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31.
Ansari , A. Q., and W. E. Loomis . (Iowa State University, Ames.) Leaf temperatures. Amer. Jour. Bot. 46(10): 713–717. Illus. 1959.—Leaf temperatures were measured with a thermocouple and potentiometer. Readings were taken on leaves of varying thickness, under varying environmental and plant conditions, and during alternating heating and cooling cycles in sun and shade. Leaves tended to assume air temperature. Sunshine heated thin leaves 6–10°C. above the air in about 1 min. Very thick leaves were heated 20°C. above air in 20–30 min. Cooling in still air in shade was at the same rate as heating in sunshine, and the product of this rate times leaf mass in g./cm.2 was constant for all leaves tested. Wind at 5 m.p.h. lowered leaf temperature in the sun about half way to air temperature. This cooling effect can result in a reduction of transpiration by wind. Transpiration had a minor effect on leaf temperature. Wilted leaves showed nearly the same temperature response as turgid ones. Dried leaves heated less and cooled faster in shade than transpiring leaves. Vaselined leaves were 1–3°C. warmer than transpiring leaves but showed similar heating and cooling curves. 相似文献
32.
1. Three random linear copolymers composed of two or three of the amino acids d-tyrosine, d-glutamic acid, d-alanine and d-lysine, and a branched multichain copolymer with a poly-d-lysine backbone and polymeric side chains of d-tyrosine and d-glutamic acid, were found to be non-antigenic in rabbits, by precipitin and passive cutaneous anaphylaxis, and in guinea pigs, by delayed hypersensitivity tests. The corresponding four copolymers of l-amino acids were shown to be antigenic by all the three criteria. 2. No immunological cross-reactions were observed between the polypeptides composed of d-amino acids and the corresponding l-amino acid copolymers. 3. Similarly, an azobenzenearsonic acid conjugate of poly-d-tyrosine was shown to be non-antigenic in guinea pigs, in contrast with an analogous conjugate of poly-l-tyrosine. Animals sensitized with the conjugate of poly-l-tyrosine did not exhibit delayed skin reactions, when cross-tested with the d-conjugate. 4. A linear polymer composed of d-tyrosine, l-glutamic acid and l-alanine was found to be immunogenic and to cross-react with the corresponding polymer composed exclusively of d-amino acids. 相似文献
33.
The covalent interaction of chloroacetic acid with rat liver lipids was studied in vivo. Rats were given a single oral dose (8.75 mg/kg, 50 microCi) of 1-[14C]chloroacetic acid and sacrificed after 24 hours. Lipids extracted from the livers were separated into neutral lipids and phospholipids by solid-phase extraction using sep-pak silica cartridges. The neutral lipid fraction was further fractionated by preparative thin-layer chromatography followed by reverse-phase high-performance liquid chromatography. The fraction corresponding to the retention time of standard cholesteryl chloroacetate gave a pseudomolecular ion peak at m/z 480/482 ratio: (3:1) on ammonia chemical ionization mass spectrometry, and the fragmentation pattern was found to be similar to that of the standard sample. Under similar conditions, acetic acid resulted in the formation of cholesteryl acetate. The effect of such conjugation reactions on the cell membrane and their contribution to toxicity is presently unknown. 相似文献
34.
J B Das S Ghosh C M Cosentino G G Ansari 《Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)》1990,195(2):274-278
Plasma disappearance of sulfobromophthalein (BSP) after an intravenous bolus (5 mg/kg) was determined in six lab chow-fed (LCF) rabbits and in six rabbits maintained on total parenteral nutrition (TPN) for 5 days. A common bile duct cannula enabled measurements of bile flow and biliary BSP excretion. Compartmental analysis of the biexponential plasma disappearance curve yielded three fractional transfer rates, plasma to liver (hepatic uptake), liver to plasma (reflux), and liver to bile (canalicular excretion). The transfer rates for hepatic uptake were 0.253 +/- 0.061/min for LCF and 0.147 +/- 0.040/min for TPN (P less than 0.01) and for the canalicular excretion of BSP were 0.038 +/- 0.019/min for LCF and 0.019 +/- 0.002/min for TPN (P less than 0.05). Model-computed rates for BSP excretion in bile over 60 min were lower with TPN (61%) than with LCF (80%); the measured excretory rates were 53% for TPN rabbits and 75% of injected dose for LCF animals. Basal biliary flow was reduced by 50% in the TPN group. With a two-compartmental model, assuming two pools and three transfer rates, we have demonstrated for the first time significant decreases in hepatic uptake and canalicular excretion of the organic anion BSP during TPN. A decrease in hepatic blood flow due to the enteral fast of TPN could have contributed in part to the decreased hepatic uptake. But, because the second exponent of the biexponential curve is independent of hepatic blood flow, the decrease in liver to bile transfer rate is a true approximation of a diminished canalicular excretory capacity during TPN. It is concluded that the movement of organic anions along the hepatic BSP/bilirubin transport system is impaired early during TPN. 相似文献
35.
