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21.
Transducer of regulated CREB activity 2 (TORC2) is a coactivator of CREB and an important regulator of energy balance in mammals through control of gluconeogenesis in the liver. In this issue of Cell Metabolism, Wang and coworkers (2008) report an intriguing role for Drosophila TORC in the neuronal regulation of metabolism. 相似文献
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Distinguishing driver and passenger mutations in an evolutionary history categorized by interference
In many biological scenarios, from the development of drug resistance in pathogens to the progression of healthy cells toward cancer, quantifying the selection acting on observed mutations is a central question. One difficulty in answering this question is the complexity of the background upon which mutations can arise, with multiple potential interactions between genetic loci. We here present a method for discerning selection from a population history that accounts for interference between mutations. Given sequences sampled from multiple time points in the history of a population, we infer selection at each locus by maximizing a likelihood function derived from a multilocus evolution model. We apply the method to the question of distinguishing between loci where new mutations are under positive selection (drivers) and loci that emit neutral mutations (passengers) in a Wright-Fisher model of evolution. Relative to an otherwise equivalent method in which the genetic background of mutations was ignored, our method inferred selection coefficients more accurately for both driver mutations evolving under clonal interference and passenger mutations reaching fixation in the population through genetic drift or hitchhiking. In a population history recorded by 750 sets of sequences of 100 individuals taken at intervals of 100 generations, a set of 50 loci were divided into drivers and passengers with a mean accuracy of >0.95 across a range of numbers of driver loci. The potential application of our model, either in full or in part, to a range of biological systems, is discussed. 相似文献
24.
The two ADF-H domains of twinfilin play functionally distinct roles in interactions with actin monomers 下载免费PDF全文
Ojala PJ Paavilainen VO Vartiainen MK Tuma R Weeds AG Lappalainen P 《Molecular biology of the cell》2002,13(11):3811-3821
Twinfilin is a ubiquitous and abundant actin monomer-binding protein that is composed of two ADF-H domains. To elucidate the role of twinfilin in actin dynamics, we examined the interactions of mouse twinfilin and its isolated ADF-H domains with G-actin. Wild-type twinfilin binds ADP-G-actin with higher affinity (K(D) = 0.05 microM) than ATP-G-actin (K(D) = 0.47 microM) under physiological ionic conditions and forms a relatively stable (k(off) = 1.8 s(-1)) complex with ADP-G-actin. Data from native PAGE and size exclusion chromatography coupled with light scattering suggest that twinfilin competes with ADF/cofilin for the high-affinity binding site on actin monomers, although at higher concentrations, twinfilin, cofilin, and actin may also form a ternary complex. By systematic deletion analysis, we show that the actin-binding activity is located entirely in the two ADF-H domains of twinfilin. Individually, these domains compete for the same binding site on actin, but the C-terminal ADF-H domain, which has >10-fold higher affinity for ADP-G-actin, is almost entirely responsible for the ability of twinfilin to increase the amount of monomeric actin in cosedimentation assays. Isolated ADF-H domains associate with ADP-G-actin with rapid second-order kinetics, whereas the association of wild-type twinfilin with G-actin exhibits kinetics consistent with a two-step binding process. These data suggest that the association with an actin monomer induces a first-order conformational change within the twinfilin molecule. On the basis of these results, we propose a kinetic model for the role of twinfilin in actin dynamics and its possible function in cells. 相似文献
25.
Mei Li Zhong Wei Jianing Wang Alexandre Jousset Ville‐Petri Friman Yangchun Xu Qirong Shen Thomas Pommier 《Ecology letters》2019,22(1):149-158
While several studies have established a positive correlation between community diversity and invasion resistance, it is less clear how species interactions within resident communities shape this process. Here, we experimentally tested how antagonistic and facilitative pairwise interactions within resident model microbial communities predict invasion by the plant–pathogenic bacterium Ralstonia solanacearum. We found that facilitative resident community interactions promoted and antagonistic interactions suppressed invasions both in the lab and in the tomato plant rhizosphere. Crucially, pairwise interactions reliably explained observed invasion outcomes also in multispecies communities, and mechanistically, this was linked to direct inhibition of the invader by antagonistic communities (antibiosis), and to a lesser degree by resource competition between members of the resident community and the invader. Together, our findings suggest that the type and strength of pairwise interactions can reliably predict the outcome of invasions in more complex multispecies communities. 相似文献
26.
