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91.
Cottnam CF Hemsley AR Rössler R Collinson ME Brain AP 《Review of Palaeobotany and Palynology》2000,109(1):33-44
Studies of wall structure in Mesozoic and Recent selaginellalean megaspores have been well documented. However, Palaeozoic examples have received minimal attention. The principal Palaeozoic megaspore genus of likely selaginellalean affinity is Triangulatisporites, extending from the Upper Devonian to the Upper Carboniferous. The particulate wall ultrastructure of a previously published Carboniferous (Duckmantian) megaspore assigned to this genus suggested that this form of wall construction may have been the ancestral wall structure of the group, an observation which posed difficulties in relating selaginellalean ultrastructure to that of other contemporaneous lycopsid megaspores. Subsequent investigation showed that the genus also contains more laminate exines similar to those of other extinct lycopsids and extant Selaginella species. Our new examples of Triangulatisporites ultrastructure from the Langsettian, Duckmantian and Westphalian D yield more information regarding early variation of wall structure within Carboniferous selaginellalean megaspores and suggest that a more laminate wall composition is at least as old as the particulate form. However, without further investigation of Lower Carboniferous forms, we are unable to state which is indeed ancestral. The laminate structure reported here and elsewhere is, none the less, more easily related to comparable ultrastructure in other groups of Carboniferous lycopsid megaspores and could suggest a link with such genera as Zonalesporites and early Lagenicula. This would be in keeping with current concepts regarding the most primitive ultrastructural type within lycopsid megaspore walls. 相似文献
92.
Dynamic and transient interactions of Atg9 with autophagosomes, but not membrane integration, are required for autophagy 总被引:1,自引:0,他引:1
Orsi A Razi M Dooley HC Robinson D Weston AE Collinson LM Tooze SA 《Molecular biology of the cell》2012,23(10):1860-1873
Autophagy is a catabolic process essential for cell homeostasis, at the core of which is the formation of double-membrane organelles called autophagosomes. Atg9 is the only known transmembrane protein required for autophagy and is proposed to deliver membrane to the preautophagosome structures and autophagosomes. We show here that mammalian Atg9 (mAtg9) is required for the formation of DFCP1-positive autophagosome precursors called phagophores. mAtg9 is recruited to phagophores independent of early autophagy proteins, such as ULK1 and WIPI2, but does not become a stable component of the autophagosome membrane. In fact, mAtg9-positive structures interact dynamically with phagophores and autophagosomes without being incorporated into them. The membrane compartment enriched in mAtg9 displays a unique sedimentation profile, which is unaltered upon starvation-induced autophagy. Correlative light electron microscopy reveals that mAtg9 is present on tubular-vesicular membranes emanating from vacuolar structures. We show that mAtg9 resides in a unique endosomal-like compartment and on endosomes, including recycling endosomes, where it interacts with the transferrin receptor. We propose that mAtg9 trafficking through multiple organelles, including recycling endosomes, is essential for the initiation and progression of autophagy; however, rather than acting as a structural component of the autophagosome, it is required for the expansion of the autophagosome precursor. 相似文献
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S K Collinson S C Clouthier J L Doran P A Banser W W Kay 《Journal of bacteriology》1996,178(3):662-667
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J Collinson 《BMJ (Clinical research ed.)》1976,2(6031):367-368
97.
Wendy J. Collinson Daniel M. Parker Ric T. F. Bernard Brian K. Reilly Harriet T. Davies‐Mostert 《Ecology and evolution》2014,4(15):3060-3071
Previous assessments of wildlife road mortality have not used directly comparable methods and, at present, there is no standardized protocol for the collection of such data. Consequently, there are no internationally comparative statistics documenting roadkill rates. In this study, we used a combination of experimental trials and road transects to design a standardized protocol to assess roadkill rates on both paved and unpaved roads. Simulated roadkill were positioned over a 1 km distance, and trials were conducted at eight different speeds (20–100 km·h−1). The recommended protocol was then tested on a 100-km transect, driven daily over a 40-day period. This recorded 413 vertebrate roadkill, comprising 106 species. We recommend the protocol be adopted for future road ecology studies to enable robust statistical comparisons between studies. 相似文献
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Ian Collinson Robin A. Corey William J. Allen 《Philosophical transactions of the Royal Society of London. Series B, Biological sciences》2015,370(1679)
The structure of the first protein-conducting channel was determined more than a decade ago. Today, we are still puzzled by the outstanding problem of protein translocation—the dynamic mechanism underlying the consignment of proteins across and into membranes. This review is an attempt to summarize and understand the energy transducing capabilities of protein-translocating machines, with emphasis on bacterial systems: how polypeptides make headway against the lipid bilayer and how the process is coupled to the free energy associated with ATP hydrolysis and the transmembrane protein motive force. In order to explore how cargo is driven across the membrane, the known structures of the protein-translocation machines are set out against the background of the historic literature, and in the light of experiments conducted in their wake. The paper will focus on the bacterial general secretory (Sec) pathway (SecY-complex), and its eukaryotic counterpart (Sec61-complex), which ferry proteins across the membrane in an unfolded state, as well as the unrelated Tat system that assembles bespoke channels for the export of folded proteins. 相似文献