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71.
Autologous disc cell implantation, growth factors and gene therapy appear to be promising therapies for disc regeneration. Unfortunately, the replicative lifespan and growth kinetics of human nucleus pulposus (NP) cells related to host age are unclear. We investigated the potential relations among age, replicative lifespan and growth rate of NP cells, and determined the age range that is suitable for cell-based biological therapies for degenerative disc diseases. We used NP tissues classified by decade into five age groups: 30s, 40s, 50s, 60s and 70s. The mean cumulative population doubling level (PDL) and population doubling rate (PDR) of NP cells were assessed by decade. We also investigated correlations between cumulative PDL and age, and between PDR and age. The mean cumulative PDL and PDR decreased significantly in patients in their 60s. The mean cumulative PDL and PDR in the younger groups (30s, 40s and 50s) were significantly higher than those in the older groups (60s and 70s). There also were significant negative correlations between cumulative PDL and age, and between PDR and age. We found that the replicative lifespan and growth rate of human NP cells decreased with age. The replicative potential of NP cells decreased significantly in patients 60 years old and older. Young individuals less than 60 years old may be suitable candidates for NP cell-based biological therapies for treating degenerative disc diseases.  相似文献   
72.
The course of the vascular system in the proximal end of Dolerotheca formosa is described. Vascular bundles flare outward and downward immediately upon entering from the peduncle. These bundles are located in radiating septa just beneath the cover and give off small lateral bundles pinnately. Laterals from adjacent septal bundles meet, fuse, and extend downward in the parenchyma plate separating paired sporangia. The septal bundles, therefore, alternate in position with the parenchyma plate bundles and are interpreted as remnants of an ancestral bifurcating pinna system, which bore pendent sporangia along each side of supporting rachises. This interpretation differs from both the Codonotheca aggregation and plicated Whittleseya hypotheses recently advanced to explain the evolutionary pathway by which this complex pteridosperm pollen organ evolved.  相似文献   
73.
Capsule In years with low vole abundance birds visited hunting grounds more frequently and for longer.

Aims To describe diet composition, hunting behaviour, habitat choice and reproductive success of urban Kestrels during changing vole abundance.

Methods For five years, we studied the hunting effort of Kestrels in a medium-sized city during the breeding season. Pitfall traps were used for determining vole abundance. Kestrel diet composition was determined from pellet analyses. The number of eggs and offspring was recorded during at least two consecutive visits for each nest and each breeding stage.

Results In contrast to larger European cities, the Common Vole Microtus arvalis was a key part of the Kestrels' diet and did not fluctuate significantly according to vole availability. Reproductive success was quite high and stable throughout years with different vole abundance. In years of low vole abundance, the arrival frequency at hunting grounds and time spent there increased. During years with a low vole population, Kestrels had less hunting success and the rate of successful visits decreased. Therefore, Kestrels probably had to change hunting grounds more frequently. During low vole years Kestrels used less demanding techniques, e.g. perching, despite the lower success of these hunting techniques, to avoid extremely high energetic costs.

Conclusions An increase in hunting helps to maintain a proper diet and consequently reproductive success. Vole abundance did not change dramatically during the study period, as reported by studies from western and northern Europe. The proportion of ruderal habitats on the city periphery is higher than in more monotonous farmland habitats. Ruderal habitats can be important when Kestrels look for mammals other than voles, especially during vole scarcity.  相似文献   
74.
Endo- β-N-acetylgucosaminidases (ENGases) are the enzymes that catalyze both hydrolysis and transglycosylation reactions. It is of interest to study ENGases because of their ability to synthesize glycopeptides. Homology models of Human, Arabidopsis thaliana and Sorghum ENGases were developed and their active sites marked based on information available from Arthrobacter protophormiae (PDB ID: 3FHQ) ENGase. Further, these models were docked with the natural substrate GlcNAc-Asn and the inhibitor Man3GlcNAc-thiazoline. The catalytic triad of Asn, Glu and Tyr (N171, E173 and Y205 of bacteria) were found to be conserved across the phyla. The crucial Y299F mutation showing 3 times higher transglycosylation activity than in wild type Endo-A is known. The hydrolytic activity remained unchanged in bacteria, while the transglycosylation activity increased. This Y to F change is found to be naturally evolved and should be attributing higher transglycosylation rates in human and Arabidopsis thaliana ENGases. Ligand interactions Ligplots revealed the interaction of amino acids with hydrophobic side chains and polar uncharged side chain amino acids. Thus, structure based molecular model-ligand interactions provide insights into the catalytic mechanism of ENGases and assist in the rational engineering of ENGases.  相似文献   
75.
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