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81.
Isolation and complete nucleotide sequence of the gene for bovine parathyroid hormone 总被引:7,自引:0,他引:7
The structure of the bovine parathyroid hormone (PTH) gene has been analyzed by Southern blot hybridization of genomic DNA and by nucleotide sequence analysis of a cloned PTH gene. In the Southern analysis, several restriction enzymes produced single fragments that hybridized to PTH cDNA suggesting that there is a single bovine PTH gene. The restriction map of the cloned gene is the same as that determined by Southern blot analysis of bovine DNA. The sequence of 3154 bp of the cloned gene has been determined including 510 bp and 139 bp in the 5' and 3' flanking regions, respectively. The gene contains two introns which separate three exons that code primarily for: (i) the 5' untranslated region, (ii) the pre-sequence of preProPTH, and (iii) PTH and the 3' untranslated region. The gene contains 68% A + T and unusually long stretches of 100- to 150-bp sequences containing alternating A and T nucleotides in the 5' flanking region and intron A. The 5' flanking region contains two TATA sequences, both of which appear to be functional as determined by S1 nuclease mapping. Compared to the rat and human genes, the locations of the introns are identical but the sizes differ. Comparable human and bovine sequences in the flanking regions and introns are about 80% homologous. 相似文献
82.
James A. McAteer Orion D. Hegre 《In vitro cellular & developmental biology. Plant》1978,14(9):795-803
Summary A method of perfusion organ culture is described in which explants cultured at the airmedium interface are bathed by a continuous
flow of nutrient medium. Morphological studies on the fetal rat lung indicate that explant development in this system is comparable
to that obtained using standard organ-culture dishes. Medium supply is easily manipulated and continuous sampling of the effluent
stream is possible without disturbing the immediate explant environment. The basic design facilitates secretory-response studies
on cultured organ explants as demonstrated by a study of glucose-stimulated insulin release by the neonatal rat pancreas.
This work was supported by U. S. Public Health Service Training Grant No. GM 00114. 相似文献
83.
Localization of retinoic acid-binding protein in nuclei 总被引:5,自引:0,他引:5
B P Sani 《Biochemical and biophysical research communications》1977,75(1):7-12
Retinoic acid-binding component has been detected in the nuclei of chick embryo skin. The physicochemical properties of this macromolecule are in agreement with the properties of the retinoic acid-binding protein isolated from tissue cytosol. Although no binding protein could be detected in normal colon or lung tissue, nuclei isolated from a transplantable colon tumor and Lewis lung carcinoma contained this protein. 相似文献
84.
Summary Insulin release and membrane potential fluctuations in response to increased extracellular potassium [K+]
o
have been measured in single perifused islets of Langerhans from normal mice. An increase in [K+]
o
from 5mm to 50mm induced a transient insulin release with a peak at about 1 min. The peak value was [K+]
o
-dependent but the half-timet
1/2 for the decline was constant at nearly 1 min. 2.5mm cobalt completely inhibited the potassium-induced stimulation of insulin release. The insulin release elicited by 28 and 50mm [K+]
o
was similar in terms of peak, total release and half-time from maximum release. Stepwise increase in [K+]
o
from 10 to 28 to 50mm resulted in a normal response to 28mm but no peak of release after the 28 to 50mm increase. The results indicate good correlation between excess voltage noise, thought to reflect calcium channel activity, and insulin release evoked by changing extracellular potassium. 相似文献
85.
Chondrocytes obtained from epiphyseal cartilage of fetal guinea pigs or ear cartilage of young rabbits were cultured in monolayer. The influence of colchicine, cytochalasin B, and p-nitrophenyl-β-d-xylopyranoside on secretion of proteoglycans was investigated. Radioactive sulfate was used as a precursor. As observed previously in other systems, β-d-xylosides initiated the synthesis of free chondroitin sulfate chains, competing with the endogenous proteoglycan core protein acceptor. The molecular weights of the chondroitin sulfate chains synthesized both on the xyloside and on the core-protein acceptor in maximally stimulated cells were similar and significantly lower than in proteoglycans synthesized in the absence of xyloside. The size of the chondroitin sulfate chains synthesized on the xyloside was inversely related to the concentration of this compound. This finding suggests that the chain length is dependent on the ratio between available acceptor and chain-lengthening enzymes or precursors. Cytochalasin B, a microfilament-modifying agent, inhibited proteoglycan synthesis, without any effect on secretion. Cells treated with cytochalasin B could be stimulated with β-d-xyloside to synthesize free chondroitin sulfate chains to the same relative degree as cells with intact microfilaments. Colchicine, an antimicrotubular agent, partially inhibited synthesis and secretion of proteoglycan. However, cells treated with colchicine could be stimulated with β-d-xyloside to synthesize and secrete free chondroitin sulfate chains to about the same relative degree as cells with intact microtubules. The data suggest that microtubules may have a facilitatory rather than an obligatory role in the secretion of proteoglycans and that at least part of the effect of colchicine is located at or after the site of glycosaminoglycan synthesis. 相似文献
86.
