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1.
I. A. Catalán † E. Berdalet † M. P. Olivar † C. Roldán † 《Journal of fish biology》2007,70(2):391-405
Six condition indices based on RNA, total soluble protein and two metabolic enzymes [lactate dehydrogenase (LDH) and citrate synthase (CS)] were analysed in muscle tissue of individual larvae, post-flexion reared sea bass Dicentrarchus labrax using DNA and total soluble protein as standards for size. In addition, the effect of 2 days of food deprivation on the cell proliferation rates was assessed. The RNA:DNA best reflected short-term changes in feeding conditions. If standardized by DNA content, LDH activity was a better indicator of condition than any other index but RNA:DNA. Further, the analysis of cell proliferation rates in muscle from 26 day-old larvae proved useful in distinguishing continuously fed larvae from individuals subjected to 2 days of fast. 相似文献
2.
Rat kidney (NRK) cells infected with a temperature-sensitive mutant of the Kirsten sarcoma virus were arrested in the G0/G1 phase of their cell cycle by incubation in serum-deficient medium at a p21-inactivating temperature of 41 degrees C. These quiescent ts K-NRK cells were then stimulated to transit G1 and initiate DNA replication by lowering the temperature to 36 degrees C, which rapidly reactivated p21. Reactivating the viral Ki-RAS protein by temperature shift led to an increase in adenylate cyclase activity in early G1 phase. The Ki-RAS protein increased the sensitivity of adenylate cyclase to guanyl nucleotides by a mechanism that seemed to involve inactivation of the enzyme's inhibitory G1 regulatory protein. 相似文献
3.
I. D. Bassukas G. Vester B. Maurer-Schultze 《Virchows Archiv. B, Cell pathology including molecular pathology》1990,59(1):251-256
Cell kinetic studies of endothelial cells in the adenocarcinoma EO 771 growing in C57bl/6j mice and after transplantation
into Balb/c-nu/nu mice, as well as of the effect of cyclophosphamide treatment have been carried out. The3H-thymidine labelling index of endothelial cells decreases from about 8% 3–6 days after tumour inoculation to about 3% at
18 days. This decrease parallels that of the labelling index of tumour cells, i.e. there is a positive correlation between
the labelling index of endothelial cells and that of tumour cells. The labelling index of endothelial cells in the tumour
periphery is two to three times as high as that in the tumour centre reflecting corresponding differences in the rate of proliferation.
There is no difference in the proliferation of endothelial cells whether the tumour grows in C57bl/6j or in Balb/c-nu/nu mice.
After treatment with cyclophosphamide the labelling index of endothelial cells decreases within 2 days to 1–2% and remains
that low despite regrowth of the tumour with increased tumour cell proliferation, indicating that tumour relapse does not
depend on tumour angiogenesis. 相似文献
4.
G. Wiedemann R. Pabst T. Wagner F. Trepel 《Virchows Archiv. B, Cell pathology including molecular pathology》1988,56(1):407-412
Labelling index after one or repeated intravenous injections of 3H-thymidine was measured for various subpopulations of lymphatic
cells in different canine lymphoid compartments and correlated with cell morphology. High doses of tritiated thymidine were
injected and exposure times of up to 211 days were used. The labelling indices of lymphoid blasts were comparable in all tissues
investigated. Labelling index varied from 100% in immunoblasts to 4% in small-sized lymphocytes. Approximately 80% of immunoblasts
were labelled 1 h after 3H-thymidine application and 100% labelling was obtained after 12 h repetitive 3H-thymidine labelling.
In contrast with mediumsized and large lymphocytes, immunoblasts seem to be rapidly proliferating cells in the dog with almost
no Go cells.
Supported by the Deutsche Forschungsgemeinschaft DFG Grant SFB 112 相似文献
5.
