane and that the bound Con A was associated with those nanoscale features.

Published
2003

218. Crown Ether Functionalized Lipid Membranes:  Lead Ion Recognition and Molecular Reorganization

Author

Sasaki, D. Y., Waggoner, T. A., Last, J. A., and Alam, T. M.

Abstract

A fluorescent lipid bilayer, functionalized with 18-crown-6, was developed to examine the mechanism of chemical recognition-induced molecular reorganization events in a membrane system. The synthetic receptor-lipid, PS18C6, was prepared with the crown ether at the headgroup position and a pyrene fluorescent tag on the hydrophobic tail. When incorporated into bilayers of distearylphosphatidylcholine, the receptor-lipid aggregated into domains, evidenced by the relatively large pyrene excimer emission from the bilayer. Langmuir pressure−area (π−A) isotherm measurements and atomic force microscopy (AFM) further aided in characterizing the receptor aggregation at the macro- and nanoscale, respectively. The functionalized bilayer exhibited selective affinity for mercuric and lead ions in aqueous buffered solution (pH 7.4), with a fluorescence response that was linear over the concentration range 10-7 to 10-4 M metal ions. 1H NMR studies established that the binding stoichiometry of PS18C6 with lead was 1:1, with Ka = 105 M-1 in methanol. Recognition and binding of lead ions at the membrane surface resulted in a rapid and prominent reorganization of the receptor-lipids in the membrane that was measurable at both the macro- and nanoscales. Removal of the lead ions, through the addition of EDTA, resulted in recovery of the original fluorescence and the reaggregation of structures in the membrane.

Published
2002
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220. Lateral-flow assay for rapid serodiagnosis of human leptospirosis.

Author

Smits, H L, Eapen, C K, Sugathan, S, Kuriakose, M, Gasem, M H, Yersin, C, Sasaki, D, Pujianto, B, Vestering, M, Abdoel, T H, and Gussenhoven, G C

Abstract

An assay device for the rapid detection of Leptospira-specific immunoglobulin M (IgM) antibodies in human sera is presented. The sensitivity (85.8%) and specificity (93.6%) of the assay compared well (91.9% agreement) with those of an IgM enzyme-linked immunosorbent assay routinely used in the serodiagnosis of leptospirosis. The sensitivity of the assay varied with the stage of the disease. The assay uses stabilized components and is simply performed by the addition of serum and sample fluid to the sample well of the assay device. The assay is read after 10 min, and a positive result is obtained when staining of the test line is observed.

Published
2001
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221. Solid-State <SUP>31</SUP>P NMR Study of Phosphonate Binding Sites in Guanidine-Functionalized, Molecular Imprinted Silica Xerogels

Author

Sasaki, D. Y. and Alam, T. M.

Abstract

Phosphonate binding sites in guanidine and ammonium surface-functionalized silica xerogels were prepared via the molecular imprinting technique and characterized using solid-state 31P MAS NMR. One-point, two-point, and nonspecific host−guest interactions between phenylphosphonic acid (PPA) and the functionalized gels were distinguished by characteristic chemical shifts of the observed absorption peaks. Using solid-state as well as solution-phase NMR analyses, absorptions observed at 15.5 and 6.5 ppm were identified as resulting from the 1:1 (one-point) and 2:1 (two-point) guanidine to phosphonate interactions, respectively. Similar absorptions were observed with the ammonium functionalized gels. By examining the host−guest interactions within the gels, the efficiency of the molecular imprinting procedure with regard to the functional monomer-to-template interaction could be readily assessed. Template removal followed by substrate adsorption studies conducted on the guanidine-functionalized gels provided a method to evaluate the binding characteristics of the receptor sites to a phosphonate substrate. During these experiments, 29Si and 31P MAS NMR acted as diagnostic monitors to identify structural changes occurring in the gel matrix and at the receptor site from solvent-mediated processes.

