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91.
Autophagy fights disease through cellular self-digestion 总被引:3,自引:0,他引:3
Autophagy, or cellular self-digestion, is a cellular pathway involved in protein and organelle degradation, with an astonishing number of connections to human disease and physiology. For example, autophagic dysfunction is associated with cancer, neurodegeneration, microbial infection and ageing. Paradoxically, although autophagy is primarily a protective process for the cell, it can also play a role in cell death. Understanding autophagy may ultimately allow scientists and clinicians to harness this process for the purpose of improving human health. 相似文献
92.
Heterodimeric JAK-STAT activation as a mechanism of persistence to JAK2 inhibitor therapy 总被引:1,自引:0,他引:1
P Koppikar N Bhagwat O Kilpivaara T Manshouri M Adli T Hricik F Liu LM Saunders A Mullally O Abdel-Wahab L Leung A Weinstein S Marubayashi A Goel M Gönen Z Estrov BL Ebert G Chiosis SD Nimer BE Bernstein S Verstovsek RL Levine 《Nature》2012,489(7414):155-159
The identification of somatic activating mutations in JAK2 (refs?1–4) and in the thrombopoietin receptor gene (MPL) in most patients with myeloproliferative neoplasm (MPN) led to the clinical development of JAK2 kinase inhibitors. JAK2 inhibitor therapy improves MPN-associated splenomegaly and systemic symptoms but does not significantly decrease or eliminate the MPN clone in most patients with MPN. We therefore sought to characterize mechanisms by which MPN cells persist despite chronic inhibition of JAK2. Here we show that JAK2 inhibitor persistence is associated with reactivation of JAK–STAT signalling and with heterodimerization between activated JAK2 and JAK1 or TYK2, consistent with activation of JAK2 in trans by other JAK kinases. Further, this phenomenon is reversible: JAK2 inhibitor withdrawal is associated with resensitization to JAK2 kinase inhibitors and with reversible changes in JAK2 expression. We saw increased JAK2 heterodimerization and sustained JAK2 activation in cell lines, in murine models and in patients treated with JAK2 inhibitors. RNA interference and pharmacological studies show that JAK2-inhibitor-persistent cells remain dependent on JAK2 protein expression. Consequently, therapies that result in JAK2 degradation retain efficacy in persistent cells and may provide additional benefit to patients with JAK2-dependent malignancies treated with JAK2 inhibitors. 相似文献
93.
IDH mutation impairs histone demethylation and results in a block to cell differentiation 总被引:1,自引:0,他引:1
Lu C Ward PS Kapoor GS Rohle D Turcan S Abdel-Wahab O Edwards CR Khanin R Figueroa ME Melnick A Wellen KE O'Rourke DM Berger SL Chan TA Levine RL Mellinghoff IK Thompson CB 《Nature》2012,483(7390):474-478
Recurrent mutations in isocitrate dehydrogenase 1 (IDH1) and IDH2 have been identified in gliomas, acute myeloid leukaemias (AML) and chondrosarcomas, and share a novel enzymatic property of producing 2-hydroxyglutarate (2HG) from α-ketoglutarate. Here we report that 2HG-producing IDH mutants can prevent the histone demethylation that is required for lineage-specific progenitor cells to differentiate into terminally differentiated cells. In tumour samples from glioma patients, IDH mutations were associated with a distinct gene expression profile enriched for genes expressed in neural progenitor cells, and this was associated with increased histone methylation. To test whether the ability of IDH mutants to promote histone methylation contributes to a block in cell differentiation in non-transformed cells, we tested the effect of neomorphic IDH mutants on adipocyte differentiation in vitro. Introduction of either mutant IDH or cell-permeable 2HG was associated with repression of the inducible expression of lineage-specific differentiation genes and a block to differentiation. This correlated with a significant increase in repressive histone methylation marks without observable changes in promoter DNA methylation. Gliomas were found to have elevated levels of similar histone repressive marks. Stable transfection of a 2HG-producing mutant IDH into immortalized astrocytes resulted in progressive accumulation of histone methylation. Of the marks examined, increased H3K9 methylation reproducibly preceded a rise in DNA methylation as cells were passaged in culture. Furthermore, we found that the 2HG-inhibitable H3K9 demethylase KDM4C was induced during adipocyte differentiation, and that RNA-interference suppression of KDM4C was sufficient to block differentiation. Together these data demonstrate that 2HG can inhibit histone demethylation and that inhibition of histone demethylation can be sufficient to block the differentiation of non-transformed cells. 相似文献
94.
95.
Estimation of secondary structure in ribonucleic acids 总被引:89,自引:0,他引:89
96.
M Alavaikko A Rinne M J?rvinen V K Hopsu-Havu P R Meyer A M Levine R J Lukes 《Experientia》1985,41(9):1173-1175
One of two cases of acquired immune deficiency syndrome-related persistent generalized lymphadenopathy revealed a profoundly altered pattern of dendritic reticulum cells as demonstrated by immunoreactive acid cysteine proteinase inhibitor. The alterations could be related to totally or partially destructed lymphoid secondary follicles. 相似文献
97.
Structure of pyruvate kinase and similarities with other enzymes: possible implications for protein taxonomy and evolution 总被引:4,自引:0,他引:4
The structure determination of pyruvate kinase shows that each subunit of the tetrameric molecule consists of three domains. The largest of these domains has a remarkable similarity to the structure of triosephosphate isomerase. Another domain shows similarities to many other nucleotide binding proteins. We discuss these similarities and their implications for current arguments on protein taxonomy and evolution. 相似文献
98.
99.
Résumé Nous avons constaté que chez les souris l'insuline possède une sensibilité élevée au peptone anaphylactoïde non-carbohydraté. Ce résultat concorde avec l'hypothèse d'une relation inverse entre la quantité de glucose dans le sang et la sensibilité d'un hôte à une grande variété de «stressors». 相似文献
100.