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81.
Elizabeth M. P. Madin Joshua S. Madin Aaron M. T. Harmer Neville S. Barrett David J. Booth M. Julian Caley Alistair J. Cheal Graham J. Edgar Michael J. Emslie Steven D. Gaines Hugh P. A. Sweatman 《Ecology and evolution》2020,10(14):6954-6966
The relative roles of top‐down (consumer‐driven) and bottom‐up (resource‐driven) forcing in exploited marine ecosystems have been much debated. Examples from a variety of marine systems of exploitation‐induced, top‐down trophic forcing have led to a general view that human‐induced predator perturbations can disrupt entire marine food webs, yet other studies that have found no such evidence provide a counterpoint. Though evidence continues to emerge, an unresolved debate exists regarding both the relative roles of top‐down versus bottom‐up forcing and the capacity of human exploitation to instigate top‐down, community‐level effects. Using time‐series data for 104 reef communities spanning tropical to temperate Australia from 1992 to 2013, we aimed to quantify relationships among long‐term trophic group population density trends, latitude, and exploitation status over a continental‐scale biogeographic range. Specifically, we amalgamated two long‐term monitoring databases of marine community dynamics to test for significant positive or negative trends in density of each of three key trophic levels (predators, herbivores, and algae) across the entire time series at each of the 104 locations. We found that trophic control tended toward bottom‐up driven in tropical systems and top‐down driven in temperate systems. Further, alternating long‐term population trends across multiple trophic levels (a method of identifying trophic cascades), presumably due to top‐down trophic forcing, occurred in roughly fifteen percent of locations where the prerequisite significant predator trends occurred. Such alternating trophic trends were significantly more likely to occur at locations with increasing predator densities over time. Within these locations, we found a marked latitudinal gradient in the prevalence of long‐term, alternating trophic group trends, from rare in the tropics (<5% of cases) to relatively common in temperate areas (~45%). Lastly, the strongest trends in predator and algal density occurred in older no‐take marine reserves; however, exploitation status did not affect the likelihood of alternating long‐term trophic group trends occurring. Our data suggest that the type and degree of trophic forcing in this system are likely related to one or more covariates of latitude, and that ecosystem resiliency to top‐down control does not universally vary in this system based on exploitation level. 相似文献
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83.
Stephanie Ringeissen Susan C Connor H Roger Brown Brian C Sweatman Mark P Hodson Steve P Kenny Richard I Haworth Paul McGill Mark A Price Mike C Aylott Derek J Nunez John N Haselden Catherine J Waterfield 《Biomarkers》2003,8(3-4):240-271
This study identified two potential novel biomarkers of peroxisome proliferation in the rat. Three peroxisome proliferator-activated receptor (PPAR) ligands, chosen for their high selectivity towards the PPARalpha, -delta and -gamma subtypes, were given to rats twice daily for 7 days at doses known to cause a pharmacological effect or peroxisome proliferation. Fenofibrate was used as a positive control. Daily treatment with the PPARalpha and -delta agonists produced peroxisome proliferation and liver hypertrophy. 1H nuclear magnetic resonance spectroscopy and multivariate statistical data analysis of urinary spectra from animals given the PPARalpha and -delta agonists identified two new potential biomarkers of peroxisome proliferation--N-methylnicotinamide (NMN) and N-methyl-4-pyridone-3-carboxamide (4PY)--both endproducts of the tryptophan-nicotinamide adenine dinucleotide (NAD+) pathway. After 7 days, excretion of NMN and 4PY increased 24- and three-fold, respectively, following high doses of fenofibrate. The correlation between total NMN excretion over 7 days and the peroxisome count was r=0.87 (r2=0.76). Plasma NMN, measured using a sensitive high performance liquid chromatography method, was increased up to 61-fold after 7 days' treatment with high doses of fenofibrate. Hepatic gene expression of aminocarboxymuconate-semialdehyde decarboxylase (EC 4.1.1.45) was downregulated following treatment with the PPARalpha and -delta agonists. The decrease was up to 11-fold compared with controls in the groups treated with high doses of fenofibrate. This supports the link between increased NMN and 4PY excretion and regulation of the tryptophan-NAD+ pathway in the liver. In conclusion, NMN, and possibly other metabolites in the pathway, are potential non-invasive surrogate biomarkers of peroxisome proliferation in the rat. 相似文献
84.
Thirty-three dairy farms in the Norwegian counties of ?stfold and Akershus in which cubicle sheds had been in use for at least
one year and with a herd size of less than 60 cows, were contacted and asked to participate in a study. The study focused
on heifers' use of cubicles and concentrate dispenser just after being transferred from rearing accommodation to the milking
herd. For each heifer, the farmer recorded cubicle use once nightly between 9 and 11 pm. The daily amount of concentrate released
in the dispenser and the allotted daily ration were also recorded. The recording period was 15 consecutive days for cubicle
use and 7 days for concentrate dispenser use. Cubicle refusal behaviour, i.e. lying outside the cubicles, was analysed by
logistic regression using rearing accommodation of heifers, herd size, heifer age, and housing layout as independent variables,
and herd as a clustering variable. On Day 2 after transfer, 34% of the heifers were showing cubicle refusal behaviour (N =
340). By Day 15 this percentage had dropped to 23. Cubicle refusal was lower throughout the whole period among heifers which
used the cubicles on the 3 first days after transfer compared to those which did not. This tendency could also be detected
several months later. The analysis showed cubicle refusal to be significantly associated with rearing accommodation (OR =
6.1, c.i.95%OR = 1.5–24.3, P = 0.01) and cubicle layout in the shed (OR = 0.2, c.i.95%OR = 0.0–0.7, P = 0.01). None of the tested variables were found to be significant for failure to use the concentrate dispenser,
a behaviour which was less frequent than cubicle refusal. However, 8 percent of the heifers did not visit the dispenser at
all throughout the 7 days of observation. 相似文献
85.