WALTER C. QUEVEDO JACOB DYCKMAN RUTH HALABAN GISELA E. MOELLMANN JANET M. COWAN THOMAS J. HOLSTEIN 《Pigment cell & melanoma research》1988,1(Z1):124-131
The BULT melanoma originated at Brown University as a spontaneous, small black nodule on the tail of an adult female mouse of the LT/Ch strain. Histological examination of a portion of the tumor indicated that it was intradermal and consisted predominantly of heavily melanized, ovoid to fusiform cells with melanin-laden macrophages scattered among them. The BULT melanoma has been maintained in LT/Ch mice for approximately 5 years by periodic transplantation, at first subcutaneously on the flanks and, more recently, intramuscularly in the hind legs. The shift in transplantation site was made following a marked decline in the growth of subcutaneous grafts. The transplants have retained the uniform deep-black melanization and general histology of the primary melanoma. Numerous melanosomes at all stages of development are found within the melanoma cells. DOPA-positive cytoplasmic vesicles are abundant. Occasional autophagic vacuoles containing clusters of melanosomes are also present. A few metastases from the transplanted melanoma have been observed in lymph nodes and on one occasion in the lungs. When grown in vitro, BULT melanoma cells do not require special growth promoting agents (e.g., TPA; cAMP) in order to proliferate. The BULT melanoma differs in one or more respects from each of the other three transplantable spontaneous mouse melanomas widely used in cancer research. In addition, it arose in a strain of mice characterized by the spontaneous death of melanocytes while the latter are engaged in synthesizing eumelanin within hair follicles. Karyotypic analysis of cultured cells showed a modal chromosome number of 68 with a range of 58–72 chromosomes. 相似文献
6.
A range of surfactants, including the anionic sodium dodecyl sulfate, the cationic cetyltrimethylammonium bromide and the nonionics octylphenoxy polyethoxyethanol (Triton X100) and polyoxyethylene 20 sorbitan monoleate (Tween 80) was studied for effects on proliferation, contractibility and attachment of cultured human fibroblasts. Only ionic surfactants exhibited a stimulatory effect on fibroblast proliferation, whereas all the surfactants tested increased the contraction of collagen gels containing fibroblasts, with the greatest effect from the non-ionic surfactants. This activity was not correlated with an increase of cell population or cell attachment within the collagenous matrix. The activity of the surfactants was seen only at levels close to their LD50 values and in a narrow range of concentrations. Thus, we consider that they are the result of the so-called hormesis phenomenon.Abbreviations CTAB
cetyltrimethyl-ammonium bromide
- FCS
fetal calf serum
- LD100
dose lethal to 100% of exposed
- MCD
maximal contraction dose
- PDL
population doubling level
- SDS
sodium dodecyl sulfate 相似文献
7.
Masamitsu Wada 《Journal of plant research》1988,101(4):519-528
Chloroplast proliferation was investigated inAdiantum protonemata growing under continuous red light. Cell division is absent when cells are grown under red light. The chloroplast
number increases as the cell length increases, therefore the chloroplasts divide in the absence of cell division. Chloroplasts
in the basal part of the filamentous protonemal cell migrate gradually toward the cell apex, but there is no large net migration
from the tip to the base or vice versa, indicating that chloroplast division takes place in the apical part of the protonemata.
Chloroplast number in the apical 100 μm was maintained at about 200 during cell growth at least over eight days. The chloroplasts
were either dumbbell- or ellipsoid-shaped. Dumbbell-shaped chloroplasts are abundant everywhere in a protonema, ranging from
30 to 50% of the total chloroplasts. The dumbbell-shaped chloroplasts attached to or very close to the plasma membrane seem
to be the ones that are dividing but the dumbbell-shaped ones in the other regions do not divide. These data support the hypothesis
that a signal from the plasma membrane induces the dumbbell-shaped chloroplasts to divide. 相似文献
8.
A rapid fluorometric DNA assay for the measurement of cell density and proliferation in vitro 总被引:4,自引:0,他引:4
Timothy A. McCaffrey Lily A. Agarwal Babette B. Weksler 《In vitro cellular & developmental biology. Plant》1988,24(3):247-252
Summary Many research efforts require the accurate determination of cell density in vitro. However, physical cell counting is inaccurate,
time-intensive and requires removal of the cells from their growth environment, thereby introducing a host of potential artifacts.
The current studies document a very simple method of determining cell density in microtiter wells via DNA-enhanced fluorescence.