Hillard S. Kaplan Jane B. Lancaster Sara E. Johnson John A. Bock 《Human nature (Hawthorne, N.Y.)》1995,6(4):325-360
Our objective is to test an optimality model of human fertility that specifies the behavioral requirements for fitness maximization
in order (a) to determine whether current behavior does maximize fitness and, if not, (b) to use the specific nature of the behavioral deviations from fitness maximization towards the development of models of evolved
proximate mechanisms that may have maximized fitness in the past but lead to deviations under present conditions. To test
the model we use data from a representative sample of 7,107 men living in Albuquerque, New Mexico, between 1990 and 1993.
The model we test proposes that low fertility in modern settings maximizes number of grandchildren as a result of a trade-off
between parental fertility and next generation fertility. Results do not show the optimization, although the data do reveal
a trade-off between parental fertility and offspring education and income.
We propose that two characteristics of modern economies have led to a period of sustained fertility reduction and to a corresponding
lack of association between income and fertility. The first is the direct link between costs of investment and wage rates
due to the forces of supply and demand for labor in competitive economies. The second is the increasing emphasis on cumulative
knowledge, skills, and technologies in the production of resources. Together they produce historically novel conditions. These
two features of modern economies may interact with evolved psychological and physiological mechanisms governing fertility
and parental investment to produce behavior that maximizes the economic productivity of lineages at the expense of fitness.
If cognitive processes evolved to track diminishing returns to parental investment and if physiological processes evolved
to regulate fertility in response to nutritional state and patterns of breast feeding, we might expect non-adaptive responses
when returns from parental investment do not diminish until extremely high levels are reached. With high economic payoffs
from parental investment, people have begun to exercise cognitive regulation of fertility through contraception and family
planning practices. Those cognitive processes maynot have evolved to handle fitness trade-offs between fertility and parental investment.
A preliminary presentation of this data was published in R. I. M. Dunbar, ed.,Human Reproduction Decisions: Biological and Social Perspectives. New York: St. Martin’s Press, 1995. Support for the research project, “Male Fertility and Parenting in New Mexico,” began
with two seed grants from the University of New Mexico’s Biomedical Research Grants Program, 1988 and 1989, and one from the
University of New Mexico Research Allocations Committee, 1988. Further seed money as well as interim funding came from the
William T. Grant Foundation (#89130589 and #91130501). The major support for the project came from the National Science Foundation
from 1990 to 1993 (#BNS-9011723 and #DBS-911552). Both National Science Foundation grants included Research Experience for
Undergraduates supplements.
Hillard S. Kaplan is an Associate Professor of Anthropology at the University of New Mexico. His earlier research and publications
focused on food sharing, time allocation, parental investment, and reproductive strategies among Ache hunter-gatherers in
Paraguay, Machiguenga and Piro forager-horticulturalists in Peru, and villagers of several ethnicities in Botswana. New research
and theory concern fertility, parental investment, and mating strategies in developed and developing nations. This research
formulates a new theory of reproductive decision-making and the demographic transition, integrating human capital and parental
investment theory in a synthesis of economic and evolutionary approaches.
Jane B. Lancaster is a Professor of Anthropology at the University of New Mexico. Her research and publications are on human
reproductive biology and behavior, especially human parental investment; women’s reproductive biology of pregnancy, lactation,
and child-spacing; and male fertility and investment in children. Current research with Hillard S. Kaplan is on male life
history strategies among a large sample of men in New Mexico. She has coedited three books on human parental investment:School-Age Pregnancy and Parenthood (with B. Hamburg),Parenting across the Life Span (with J. Altmann, A. Rossi, and L. Sherrod), andOffspring Abuse and Neglect (with R. Gelles). She is scientific editor of a quarterly journal,Human Nature: An Interdisciplinary, Biosocial Perspective published by Aldine de Gruyter. She is also a council member of the newly formed Human Behavior and Evolution Society.
John A. Bock is Andrew W. Mellon Post-Doctoral Fellow in Epidemiology and Population Health at the National Centre for Epidemiology
and Population Health, The Australian National University. His research focuses on the allocation of parental investment and
the determinants of children’s activities, integrating aspects of economic and evolutionary theory. He has ongoing field research
with Bantu and Bushmen agro-pastoralists and forager-horticulturalists in the Okavango Delta, Botswana. He is also collaborating
with Lancaster and Kaplan on the determinants of progeny distribution and homosexuality among New Mexican men.
Sara E. Johnson is a Ph.D. candidate at the University of New Mexico. Her major research trajectory focuses on trade-offs
in life history characters. Her research experience includes participation in a study of variation in growth and development
among children in a multi-ethnic community in the Okavango Delta, Botswana, in addition to her dissertation work on individual
variation in growth and mortality among juvenile baboons. She is collaborating with Lancaster and Kaplan on the association
between survival and fertility among Albuquerque men. 相似文献
36.
