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41.
The effective population size of Anopheles gambiae in Kenya: implications for population structure 总被引:4,自引:0,他引:4
We estimated current and long-term effective population size (Ne) of two
Anopheles gambiae (savanna cytotype) populations in Kenya. Temporal
variation at nine microsatellite loci in each population sampled 7 and 9
years apart and genetic diversity in each sample were analyzed to answer
the following questions. (1) Do bottlenecks occur in Kenyan populations of
A. gambiae? (2) How variable are different populations with respect to
their current and long-term Ne values? (3) What are the implications of
these results on population structure and history? The estimates of Ne of
Asembo and Jego were 6,359 and 4,258, respectively, and the lower 95%
limits were 2,455 and 1,669, respectively. Thus, despite the typical
observation of low density at the village level during the dry season,
large populations are maintained annually. Large current Ne is consistent
with previous studies showing low differentiation across the continent,
especially under Wright's isolation-by-distance model. Current Ne in Asembo
was 1.5-fold higher than in Jego, but this difference was not significant.
Long-term Ne in Asembo (22,667) was 2.9-fold higher than that in Jego
(7,855) based on the stepwise mutation model. The difference between
populations was significant at both time points regardless of whether
long-term Ne values were calculated based on the stepwise mutation model or
the infinite-alleles model. Heterozygosity in Jego declined significantly
between 1987 (59%) and 1996 (54%), whereas heterozygosity in Asembo was
stable (66%-65%). Despite the relatively high and significant
differentiation between Asembo and Jego (FST = 0.072-0.10, RST = 0.037-
0.038), all alleles in Jego were found in Asembo but not vice versa. All of
these findings suggest that lower Ne in Jego magnifies differentiation
between the two populations. The long-term Ne was biased downward, because
its calculation was based on an upper bound estimate of microsatellite
mutation rate. Ne values based on mtDNA and allozymes were an order of
magnitude higher. Long-term Ne therefore, is probably measured in hundreds
of thousands and hence does not support a recent expansion of this species
from a small population.
相似文献
42.
The plasmalemma and hyaline ectoplasm together constitute the sensory and motor organ of macrophages. The purpose of this study was to isolate this cell fraction in order to analyze it biochemically and functionally. Brief sonification of warmed rabbit lung macrophages caused release of heterodisperse hyaline blebs and filopodia, which were easily collected by differential centrifugation. Viewed in the electron microscope, these structures consisted of membrane-bounded sacs principally containing actin filaments. Some contained secondary lysosomes. They were enriched threefold over whole cell homogenates in specific adenylate cyclase activity and in trichloroacetic-acid-precipitable (125)I when derived from cells labeled with 125(I) by means of a lactoperoxidase-catalyzed reaction. These markers were found to have identical isopycnic densitites when macrophage homogenates were subjected to sedimentation in a focusing sucrose density gradient system, and these markers had densities distinct from those of other cytoplasmic organelles. These markers were therefore assumed to be associated with macrophage plasma membranes. The specific β- glucuronidase activity of the bleb fraction was similar to that of homogenates, but the blebs had considerably lower specific succinic dehydrogenase activity and RNA content, and DNA was undetectable. Electrophoresis of blebs solubilized in sodium dodecyl sulfate on polyacrylamide gels revealed polypeptides co-migrating with macrophage actin-binding protein, myosin, and actin; blebs also had EDTA-activated adenosine triphosphatase activity characteristic of myosin. The concentrations of actin-binding protein and myosin were higher in blebs than in cells or cytoplasmic extracts, whereas actin concentrations were similar (relative to extracts) or only slightly greater (than in cells). Blebs and intact cells had high lactate dehydrogenase activities in the presence but not the absence of Triton X-100. Blebs and cells oxidased 1-[(14)C]glucose, and the rate of glucose oxidation was increased substantially in the presence of latex beads. We conclude that intact sacs of plasmalemma encasing contractile proteins and cytoplasmic enzymes can be isolated from macrophages. They are enriched in myosin and actin-binding protein, indicating that the contractile apparatus is regulated in the cell periphery. These structures have the capacity to respond to environmental signals. We suggest the name "podosomes" for them because of their resemblance to macrophage pseudopodia. We propose that podosome formation results from rapid dissolution of the cortical gel when the membrane is in an actively extended configuration. 相似文献
43.
44.