Published
2000

224. Production of functional human T-T hybridomas in selection medium lacking aminopterin and thymidine.

Author

Foung, S K, Sasaki, D T, Grumet, F C, and Engleman, E G

Abstract

The production of hybridomas between immunologically activated T cells and malignant T-cell lines offers a potentially unlimited source of soluble T-cell-derived products. Recently, human T-T hybrids have been described; however, their use has been hampered by slow growth and chromosomal instability due at least in part to the presence of thymidine in the traditional hypoxanthine/aminopterin/thymidine (HAT) selection medium. In this report, we describe the development of a rapidly growing hypoxanthine phosphoribosyltransferase-deficient human T-cell line designated J3R7, the use of azaserine/hypoxanthine (AH) medium as an alternative selection medium to HAT medium, and the production of functional T-T hybrids by using the J3R7 line and the AH selection technique. Hybrids selected in AH medium were 4-fold greater in number and 3-fold faster in growth rate than hybrids grown in HAT medium. No stable clones were obtained from HAT cultures whereas AH-derived hybrids could be readily cloned by the method of limiting dilution. Evidence for hybridization included (i) the presence of approximately twice the number of chromosomes in hybrids than in J3R7 cells; (ii) the presence on hybrid cells of the Leu-3a surface antigen, present on normal helper T cells but not on J3R7 cells; (iii) the expression of HLA antigens of both the normal T-cell partner and the J3R7 line; and (iv) the constitutive secretion of interleukin 2 from multiple hybrid clones but not from the J3R7 cell line. Thus far, these clones have maintained their rapid growth, chromosome number, surface phenotype, and constitutive secretion of interleukin 2 for 4 months.

Published
1982
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225. Leptospirosis on Oahu: an outbreak among military personnel associated with recreational exposure.

Author

Katz, A R, Sasaki, D M, Mumm, A H, Escamilla, J, Middleton, C R, and Romero, S E

Abstract

In December 1992, a common-source waterborne outbreak of leptospirosis occurred on the island of Oahu in the state of Hawaii. Two male service persons were hospitalized with culture-confirmed leptospirosis. Eighteen others had similar histories of exposure to the same freshwater swimming site. Although six men developed signs and symptoms comparable to those of the two confirmed cases, none manifested culture or serologic evidence of leptospirosis. The increased incidence of leptospirosis in Hawaii coupled with an increased risk in young males characterize the military population in Hawaii as a high-risk population with respect to leptospirosis.

Published
1997

226. Solid Phase Immobilization of Optically Responsive Liposomes in Sol-Gel Materials for Chemical and Biological Sensing

Author

Yamanaka, S. A., Charych, D. H., Loy, D. A., and Sasaki, D. Y.

Abstract

Liposomes enhanced with surface recognition groups have previously been found to have high affinity for heavy metal ions and virus particles with unique fluorescent and colorimetric responses, respectively. These lipid aggregate systems have now been successfully immobilized in a silica matrix via the sol-gel method, affording sensor materials that are robust, are easily handled, and offer optical clarity. The mild processing conditions allow quantitative entrapment of preformed liposomes without modification of the aggregate structure. Lipid extraction studies of immobilized nonpolymerized liposomes showed no lipid leakage in aqueous solution over a period of 3 months. Heavy metal fluorescent sensor materials prepared with 5% N-[8-[1-octadecyl-2-(9-(1-pyrenyl)nonyl)-rac-glyceroyl]-3,6-dioxaoctyl]iminodiacetic acid/distearylphosphatidylcholine liposomes exhibited a 4−50-fold enhancement in sensitivity to various metal ions compared to that of the liposomes in free solution. Through ionic attraction the anionic silicate surface, at the experimental pH of 7.4, may act as a preconcentrator of divalent metal ions, boosting the gel's internal metal concentration. Entrapped sialic acid-coated polydiacetylene liposomes responded with colorimetric signaling to influenza virus X31, although slower than the free liposomes in solution. The successful transport of the virus (50−100 nm diameter) reveals a large pore diameter of the gel connecting the liposome to the bulk solution. The porous and durable silica matrix additionally provides a protective barrier to biological attack (bacterial, fungal) and allows facile recycling of the liposome heavy metal sensor.

