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61.
Vaughan JA 《Trends in parasitology》2007,23(2):63-70
Malaria transmission relies on the sporogonic development of Plasmodium parasites within insect vectors. Sporogony is a complex process that involves several morphologically distinct life-stages and can be described in terms of population dynamics: changes in the abundance and distribution of successive life-stages throughout development. Recent publications on the population dynamics of sporogony are reviewed, with special attention to the differences and similarities among the parasite-vector systems examined thus far. Understanding the population dynamics of malaria parasites within their natural vectors will lead to a better understanding of how malaria parasites survive and are maintained within mosquitoes. 相似文献
62.
Francinaldo Soares Silva Jefferson Mesquita Brito Benedita Maria Costa Neta Shelre Emile Pereira Duarte Lobo 《Memórias do Instituto Oswaldo Cruz》2015,110(6):801-803
Hoover Pugedo light traps were modified for use with green and blue-light-emitting
diodes to trap phlebotomine sandflies in northeastern Brazil. A total of 2,267
specimens belonging to eight genera and 15 species were sampled. The predominant
species were Nyssomyia whitmani(34.41%) and Micropygomyia
echinatopharynx(17.25%).The green LED trap prevailed over the blue and
control lights; however, no statistically significant difference could be detected
among the three light sources. Even without statistical significance, we suggest
using LEDs as an attractant for the capture of sandflies because of several
advantages over the conventional method with incandescent lamps. 相似文献
63.
Jefferson José da Silva Santos Tereza Magalh?es José Valter Joaquim Silva Junior Andréa Nazaré Monteiro Rangel da Silva Marli Tenório Cordeiro Laura Helena Vega Gonzales Gil 《Memórias do Instituto Oswaldo Cruz》2015,110(5):677-683
Full-length dengue virus (DENV) cDNA clones are an invaluable tool for many studies,
including those on the development of attenuated or chimeric vaccines and on
host-virus interactions. Furthermore, the importance of low passage DENV infectious
clones should be highlighted, as these may harbour critical and unique
strain-specific viral components from field-circulating isolates. The successful
construction of a functional Brazilian low passage DENV serotype 2 full-length clone
through homologous recombination reported here supports the use of a strategy that
has been shown to be highly useful by our group for the development of flavivirus
infectious clones and replicons. 相似文献
64.
A global plastid phylogeny of the brake fern genus Pteris (Pteridaceae) and related genera in the Pteridoideae 下载免费PDF全文
65.
Haitian Fan Joseph Hahm Stephen Diggs J. Jefferson P. Perry Gregor Blaha 《The Journal of biological chemistry》2015,290(34):20856-20864
The translational GTPase BipA regulates the expression of virulence and pathogenicity factors in several eubacteria. BipA-dependent expression of virulence factors occurs under starvation conditions, such as encountered during infection of a host. Under these conditions, BipA associates with the small ribosomal subunit. BipA also has a second function to promote the efficiency of late steps in biogenesis of large ribosomal subunits at low temperatures, presumably while bound to the ribosome. During starvation, the cellular concentration of stress alarmone guanosine-3′, 5′-bis pyrophosphate (ppGpp) is increased. This increase allows ppGpp to bind to BipA and switch its binding specificity from ribosomes to small ribosomal subunits. A conformational change of BipA upon ppGpp binding could explain the ppGpp regulation of the binding specificity of BipA. Here, we present the structures of the full-length BipA from Escherichia coli in apo, GDP-, and ppGpp-bound forms. The crystal structure and small-angle x-ray scattering data of the protein with bound nucleotides, together with a thermodynamic analysis of the binding of GDP and of ppGpp to BipA, indicate that the ppGpp-bound form of BipA adopts the structure of the GDP form. This suggests furthermore, that the switch in binding preference only occurs when both ppGpp and the small ribosomal subunit are present. This molecular mechanism would allow BipA to interact with both the ribosome and the small ribosomal subunit during stress response. 相似文献
66.
Washington J. Gapare Brian S. Baltunis Milo? Ivkovi? Charlie B. Low Paul Jefferson Harry X. Wu 《Tree Genetics & Genomes》2011,7(2):409-419
Growth and form traits from a series of three provenance trials of Pinus radiata D. Don planted in New Zealand and Australia were analysed at age 9 years from planting. The trials included selections from
three mainland California natural populations—A?o Nuevo, Monterey and Cambria. Monterey and Cambria performed better than
A?o Nuevo at two New Zealand sites, but Monterey and A?o Nuevo were almost identical in growth, whereas Cambria grew less
vigorously at the Australian site. We detected significant provenance differences for diameter at breast height (DBH) growth
and stem straightness across countries (p < 0.001). Estimated heritability for DBH ranged from 0.19 to 0.26 within sites, while heritability estimates for stem straightness
and branching frequency ranged from 0.10 to 0.24. Estimated type B genetic correlations for DBH were always higher between
the two trials in New Zealand trials than between pairs of trials in New Zealand and the Australian site. The genetic coefficient
of variation (CVA) for DBH was around 8–10% compared to ca. 5% for the current breeding population. These results suggested that there is appreciable
genetic variation in the native populations, and infusion of these materials would increase the genetic variation in current
breeding populations. Ten unrelated parents ranked above control seedlots from the older open-pollinated seed orchard stock
for DBH growth and would be potential candidates for infusion. The promising performance of the Cambria material is an important
result because the genetic base of the present Australian and New Zealand plantations is principally derived from A?o Nuevo
and Monterey. 相似文献
67.
