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81.
Richard W. Joy IV Edward C. Yeung Lisheng Kong Trevor A. Thorpe 《In vitro cellular & developmental biology. Plant》1991,27(1):32-41
Summary The growth and development of white spruce somatic embryos was followed from the filamentous immature to the mature cotyledonary
embryo stage. Histochemical examination of the various stages of embryo development showed that lipids, proteins, and polysaccharides
were produced to varying degrees during the process. During early stages (1 to 2 wk on ABA), mostly polysaccharide was produced,
whereas during later stages, polysaccharides, lipids, and protein accumulated. Electron microscopy indicated that lipid deposition
in somatic embryos started during the first week after transfer to ABA-containing medium. Deposition of the storage products
began at the basal end of the embryonal mass and within the proximal zone of the suspensors. Accumulation continued to the
peripheral regions and then inward toward the cortex of the developing embryo. In all cases, polysaccharide accumulated first,
followed by lipid and lastly, protein. Quantitatively, cotyledonary stage somatic embryos had less lipid and protein and more
starch when compared to zygotic embryos at the same developmental stage. Total protein profiles elucidated by sodium dodecyl
sulfate-polyacrylamide gel electrophoresis indicated that the majority of proteins were similar in zygotic and somatic embryos.
Prominent protein bands were found at 30, 20, 19.5, 15, 14.4, 12, and 10 Kd. However, protein bands at 40, 15, and 12 Kd in
total protein from somatic embryos were either absent or highly underexpressed. 相似文献
82.
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84.
Erik A Karlsson Christopher T Small Pamela Freiden MM Feeroz Frederick A Matsen IV Sorn San M Kamrul Hasan David Wang Lisa Jones-Engel Stacey Schultz-Cherry 《PLoS pathogens》2015,11(11)
Astroviruses (AstVs) are positive sense, single-stranded RNA viruses transmitted to a wide range of hosts via the fecal-oral route. The number of AstV-infected animal hosts has rapidly expanded in recent years with many more likely to be discovered because of the advances in viral surveillance and next generation sequencing. Yet no study to date has identified human AstV genotypes in animals, although diverse AstV genotypes similar to animal-origin viruses have been found in children with diarrhea and in one instance of encephalitis. Here we provide important new evidence that non-human primates (NHP) can harbor a wide variety of mammalian and avian AstV genotypes, including those only associated with human infection. Serological analyses confirmed that >25% of the NHP tested had antibodies to human AstVs. Further, we identified a recombinant AstV with parental relationships to known human AstVs. Phylogenetic analysis suggests AstVs in NHP are on average evolutionarily much closer to AstVs from other animals than are AstVs from bats, a frequently proposed reservoir. Our studies not only demonstrate that human astroviruses can be detected in NHP but also suggest that NHP are unique in their ability to support diverse AstV genotypes, further challenging the paradigm that astrovirus infection is species-specific. 相似文献
85.
The parasite fauna of the burbot (Lota lota) within its natural range is reviewed. The sent paper summarizes the data on parasites of the burbot from water bodies of Eurasia and North America, based on published monographs, reviewed journals, scientific reports, conference contributions, and PhD theses. The checklist includes all protozoan and metazoan parasites of the burbot. A total of 242 parasite species/taxa were recorded in the burbot (Ki-netoplastomonada--4, Parasitomonada--3, Coccidiomorpha--1. Microsporidea--3, Myxosporidia--35, Pleurostomata--1. Cyrtostomata--3, Peritricha--20. Protozoa incertae sedis--1. Monogenea--8, Cestoda--23, Digenea--50. Nematoda--36, Acanthocephala--28, Hirudinea--11. Bivalvia--5, Crustacea--10). Most parasites belong to digenean trematodes. Most of these species (183 species/taxa) were recorded on Eurasian and only 92--in North America fishes. Several parasite species recorded from the burbot are discussed in relation to host specificity and their geographical distribution. 相似文献
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87.