Published
1997

227. Intracellular processing of procollagen induced by the action of colchicine

Author

Fernandez-Madrid, F, Noonan, S, Riddle, J, Karvonen, R, and Sasaki, D

Subjects
Microscopy, Electron, integumentary system, Depression, Chemical, Vacuoles, Animals, Electrophoresis, Polyacrylamide Gel, Chick Embryo, Fibroblasts, In Vitro Techniques, Colchicine, Secretory Rate, Procollagen, Research Article
Abstract

Corium fragments incubated in vitro with colchicine or obtained from chick embryos 11 days old after in vivo injection of this alkaloid were studied with the electron microscope. The well known effect of colchicine in producing an accumulation of procollagen was demonstrated by electrophoretic separation of the collagenous products in polyacrylamide gels after incubation of corium fragments in vitro with labelled amino acids. Electron microscopical studies showed various types of cytoplasmic vacuoles containing collagenous fibrillar structures. Some of these vacuoles contained non-striated filaments, fibres with the periodicity of native collagen, and segment long spacing (SLS) crystallites, embedded in an electrondense substance. The central aspect of this communication is the finding of intracellular SLS in cytoplasmic vacuoles. These crystallites were morphologically intact, and had no additional bands at the NH2 or COOH ends, suggesting that they were formed by the aggregation of tropocollagen molecules. Since the presence of intact SLS in cytoplasmic vacuoles suggests that these are secretory, we believe that inhibition of the transcellular transport system by colchicine permitted the visualization of vacuoles containing the products of tropocollagen interconversions. We interpret these findings as an example of autophagocytosis, with intracellular processing of procollagen, occurring in chick embryo fibroblasts when the secretion of procollagen is inhibited by colchicine.

Published
1980

231. Structural, physiognomic and aboveground biomass variation in savanna-forest transition zones on three continents. How different are co-occuring savanna and forest formations?

Author

Veenendaal, E.M., Torello-Raventos, M., Feldpausch, T.R., Domingues, T.F., Gerard, F., Schrodt, F., Saiz, G., Quesada, C.A., Djagbletey, G., Ford, A., Kemp, J., Marimon, B.S., Marimon-Junior, B.H., Lenza, E., Ratter, J.A., Maracahipes, L., Sasaki, D., Sonke, B., Zapfack, L., Villaroel, D., Schwarz, M., Ishida, F.Y., Gilpin, M., Nardoto, G.B., Affum-Baffoe, K., Arroyo, L., Bloomfield, K., Ceca, G., Compaore, H., Davies, K., Diallo, A., Fyllas, N.M., Gignoux, J., Hien, F., Johnson, M., Mugin, E., Hiernaux, P., Killeen, T., Metcalfe, D., Miranda, H.S., Steininger, M., Sykora, K., Bird, M.I., Grace, J., Lewis, S., Phillips, O.L., and Lloyd, J.

Subjects
13. Climate action, 15. Life on land

232. Cytokine-mobilized peripheral blood CD34+Thy-1+Lin- human hematopoietic stem cells as target cells for transplantation-based gene therapy

Author

Bp, Chen, Fraser C, Reading C, Murray L, Uchida N, Anne GALY, Sasaki D, Tricot G, Jagannath S, and Barlogie B

Subjects
Adult, Transplantation, Heterologous, Hematopoietic Stem Cell Transplantation, Antigens, CD34, Bone Marrow Cells, Genetic Therapy, Mice, SCID, Thymus Gland, HLA-A3 Antigen, Flow Cytometry, Hematopoietic Stem Cells, Polymerase Chain Reaction, Transplantation, Autologous, Colony-Forming Units Assay, Mice, Fetus, Antigens, CD, Bone Marrow, Neoplasms, Animals, Cytokines, Humans, Thy-1 Antigens, Biomarkers
Abstract

