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991.
Isolation of a Specialized Lambda Transducing Bacteriophage Carrying the Beta Subunit Gene for Escherichia coli Ribonucleic Acid Polymerase 总被引:45,自引:24,他引:21 下载免费PDF全文
A heat-inducible lysis-defective lambda prophage has been integrated directly into the E. coli chromosome at a site (bfe) very closely linked to the ribonucleic acid polymerase mutation rif(d), a dominant rifampin resistance allele. This unusual lysogen has facilitated the isolation of specialized transducing phages conferring rifampin resistance to sensitive cells, and carrying at least the beta subunit gene of RNA polymerase in intact form. 相似文献
992.
Light-Evoked and Spontaneous Discrete Waves in the Ventral Nerve Photoreceptor of Limulus 总被引:20,自引:19,他引:1 下载免费PDF全文
Discrete waves, recorded from the ventral nerve photoreceptor, occur in the light and in the dark. Spontaneous waves, on the average, are smaller than light-evoked waves. This suggests that not all spontaneous waves can arise from spontaneous changes in the visual pigment molecule identical to changes induced by photon absorption. Spontaneous and light-evoked waves are statistically independent of each other. This is shown by determination of frequency of response as a function of pulse energy for short pulses and determination of the distribution of intervals between waves evoked by steady lights. The available data can be explained by two models. In the first each photon produces a time-dependent excitation that goes to zero the instant the wave occurs so that the number of effective absorptions from a short light pulse equals the number of waves produced by the light pulse. In the second the excitation produced by photon absorption is unaffected by the occurrence of the waves so that the number of waves produced from a short light pulse may be different from the number of effective absorptions. Present results do not allow a choice between the two models. 相似文献
993.
994.
Kinetic modeling of [18F]VAT,a novel radioligand for positron emission tomography imaging vesicular acetylcholine transporter in non‐human primate brain 下载免费PDF全文
Hongjun Jin Xuyi Yue Hui Liu Junbin Han Hubert Flores Yi Su Stanley M. Parsons Joel S. Perlmutter Zhude Tu 《Journal of neurochemistry》2018,144(6):791-804
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996.
Invasive Ruffe (Gymnocephalus cernua) has caused substantial ecological damage in North America, parts of Western Europe, Scandinavian countries, and the United Kingdom. The objectives of this review are to define Ruffe’s native and non-native range, examine life history requirements, explore the life cycle, and differentiate between life stages. We compare data from its native and non-native ranges to determine if there are any differences in habitat, size, age, genotype, or seasonal migration. Literature from both the native and non-native ranges of Ruffe, with some rare, translated literature, is used. In each life stage, Ruffe exhibit plasticity with regard to chemical, physical, biological, and habitat requirements. Adult Ruffe has characteristics that allow them to adapt to a range of environments, including rapid maturation, relatively long life and large size (allowing them to reproduce many times in large batches), batch spawning, genotype and phenotype (having plasticity in their genetic expression), tolerance to a wide range of water quality, broad diet, and multiple dispersal periods. There is, however, variability among these characteristics between the native, non-native North American, and European non-native populations, which presents a challenge to managing populations based on life history characteristics. Monitoring and preventative strategies are important because, based on Ruffe’s variable life history strategies and its recent range expansion, all of the Laurentian Great Lakes and many other water bodies in the UK, Europe, and Norway are vulnerable to Ruffe establishment. 相似文献
997.
Andrea Gloria‐Soria Diego Ayala Ambicadutt Bheecarry Olger Calderon‐Arguedas Dave D. Chadee Marina Chiappero Maureen Coetzee Khouaildi Bin Elahee Ildefonso Fernandez‐Salas Hany A. Kamal Basile Kamgang Emad I. M. Khater Laura D. Kramer Vicki Kramer Alma Lopez‐Solis Joel Lutomiah Ademir Martins Jr Maria Victoria Micieli Christophe Paupy Alongkot Ponlawat Nil Rahola Syed Basit Rasheed Joshua B. Richardson Amag A. Saleh Rosa Maria Sanchez‐Casas Gonçalo Seixas Carla A. Sousa Walter J. Tabachnick Adriana Troyo Jeffrey R. Powell 《Molecular ecology》2016,25(21):5377-5395
Mosquitoes, especially Aedes aegypti, are becoming important models for studying invasion biology. We characterized genetic variation at 12 microsatellite loci in 79 populations of Ae. aegypti from 30 countries in six continents, and used them to infer historical and modern patterns of invasion. Our results support the two subspecies Ae. aegypti formosus and Ae. aegypti aegypti as genetically distinct units. Ae. aegypti aegypti populations outside Africa are derived from ancestral African populations and are monophyletic. The two subspecies co‐occur in both East Africa (Kenya) and West Africa (Senegal). In rural/forest settings (Rabai District of Kenya), the two subspecies remain genetically distinct, whereas in urban settings, they introgress freely. Populations outside Africa are highly genetically structured likely due to a combination of recent founder effects, discrete discontinuous habitats and low migration rates. Ancestral populations in sub‐Saharan Africa are less genetically structured, as are the populations in Asia. Introduction of Ae. aegypti to the New World coinciding with trans‐Atlantic shipping in the 16th to 18th centuries was followed by its introduction to Asia in the late 19th century from the New World or from now extinct populations in the Mediterranean Basin. Aedes mascarensis is a genetically distinct sister species to Ae. aegypti s.l. This study provides a reference database of genetic diversity that can be used to determine the likely origin of new introductions that occur regularly for this invasive species. The genetic uniqueness of many populations and regions has important implications for attempts to control Ae. aegypti, especially for the methods using genetic modification of populations. 相似文献
998.