Thompson-Torgerson CS Holowatz LA Flavahan NA Kenney WL 《American journal of physiology. Heart and circulatory physiology》2007,292(4):H1700-H1705
Cutaneous vasoconstriction (VC) is the initial thermoregulatory response to cold exposure and can be elicited through either whole body or localized skin cooling. However, the mechanisms governing local cold-induced VC are not well understood. We tested the hypothesis that Rho kinase participates in local cold-induced cutaneous VC. In seven men and women (20-27 yr of age), up to four ventral forearm skin sites were instrumented with intradermal microdialysis fibers for localized drug delivery during cooling. Skin blood flow was monitored at each site with laser-Doppler flowmetry while local skin temperature was decreased and maintained at 24 degrees C for 40 min. Cutaneous vascular conductance (CVC; laser-Doppler flowmetry/mean arterial pressure) was expressed as percent change from 34 degrees C baseline. During the first 5 min of cooling, CVC decreased at control sites (lactated Ringer solution) to -45 +/- 6% (P < 0.001), increased at adrenoceptor-antagonized sites (yohimbine + propranolol) to 15 +/- 14% (P = 0.002), and remained unchanged at both Rho kinase-inhibited (fasudil) and adrenoceptor-antagonized + Rho kinase-inhibited sites (yohimbine + propranolol + fasudil) (-9 +/- 1%, P = 0.4 and -6 +/- 2%, P = 0.4, respectively). During the last 5 min of cooling, CVC further decreased at all sites when compared with baseline values (control, -77 +/- 4%, P < 0.001; adrenoceptor antagonized, -61 +/- 3%, P < 0.001; Rho kinase inhibited, -34 +/- 7%, P < 0.001; and adrenoceptor antagonized + Rho kinase inhibited sites, -35 +/- 3%, P < 0.001). Rho kinase-inhibited and combined treatment sites were significantly attenuated when compared with both adrenoceptor-antagonized (P < 0.01) and control sites (P < 0.0001). Rho kinase mediates both early- and late-phase cold-induced VC, supporting in vitro findings and providing a putative mechanism through which both adrenergic and nonadrenergic cold-induced VC occurs in an in vivo human thermoregulatory model. 相似文献
45.
Arvid WA Kamps Dick Hendriks Jan W Smit Edo Vellenga 《Cancer immunology, immunotherapy : CII》1999,16(1):46-52
The present study focused on whether it is possible to expand monocytic cells from CD34+ progenitor cells by using macrophage colony-stimulating factor (M-CSF) in the absence and presence of mast cell growth factor
(MGF) and IL-6. It was demonstrated that CD34+ cells differentiate without expansion to functional mature monocytic cells in the presence of M-CSF or combinations of M-CSF
plus IL-6 and MGF. A different response pattern was observed for the number of clonogenic cells. The addition of IL-6 or both
IL-6 and MGF to M-CSF containing cultures resulted in significant higher numbers of colony-forming unit-macrophage (CFU-M)
as tested in clonogenic and3H-thymidine assays. Furthermore, M-CSF plus both IL-6 and MGF appeared to be the most potent combination to preserve the monocytic
precursor in cell suspension culture assays. These results indicate that IL-6 and MGF in conjunction with M-CSF affect CD34+ cells especially at precursor level without distinct effect on the more mature stages. Secondly we studied whether M-CSF
is only critical for the monocytic lineage or also affects dendritic cell (DC) development. Indeed, we were able to culture
CD83+ DC from CD34+ progenitor cells in the presence of M-CSF in conjunction with TNF-α, IL-4, and MGF although their absolute number is almost
threefold lower than the number of CD83+ cells yielded from GM-CSF plus TNF-α, IL-4, and MGF stimulated CD34+ cells. 相似文献
46.
A gas chromatographic-electron capture detection (GC-ECD) method for the analysis of deoxynivalenol (DON) in cereals was investigated.
The sample was extracted with a mixture of acetonitrile-water and purified with a MycoSep #225 column. The silylation was
performed with Tri-Sil-TBT reagent, followed by dilution with hexane and a washing step with buffer. By using Tri-Sil-TBT
reagent no double peaks were observed for DON in the gas chromatograms, in comparison with two other silylation reagents TMSI
and Tri-Sil-Z. The use of trichothecolone (TRI) as an internal standard for DON was studied in order to indicate possible
problems in the derivatisation reaction. TRI proved to be a relatively good internal standard for DON in cereal samples, as
well as 1,1-bis-(4-chlorophenyl)-2,2-dichloroethylene (DDE), which was used as a GC standard for ensuring the function of
GC-ECD. During the study, a matrix effect was clearly observed between the cereal matrix-assisted calibration curve and the
calibration curve prepared without cereal matrix. The results of spiked and reference material samples, quantified with the
calibration curve prepared without and with matrix, demonstrated that the matrix affects the results. However, after recovery
correction the results were comparable. The validation results demonstrated that the GC-ECD method for DON analysis in cereals
is sufficiently reliable. 相似文献
47.
