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181.
182.
Landscape of transcription in human cells 总被引:3,自引:0,他引:3
S Djebali CA Davis A Merkel A Dobin T Lassmann A Mortazavi A Tanzer J Lagarde W Lin F Schlesinger C Xue GK Marinov J Khatun BA Williams C Zaleski J Rozowsky M Röder F Kokocinski RF Abdelhamid T Alioto I Antoshechkin MT Baer NS Bar P Batut K Bell I Bell S Chakrabortty X Chen J Chrast J Curado T Derrien J Drenkow E Dumais J Dumais R Duttagupta E Falconnet M Fastuca K Fejes-Toth P Ferreira S Foissac MJ Fullwood H Gao D Gonzalez A Gordon H Gunawardena C Howald S Jha R Johnson P Kapranov B King 《Nature》2012,489(7414):101-108
Eukaryotic cells make many types of primary and processed RNAs that are found either in specific subcellular compartments or throughout the cells. A complete catalogue of these RNAs is not yet available and their characteristic subcellular localizations are also poorly understood. Because RNA represents the direct output of the genetic information encoded by genomes and a significant proportion of a cell's regulatory capabilities are focused on its synthesis, processing, transport, modification and translation, the generation of such a catalogue is crucial for understanding genome function. Here we report evidence that three-quarters of the human genome is capable of being transcribed, as well as observations about the range and levels of expression, localization, processing fates, regulatory regions and modifications of almost all currently annotated and thousands of previously unannotated RNAs. These observations, taken together, prompt a redefinition of the concept of a gene. 相似文献
183.
壬二酸的性质、合成和应用 总被引:3,自引:0,他引:3
本综述了壬二酸的性质,用途及合成方法。介绍了国内外采用臭氧氧化法合成壬二酸的研究进展。对臭氧氧化法合成壬二酸的反应机理,合成工艺做了较为系统的总结并对臭氧氧化法在精细化工中的应用做了展望:臭氧氧化法作为一种清洁工艺在油脂深加工和精细化工产品的开发方面大有可为。 相似文献
184.
Understanding of the crystal chemistry of the Earth's deep mantle has evolved rapidly recently with the gradual acceptance of the importance of the effect of minor elements such as aluminium on the properties of major phases such as perovskite. In the early Earth, during its formation and segregation into rocky mantle and iron-rich core, it is likely that silicate liquids played a large part in the transport of volatiles to or from the deep interior. The importance of aluminium on solubility mechanisms at high pressure has so far received little attention, even though aluminium has long been recognized as exerting strong control on liquid structures at ambient conditions. Here we present constraints on the solubility of argon in aluminosilicate melt compositions up to 25 GPa and 3,000 K, using a laser-heated diamond-anvil cell. The argon contents reach a maximum that persists to pressures as high as 17 GPa (up to 500 km deep in an early magma ocean), well above that expected on the basis of Al-free melt experiments. A distinct drop in argon solubility observed over a narrow pressure range correlates well with the expected void loss in the melt structure predicted by recent molecular dynamics simulations. These results provide a process for noble gas sequestration in the mantle at various depths in a cooling magma ocean. The concept of shallow partial melting as a unique process for extracting noble gases from the early Earth, thereby defining the initial atmospheric abundance, may therefore be oversimplified. 相似文献
185.
I. R. C. Bick J. B. Bremner A. Razak bin Modh Ali Le Van Thuc 《Cellular and molecular life sciences : CMLS》1980,36(10):1135-1135
Summary A novel series of alkaloids has been obtained from the Tasmanian plantAthrotaxis selaginoides, the first to be isolated from the plant family Taxodiaceae. 相似文献
186.
UV-irradiation of phenylalanine by 253.7 nm light in the presence of hydrogen peroxide formed 5 ninhydrin reactive products and ammonia. Four of them were identified as aspartic acid, serine, alanine and lysine. 相似文献
187.
188.
A. Ali M. A. Guidicci D. Stevenson 《Cellular and molecular life sciences : CMLS》1976,32(12):1503-1504
Summary This synthesis is especially suitable for production of highly-purified bradykinin-potentiating pentapeptide (BPP5a) because of the high yields of the coupling and deprotection reactions, accompanied by minimal side reactions, and the need for only one simple final purification step.The authors wish to thankJ. Pallak for carrying out the aminoacid analyses and bio-assays. 相似文献
189.
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy 总被引:17,自引:0,他引:17
Ali RR Sarra GM Stephens C Alwis MD Bainbridge JW Munro PM Fauser S Reichel MB Kinnon C Hunt DM Bhattacharya SS Thrasher AJ 《Nature genetics》2000,25(3):306-310
The gene Prph2 encodes a photoreceptor-specific membrane glycoprotein, peripherin-2 (also known as peripherin/rds), which is inserted into the rims of photoreceptor outer segment discs in a complex with rom-1 (ref. 2). The complex is necessary for the stabilization of the discs, which are renewed constantly throughout life, and which contain the visual pigments necessary for photon capture. Mutations in Prph2 have been shown to result in a variety of photoreceptor dystrophies, including autosomal dominant retinitis pigmentosa and macular dystrophy. A common feature of these diseases is the loss of photoreceptor function, also seen in the retinal degeneration slow (rds or Prph2 Rd2/Rd2) mouse, which is homozygous for a null mutation in Prph2. It is characterized by a complete failure to develop photoreceptor discs and outer segments, downregulation of rhodopsin and apoptotic loss of photoreceptor cells. The electroretinograms (ERGs) of Prph2Rd2/Rd2 mice have greatly diminished a-wave and b-wave amplitudes, which decline to virtually undetectable concentrations by two months. Subretinal injection of recombinant adeno-associated virus (AAV) encoding a Prph2 transgene results in stable generation of outer segment structures and formation of new stacks of discs containing both perpherin-2 and rhodopsin, which in many cases are morphologically similar to normal outer segments. Moreover, the re-establishment of the structural integrity of the photoreceptor layer also results in electrophysiological correction. These studies demonstrate for the first time that a complex ultrastructural cell defect can be corrected both morphologically and functionally by in vivo gene transfer. 相似文献
190.
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome 总被引:23,自引:0,他引:23
Chavanas S Bodemer C Rochat A Hamel-Teillac D Ali M Irvine AD Bonafé JL Wilkinson J Taïeb A Barrandon Y Harper JI de Prost Y Hovnanian A 《Nature genetics》2000,25(2):141-142
We describe here eleven different mutations in SPINK5, encoding the serine protease inhibitor LEKTI, in 13 families with Netherton syndrome (NS, MIM256500). Most of these mutations predict premature termination codons. These results disclose a critical role of SPINK5 in epidermal barrier function and immunity, and suggest a new pathway for high serum IgE levels and atopic manifestations. 相似文献