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944.
Zhongcai Ma Kenny Y.C. Kwong David Paek 《Biochemical and biophysical research communications》2010,400(4):569-574
Plaminogen activator inhibitor-1 (PAI-1), the key physiological inhibitor of the plasmin fibrinolytic system, plays important roles in the pathogenesis of asthma. Mast cells (MCs) are crucial effector cells and a major source of PAI-1 for asthma. Cyclic adenosine monophosphate (cAMP) is the important regulator of MCs; however, its effects on PAI-1 expression in MCs remain unknown. We reported cAMP/protein kinase A pathway positively regulates PAI-1 expression through cAMP-response element binding protein binding to hypoxia response element-1 at −158 to −153 bp of human PAI-1 promoter in human MCs. Moreover, cAMP synergistically augments PAI-1 expression with ionomycin- or IgE receptor cross-linking-mediated stimulation. 相似文献
945.
Barbara Mantovani Valerio Scali 《Evolution; international journal of organic evolution》1992,46(3):783-796
In northwestern Sicily interspecific hybrid females between Bacillus rossius and B. grandii benazzii (Insecta, Phasmatodea) are sympatric with facultatively parthenogenetic demes of the former and bisexual populations of the latter. Preliminary observations suggested that hybrid females are maintained by hybridogenetic reproduction, not by current F1 hybrid production nor through parthenogenesis. Being hybridogens, a complex of hemiclonal lineages, we informally refer to them as B. rossius-grandii benazzii, according to Schultz's proposal. In this study B. rossius-g. benazzii females were crossed with males of B. g. benazzii, B. g. grandii, B. g. maretimi, and B. rossius. Allozyme analysis of the progeny showed that the great majority of them were actually produced by hybridogenesis with a hemiclonal inheritance of the maternal B. rossius genotype (Brm) and actual syngamy with a sperm from the fathering male, so that Brm-gbp, Brm-ggp, Brm-gmp, and Brm-rp offspring were obtained in the respective crosses. All-paternal progeny (androgenetics) were also produced (Bgbpgbp, Bgmpgmp, Brprp) and two gynogenetic descendants were observed. Cytological investigations on virgin eggs that failed to hatch revealed in most of them a haploid-diploid blocked blastoderm; this rudimentary parthenogenesis appears to be an important prerequisite for further evolution of this hybridogen. Reproductive modes of descendants were also analyzed; although Brm-gp hybrids are still able to reproduce by hybridogenesis, a progressive disruption of the hybridogenetic-androgenetic system takes place in synthetic B. rossius (Brm-rp, Brprp) and abundant thelytokous parthenogenetic offspring are obtained from females of androgenetic origin. The evolutionary role of these hybridogens appears to be linked to their shift towards parthenogenesis; this has apparently occurred in the southeastern Sicilian hybrid B. whitei (=B. rossius/g. grandii), which exhibits both hybridogenesis and parthenogenesis. 相似文献
946.
A novel type of DNA-binding protein interacts with a conserved sequence in an early nodulin ENOD12 promoter 总被引:3,自引:0,他引:3
947.
C. Rabarivola B. Meier C. Langer W. Scheffrahn Y. Rumpler 《Primates; journal of primatology》1996,37(2):215-225
Analysis for genetic variation of insular and mainland populations ofEulemur macaco has revealed: (1) a different degree of genetic variation between populations; and (2) the phylogenetic relationships between
groups, on the islands of Nosy-Be and Nosy-Komba, and in the Peninsula of Ambato (Madagascar). Eleven systems of blood proteins
from 157 animals were used as genetic markers. The genetic variation was lower on the island of Nosy-Komba than in the mainland
of Ambato. This is consistent with the expectation that genetic variation is lower on islands than on mainlands. In contrast,
the genetic variation on the island of Nosy-Be was the highest of the three populations. This finding can best be explained
by assuming that the sample of Nosy-Be consists of individuals of several small isolated groups, where genetic drift computation
showed the population of Nosy-Be to be distinct, and the populations of Nosy-Komba and Ambato to be close within the same
branch of the dendrogram. These findings give an insight into the population history of the island of Nosy-Komba, which might
have been populated by mainland groups from Ambato. 相似文献
948.
上海轨道交通对城市土地利用变化的影响 总被引:3,自引:0,他引:3
利用1989、2005年上海市1∶50 000彩红外航空遥感影像解译的土地利用数据,基于GIS技术,定量研究了上海轨道交通对城市土地利用动态变化的影响,并用Markov模型对研究区2010—2025年间的土地利用变化进行了初步预测.结果表明:轨道交通加快了上海市土地利用的转化,促进了以耕地为主的自然景观向居住、公共设施用地等土地获益较高的人工景观转化;轨道交通增加了研究区的土地利用程度;1989—2005年,研究区其他用地(以在建用地为主,下同)、公共设施用地、绿地、耕地、水域的转化率较大,其中,其他用地的变化速度最快,水域的变化速度最慢;2010—2025年,耕地、水域的面积和比例将继续减少,居住、公共设施用地等人工景观的面积则呈继续增加的趋势.从提高土地利用程度和土地获益的角度,轨道交通沿线的这种土地利用结构仍需要进一步调整,以增加土地的集约化程度和实现土地资源的可持续利用. 相似文献
949.
950.
Abidi O Boulouiz R Nahili H Imken L Rouba H Chafik A Barakat A 《Biochemical and biophysical research communications》2008,377(3):971-974
In Caucasian populations a single mutation, 35delG, accounts for the majority of GJB2 gene mediated hearing loss, with carrier frequencies estimated between 2-4%, possibly resulting from a founder effect rather than from a mutational hot spot. In Moroccan population, the 35delG mutation accounts for 90.8% of all GJB2 mutated alleles in deaf patients with a carrier frequency of 2.65%. The aim of this study was to evaluate whether the 35delG mutation has derived from a single origin in the Moroccan population. We enrolled 30 unrelated deaf patients homozygous for the 35delG mutation and 165 unrelated control individuals negative for this mutation, and genotyped three microsatellite markers flanking the GJB2 region: D13S141, D13S175 and D13S143. Data analysis revealed that the 35delG mutation is associated with particular alleles of these markers, with significant linkage disequilibrium for the 125 and 105 nucleotide long alleles of D13S141 and D13S175, and that a single specific haplotype accounts for 68% of the chromosomes carrying the 35delG mutation. The estimate age of 35delG mutation is 135 generations or approximately 2700 years old. Like in other Mediterranean populations, our results suggest that in the Moroccan population the 35delG mutation has derived from a single origin in a common founder process. 相似文献