Gene-therapy of blood-borne disorders may be best achieved using hematopoietic stem cells (HSC) which have extensive self renewal potential as well as multilineage repopulating potential as a cellular target. The human HSC, which is CD34+Thy-1+Lin- has been isolated from fetal, adult bone marrow and cytokine-mobilized peripheral blood (MPB) (1-3). Results presented in this study show that the degree of mobilization of HSC into peripheral blood of cancer patients is highly variable and that the combined use of high dose chemotherapy and GM-CSF as a mobilization strategy is superior to the use of G-CSF with regard to the mobilization of true HSC. A multistep cell isolation procedure has been developed which utilizes high speed flow-cytometric cell sorting and allows the isolation of sufficient numbers of HSC from MPB to permit their use as an hematopoietic graft for clinical transplantation. Hematopoietic stem cells isolated from MPB are capable of self-renewal and differentiation into multiple hematopoietic lineages as shown by their behavior in both in vitro and in vivo assays. Mobilized PB mononuclear cells isolated from cancer patients are frequently contaminated with tumor cells. Using this cell isolation procedure, HSC preparations from patients with multiple myeloma have been created with greatly reduced tumor cell burdens. These CD34+Thy-1+Lin- cells are capable of being stably transduced at high efficiency (32-75%) by co-culture on a cell line producing recombinant retroviruses containing the neomycin-resistant gene. These HSC cell populations are likely ideal targets for hematopoietic cell-based gene therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

234. Report on geological, geomorphological and meteorite fieldwork in the Sør Rondane Mountains, Eastern Dronning Maud Land, 2009-2010 (JARE-51)

Author

Tsuchiya, N., MASAHIRO ISHIKAWA, Satish-Kumar, M., Kawakami, T., Kojima, H., Kaiden, H., Miura, H., Suganuma, Y., Abe, M., Sasaki, D., Chiba, M., Okada, Y., Hashizume, F., Grantham, G., Goderis, S., Analytical, Environmental & Geo-Chemistry, and Earth System Sciences

Subjects
Earth and Planetary Sciences(all), lcsh:G1-922, Aquatic Science, lcsh:Geography (General)
Abstract

Earth science-related field activities, involving geology, geomorphology and meteorite searches, were carried out in the Sor Rondane Mountains, Eastern Dronning Maud Land, during the 2009-2010 summer season as a part of the 51st Japanese Antarctic Research Expedition (JARE-51), in collaboration with the Belgian Antarctic Research Expedition (BELARE). Geology and geomorphology parties accessed the Sør Rondane Mountains using the Dronning Maud Land Air Network (DROMLAN), and the meteorite search party to Antarctica on the maiden voyage by the new Japanese icebreaker Shirase. The geology party covered the entire area of the Sør Rondane Mountains, although with an emphasis on the eastern part. The geomorphology party carried out fieldwork in western and central parts of the mountains, and the meteorite search party performed a survey in the eastern part. All field activities were successfully carried out. Some of the geology members returned to Japan by DROMLAN, while others flew to Syowa Station from the Sør Rondane Mountains by DROMLAN, and then returned to Japan on board Shirase. This report provides a summary of the field operations, including logistics and weather records.