Grace S. Tan Barry G. Garchow Xuhang Liu Jennifer Yeung John P. Morris IV Trinna L. Cuellar Michael T. McManus Marianthi Kiriakidou 《Nucleic acids research》2009,37(22):7533-7545
Mammalian Argonaute 2 (Ago2) protein associates with microRNAs (miRNAs) or small interfering RNAs (siRNAs) forming RNA-induced silencing complexes (RISCs/miRNPs). In the present work, we characterize the RNA-binding and nucleolytic activity of recombinant mouse Ago2. Our studies show that recombinant mouse Ago2 binds efficiently to miRNAs forming active RISC. Surprisingly, we find that recombinant mouse Ago2 forms active RISC using pre-miRNAs or long unstructured single stranded RNAs as guides. Furthermore, we demonstrate that, in vivo, endogenous human Ago2 binds directly to pre-miRNAs independently of Dicer, and that Ago2:pre-miRNA complexes are found both in the cytoplasm and in the nucleus of human cells. 相似文献
88.
Roman Aranda IV Shauna M. Dineen Rhonda L. Craig James M. Robertson 《Analytical biochemistry》2009,387(1):122-127
Quantification of RNA is essential for various molecular biology studies. In this work, three quantification methods were evaluated: ultraviolet (UV) absorbance, microcapillary electrophoresis (MCE), and fluorescence-based quantification. Viral, bacterial, and eukaryotic RNA were measured in the 500 to 0.05-ng μl−1 range via an ND-1000 spectrophotometer (UV), Agilent RNA 6000 kits (MCE), and Quant-iT RiboGreen assay (fluorescence). The precision and accuracy of each method were assessed and compared with a concentration derived independently using inductively coupled plasma-optical emission spectroscopy (ICP-OES). Cost, operator time and skill, and required sample volumes were also considered in the evaluation. Results indicate an ideal concentration range for each quantification technique to optimize accuracy and precision. The ND-1000 spectrophotometer exhibits high precision and accurately quantifies a 1-μl sample in the 500 to 5-ng μl−1 range. The Quant-iT RiboGreen assay demonstrates high precision in the 1 to 0.05-ng μl−1 range but is limited to lower RNA concentrations and is more costly than the ND-1000 spectrophotometer. The Agilent kits exhibit less precision than the ND-1000 spectrophotometer and Quant-iT RiboGreen assays in the 500 to 0.05-ng μl−1 range. However, the Agilent kits require 1 μl of sample and can determine the integrity of the RNA, a useful feature for verifying whether the isolation process was successful. 相似文献
89.
Background
Rho1 is a small GTPase of the Ras superfamily that serves as the central component in a highly conserved signaling pathway that regulates tissue morphogenesis during development in all animals. Since there is tremendous diversity in the upstream signals that can activate Rho1 as well as the effector molecules that carry out its functions, it is important to define relevant Rho1-interacting genes for each morphogenetic event regulated by this signaling pathway. Previous work from our lab and others has shown that Rho signaling is necessary for the morphogenesis of leg imaginal discs during metamorphosis in Drosophila, although a comprehensive identification of Rho1-interacting genes has not been attempted for this process.Methodology/Principal Findings
We characterized an amorphic allele of Rho1 that displays a poorly penetrant dominant malformed leg phenotype and is capable of being strongly enhanced by Rho1-interacting heterozygous mutations. We then used this allele in a second-site noncomplementation screen with the Exelixis collection of molecularly defined deficiencies to identify Rho1-interacting genes necessary for leg morphogenesis. In a primary screen of 461 deficiencies collectively uncovering ∼50% of the Drosophila genome, we identified twelve intervals harboring Rho1-interacting genes. Through secondary screening we identified six Rho1-interacting genes including three that were previously identified (RhoGEF2, broad, and stubbloid), thereby validating the screen. In addition, we identified Cdc42, Rheb and Sc2 as novel Rho1-interacting genes involved in adult leg development.Conclusions/Significance
This screen identified well-known and novel Rho1-interacting genes necessary for leg morphogenesis, thereby increasing our knowledge of this important signaling pathway. We additionally found that Rheb may have a unique function in leg morphogenesis that is independent of its regulation of Tor. 相似文献90.
Saul Lozano-Fuentes Ildefonso Fernandez-Salas Maria de Lourdes Munoz Julian Garcia-Rejon Ken E. Olson Barry J. Beaty William C. Black IV 《PLoS neglected tropical diseases》2009,3(6)