Fixed cells are stained with the A-T intercalating DNA stains DAPI or Hoechst 33342 and then fluorescence is quantified in
a plate fluorometer. Fluorescence is shown to be linearly related to cell density as determined by two physical counting methods.
The validity of the method is established in determining serum-stimulated growth of smooth muscle cells and in mitogen-induced
growth of endothelial cells. The fixed cells can be stored for prolonged periods, thus allowing time-course proliferation
assays without interassay variations. The fixed cells are also suitable for determinations of antigens of interest by ELISA.
This method is potentially valuable in many in vitro systems where the quantification of cell density and proliferation is
necessary.
This work supported in part by NIH Cardiovascular Training Grant HL07423 and a grant from the American Federation for Aging
Research to T. M. and HL35724 to B. W.
EDITOR’S STATEMENT The technique described in this paper represents an approach to quantifying cell density in adherent monolayers
of cultured cells in microtiter wells that is rapid and simple and does not require radioisotopes or removal of cells. 相似文献
9.
Culture conditions for arresting and stimulating the proliferation of a rainbow trout fibroblast cell line,RTG-2 总被引:1,自引:0,他引:1
L. E. J. Lee A. Martinez N. C. Bols 《In vitro cellular & developmental biology. Plant》1988,24(8):795-802
Summary Conditions for arresting and stimulating the proliferation of the rainbow trout fibroblast cell line RTG-2 have been examined
and the time course of events after stimulation determined. Quiescent populations were achieved in two ways. Cultures grown
to confluency without a medium change for at least 7 d had fewer than 5% of the cells in S phase and few mitotic figures.
Cultures deprived of serum, which could be done for up to 3 d without a loss in cell number, also achieved quiescence. After
3 d without serum, less than 1% of cells were in S phase and mitotic figures were infrequent. Addition to these cultures of
fresh serum-containing medium brought about the synchronous entry of cells into S phase and mitosis. For cultures in which
either the medium had been changed after 7 d without a change or serum-containing medium had been added after 3 d of serum
deprivation, DNA synthesis increased after a lag period of 20 to 24 h, was pronounced between 30 and 45 h, and then declined.
This was followed by a peak in the mitotic index. These protocols for arresting and subsequently stimulating RTG-2 proliferation
should allow the G1-S transition to be studied in a representative of teleosts.
This research was supported by Natural Sciences and Engineering Research Council of Canada grant to N. C. B. 相似文献
10.
Expression of c-myc protooncogene in rat lens cells during development,maturation and reversal of galactose cataracts 总被引:2,自引:0,他引:2
Yi Wen Songtao Shu Nalin J. Unakar Isaac Bekhor 《Molecular and cellular biochemistry》1992,112(1):73-79
It is well established that normal patterns of epithelial cell proliferation and metabolism, and of fiber cell differentiation and maturation are essential for the maintenance of transparency in the ocular lens. Several factors, including exposure to high levels of sugars, have been known to result in the compromise of lens transparency. For example, initiation of lens cell damage by galactose induces lens epithelial cells to proliferate. Elevated levels of c-myc mRNA have usually been correlated with rapid cell growth and increased entry of cells into the S phase. Therefore, changes in c-myc mRNA levels may provide an early indication of the stimulation of lens epithelial cells to proliferate and differentiate, which has been postulated to be an early and important event in response to lens cell injury by galactose. By Northern blot hybridization analysis we quantitated c-myc mRNA levels in the lens capsule epithelia of rats (1) exposed to galactose, and (2) undergoing a partial recovery from the galactose-induced cell damage. At the onset of lens cell damage, we find c-myc mRNA to elevate to 6-fold by 24 hr, and by 48 hr decreases to about 3-fold the normal levels. During recovery, c-myc mRNA continues to be expressed at high levels approaching a 10-fold increase by day 12, then decreasing to levels of about 8-fold the control by day 30. The 24 h transitory elevation in c-myc mRNA in lens epithelial cells is in accord with our previous observations on the 24 h increase in MP26, crystallin and aldose reductase mRNAs following a high influx of galactose. Therefore, the elevation in c-myc mRNA as well suggest that galactose appears to cause lens cells to undergo an early transitory period of gene induction following the exposure of lens cells to galactose. 相似文献