243. General lectures (II)

Author

Karasawa, Y., primary, Ōnuma, H., additional, Suzuki, H., additional, Okazaki, T., additional, Yasui, A., additional, Murakami, T., additional, Furuya, K., additional, Ohtsuki, M., additional, Sata, H., additional, Kondo, T., additional, Takada, H., additional, Kawaguchi, K., additional, Sai, S., additional, Takeda, S., additional, Kitagawa, M., additional, Morooka, T., additional, Shiraishi, T., additional, Namiki, M., additional, Kawauchi, H., additional, Nakagawa, K., additional, Kuramata, H., additional, Yamaguchi, Y., additional, Kabakino, T., additional, Inokuchi, T., additional, Wakisaka, J., additional, Yamauchi, Y., additional, Debuchi, T., additional, Ogo, W., additional, Yamasaki, C., additional, Sigemori, M., additional, Hashimoto, K., additional, Shirozu, T., additional, Kaibara, N., additional, Inokuchi, K., additional, Soejima, K., additional, Hiyama, T., additional, Wakita, M., additional, Ikemoto, T., additional, Hayasaka, H., additional, Fukui, S., additional, Takeda, T., additional, Aoyama, N., additional, Takada, Y., additional, Saheki, Y., additional, Yoshida, Y., additional, Minagawa, K., additional, Okuyama, T., additional, Yamamitsu, S., additional, Konishi, Y., additional, Ishimatsu, N., additional, Murai, S., additional, Nukaga, A., additional, Toyama, S., additional, Watanabe, Y., additional, Mizushima, N., additional, Abe, M., additional, Maruyama, K., additional, Yoshino, K., additional, Suzuki, T., additional, Akisato, K., additional, Kitajima, M., additional, Tabata, T., additional, Hashimoto, M., additional, Tanaka, T., additional, Nakagawa, Y., additional, Ishii, Y., additional, Inoue, M., additional, Katayama, S., additional, Nakano, Y., additional, Fukuda, M., additional, Takaki, M., additional, Hyodo, H., additional, Kobayashi, J., additional, Nishikawa, H., additional, Morimoto, K., additional, Takagi, T., additional, Sako, S., additional, Tomoda, H., additional, Furusawa, M., additional, Sassa, R., additional, Unuma, T., additional, Iwase, T., additional, Yoshioka, T., additional, Kusakabe, M., additional, Iio, M., additional, Kobayashi, S., additional, Kizu, M., additional, Kasugai, T., additional, Yoshida, K., additional, Kembo, T., additional, Yoshida, T., additional, Suga, Y., additional, Suguro, T., additional, Kono, Y., additional, Mitsui, S., additional, Nagamachi, Y., additional, Nakamura, T., additional, Suto, H., additional, Higuchi, T., additional, Onai, M., additional, Isizuka, K., additional, Takei, A., additional, Simoda, M., additional, Sekiguchi, T., additional, Shichijo, K., additional, Akashi, Y., additional, Mori, K., additional, Ogasawara, K., additional, Tanaka, R., additional, Yoshikawa, K., additional, Takahashi, T., additional, Ogata, T., additional, Tanaka, S., additional, Seito, T., additional, Matsuda, H., additional, Imajo, T., additional, Moriyasu, K., additional, Takata, Y., additional, Kamei, H., additional, Murai, H., additional, Takemitsu, T., additional, Kanemitsu, T., additional, Ishii, M., additional, Imaizumi, M., additional, Inada, M., additional, Glass, G. B. J., additional, Ebata, K., additional, Yamanaka, N., additional, Watanabe, S., additional, Mori, H., additional, Tsukasa, S., additional, Sato, H., additional, Chuman, Y., additional, Nakahara, N., additional, Taniguchi, H., additional, Ehira, S., additional, Hori, M., additional, Irisa, T., additional, Yokoyama, H., additional, Kunieda, T., additional, Ogushi, Y., additional, Kawakami, K., additional, Kuroda, M., additional, Sasaki, D., additional, SŌma, S., additional, Yanagiya, S., additional, Munakata, A., additional, Matsunaga, F., additional, Abiko, M., additional, Ohuchi, H., additional, Tai, C., additional, Kawashima, T., additional, Oosawa, W., additional, Asakura, H., additional, Senba, H., additional, Hatayama, T., additional, Yukawa, K., additional, Konishi, T., additional, Miyata, M., additional, Shimazu, H., additional, Kinoshita, T., additional, Nukada, K., additional, Yamagishi, T., additional, Harada, K., additional, Nakano, S., additional, Sakai, T., additional, Shindo, K., additional, Fukushima, K., additional, Odagiri, S., additional, Tarao, K., additional, Saito, Y., additional, Ohara, K., additional, Sasaki, S., additional, Tomoda, T., additional, Kaneda, N., additional, Yamaguchi, H., additional, Hayashi, T., additional, Suzuki, J., additional, Kofune, Y., additional, Urase, A., additional, Yamagata, A., additional, Sugino, N., additional, Hatano, M., additional, Oshima, K., additional, Tanabe, T., additional, Ohto, M., additional, Okuda, K., additional, Mitani, E., additional, Yamamoto, S., additional, Kobayashi, K., additional, Ono, T., additional, Kamata, T., additional, Mohri, S., additional, Makiishi, H., additional, Kitano, A., additional, Tatumi, S., additional, Mizuno, S., additional, Tsumori, K., additional, Shimizu, T., additional, Nomatsu, K., additional, Hiratsuka, H., additional, Ichinose, M., additional, Morishita, T., additional, Morita, A., additional, Matsuzaki, S., additional, Oda, M., additional, Kamegaya, K., additional, Tuchiya, M., additional, Sambe, K., additional, Murakami, Y., additional, Machii, A., additional, Nitta, Y., additional, Aiso, Y., additional, Kitahara, N., additional, Sato, M., additional, Yoshizawa, Y., additional, Hishinuma, Y., additional, Nagasako, H., additional, Nao, Y., additional, Harada, H., additional, Mishima, K., additional, Yamagata, Y., additional, Mandai, M., additional, Kondo, Y., additional, Uchida, Y., additional, Takizawa, S., additional, Kinoshita, S., additional, Kurihara, T., additional, Sakumoto, K., additional, Okamoto, H., additional, Sakurai, S., additional, Ishitobi, S., additional, Tanaka, H., additional, Ishihara, K., additional, Kuno, N., additional, Aoki, I., additional, Horiguchi, Y., additional, Kitamura, K., additional, Miwa, M., additional, Okada, K., additional, Endo, Y., additional, Tatsuta, M., additional, Morii, T., additional, Okuda, S., additional, Tamura, H., additional, Fukuda, K., additional, Sato, K., additional, Koizumi, K., additional, Takebe, T., additional, Yamagata, S., additional, Noda, S., additional, Toda, Y., additional, Hayakawa, T., additional, Nakajima, S., additional, Hitokawa, S., additional, Sawabu, N., additional, Hirose, S., additional, Takada, A., additional, Takeuchi, J., additional, Kuniyasu, Y., additional, Kakehi, H., additional, Uchiyama, G., additional, Arimizu, N., additional, Kuroda, T., additional, Saishyo, H., additional, Takashima, T., additional, Shin, M., additional, Akashi, M., additional, Moriyama, T., additional, Uchimura, M., additional, Tsuchiya, R., additional, Kakizaki, G., additional, Noto, N., additional, Oizumi, T., additional, Soeno, T., additional, Maeta, T., additional, Saito, T., additional, Naito, S., additional, Shimizu, K., additional, Nakajima, T., additional, Tanaka, M., additional, Kin, T., additional, Sugiyama, S., additional, Takayama, H., additional, Tomono, T., additional, Kamijo, N., additional, Kimura, Y., additional, Matsuo, T., additional, Shimada, M., additional, Terashima, B., additional, Furuta, S., additional, Kashiwabara, K., additional, Oka, S., additional, Sugiura, M., additional, Karasawa, M., additional, Ito, K., additional, Takei, K., additional, Ishihara, Y., additional, Kuroda, A., additional, Sato, N., additional, Noro, T., additional, Ishikawa, H., additional, Tajima, Y., additional, Hashihira, S., additional, Nishii, T., additional, Mori, R., additional, Takeda, Y., additional, Yamadori, T., additional, Wakabayashi, A., additional, Iwata, S., additional, Shiraso, M., additional, Tokutake, K., additional, Matsuno, S., additional, Haga, N., additional, Suda, Y., additional, Sato, T., additional, Tsunoda, T., additional, Kanno, H., additional, Aneha, Y., additional, Kikuchi, K., additional, Imamura, K., additional, Kondo, O., additional, Yuki, Y., additional, Omata, S., additional, Okamoto, S., additional, Nagahara, H., additional, Motoyama, H., additional, Watanabe, H., additional, Maekawa, T., additional, Miyakawa, T., additional, Anazawa, Y., additional, Motoyama, T., additional, Kawamura, T., additional, Kusaka, Y., additional, Shima, F., additional, Abe, S., additional, Ichihara, S., additional, Nomura, M., additional, Ushiyama, T., additional, Futagawa, S., additional, Ishida, M., additional, Obata, G., additional, Sugiyama, Y., additional, Suzuki, K., additional, Abo, M., additional, Takeuchi, M., additional, Tann, E., additional, Kimura, K., additional, Iwaya, A., additional, Takahashi, H., additional, Ono, K., additional, Inoue, J., additional, Miyaishi, S., additional, Sasaki, T., additional, Kuroyanagi, Y., additional, Kato, H., additional, Kido, C., additional, Hibino, K., additional, Kishikawa, M., additional, Takeuchi, T., additional, Murate, H., additional, Tanabe, A., additional, Kozuka, M., additional, Ito, M., additional, Kato, N., additional, Yazaki, Y., additional, Goto, K., additional, Miyaji, M., additional, Yokoi, J., additional, Endo, I., additional, Kato, S., additional, Miyazaki, M., additional, Murayama, N., additional, Kawamura, A., additional, Murohisa, B., additional, Hirai, S., additional, Furukawa, M., additional, Nakashima, G., additional, Furuse, H., additional, Fukuda, T., additional, Hanyu, F., additional, Sakakibara, N., additional, Ide, H., additional, Momma, K., additional, Nagashima, H., additional, Matsushiro, T., additional, Suzuki, N., additional, Saitoh, T., additional, Nakamura, N., additional, Takahashi, W., additional, Hatanaka, T., additional, Kobayashi, N., additional, Hagano, M., additional, Furusawa, T., additional, Osuga, T., additional, Portman, O. W., additional, Takahashi, K., additional, Kibayashi, H., additional, Yamazaki, H., additional, Komaki, K., additional, Tanimura, H., additional, Hikasa, Y., additional, Ogawa, R., additional, Nakagawa, H., additional, Osada, M., additional, Koizumi, H., additional, Katayama, M., additional, Sakamoto, H., additional, Manome, T., additional, Sesoko, M., additional, Kobayashi, M., additional, Komine, Y., additional, Watanabe, N., additional, Okabe, Y., additional, Ogino, M., additional, Naruke, T., additional, Hoshika, T., additional, Miyano, T., additional, Tsuneoka, K., additional, Kitajima, S., additional, Nakada, I., additional, Sasamori, Y., additional, Munakata, H., additional, Tanaka, K., additional, Oguro, H., additional, Numata, T., additional, Oh-Uti, K., additional, Goto, S., additional, Takashina, K., additional, Sasaki, G., additional, Kimura, A., additional, Sasagawa, T., additional, Takahashi, G., additional, Sugiyama, H., additional, Iwaki, K., additional, Okada, S., additional, Iwasaki, M., additional, Kawashima, Y., additional, Kaneda, H., additional, Honda, T., additional, Ariga, K., additional, Sa, Woo pak, additional, Hozawa, H., additional, Susuki, T., additional, Kato, Y., additional, Mizuno, T., additional, Oya, H., additional, Yoshino, S., additional, and Hattori, T., additional

Published
1973
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248. A panel-sized TFT-LCD scan driver

Author

Sasaki, D., primary, Ishibashi, O., additional, Toba, T., additional, Noda, S., additional, Yanase, J., additional, Takaoka, H., additional, Sato, Y., additional, Kamon, Y., additional, Tsuchi, H., additional, Okumura, H., additional, Kanoh, H., additional, and Hayama, H., additional

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