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991.
Anwar T. Mankarios Michael A. Hall Michael C. Jarvis David R. Threlfall John Friend 《Phytochemistry》1980,19(8):1731-1733
Onion (Allium cepa) cell walls were fractionated by successive extraction with oxalate-citrate buffer and with alkali. The substantial oxalate-citrate extracted fraction comprised a range of pectic polysaccharides with varying proportions of neutral side-chains. Methylation analysis of the alkali extract indicated that (1,4′)-linked galactans and a substituted xyloglucan were probably major components. Onions thus resemble dicotyledonous plants more than the Gramineae in their cell wall composition. 相似文献
992.
Summary Gastric parietal cells of rats maintained under standardized conditions and fed ad libitum were examined by electron microscopy at 6 time points of the 24-h day. Morphometric determinations were made on 4 cell characteristics. The volume density of secretory canaliculi was maximal at the mid-dark sampling point and decreased during the light phase; a secondary peak was seen 1 h before the onset of darkness. The surface density of microvesicles and RER fluctuated inversely with the pattern displayed by secretory canaliculi. The number of multivesicular bodies per cytoplasmic area exhibited a single peak, 1 h after the onset of darkness. It was further noted that parietal cells in the necks and bases of glands differed morphologically and that their organelle populations varied at individual circadian rates. 相似文献
993.
Peter F. Davies 《Journal of cellular biochemistry》1980,13(2):211-217
In sub-confluent cultures of Balb/c-3T3 cells, pinocytosis rates were increased after exposure to specific growth factors (serum; platelet-derived growth factor, PDGF; epidermal growth factor, EGF). Conversely, as cells became growth-inhibited with increasing culture density, there was a corresponding decline in pinocytosis rate per cell. In order to test whether density-inhibition of pinocytosis was influenced either by the growth cycle or by cell contact independently of growth, cells were induced into a quiescent state at a range of subconfluent and confluent densities. Under such conditions, cell density did not significantly inhibit pinocytosis rate. When confluent quiescent cultures in 2.5% serum were exposed to 10% serum, the resulting round of DNA synthesis was accompanied by enhanced pinocytosis per cell, even though the cells were incontact with one another. Furthermore, in a SV40-viral transformed 3T3 cell line, both the growth fraction and the pinocytosis rate per cell remained unchanged over a wide range of culture densities. These studies indicate that density-dependent inhibition of pinocytosis in 3T3 cells appears to be secondary to growth-inhibition rather than to any direct physical effects of cell–cell contact. 相似文献
994.
The BALB/3T3 clone A31 mouse embryo cell line has been used by many investigators as a model “normal” “fibroblast” line for a variety of in vitro studies. It has been shown, however, that these cells are not “normal” because they will produce tumors within 2–4 months if 3 × 104 cells are implanted subcutaneously in BALB/c mice attached to 0.2 × 5 × 10-mm plastic plates. Previous studies also suggested that these cells were not fibroblasts because they gave rise to tumors with the characteristics of vascular endothelium not fibroblasts. We now report that BALB/3T3 (clone A31), BALB/3T3-T, a proadipocyte subclone of clone A31 cells, and six recent subclones of BALB/3T3-T cells show additional differentiation patterns when tumors derived by implantation of these cells attached to plastic plates are examined. Differentiation into pericytes, chondrocytes, and fibroblasts was observed. We conclude that the BALB/3T3 clone A31 cell line and related lines are multipotent mesenchymal cells which are capable of differentiation into a variety of cell types. 相似文献
995.
Darrell H. Carney 《Journal of cellular biochemistry》1980,13(4):467-478
The localization of thrombin receptors on mouse embryo (ME) cells has been examined by direct fluorescence microscopy using a fluorescein aminelabeled thrombin. Two fluorescein amines, 4-(N-6-aminoethyl thioureal)-fluorescein and 4-(N-6-aminohexyl thioureal)-fluorescein, were synthesized and attached to the carbohydrate moiety of highly purified human α-thrombin by periodate oxidation of the carbohydrate and selective reduction of the Schiff's base using sodium cyanoborohydride. Preparations of fluorescent thrombin with from 1 to 4 fluoresceins per molecule of thrombin retained their ability to proteolytically cleave fibrinogin to form fibrin clots, to bind to thrombin receptors on ME cells, and to initiate cell division. After incubating mitogenic concentrations of the fluorescein amine labeled thrombin with ME cells at 4°C, a diffuse fluorescent pattern was observed over the surface of the ME cells. This diffuse pattern was specific: it was not observed on cells from parallel cultures incubated with fluorescent thrombin plus a 20-fold excess of unlabeled thrombin. Thus, thrombin receptors appear to be distributed randomly over the surface of ME cells prior to interaction with thrombin. Increasing the temperature to 37°C following binding at 4° C resulted in a rapid dissociation of the fluorescent pattern from the cells leaving only the autofluorescent vesicles. This result may reflect the unique ability of thrombin to proteolytically cleave its own receptor. 相似文献
996.
Selective isolation and culture of a proliferating epithelial cell population from the hamster trachea 总被引:7,自引:0,他引:7
William E. Goldman Joel B. Baseman 《In vitro cellular & developmental biology. Plant》1980,16(4):313-319
Summary A reliable cell isolation technique was developed to allow the cultivation of cells from the hamster respiratory tract. Repeated
thermolysin treatments and gradient centrifugation yielded a cell culture completely free from contamination by fibroblasts.
