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11.
Elissavet Kardami 《Molecular and cellular biochemistry》1990,92(2):129-135
Summary We have examined the effect of crude cardiac tissue extracts as well as that of several growth factors and triiodothyronin (T3) on DNA synthesis of cardiac myocytes in culture. Extracts from embryonic and adult cardiac tissue stimulated DNA synthesis of myocytes. Atrial myocytes exhibited overall higher degree of stimulation than their ventricular counterparts and extracts from adult atrial tissue had the highest apparent mitogenic activity for atrial myocytes. We have shown that adult heart contains basic fibroblast growth factor (bFGF), especially in the atria [1]. Transforming growth factor (TGF) and insulin-like growth factors (IGFs) are also accumulated in cardiac tissues [2, 3]. We found that bFGF and the IGFs stimulate myocyte cell proliferation and DNA synthesis. These factors also stimulate cardiac non-muscle proliferation, especially in the presence of serum. TGF inhibited proliferation and DNA synthesis and cancelled the effect of bFGF or IGFs on the myocytes. T3 also diminished the bFGF-induced mitogenic stimulation of cardiomyocytes. Our data suggest that these factors may be involved in the regulation of cardiomyocyte proliferation in vivo.Abbreviations bFGF
basic Fibroblast Growth Factor
- BSA
Bovine Serum Albumin
- DM
Defined Medium
- Fes
Fetal calf serum
- FITC
Fluorescein
- IGF
Insulin-like Growth Factor
- IgG
Immunoglobulin
- LI
Labeling Index
- PBS
Phosphate Buffered Saline
- T3
Triiodothyronine
- TGF
Transforming Growth Factor 相似文献
12.
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
13.
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
14.
Øyvind Skraastad Karl L. Reichelt 《Virchows Archiv. B, Cell pathology including molecular pathology》1988,56(1):321-325
Previous work indicates that the colonic epithelial cell proliferation in mice is reversibly inhibited by the tripeptide pGlu-His-GlyOH
found in aqueous extracts of the intestine. In the present study we examined the possible tissue specificity of the colon
mitosis inhibitor. The mitotic rate in the small intestine, epidermis and forestomach in mice was registered after a single
i.p. injection of the tripeptide. A significantly reduced rate of cell renewal was found at 18 h in the epidermis whereas
no inhibition was observed in the forestomach or ileal epithelium. To investigate whether the amino acid sequence of the tripeptide
is essential for the inhibitory effect, three structurally related bioactive peptides were tested and compared to the effect
of CMI. CMI showed a bell-shaped dose-response relationship as previously shown, whereas the mitotic rate was not reduced
in the colonie epithelium after treatment with either an epidermal mitosis inhibitory pentapeptide, or the dipeptide pGlu-GlyOH,
or an analogue of luteinizing hormone-releasing hormone. The efficacy of the tripeptide was dependent on the basal rate of
cell renewal in the colonie epithelium. When the tripeptide was given at the circadian nadir of cell proliferation a delayed
reduction of the proliferative activity was observed at 6 h after treatment, whereas treatment when the rate of cell proliferation
was at its circadian zenith gave an immediate mitotic inhibition. 相似文献
15.
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
16.
Human alpha or beta interferons inhibit the proliferation of Daudi Burkitt lymphoma cells and induce the differentiation of these cells towards a mature plasma cell phenotype. Similar responses are seen when Daudi cells are treated with the phorbol ester, TPA. Both interferons and TPA down-regulate expression of the c-myc oncogene in these cells. Although TPA can mimic the effect of interferon on cell differentiation, it does not induce 2'5' oligoadenylate synthetase or the interferon-sensitive mRNAs, 6-16 or 9-27. Thus chronic stimulation of protein kinase C by TPA cannot mimic all of the effects of interferon treatment on gene expression. Inhibition of ADP-ribosyl transferase activity by 3-methoxybenzamide impairs interferon- or TPA-induced differentiation of Daudi cells. This agent induces a higher level of c-myc mRNA in the cells and stimulates the incorporation of [3H]thymidine into DNA; although these effects are partially counteracted by interferon or TPA treatment, the elevated expression of the c-myc gene may be sufficient to prevent terminal differentiation and allow cell proliferation to continue. 相似文献
17.
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
18.
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
19.
测定了3T3细胞、人和大鼠一些组织中DNA拓扑异构酶Ⅰ的活性;估计了核酸内切酶对拓扑酶Ⅰ松弛活性测定的干扰程度;发现增殖组织全细胞抽提液中酶比活高于正常分化组织,而且在异常增殖组织中酶比活的增高更为显著。 相似文献
20.
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