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21.
S M Kappes M D Bishop J W Keele M C T Penedo H C Hines M D Grosz G A Hawkins R T Stone S L F Sunden C W Beattie 《Animal genetics》1994,25(3):133-140
Seven bovine erythrocyte antigen loci and three serum protein loci were tentatively assigned to chromosomes or synteny groups by linkage analysis to previously assigned microsatellite DNA markers. The erythrocyte antigen locus EAB was mapped to synteny group U27; EAC to chromosome 18, synteny group U9; EAL to chromosome 3, synteny group U6; EAS to chromosome 21, synteny group U4; EAZ to chromosome 10, synteny group U5; EAR' to chromosome 16, synteny group U1; and EAT' to chromosome 19, synteny group U21. The vitamin D binding protein (GC) and albumin (ALB) loci were assigned to chromosome 6, synteny group U15 and post-transferrin 2 (PTF 2) to chromosome 19, synteny group U21. 相似文献
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26.
F Velge-Roussel C Verwaerde J M Grzych A Auriault A Capron 《Journal of immunology (Baltimore, Md. : 1950)》1989,142(7):2527-2532
A rat IgE mAb specific for larval Ag (26 kDa, 56 kDa) has been shown to protect rats against Schistosoma mansoni infection. Immunizations of Lou/M rats performed with this IgE (Ab1) induced the production of antiidiotypic antibodies (Ab2). Moreover, after this Ab2 production, anti-antiidiotypic antibodies (Ab3) were revealed. The screening of Ab3 isotypes showed the presence of IgG Ab3 and more interestingly of IgE Ab3, i.e., the same isotype as Ab1. These IgE and IgG antibodies recognized predominantly the 26-kDa Ag and were cytotoxic for schistosomula in the presence of platelets for IgE Ab3 and eosinophils for IgG Ab3. Both IgE and IgG Ab3 conferred by passive transfer protective immunity to infected rats (up to 50%). Thus the immunization with an IgE mAb led in part to the production of Ab3 of the same isotype as Ab1. In conclusion, these results suggest that the isotype selection of the antibodies of the third generation (Ab3) might be influenced by the Ab1. The respective role of the idiotope and isotype of Ab1 in isotype regulation is discussed. 相似文献
27.
T. Friedel F. G. Barth 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1997,180(3):223-233
Spiders can use air particle movements to localize moving prey. We studied the responses of 32 wind-sensitive interneurones
in the hunting spider Cupiennius salei to prey stimuli.
Stimulation with a tethered flying fly or with artificial air pulses activated plurisegmental interneurones that responded
to changes in air movement velocity and were thus well suited to represent the highly fluctuating air stream typical of prey
stimuli. In most interneurones (n = 18) the responses to the stimulation of different legs were not significantly different from each other.
Different interneurones had different response characteristics and their latencies largely overlapped suggesting that there
is parallel processing of the signals by populations of interneurones with different response characteristics.
In two interneurones the number of spikes and the spiking pattern elicited by stimulation of each of the eight legs markedly
differed depending on the leg stimulated. These neurones may play an important role in directional information processing.
Stimulation of the adjacent legs from front to back or from back to front revealed two interneurones sensitive to the direction
of successive stimulation of the legs. These neurones may be able to detect the motion of an air movement source in a preferred
direction and thus act as nearfield motion detectors to localize a moving prey item.
Accepted: 28 September 1996 相似文献
28.
