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DNA aneuploidy has been identified as a prognostic factor in the majority of epithelial malignancies. We aimed at identifying ploidy-associated protein expression in endometrial cancer of different prognostic subgroups. Comparison of gel electrophoresis-based protein expression patterns between normal endometrium (n?=?5), diploid (n?=?7), and aneuploid (n?=?7) endometrial carcinoma detected 121 ploidy-associated protein forms, 42 differentially expressed between normal endometrium and diploid endometrioid carcinomas, 37 between diploid and aneuploid endometrioid carcinomas, and 41 between diploid endometrioid and aneuploid uterine papillary serous cancer. Proteins were identified by mass spectrometry and evaluated by Ingenuity Pathway Analysis. Targets were confirmed by liquid chromatography/mass spectrometry. Mass spectrometry identified 41 distinct polypeptides and pathway analysis resulted in high-ranked networks with vimentin and Nf-κB as central nodes. These results identify ploidy-associated protein expression differences that overrule histopathology-associated expression differences and emphasize particular protein networks in genomic stability of endometrial cancer.  相似文献   
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Summary A new method for the classification of antiphlogistics is described using the growth inhibition ofLactobacillus casei. In this test the fenamic acids and particularly the new class of the Cinnopentazon-antiphologistics (Scha 306, Scha 764 etc.) exhibit bacteriostatic properties of a medium intensity.

Alexander von Muralt zum 65. Geburtstag gewidmet.  相似文献   
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Research on aging in model organisms has revealed different molecular mechanisms involved in the regulation of the lifespan. Studies on Saccharomyces cerevisiae have highlighted the role of the Sir2 family of genes, human Sirtuin homologs, as the longevity factors. In Caenorhabditis elegans, the daf-16 gene, a mammalian homolog of FoxO genes, was shown to function as a longevity gene. A wide array of studies has provided evidence for a role of the activation of innate immunity during aging process in mammals. This process has been called inflamm-aging. The master regulator of innate immunity is the NF-κB system. In this review, we focus on the several interactions of aging-associated signaling cascades regulated either by Sirtuins and FoxOs or NF-κB signaling pathways. We provide evidence that signaling via the longevity factors of FoxOs and SIRT1 can inhibit NF-κB signaling and simultaneously protect against inflamm-aging process. Received 4 October 2007; received after revision 7 November 2007; accepted 9 November 2007  相似文献   
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The HERG (KCNH2) channel is a voltage-sensitive potassium channel mainly expressed in cardiac tissue, but has also been identified in other tissues like neuronal and smooth muscle tissue, and in various tumours and tumour cell lines. The function of HERG has been extensively studied, but it is still not clear what mechanisms regulate the surface expression of the channel. In the present report, using human embryonic kidney cells stably expressing HERG, we show that diacylglycerol potently inhibits the HERG current. This is mediated by a protein kinase C-evoked endocytosis of the channel protein, and is dependent on the dynein–dynamin complex. The HERG protein was found to be located only in early endosomes and not lysosomes. Thus, diacylglycerol is an important lipid participating in the regulation of HERG surface expression and function.  相似文献   
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Mitchell-Olds T  Schmitt J 《Nature》2006,441(7096):947-952
Genomic studies of natural variation in model organisms provide a bridge between molecular analyses of gene function and evolutionary investigations of adaptation and natural selection. In the model plant species Arabidopsis thaliana, recent studies of natural variation have led to the identification of genes underlying ecologically important complex traits, and provided new insights about the processes of genome evolution, geographic population structure, and the selective mechanisms shaping complex trait variation in natural populations. These advances illustrate the potential for a new synthesis to elucidate mechanisms for the adaptive evolution of complex traits from nucleotide sequences to real-world environments.  相似文献   
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Arthropods play a significant role in ecosystems as prey for animals such as insectivorous primates. The venomous Javan slow loris (Nycticebus javanicus) is a nocturnal primate endemic to the island of Java, Indonesia. It remains unknown if its venom is partially sequestered from noxious arthropod prey. We studied the little-known arthropod community in a rural agriculture system in West Java, Indonesia, in order to investigate the potential prey and source for sequestration of venom. We found specimens of the partially noxious insect orders Lepidoptera, Hemiptera, Coleoptera, Hymenoptera, Orthoptera and of the class Arachnida in slow loris foraging trees in an agricultural area in West Java, Indonesia. To examine the effects of environmental conditions on the abundance of this food source, arthropods were trapped every two weeks for five months, using sweep net transects, Malaise and pitfall traps. Trap type had a significant effect on taxa caught. Wind strength negatively affected the number of Lepidoptera captured in the Malaise trap and humidity had a confounding effect on Orthoptera caught by sweep net. Despite the short-term nature of our study, by using a combination of trapping methods, we identified a relatively high diversity of insects in a human-dominated landscape. Our results can be used as a basis to understand the proximate and ultimate factors shaping the use of venom by the slow loris as a primate.  相似文献   
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The identification of tumor-suppressor genes in solid tumors by classical cancer genetics methods is difficult and slow. We combined nonsense-mediated RNA decay microarrays and array-based comparative genomic hybridization for the genome-wide identification of genes with biallelic inactivation involving nonsense mutations and loss of the wild-type allele. This approach enabled us to identify previously unknown mutations in the receptor tyrosine kinase gene EPHB2. The DU 145 prostate cancer cell line, originating from a brain metastasis, carries a truncating mutation of EPHB2 and a deletion of the remaining allele. Additional frameshift, splice site, missense and nonsense mutations are present in clinical prostate cancer samples. Transfection of DU 145 cells, which lack functional EphB2, with wild-type EPHB2 suppresses clonogenic growth. Taken together with studies indicating that EphB2 may have an essential role in cell migration and maintenance of normal tissue architecture, our findings suggest that mutational inactivation of EPHB2 may be important in the progression and metastasis of prostate cancer.  相似文献   
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