Eun-Jin Cheon Bon-Hoon Koo Joong-Hyun Choi 《Applied psychophysiology and biofeedback》2016,41(1):103-110
The purpose of this study was to evaluate the effect of neurofeedback on depressive symptoms and electrophysiological disturbances in patients with major depressive disorder. We recruited participants suffering from depression to evaluate efficacy of left prefrontal beta with alpha/theta training. An 8-week, prospective, open-label study was undertaken. Twenty participants were recruited. The treatment protocol was twice or three times a week training of beta at F3 with alpha/theta at Pz for 8 weeks. When every visit, patients were received beta training for 30 min, and then alpha/theta training for 30 min. Baseline, 4 and 8 week scores of; the Hamilton rating scale for Depression (HAM-D), the Hamilton rating scale for Anxiety (HAM-A), the Beck Depression Inventory (BDI)-II, the Beck Anxiety Inventory (BAI), Clinical global impression-severity (CGI-S), and pre- and post-treatment resting state EEGs were compared. Interhemispheric alpha power asymmetry (A score) was computed for homologous sites F3–F4. Pre- and post-training clinical assessments revealed significant improvements in HAM–D, HAM-A, BDI, and CGI-S scores. Cumulative response rates by HAM-D were 35.0 and 75.0 % at 4 and 8 weeks, respectively, corresponding cumulative remission rates by HAM-D were 15.0 and 55.0 %, respectively. No significant differences were found between pre- and post-treatment A score. Neurofeedback treatment could improve depressive symptoms significantly. In addition, anxiety symptoms and clinical illness severity decreased significantly after neurofeedback treatment. Despite its several limitations, such as, small sample size and lack of a control group, this study suggested neurofeedback has significant effects in patients with major depressive disorder. 相似文献
999.
1000.
Joel Ramos da Palma Laura Cendron Nabil Georges Seidah Antonella Pasquato Stefan Kunz 《The Journal of biological chemistry》2016,291(5):2055-2066
The proprotein convertase subtilisin kexin isozyme-1 (SKI-1)/site-1 protease (S1P) is implicated in lipid homeostasis, the unfolded protein response, and lysosome biogenesis. The protease is further hijacked by highly pathogenic emerging viruses for the processing of their envelope glycoproteins. Zymogen activation of SKI-1/S1P requires removal of an N-terminal prodomain, by a multistep process, generating the mature enzyme. Here, we uncover a modular structure of the human SKI-1/S1P prodomain and define its function in folding and activation. We provide evidence that the N-terminal AB fragment of the prodomain represents an autonomous structural and functional unit that is necessary and sufficient for folding and partial activation. In contrast, the C-terminal BC fragment lacks a defined structure but is crucial for autoprocessing and full catalytic activity. Phylogenetic analysis revealed that the sequence of the AB domain is highly conserved, whereas the BC fragment shows considerable variation and seems even absent in some species. Notably, SKI-1/S1P of arthropods, like the fruit fly Drosophila melanogaster, contains a shorter prodomain comprised of full-length AB and truncated BC regions. Swapping the prodomain fragments between fly and human resulted in a fully mature and active SKI-1/S1P chimera. Our study suggests that primordial SKI-1/S1P likely contained a simpler prodomain consisting of the highly conserved AB fragment that represents an independent folding unit. The BC region appears as a later evolutionary acquisition, possibly allowing more subtle fine-tuning of the maturation process. 相似文献