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Summary Observations are presented on the patterns of DNA synthesis and mitotic activity in medullary parenchyma cells excised from tubers ofHelianthus tuberosus in four different periods of dormancy. Dormancy break (activation) was induced byin vitro culture on media added with 2,4-dichlorophenoxyacetic acid. The cell cycle responsein vitro to different combinations of growth substances has also been investigated.The results show that remarkable changes in the timing of the first and second cell cycles and their phases occur with the progression of dormancy. With increasing time after tuber harvest, the following behaviours are observed: (i) a lengthening of the first cell cycle, chiefly due to a lengthening of the G2 phase (G2 is absent at the beginning of dormancy) and an increase in the time interval between the start of thein vitro culture and the onset of the first mitotic wave; (ii) an increased duration of the S phase; (iii) a remarkable reduction in the cell synchrony.These behaviours, as indicated also by their comparison with thein vitro response of the cell cycle to different hormonal treatments, seem to depend on the physiological status of the tubers at the time of explant. It is concluded that the analysis of the cell cycle is an useful tool for understanding some aspects of such a complex physiological situation as dormancy.Istituto di Mutagenesi e Differenziamento del C.N.R., Pisa, Italy, publication no. 321. 相似文献
65.
66.
The time evolution of slowly evolving discrete dynamical systems x
i + 1
= T(r
i
,x
i
), defined on an interval [0, L], where a parameter r
ichanges slowly with respect to i is considered. For certain transformations T, once r
i reaches a critical value the system faces a non-zero probability of extinction because some x
j [0, L]. Recent ergodic theory results of Ruelle, Pianigiani, and Lasota and Yorke are used to derive a simple expression for the probability of survival of these systems. The extinction process is illustrated with two examples. One is the quadratic map, T(r, x) = rx(1 – x), and the second is a simple model for the growth of a cellular population. The survival statistics for chronic myelogenous leukemia patients are discussed in light of these extinction processes. Two other dynamical processes of biological importance, to which our results are applicable, are mentioned. 相似文献
67.
Undifferentiated Friend erythroleukemic cells (FL cells) acquire membrane microviscosity (
), in accord with the culture cell density. At low cell density
poise, whereas at confluency it increases to
poise. Concomitantly, the total number of available transferrin receptors per cell decreases by about 80% upon increase in
cell density. Modulation of membrane microviscosity, by artificial alteration of the membrane cholesterol level, mediates
similar modulations of the availability of the transferrin receptors. The correlation between the availability of the transferrin
receptors and the membrane lipid fluidity may take part in the overt decrease in iron uptake by erythroid cells along the
erythropoiesis pathway. 相似文献
68.
Summary Electron probe microanalysis of unfixed freeze-substituted rat liver tissue embedded in Spurr's low viscosity epoxy resin demonstrated the occurrence of Si as well as P, S, and Cl in the nucleus, nucleolus, mitochondria, and rough endoplasmic reticulum. Chemical analysis confirmed that the Si in the organelles did not originate from instrumental contaminants. This suggests that Si may be involved in the biochemistry of these subcellular organelles.Supported by Grant GM-08229-12-13 from the National Institutes of Health, USPHS.We are grateful to the Kevex Corporation and Mr. Glenn W. Meyer, Sales Engineer, for the use of the Kevex X-ray spectrometer; we wish to thank as well the Perkin-Elmer Corporation and their Western Branch Manager, Mr. Michael E. Mullen and Senior Microscopist, Mr. Minoru Shinorhara, for use of and assistance with the Hitachi HU 12 A transmission electron microscope. We also wish to acknowledge Mary Louise Chiappino for her technical assistance in preparing the thin sections, the final micrographs and the X-ray photographs, and Darlene Lum for technical assistance in the laboratory. 相似文献
69.
A. Debec 《Development genes and evolution》1976,180(2):107-119
Summary Our previous isoenzyme investigation ofDrosophila melanogaster cell lines in vitro has been completed with twelve further enzyme systems. The enzyme profiles seem to be in good agreement with a previous hypothesis concerning the precise origin of these cell lines (probably from imaginal discs or nervous tissues). Our results have been summarized with reference to the biochemical genetic map ofDrosophila melanogaster in order to consider a possible functional organization of the genome.Abbreviations NAD
nicotine adenine nucleotide
- NADP
nicotine adenine nucleotide phosphate
- NBT
nitroblue tetrazolium
- PMS
phenazine methosulfate
- EDTA
ethylene diamine tetraacetic acid
- GOT
Glutamate-oxaloacetate transaminase
- PGK
Phosphoglycerate kinase
- GPDH
-glycerophosphate dehydrogenase
- MDH
Malate dehydrogenase
- PGM
Phosphoglucomutase
- Aph
Alkaline phosphatase
- MDH-NADP
Malic enzyme
- Lap
Leucine Amino-Peptidase
- LDH
Lactate dehydrogenase
- -1-OHDH
L-3-hydroxyacid dehydrogenase
- ADH
Alcohol dehydrogenase
- Aldox
Aldehyde oxydase
- 6PGD
6 Phosphogluconate dehydrogenase
- G6PD
Glucose-6-Phosphate dehydrogenase
- Hex3
Fructokinase
- IDH
Isocitrate dehydrogenase
- Est 6
Esterase 6
- Est C
Esterase C
- ODH
Octanol dehydrogenase
- XDH
Xanthine dehydrogenase
- AcPh
Acid Phosphatase 1 相似文献
70.
Hepatocytes from rats were isolated by treatment with trypsin and cultured. Plasma membranes at different culture stages were observed by electron microscopy. The activities of 5' nucleotidase and adenosinetriphosphatase on the plasma membranes were examined. The cell coat was also studied by use of the concanavalin A-peroxidase technique. The surfaces of single cells, covered with microvilli, are the site of adenosinetriphosphatase activity only and are devoid of 5'-nucleotidase activity. After a few h of culture, the cells are grouped together in tight clusters or long trails and are separated by an intercellular space of 250 A, partially permeable to lanthanum nitrate. The juxtaposed plasma membranes on which 5'-nucleotidase and adenosinetriphosphatase activities occur also delimit spaces similar to bile canaliculi. The formation of junction complexes and their permeability to lanthanum nitrate was also studied. No enzymatic activity is observed at the junctions. The numerous tight junctions, impervious to the tracer, are always accompanied by a profusion of microfilaments. Mature desmosomes are rare, and are present only in the form of "maculae adhaerentes diminutae." The gap junctions, nearly always permeable to the tracer, form rapidly and assume a variety of shapes (trail, bulge and ring-like), the significance of which is open to discussion. The use of concanavalin A permits localization of the free sugar sites on the surface of the cells, in the pinocytotic vesicles and in the internal space of the gap junctions. 相似文献