68.
Williamson DL Kimball SR Jefferson LS 《American journal of physiology. Endocrinology and metabolism》2005,289(1):E95-104
Insulin and TNF-alpha exert opposing effects on skeletal muscle protein synthesis that are mediated in part by the rapamycin-sensitive mammalian target of rapamycin (mTOR) pathway and the PD-98059-sensitive, extracellular signal-regulated kinase (ERK)1/2 pathway. The present study examined the separate and combined effects of insulin (INS), TNF, PD-98059, or dnMEK1 adenovirus on the translational control of protein synthesis in C(2)C(12) myotubes. Cultures were treated with INS, TNF, PD-98059, dnMEK1, or a combination of INS + TNF with PD-98059 or dnMEK1. INS stimulated protein synthesis, enhanced eIF4E.eIF4G association, and eIF4G phosphorylation and repressed eIF4E.4E-BP1 association vs. control. INS also promoted phosphorylation of ERK1/2, S6K1, and 4E-BP1 and dephosphorylation of eIF4E. TNF alone did not have an effect on protein synthesis (vs. control), eIF4E.eIF4G association, or the phosphorylation of eIF4G, S6K1, or 4E-BP1, although it transiently increased ERK1/2 and eIF4E phosphorylation. When myotubes were treated with TNF + INS, the cytokine blocked the insulin-induced stimulation of protein synthesis. This appeared to be due to an attenuation of insulin-stimulated eIF4E.eIF4G association, because other stimulatory effects of INS, e.g., phosphorylation of ERK1/2, 4E-BP1, S6K1, eIF4G, and eIF4E and eIF4E.4E-BP1 association, were unaffected. Finally, treatment of myotubes with PD-98059 or dnMEK1 adenovirus before TNF + INS addition resulted in a derepression of protein synthesis and the association of eIF4G with eIF4E. These findings suggest that TNF abrogates insulin-induced stimulation of protein synthesis in myotubes through a decrease in eIF4F complex assembly independently of S6K1 and 4E-BP1 signaling and dependently on a MEK1-sensitive signaling pathway. 相似文献
69.
Smith JJ Conrad DW Cuneo MJ Hellinga HW 《Protein science : a publication of the Protein Society》2005,14(1):64-73
Covalent modification is an important strategy for introducing new functions into proteins. As engineered proteins become more sophisticated, it is often desirable to introduce multiple, modifications involving several different functionalities in a site-specific manner. Such orthogonal labeling schemes require independent labeling of differentially reactive nucleophilic amino acid side chains. We have developed two protein-mediated protection schemes that permit independent labeling of multiple thiols. These schemes exploit metal coordination or disulfide bond formation to reversibly protect cysteines in a Cys(2)His(2) zinc finger domain. We constructed a variety of N- and C-terminal fusions of these domains with maltose-binding protein, which were labeled with two or three different fluorophores. Multiple modifications were made by reacting an unprotected cysteine in MBP first, deprotecting the zinc finger, and then reacting the zinc finger cysteines. The fusion proteins were orthogonally labeled with two different fluorophores, which exhibited intramolecular fluorescene resonance energy transfer (FRET). These conjugates showed up to a threefold ratiometric change in emission intensities in response to maltose binding. We also demonstrated that the metal- and redox-mediated protection methods can be combined to produce triple independent modifications, and prepared a protein labeled with three different fluorophores that exhibited a FRET relay. Finally, labeled glucose-binding protein was covalently patterned on glass slides using thiol-mediated immobilization chemistries. Together, these experiments demonstrated that reversible thiol protection schemes provide a rapid, straightforward method for producing multiple, site-specific modifications. 相似文献
70.
Outbred female CD-1 mice were treated with genistein (Gen), the primary phytoestrogen in soy, by s.c. injections on Neonatal Days 1-5 at doses of 0.5, 5, or 50 mg/kg per day (Gen-0.5, Gen-5, and Gen-50). The day of vaginal opening was observed in mice treated with Gen and compared with controls, and although there were some differences, they were not statistically significant. Gen-treated mice had prolonged estrous cycles with a dose- and age-related increase in severity of abnormal cycles. Females treated with Gen-0.5 or Gen-5 bred to control males at 2, 4, and 6 mo showed statistically significant decreases in the number of live pups over time with increasing dose; at 6 mo, 60% of the females in the Gen-0.5 group and 40% in the Gen-5 group delivered live pups compared with 100% of controls. Mice treated with Gen-50 did not deliver live pups. At 2 mo, >60% of the mice treated with Gen-50 were fertile as determined by uterine implantation sites, but pregnancy was not maintained; pregnancy loss was characterized by fewer, smaller implantation sites and increased reabsorptions. Mice treated with lower doses of Gen had increased numbers of corpora lutea compared with controls, while mice treated with the highest dose had decreased numbers; however, superovulation with eCG/hCG yielded similar numbers of oocytes as controls. Serum levels of progesterone, estradiol, and testosterone were similar between Gen-treated and control mice when measured before puberty and during pregnancy. In summary, neonatal treatment with Gen caused abnormal estrous cycles, altered ovarian function, early reproductive senescence, and subfertility/infertility at environmentally relevant doses. 相似文献