Serum beta 2 microglobulin levels, measured by radioimmunoassay (Phadebas test), were found increased in acute myeloid leukemias at diagnosis. Serum beta 2 microglobulin levels were significantly higher in patients with monocytic leukemias (13 patients, M4-M5 FAB classification) than in those with other cytological types (18 patients). Beta 2 microglobulin levels at diagnosis were correlated with serum lysozyme levels, but they were not correlated with blood blast counts, serum LDH and ferritin levels. 195 serum beta 2 microglobulin measurements were made serially in 30 patients with acute myeloid leukemias in first remission. Compared to values at diagnosis, beta 2 microglobulin levels in remission were significantly decreased. Out of 30 patients in remission 12 had increased serum beta 2 microglobulin levels (greater than 3 mg/l). Serial measurements were not predictive for relapses. 相似文献
27.
Niina Tohmola Jouni Ahtinen Juha-Pekka Pitkänen Ville Parviainen Sakari Joenväärä Mika Hautamäki Peter Lindroos Jarno Mäkinen Risto Renkonen 《Biotechnology and Bioprocess Engineering》2011,16(2):264-272
We constructed a bioprocess environment enabling automatic sampling from a bioreactor combined with a compact on-line high
performance liquid chromatography (HPLC) unit. This setup allowed us to measure extracellular glucose, ethanol, glycerol,
and acetate concentrations automatically at 5 min intervals during the cultivation. This environment also provides mechanical
measurement of the optical density (OD) of cells and enables us to collect and store (−35°C) samples for further off-line
analyses. Among the available devices, the performance of the sampling-analysis unit is by far the best with regard to speed
and number of analytes. Both the sampling and analysis phases are easily controlled by software; thus, providing a unique
environment to perform various bioprocess activity tasks, whether they would be cell line screening or optimisation of conditions
for growth and productivity. Complex research set-ups can be created and continuous automated measurements empower long-term
cultivations with a time series. We provide evidence for the applicability of this environment by performing three comparable
batch cultivations with Saccharomyces cerevisiae yeast and show that both the on-line sampling and analysis modes produce reliable data for further use in the monitoring
and controlling of bioprocesses. On-line data provided new insight into the dynamics of the diauxic shift during aerobic glucose
batch cultivation. When cell growth and carbon dioxide production ceased for the first time during the diauxic shift, acetate
accumulation and consumption of the remaining glucose below 0.15 g/L continued to occur for 1 h. At the same time, glycerol
and ethanol began to be consumed. Samples were also collected during cultivation for later analysis of intracellular metabolites
and to collect more valuable information about metabolism. 相似文献
28.
Androgen receptor CAG polymorphism and prostate cancer risk 总被引:4,自引:0,他引:4
Mononen N Ikonen T Autio V Rökman A Matikainen MP Tammela TL Kallioniemi OP Koivisto PA Schleutker J 《Human genetics》2002,111(2):166-171
Recent studies have suggested that polymorphisms of the androgen receptor gene ( AR) may influence the risk of prostate cancer (PC) development and progression. Here, we analyzed the length of the CAG repeat of the AR gene in 1363 individuals, including patients with PC, benign prostate hyperplasia (BPH), and population controls. There was a tendency for short CAG repeats to be associated with PC. The Odds Ratio (OR) for PC was 1.47 ( P=0.05) when individuals with short CAG repeats (=18) were compared with those having long repeats (>18). CAG repeat length was not significantly associated with family history, disease stage, grade, age at diagnosis, prostate-specific antigen (PSA) level at diagnosis, or prognosis of the patients. Unexpectedly, short CAG repeats were significantly less common in patients with BPH compared with controls (OR=0.47, P=0.03). Our results suggest that the CAG polymorphism of the AR gene is unlikely to have a major role in the development or progression of PC in the Finnish population. The association of CAG repeats with the risk of BPH warrants further study. 相似文献
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Richard Nordenvall Shahram Bahmanyar Johanna Adami Ville M. Mattila Li Fell?nder-Tsai 《PloS one》2014,9(8)