Effect of bombesin upon plasma somatostatin-like immunoreactivity, insulin and glucagon in normal and chemically sympathectomized dogs 总被引:2,自引:0,他引:2
The present study was designed to determine the effects of intravenously infused bombesin (10 ng/kg/min) upon basal and postprandial plasma somatostatin-like immunoreactivity (SLI), glucagon, insulin and triglyceride levels in normal (n = 12) and chemically sympathectomized (n = 11) dogs. Basal plasma SLI, glucagon and insulin levels rose significantly during the infusion of bombesin in the normal dogs, and this was not altered by chemical sympathectomy. Bombesin infusion enhanced the postprandial SLI response, while attenuating the postprandial glucagon response by 50% and the insulin response in the early postprandial phase of the meal. Sympathectomy did not significantly alter the basal levels of these polypeptides, but augmented the postprandial plasma SLI response during the first 90 min, and reduced the postprandial glucagon response during the infusion of bombesin. The postprandial insulin response was not affected by sympathectomy. In both normal and chemically sympathectomized dogs the rise in postprandial triglyceride levels was attenuated by bombesin infusion. 相似文献
87.
Hexokinase is present in the tissues in four isoenzymic forms. Cerebral tissue contains predominantly Type I hexokinase which
is believed to be insulin-insensitive. In cerebral tissue about 60 to 70% of the hexokinase is bound to the particulate fraction.
The changes in the distribution of hexokinase Type I and Type II together with the bound and free hexokinase have been studied
in control, diabetic and diabetic animals treated with insulin. The results indicate that the presence of insulin is essential
for the normal binding of the hexokinase to the particulate fraction. In heart tissue, Type II hexokinase bound to the pellet
shows a significant decrease in diabetes, which is reversed on insulin administration. 相似文献
88.
The immune responses to several antigens were compared in the I-A mutant mouse strain B6.C-H-2bm12 and the wild-type strain C57BL/6. With a lymph node cell proliferation assay, the response to two of these antigens, beef insulin and (TG)A-L, was demonstrated to be controlled by a gene in the I-Ab region. B6.C-H-2bm12 mice failed to respond to beef insulin, while their responses to (TG)A-L, DNP-OVA and PPD were comparable with those of the wild-type strain C57BL/6. Taken together with previous studies, these data suggest that the product of a single pleiotropic I-A gene, an la molecule, functions as a histocompatibility, la, and MLR antigen, as well as a necessary component for Ir gene function. Furthermore, the data reported here demonstrate that la molecules have multiple functional “Ir determinants,” one of which has been altered in the B6.C-H-2bm12 mutant. The B6.C-H-2bm12 mice, therefore, represent a powerful analytical tool for the understanding of the cellular and molecular basis for Ir gene control of the immune response. 相似文献
89.
A review of experimental studies of the effect of zinc nutrition on insulin metabolism is presented. In addition to a short
introduction to the synthesis, secretion, and action of insulin, the effects of zinc deficiency—specifically on glucose tolerance,
insulin secretion, insulin synthesis and storage, and on total insulin-like activity—are dealt with. The concentrations of
zinc and chromium in serum, pancreas, and liver are compared to those of zinc-deficient animals and pair-fed controls.
In contrast to pair-fed controls, zinc-deficient rats had unaltered proinsulin contents after glucose stimulation, but they
showed a diminished glucose tolerance, lowered serum insulin content, and an elevated total insulin-like activity. The serum
zinc concentration of the deficient animals was greatly reduced and did not change during glucose stimulation, whereas it
rose in the case of the pair-fed controls. The serum chromium concentration increased in both groups in response to glucose
stimulation. In the pancreas of the deficient animals, the zinc concentration was reduced 60% and it increased during the
glucose tolerance test. In the liver there were no significant differences. The chromium concentrations were elevated in both
the pancreas and liver of the zinc-deficient rats by 60 and 100%, respectively, and were not influenced by glucose injection.
These studies show clearly that nutritional zinc deficiency influences insulin metabolism and action. 相似文献
90.
Eight Billroth II resected patients and 8 normal controls were given two oral glucose loads, one ingested within 2 min, and the other ingested slowly over 80 min. In the Billroth II resected group, the integrated plasma GIP release was significantly higher after the fast than after the slow glucose ingestion. In this group the integrated plasma GIP release was also significantly higher than in the control group, but only after the fast glucose ingestion. These findings indicate that the rate of glucose delivery into the intestine may be of importance in the plasma GIP response to oral glucose. 相似文献