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High concentrations of adenosine (Ado), when added to L1210 lymphocytic leukemia cells, resulted in apoptosis or programmed cell death. The apoptotic process was accompanied by distinct morphological changes including chromatin condensation and blebbing of plasma membranes. Extensive DNA fragmentation was correlated with Ado concentrations. Furthermore, apoptosis in these cells was preceded by an early but transient expression of c-myc proto-oncogene, and was not influenced by homocysteine thiolactone added to the cells. Since severe combined immunodeficiency (SCID) is associated with a deficiency of adenosine deaminase, leading to defects in both cellular and humoral immunity, Ado-induced apoptosis may thus be a contributing factor in the pathology of SCID.  相似文献   
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Classical conditioning of Hermissenda, involving paired light-rotation events, results in a 30-35% decrease in the levels of a 20-kDa G protein (cp20). To test whether a similar protein exists in vertebrates, rabbits were trained to associate a tone with periorbital electrical stimulation and G proteins were analyzed by photoaffinity labeling with [alpha-32P]GTP-azidoanilide. A 20-kDa G protein similar to cp20 decreased by 36% in the hippocampus of rabbits subjected to paired tone and electrical stimulation, but not in unpaired controls. Learning-specific decreases were also found in the amount of ras protein.  相似文献   
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Binding of interleukin-2 (IL-2) to its specific receptor induces activation of two members of Jak family protein tyrosine kinases, Jak1 and Jak3. An IL-2 receptor (IL-2R)-reconstituted NIH 3T3 fibroblast cell line proliferates in response to IL-2 only when hematopoietic lineage-specific Jak3 is ectopically expressed. However, the mechanism of Jak3-dependent proliferation in the fibroblast cell line is not known. Here, I showed that Jak3 expression is dispensable for IL-2-induced activation of Jak1 and Stat proteins and expression of nuclear proto-oncogenes in the IL-2R-reconstituted fibroblast cell line. Jak3 expression markedly enhanced these IL-2-induced signaling events. In contrast, Jak3 expression was essential for induction of cyclin genes involved in the G1-S transition. These data suggest a critical role of Jak3 in IL-2 signaling in the fibroblast cell line and may provide further insight into the cell type-specific mechanism of cytokine signaling.  相似文献   
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摘要:目的 探讨宫颈癌患者高危型人乳头瘤病毒(HPV)感染的检测及其与免疫功能和癌基因表达的相关性。方法 选择2017年9月至2018年12月在我院接受手术治疗的118例原发性宫颈癌患者为宫颈癌组,根据高危型HPV感染情况进一步分为高危型HPV组(89例)和非高危型HPV组(29例)。选择同期在我院行子宫全切术的57例子宫肌瘤患者为子宫肌瘤组。对比各组患者外周血T淋巴细胞亚群分布情况,病灶组织中原癌基因(E6/E7、c-Met、SALL4、PGRN)和抑癌基因(p53、pRb、PTEN、LKB1)表达量的差异。结果 宫颈癌组患者病灶组织中高危型HPV感染率显著高于子宫肌瘤组(75.42% vs 22.81%,2=43.764,P<0.05)。高危型HPV组患者外周血中CD4+ T淋巴细胞比例、CD4+T/CD8+ T比值低于非高危型HPV组,CD8+ T淋巴细胞比例高于非高危型HPV组(均P<0.05)。高危型HPV组患者病灶组织中E6/E7、c-Met、SALL4、PGRN mRNA的表达量高于非高危型HPV组,而p53、pRb、PTEN、LKB1 mRNA的表达量低于非高危型HPV组(均P<0.05)。结论 高危型HPV感染可导致宫颈癌患者细胞免疫功能下降及肿瘤恶性程度增加,可能是导致病情恶化、治疗效果不佳的危险因素之一。  相似文献   
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应用地高辛配体(digoxigenin)标记探针的原位杂交技术,检测了原癌基因 c-myc 和 jun在12例不同发育阶段的人胎心肌中的表达。根据胎龄,将其中9例分成三组,胎龄分别是16—17、23—24和27—28周,每组各3例。另外有32和36周及足月的大胎龄标本各例。杂交信号用图象分析仪(MIAS 300)分析处理。结果显示:c-myc mRNA 或 jun mRNA 的表达水平在3组心肌样本中的任意2组间的变化有差异显著性(P<0.01)结果表明,在胎儿早期,c-myc 和 jun 的表达都较高,随着胎龄的增加,其表达水平逐渐下降,在足月胎儿表达水平很低。结果提示,在人胎心肌的发育过程中,这两种原癌基因的表达均是一种下行调节方式,反应了 c-myc 和 jun 在心肌细胞的发育过程中与心肌细胞的生长密切相关。可能在心肌细胞的增殖与分化中起着重要调控作用。本研究也表明,地高辛配体标记探针的原位杂交技术具有灵敏度高,分辨力好和实验周期短等优点。对在体正常心肌发育的原癌基因表达的研究,有助于对正常心肌生长以及对心肌肥大发生的分子机制的了解。  相似文献   
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The cell-cycle progression of germinating embryos of maize (Zea mays L.) was studied from 0 to 72 h after the start of imbibition using DNA flow cytometry on isolated nuclei, and analyses of thymidine kinase activity, histone biosynthesis and levels of proliferating cell nulcear antigen (PCNA). At the start of germination, 75% of the cells were in G1, but this population had decreased to 25% by 72 h. The concomitant increase of cells in S-phase did not occur continuously, but stepwise, indicating that during germination most of the cells enter S-phase as a partially synchronized population. Within the initial 60 h of embryo germination the cells passed through one S-phase; the start and duration of this period of replicative DNA synthesis was further substantiated by the analysis of S-phase-associated events, the biosynthesis of core histones and the enzyme activity of thymidine kinase, which both began to increase at about 12 h after the start of differentiation. Thymidine kinase fluctuated periodically during germination with a transient maximum at 30 h and a second peak at 72 h; histone biosynthesis was not detectable until 12 h after the start of germination. The levels of PCNA protein closely resembled the pattern of thymidine kinase during germination. Together with the cytometric data this allows a clear assignment of cell cycle events to different times of embryo differentiation.Abbreviation PCNA proliferating-cell nuclear antigen Dedicated to Prof. Walter Larcher on the occasion of his 65th birthdayThe authors wish to thank Prof. G. Mikuz (Department of Pathology, University of Innsbruck, Austria) and Prof. G. Stöffler (Department of Microbiology, University of Innsbruck, Austria) for their interest and support. The technical assistance of Mrs. R. Gantschnig is gratefully acknowledged. E.I. Georgieva was recipient of short-term fellowships from the Austrian Academy of Sciences, the Austrian Forschungsgemeinschaft and the Austrian Akademischer Austauschdienst. G. López-Rodas was recipient of a postdoctoral fellowship from the Programa sectorial de Formación de Profesorado y Personal investigador del Ministerio de Educación y Ciencia (Spain). This work was supported in part by Grant SO6011 (to P.L.) from the Austrian Fonds zur Förderung der wissenschaftlichen Forschung and the Dr. Legerlotz-Foundation.  相似文献   
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