Norma L. Pucheu Norma L. Kerber Emilio A. Rivas Néstor Cortez Augusto F. Garcia 《Current microbiology》1997,34(3):155-161
Membranes from in vivo labeled cells of Rhodobacter
capsulatus U43[pTX35] grown photosynthetically carried 60% of
the [32P]-Pi in the “heavy” fraction (HM) after
sucrose gradient sedimentation. Metal-chelating chromatography of either
“heavy” or “light” (LM) membrane fractions rendered
similar Bchl-protein complex profiles after octyl-glucoside treatment,
including most of the radioactivity in the same corresponding elution
fraction (F II). Similar labeling distribution of pigment-protein complexes
was obtained for membranes of dark-grown cells induced by lowering oxygen
tension. Fractions derived from HM showed highly labeled LHIα, whereas the
same complex from LM was essentially [32P]-Pi-free, as revealed
by SDS-PAGE followed by autoradiography. Phospholipid analysis showed a
similar pattern for membranes isolated from cells photosynthetically or
semiaerobically grown, being the most abundant: phosphatidylglycerol,
phosphatidylethanolamine, cardiolipin, and phosphatidylcholine. Part of the
phospholipids from HM comigrated with LHIα during SDS-PAGE and dissociated
from the complexes only after solvent extraction and hydrophobic
chromatography. However, a small amount remained always attached to LHIα,
indicating an unusual strong interaction. These results suggest the existence
of two operationally defined membrane regions carrying LHIα complexes
differing in phosphorylation status and protein-phospholipid interaction.
Received: 10 August 1996 / Accepted: 10 September 1996 相似文献
29.
Liu Yewei; Kranias Evangelia G.; Schneider Martin F. 《American journal of physiology. Cell physiology》1997,273(6):C1915
The effects ofphosphorylation status on Ca2+release and Ca2+ removal werestudied in fast-twitch flexor digitorum brevis and slow-twitch soleusskeletal muscle fibers enzymatically isolated from wild-type andphospholamban knockout (PLBko) mice. In all fibers the adenosine3',5'-cyclic monophosphate-dependent protein kinase (PKA)inhibitor H-89 decreased the peak amplitude of the intracellularCa2+ concentration([Ca2+]) transient fora single action potential, and the PKA activator dibutyryl adenosine3',5'-cyclic monophosphate (DBcAMP) reversed this effect,indicating modulation of Ca2+release by phosphorylation status in all fibers. H-89 decreased thedecay rate constant of the[Ca2+] transient andDBcAMP reversed this effect only in phospholamban-expressing fibers(wild-type soleus), indicating modulation ofCa2+ removal only in the presenceof phospholamban. A high basal level of PKA phosphorylation in soleusfibers maintained under our control conditions was indicated bythe lack of effect of direct application of DBcAMP onCa2+ release orCa2+ removal in wild-type or PLBkosoleus fibers and was confirmed by analysis of phospholamban fromwild-type soleus fibers. 相似文献
30.
S Chwetzoff S Tsunasawa F Sakiyama A Ménez 《The Journal of biological chemistry》1989,264(22):13289-13297
The venoms of the Naja species are known to be cytotoxic. This toxicity has been attributed to the presence of small nonenzymatic polypeptides of 60 amino acid residues, designated as cardiotoxins or cytotoxins. We investigated the cytotoxic potency of Naja nigricollis venom fractions and isolated another type of cytotoxic component which is even more potent than cardiotoxins. This cytotoxic compound, which was designated as nigexine, was purified to homogeneity and its amino acid sequence was determined. Nigexine is a basic phospholipase A2 consisting of a single chain of 118 amino acids. A detailed investigation of the cytotoxic effects on epithelial FL cells, C-13T neuroblastoma cells, and promyelocytic leukemia HL 60 cells revealed that nigexine not only altered cell viability but also prevented cell proliferation. This is a property that was specific to nigexine since other phospholipases A2 from various sources had no detectable cytotoxic activity. The cytotoxic activity of nigexine was not dependent on the presence of divalent cations, unlike its enzymatic activity. In particular, the cytotoxic activity of nigexine was identical in the presence or absence of either 2 mM Ca2+ or Sr2+, or 6 mM EDTA. We also present evidence based on chemical modifications that cytotoxic activity was not correlated with enzymatic activity. Thus, modification with parabromophenacyl bromide totally abolished the enzymatic activity of nigexine, which nevertheless retained 6-20% of the cytotoxicity of native nigexine. Conversely, treatment with cyanogen bromide gave a compound that retained 7% of the enzymatic activity of the parent molecule but was devoid of detectable cytotoxicity. 相似文献