Corry-Anke Brandsma Machteld N Hylkema Barry WA van der Strate Dirk-Jan Slebos Marjan A Luinge Marie Geerlings Wim Timens Dirkje S Postma Huib AM Kerstjens 《Respiratory research》2008,9(1):17
Background
Smoking is the most important cause for the development of COPD. Since not all smokers develop COPD, it is obvious that other factors must be involved in disease development. We hypothesize that heme oxygenase-1 (HO-1), a protective enzyme against oxidative stress and inflammation, is insufficiently upregulated in COPD.The effects of HO-1 modulation on cigarette smoke induced inflammation and emphysema were tested in a smoking mouse model.Methods
Mice were either exposed or sham exposed to cigarette smoke exposure for 20 weeks. Cobalt protoporphyrin or tin protoporphyrin was injected during this period to induce or inhibit HO-1 activity, respectively. Afterwards, emphysema development, levels of inflammatory cells and cytokines, and the presence of B-cell infiltrates in lung tissue were analyzed.Results
Smoke exposure induced emphysema and increased the numbers of inflammatory cells and numbers of B-cell infiltrates, as well as the levels of inflammatory cytokines in lung tissue. HO-1 modulation had no effects on smoke induced emphysema development, or the increases in neutrophils and macrophages and inflammatory cytokines. Interestingly, HO-1 induction prevented the development of smoke induced B-cell infiltrates and increased the levels of CD4+CD25+ T cells and Foxp3 positive cells in the lungs. Additionally, the CD4+CD25+ T cells correlated positively with the number of Foxp3 positive cells in lung tissue, indicating that these cells were regulatory T cells.Conclusion
These results support the concept that HO-1 expression influences regulatory T cells and indicates that this mechanism is involved in the suppression of smoke induced B-cell infiltrates. The translation of this interaction to human COPD should now be pursued. 相似文献48.
Naeem A. Ali Alice A. Gaughan Charles G. Orosz Chris P. Baran Sara McMaken Yijie Wang Timothy D. Eubank Melissa Hunter Frank J. Lichtenberger Nicholas A. Flavahan Jack Lawler Clay B. Marsh 《PloS one》2008,3(4)
Latency Associated Peptide (LAP) binds TGF-β1, forming a latent complex.
Currently, LAP is presumed to function only as a sequestering agent for active
TGF-β1. Previous work shows that LAP can induce epithelial cell
migration, but effects on leukocytes have not been reported. Because of the
multiplicity of immunologic processes in which TGF-β1 plays a role, we
hypothesized that LAP could function independently to modulate immune responses.
In separate experiments we found that LAP promoted chemotaxis of human monocytes
and blocked inflammation in vivo in a murine model of the
delayed-type hypersensitivity response (DTHR). These effects did not involve
TGF-β1 activity. Further studies revealed that disruption of specific
LAP-thrombospondin-1 (TSP-1) interactions prevented LAP-induced responses. The
effect of LAP on DTH inhibition depended on IL-10. These data support a novel
role for LAP in regulating monocyte trafficking and immune modulation. 相似文献
49.
High risk populations and HIV-1 infection in China 总被引:1,自引:0,他引:1
Tuo Fu ZHU- * Chun Hui WANG Peng LIN Na HE Departments of Laboratory Medicine Departments of Microbiology University of Washington School of Medicine Seattle WA USA Programs in Infectious Diseases Fred Hutchinson Cancer Research Center Seattle WA - USA Guangdong Center for Disease Control Prevention Guangzhou China School of Public Health Fudan University Shanghai China 《Cell research》2005,(Z1)
INTRODUCTION HIV has spread to all of China’s 31 provinces, autono- mous regions and municipalities, creating one of the fast- est-growing HIV/AIDS epidemics in the world [1,2]. The HIV/AIDS epidemic in China has gone through three phases: the Entry Phase (1985 -1988), the Spreading Phase (1989-1994) and the Expansion Phase (1995- present). The striking increase of HIV-1 infections over the past few years may herald entry into a new fourth phase that will include much larger nu… 相似文献
50.
K Krajnak R G Dong S Flavahan D Welcome N A Flavahan 《Journal of applied physiology》2006,100(4):1230-1237
The vascular symptoms of hand-arm vibration syndrome, including cold-induced vasospasm, are in part mediated by increased sensitivity of cutaneous arteries to sympathetic stimulation. The goal of the present study was to use a rat tail model to analyze the effects of vibration on vascular function and alpha-adrenoceptor (AR) responsiveness. Rats were exposed to a single period of vibration (4 h, 125 Hz, constant acceleration 49 m/s2 root mean square). The physical or biodynamic response of the tail demonstrated increased transmissibility or resonance at this frequency, similar to that observed during vibration of human fingers. Morphological analysis demonstrated that vibration did not appear to cause structural injury to vascular cells. In vitro analysis of vascular function demonstrated that constriction to the alpha1-AR agonist phenylephrine was similar in vibrated and control arteries. In contrast, constriction to the alpha2-AR agonist UK14304 was increased in vibrated compared with control arteries, both in endothelium-containing or endothelium-denuded arteries. The alpha2C-AR antagonist MK912 (3 x 10(-10) M) inhibited constriction to UK14304 in vibrated but not control arteries, reversing the vibration-induced increase in alpha2-AR activity. Moderate cooling (to 28 degrees C) increased constriction to the alpha2-AR agonist in control and vibrated arteries, but the magnitude of the amplification was less in vibrated compared with control arteries. Endothelium-dependent relaxation to acetylcholine was similar in control and vibrated arteries. Based on these results, we conclude that a single exposure to vibration caused a persistent increase in alpha2C-AR-mediated vasoconstriction, which may contribute to the pathogenesis of vibration-induced vascular disease. 相似文献