Salek RM Colebrooke RE Macintosh R Lynch PJ Sweatman BC Emson PC Griffin JL 《Neurochemical research》2008,33(2):292-300
The vesicular monoamine transporter 2 (VMAT2) sequesters monoamines into synaptic vesicles in preparation for neurotransmission.
Samples of cerebellum, cortex, hippocampus, substantia nigra and striatum from VMAT2-deficient mice were compared to age-matched
control mice. Multivariate statistical analyses of 1H NMR spectral profiles separated VMAT2-deficient mice from controls for all five brain regions. Although the data show that
metabolic alterations are region- and age-specific, in general, analyses indicated decreases in the concentrations of taurine
and creatine/phosphocreatine and increases in glutamate and N-acetyl aspartate in VMAT2-deficient mouse brain tissues. This study demonstrates the efficacy of metabolomics as a functional
genomics phenotyping tool for mouse models of neurological disorders, and indicates that mild reductions in the expression
of VMAT2 affect normal brain metabolism.
Special issue article in honor of Dr. Frode Fonnum. 相似文献
86.
Improved quantification of cell survival on stromal monolayers by flow cytometric analyses 总被引:1,自引:0,他引:1
BACKGROUND: The ex vivo survival of leukemic cells maintained on bone marrow stroma is an important tool for the investigation of cell survival and leukemogenesis. Currently, ex vivo survival of leukemic cell survival is measured by coculture on stromal cell monolayers. In these assays, we postulated that two important sources of error might be introduced through either variations in flow volume or in donor stromal cells. METHODS: A previously reported coculture assay that maintains leukemic cells on bone marrow stromal cells was employed. RESULTS: We identified two means of optimizing the coculture assay. First, biologically inert beads having well-characterized fluorescent properties were added to each sample to mathematically adjust for flow-based variations in volume acquisition. The inclusion of fluorescent beads to the basic stromal cell assay showed a significantly lower coefficient of variation as compared to samples analyzed without beads or manually counted using a hemacytometer. Second, in order to minimize variability in bone marrow hematopoietic function between donors, an adherent stromal cell line known to support hematopoiesis (HS-5) was used. When normal human donor stromal cells were used, variability in the survival of leukemic cells was observed on stromal cells derived from different donors. In contrast, statistically significant variability in survival of leukemic cells was not seen on HS-5 monolayers. Finally, we demonstrate that patient-derived leukemic samples may be examined for cell survival using these modifications. CONCLUSIONS: The novel use of fluorescent beads and a hematopoietic-supportive stromal cell line together makes the quantification of stroma-supported cell survival more reproducible, accurate, and amenable to patient-derived samples. These improvements in flow cytometry-based cell quantification are an important step in establishing a role for stromal cell assays in the study of leukemia biology and therapy. 相似文献
87.
Peter J. Edmunds Mehdi Adjeroud Marissa L. Baskett Iliana B. Baums Ann F. Budd Robert C. Carpenter Nicholas S. Fabina Tung-Yung Fan Erik C. Franklin Kevin Gross Xueying Han Lianne Jacobson James S. Klaus Tim R. McClanahan Jennifer K. O'Leary Madeleine J. H. van Oppen Xavier Pochon Hollie M. Putnam Tyler B. Smith Michael Stat Hugh Sweatman Robert van Woesik Ruth D. Gates 《PloS one》2014,9(10)
The reduction in coral cover on many contemporary tropical reefs suggests a different set of coral community assemblages will dominate future reefs. To evaluate the capacity of reef corals to persist over various time scales, we examined coral community dynamics in contemporary, fossil, and simulated future coral reef ecosystems. Based on studies between 1987 and 2012 at two locations in the Caribbean, and between 1981 and 2013 at five locations in the Indo-Pacific, we show that many coral genera declined in abundance, some showed no change in abundance, and a few coral genera increased in abundance. Whether the abundance of a genus declined, increased, or was conserved, was independent of coral family. An analysis of fossil-reef communities in the Caribbean revealed changes in numerical dominance and relative abundances of coral genera, and demonstrated that neither dominance nor taxon was associated with persistence. As coral family was a poor predictor of performance on contemporary reefs, a trait-based, dynamic, multi-patch model was developed to explore the phenotypic basis of ecological performance in a warmer future. Sensitivity analyses revealed that upon exposure to thermal stress, thermal tolerance, growth rate, and longevity were the most important predictors of coral persistence. Together, our results underscore the high variation in the rates and direction of change in coral abundances on contemporary and fossil reefs. Given this variation, it remains possible that coral reefs will be populated by a subset of the present coral fauna in a future that is warmer than the recent past. 相似文献
88.
A 36-year-old man suffering from chronic myeloid leukemia (in chronic phase) was initially treated with busulphan. At the
end of 6 months of follow-up he developed bone marrow aplasia. He was given single foetal liver infusion therapy. The patient
recovered fully from aplasia. He continued in chronic phase for more than 7 years with intermittent busulphan therapy. 相似文献
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