巻号一覧
36 巻, 1 号
選択された号の論文の20件中1～20を表示しています
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Motohiko Murakami1987 年 36 巻 1 号 p. 2-3
発行日: 1987年
公開日: 2009/03/27
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冨田 恒男1987 年 36 巻 1 号 p. 4-18
発行日: 1987年
公開日: 2009/03/27
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Yonosuke Watanabe1987 年 36 巻 1 号 p. 22
発行日: 1987年
公開日: 2009/03/27
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J. Breton-Gorius1987 年 36 巻 1 号 p. 23-45
発行日: 1987年
公開日: 2009/03/27
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湊 啓輔, 下山 正徳1987 年 36 巻 1 号 p. 46-49
発行日: 1987年
公開日: 2009/03/27
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外山 圭輔, 川口 正人, Lung T.Yam1987 年 36 巻 1 号 p. 50-52
発行日: 1987年
公開日: 2009/03/27
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中沢 真平, 杉田 完爾1987 年 36 巻 1 号 p. 53-56
発行日: 1987年
公開日: 2009/03/27
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小出 亮, 高橋 弘剛, 恒松 由記子, 佐々木 道子, 杉田 完爾, 中沢 真平, 榎本 康弘, 渡辺 陽之輔, 金子 安比古1987 年 36 巻 1 号 p. 57-61
発行日: 1987年
公開日: 2009/03/27
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柴田 昭, 小池 正, 青木 定夫, 丸山 聡一, 石塚 利江, 大塚 武司1987 年 36 巻 1 号 p. 62-66
発行日: 1987年
公開日: 2009/03/27
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小栗 佳代子, 岡山 暎子, Bruce Caterson, 岡山 実1987 年 36 巻 1 号 p. 67-70
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーi) Rabbit femoral bone marrow was determined to contain GAGs equivalent to 220mg of hexuronate per femur and the molecular species of those were identified to be chondroitin 6-sulfate (79%) and hyaluronic acid (16%). ii) The chondroitin 6-sul-fates occurred in situ as three species of PGs with estimated molecular weights of 8, 300, 46, 000 and 16, 000, in ratio of approximately 2/5/3, and were localized only in extra-cellular matrix of the bone marrow. iii) These chondroitin 6-sulfate PGs were synthe-sized by the cells within the bone marrow and not brought out with peripheral blood cells or secreted as plasma components. iv) Together with these results, it is strongly suggested that the three species of PGs are synthesized by the stromal cells in the bone marrow and involved in construction of the extracellular matrix unique to bone marrow. These PGs present in the bone marrow were considered to play an important role in regulation of hemopoiesis as proposed by Dexter et al.3抄録全体を表示PDF形式でダウンロード (173K) -
渡辺 陽之輔, 榎本 康弘, 山田 健人, 張ヶ谷 健一1987 年 36 巻 1 号 p. 71-73
発行日: 1987年
公開日: 2009/03/27
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糸山 進次, 林 祥剛1987 年 36 巻 1 号 p. 74-80
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーThe pathogenesis of myeloproliferative disorder remains unknown, but there have been some experiments on murine myeloproliferative sarcoma induced by certain viruses. Myeloproliferative sarcoma virus which is well known among such viruses, causes myeloproliferative disorder in mice and today's work will reveal tumorigenicity of this virus in rats.
Two groups of Jar-2 rats (31 young rats and 28 newborn rats) were prepared and each rat was injected intravenously with one shot of myeloproliferative sarcoma virus (MPSV) with the helper Friend virus (F-MuLV). Only one rat of the young rat group developed erythroleukemia, whereas 14 rats of the newborn group developed myeloproliferative disorder in which trilineages of hematopoietic cells showed marked proliferation; 8 rats developed erythroleukemia and other 3 rats developed acute myelo-blastic leukemia. In addition, 15 rats of the newborn group with these hematological disorders also showed angiosarcoma of the central nervous system, mainly of the cere-bellum, and 2 of them had the same angiosarcoma in the spleen.