Viable cells could be isolated from as little tissue as a single hamster trachea, but in vitro proliferation occurred only
if the hamster was less than 4 months of age. The cultured cells could be repeatedly passaged and subcultured for weeks by
employing normal tissue culture techniques. Morphologically, the monolayers appeared to be a homogeneous population of epithelial
cells, and successful cloning of freshly isolated single cells resulted in apparently identical cultures. The epithelial origin
of these cells was also suggested by continued growth in minimum essential medium withd-valine substituted forl-valine. The relative ease with which this cell type can be isolated, cultured, and manipulated in vitro should encourage
its application as a model of the respiratory epithelium.
This research was supported by Public Health Service Grant P50-HL 19171 and Research Career Development Award 1-K04-AI 00178
to J. B. B. 相似文献
997.
Robert O. Hussa Roland A. Pattillo 《In vitro cellular & developmental biology. Plant》1980,16(7):585-590
Summary The BeWo line of trophoblastic cells, maintained in continuous culture since 1966, was employed to investigate the phenomenon
of gonadotropin α-subunit predominance that exists in several cell lines. The secretion of complete human chorionic gonadotropin
(hCG) relative to α-subunit was compared in several different BeWo sublines, all of which were derived from BeWo stock roller
tube colonies. In all of the BeWo sublines, secretion of hCG originally exceeded secretion of α-subunit. With time in culture,
however, there was a marked decline in production of hCG/hCGβ, but not in α-subunit. Thus it appears that the production of
hCGβ by BeWo choriocarcinoma cells is more labile than the production of the α-subunit. 相似文献
998.
Cystinotic and normal fibroblasts: Differential susceptibility to cysteine toxicity in vitro 总被引:2,自引:0,他引:2
Sheldon Orloff Anil B. Mukherjee Jean DeB Butler Barbara Foley Joseph D. Schulman 《In vitro cellular & developmental biology. Plant》1980,16(8):655-660
Summary Extracellular cysteine concentrations between 0.5 and 2.5 mM resulted in death of normal but not cystinotic cells grown in Eagle's minimal essential medium containing supplemental fetal
bovine serum and antibiotics. Differential cell survival was determined by viable cell counting using Trypan Blue dye exclusion.
In cocultivation experiments of [3H]thymidine-labelled cystinotic fibroblasts with nonradioactive normal fibroblasts, autoradiography confirmed the selective
survival of cystinotic cells in medium containing 1 mM cysteine. At this concentration of 1 mM cysteine, intracellular cystine content increased slightly in surviving normal cells but not in cystinotic cells, which normally
contain a high level of intracellular cystine. This comparative resistance of cystinotic fibroblasts to elevated extracellular
cysteine concentrations forms the basis for an in vitro selective system for these mutant human cells. Further exploration
of this resistance phenomenon may well expand the understanding of the molecular defect in cystinotic cells. 相似文献
999.
William C. Wright 《In vitro cellular & developmental biology. Plant》1980,16(10):875-883
Summary A new calculation of the relative efficiency of polymorphic enzyme markers, called the REB, was determined and compared with
one of Fisher's determinations of the relative efficiency called REA here. The REA estimates the chance of failing, and 1-REA
of succeeding, to show a phenotypic difference between two randomly selected persons or cultured cell lines (Case 1). In this
study it was shown that the REA also estimates the chance of detecting a cell line mislabeling or similar mixup (Case 2) and
a cell line cross-contamination leading to the complete replacement of an original line by contaminating line (Case 3). The
new REB determines the probability of failing, and 1-REB of succeeding, to detect a contamination of an original line by another
line leading to their coexistence, or at least a sufficiently long period of transitional coexistence before one overgrows
the other. The REA and REB also apply to determining the efficiency of polymorphic markers in detecting donor and recipient
cells in tissue transplants.
This work was developed from the author's involvement in the human tumor cell-line characterization project at Sloan-Kettering
Institute and he acknowledges this opportunity and the benefits of his association with Dr. J?rgen Fogh and colleagues in
the Human Tumor Cell Laboratory. 相似文献
1000.
Asynchronous 9L cells were separated into relatively homogeneously-sized populations using centrifugal elutriation with both
a conventional collection method and a long collection method. A substantial increase in the homogeneity of the volume distributions
and in the degree of synchrony of the separated fractions was obtained using the long collection method. Autoradiographic
data indicated that fractions containing ≥97% G1 cells, ≥80% S cells, and 70–75% G2 cells could be routinely recovered with this procedure. Recovery in these fractions varied from 5 to 8% of the total number
of cells elutriated. The colony forming efficiency (CFE) of cells from fractions representing each phase of the cell cycle
was a constant 60–70%, which was comparable to the 60–80% usually found for asynchronous 9L cells. The percentage of cells
in the G1, S, and G2 phases in the elutriated fractions was more accurately determined from the volume distribution than from computer fits of
the DNA histogram obtained from flow cytometry. In general, the degree of synchrony was related to the coefficient of variation
(CV) of the volume distributions of the elutriated fractions. The CV was about 14% for all elutriated fractions. When the
≥97% G1 population was allowed to progress to S and G2, the CVs were about 17 and 20.2%, respectively. Thus, the best nonperturbing method for obtaining synchronous 9L cells in
the S or G2 phases was direct elutriation with the long collection method. 相似文献