Jorge J. Casal R. Alejandra Mella Carlos L. Ballaré Sara Maldonado 《Physiologia plantarum》1994,92(4):555-562
Etiolated Vicia faba seedlings were exposed to continuous red light to investigate whether changes in extracellular peroxidase activity were correlated in time and localization with changes in extension growth and/or lignin content in the subapical region of the epicotyl. Continuous red light: (a) increased extracellular peroxidase activity after a lag of ca 0.5 h, followed by a maximum peak after 2.5 h due to slightly acidic isoforms (pI = 6–6.5, according to isoelectrofocusing gels), a minimum after 4 h and a second maximum after 8 h due to acidic isoforms (pI=4–5), (b) increased lignin content and epicotyl resistance to bending after a lag of ca 4 h, i.e. simultaneously with changes in acidic extracellular peroxidase activity, and (c) reduced extension growth to a stable rate after a lag of ca 1 h, not coinciding with the kinetics of any of the extracellular peroxidase isoforms. These effects of continuous red light were at least partially mediated by phytochrome. Tissue printing and anatomical studies revealed red light effects on extracellular peroxidase activity and lignin content mainly in the outer cortical parenchyma. The results are consistent with the involvement of phyto-chrome-mediated effects on extracellular peroxidases (acidic isoforms) in the transduction chain leading to lignin responses to red light. 相似文献
37.
T. E. Broad D. J. Burkin L. M. Cambridge D. W. Maher P. E. Lewis H. A. Ansari P. D. Pearce C. Jones 《Mammalian genome》1994,5(7):429-433
Seven new loci, casein alpha-S1 (CSN1S1), casein alpha-S2 (CSN1S2), casein beta (CSN2), the Hardy-Zuckerman 4 feline sarcoma viral (v-kit) oncogene homolog (KIT), albumin (ALB), phosphodiesterase cyclic GMP (rod receptor) beta polypeptide (PDEB), and complement component 1 (IF), were assigned to sheep Chromosome (Chr) 6 by Southern hybridization to a panel of chromosomally characterized sheep x hamster cell hybrids. By isotopic in situ hybridization, CSN2 was regionally localized to sheep Chr (OOV) 6q22–q31, anchoring this syntenic group of markers on to OOV6 and confirming its homology at a molecular and cytological level with cattle Chr 6. The assignment of these loci, from PDEB (located on human Chr 4p16.3) to IF (on HSA4q24–q25), and the observation that interleukin 2 (IL2, on HSA 4q26–q27) and tryptophan 2,3-dioxygenase (TDO2, on HSA4q31) are not located on OOV6, is further evidence of the close evolutionary relationship of sheep and cattle and the conserved synteny in these species of this extensive region of human Chr 4. On the basis of this conserved synteny, and the similar G- and Q-banding patterns of this chromosome in cattle and sheep, we propose that this sheep chromosome be numbered as 6, not 4 as recommended by ISCNDA (1990). 相似文献
38.
Anna Tramontano Elisabetta Bianchi Sara Venturini Franck Martin Antonelo Pessi Maurizio Sallozzo 《Journal of molecular recognition : JMR》1994,7(1):9-24
Conformationally constraining selectable peptides onto a suitable scaffold that enables their conformation to be predicted or readily determined by experimental techniques would considerably boost drug discovery process by reducing the gap between the discovery of a peptide lead and the design of a peptidomimetic with a more desirable pharmacological profile. With this in mind, we designed the minibody, a 61-residue β-protein aimed at retaining some desirable features of immunogloblin variable domains, such as tolerance to sequence variability in selected regions of the protein and predictability of main chain conformation of the same regions, based on the ‘canonical structures’ model. To test the ability of the minibody scaffold to support functional sites we also designed a metal binding version of the protein by suitably choosing the sequences of its loops. The minibody was produced both by chemical syntyhesis and expression in E. coli and charactgerized by size exclusion chromatography, UV CD (circular dichroism) spectroscopy and metal binding activity. All our data supported the model, but a more detailed structural characterization of the molecule was impaired by its low soubility. We were able to overcome this problem both by further; mutagenesis of the framework and by addition of a solublizing motif. The minibody is being used to select constrained human IL-6 peptidic ligands from a library displayed on the surface of the f1 bacteriophage. 相似文献
39.
Gloria del Solar Gabriela Kramer Sara Ballester Manuel Espinosa 《Molecular & general genetics : MGG》1993,241(1-2):97-105
Deletion of a region of the promiscuous plasmid pLS1 encompassing the initiation signals for the synthesis of the plasmid lagging strand led to plasmid instability in Streptococcus pneumoniae and Bacillus subtilis. This defect could not be alleviated by increasing the number of copies (measured as double-stranded plasmid DNA) to levels similar to those of the wild-type plasmid pLS1. Our results indicate that in the vicinity of, or associated with the single-stranded origin region of pLS1 there is a plasmid component involved in its stable inheritance. Homology was found between the DNA gyrase binding site within the par region of plasmid pSC101 and the pLS1 specific recombination site RSR. 相似文献
40.
Jessica N. Hightower Dolly L. Crawford Wayne E. Thogmartin Kyle R. Aldinger Sara Barker Swarthout David A. Buehler John Confer Christian Friis Jeffery L. Larkin James D. Lowe Martin Piorkowski Ronald W. Rohrbaugh Kenneth V. Rosenberg Curtis Smalling Petra B. Wood Rachel Vallender Amber M. Roth 《Diversity & distributions》2023,29(2):254-271