The myeloproliferative sarcoma virus might be useful as a new tool for studies of myeloproliferative disorders, not only in mice but also in rats.抄録全体を表示PDF形式でダウンロード (287K) -
長澤 俊郎, 中澤 正樹, 二宮 治彦, 阿部 師1987 年 36 巻 1 号 p. 81-82
発行日: 1987年
公開日: 2009/03/27
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溝口 秀昭, 片平 潤一, 赤星 雅子1987 年 36 巻 1 号 p. 83-85
発行日: 1987年
公開日: 2009/03/27
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三浦 恭定, 小松 則夫, 須田 年生, 坂田 洋一, 江口 光興, 斉藤 政樹1987 年 36 巻 1 号 p. 86-88
発行日: 1987年
公開日: 2009/03/27
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井上 健夫1987 年 36 巻 1 号 p. 89-98
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーThis experimental study was undertaken to explore the histological analysis of early thrombogenesis after aortic anastomosis. One hundred and fifty ab-dominal aortas of rats, measuring 1.2 to 1.5mm in diameter were transversely severed half way and vascular anastomosis was performed, using 10-0 monofila-ment nylon interrupted suture. After fixation with 2.5% buffered glutearaldehyde the specimens were analyzed at 3, 5, 7, 10, 15, 20 and 30 minutes after anas-tomosis under light-microscope. The following results were obtained. Thrombi formed in about half of the specimens 3 to 15 minutes after anastomosis. The thrombi reached maximum size at 7 minutes after anastomosis, then gradually decreased in size and completely disappeared at 30 minutes.抄録全体を表示PDF形式でダウンロード (4785K) -
大城 俊夫1987 年 36 巻 1 号 p. 99-111
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーThe argon, Nd: YAG and CO2 lasers have been mostly used in clinical medi-cine. Their histological changes are wavelength dependent and manifest their characteristics according to their irradiation time. Although their early skin changes appear clinically similar, there are no exact hard data to correlate their irradiation time. This study was designed to compare the irradiation time of these 3 lasers, using positive Evans blue exudation test (EBE) from the irradiated vas-cular walls as an indicator. The dorsum skin of the ddY mouse, 12 in total for each laser group, was irradiated at 3 watts of output with a spot size of 2.0mm in diameter. The EBE appeared at 0.4 seconds for the argon laser, 19 seconds for the Nd: YAG laser and 0.04 seconds for the CO2 laser, respectively. The significant difference for each laser system was demonstrated as follows: argon laser between 0.3 and 0.4 seconds (p<0.01), Nd: YAG laser between 18 and 19 seconds (p<0.01) and CO2 laser between 0.03 and 0.04 seconds (p<0.01). Histologically, all 3 lasers showed a similar homogeneous eosinophilic change of the upper dermal collagen fibers, despite the different exposure time. In con-clusion, the comparison of the irradiation time for each laser with argon stand-ardized at 1 was 47.5 for the Nd: YAG and 0.1 of the CO2. It is suggested that these correlation might be clinically useful in the medical application of these 3 lasers.抄録全体を表示PDF形式でダウンロード (17640K) -
Johannes Piiper1987 年 36 巻 1 号 p. 112-115
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーPulmonary diffusing capacity or diffusive gas/blood transfer conductance of the lungs, DL, defined as transfer rate divided by effective partial pressure difference, is a quantitative parameter for the fundamental property of lungs to allow gas exchange by diffusion. Its accurate definition and determination are complicated by a number of difficulties arising from several sources which may be grouped as follows: (1) functional inhomogeneity of parallel lung units (ventilation/diffusion/perfusion inequality); (2) heterogeneity of diffusion barrier (alveolar space; tissue layers separating blood from gas; plasma; red blood cell); (3) limitation of red cell/plasma equilibration by processes other than gas diffusion (chemical reaction; ion exchange); (4) anomalous blood/gas equilibria (for CO2).抄録全体を表示PDF形式でダウンロード (145K) -
Harold L. Kundel1987 年 36 巻 1 号 p. 116-119
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーThe anatomic and functional imaging capability of MRI is discussed. MRI will be a superb method for demonstrating anatomy, however, its real clinical impact may not become apparent until vascular imaging and functional imaging have been more fully developed.抄録全体を表示PDF形式でダウンロード (173K) -
1987 年 36 巻 1 号 p. 145
発行日: 1987年
公開日: 2009/03/27
ジャーナル フリーPDF形式でダウンロード (17K)
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