全文获取类型
收费全文 | 14217篇 |
免费 | 1113篇 |
专业分类
15330篇 |
出版年
2022年 | 101篇 |
2021年 | 177篇 |
2020年 | 122篇 |
2019年 | 156篇 |
2018年 | 223篇 |
2017年 | 167篇 |
2016年 | 337篇 |
2015年 | 558篇 |
2014年 | 554篇 |
2013年 | 819篇 |
2012年 | 991篇 |
2011年 | 949篇 |
2010年 | 667篇 |
2009年 | 521篇 |
2008年 | 783篇 |
2007年 | 856篇 |
2006年 | 854篇 |
2005年 | 822篇 |
2004年 | 802篇 |
2003年 | 732篇 |
2002年 | 745篇 |
2001年 | 163篇 |
2000年 | 113篇 |
1999年 | 163篇 |
1998年 | 218篇 |
1997年 | 151篇 |
1996年 | 131篇 |
1995年 | 140篇 |
1994年 | 122篇 |
1993年 | 118篇 |
1992年 | 138篇 |
1991年 | 97篇 |
1990年 | 79篇 |
1989年 | 98篇 |
1988年 | 88篇 |
1987年 | 79篇 |
1986年 | 83篇 |
1985年 | 96篇 |
1984年 | 128篇 |
1983年 | 102篇 |
1982年 | 113篇 |
1981年 | 109篇 |
1980年 | 98篇 |
1979年 | 65篇 |
1978年 | 69篇 |
1977年 | 64篇 |
1976年 | 60篇 |
1975年 | 50篇 |
1974年 | 58篇 |
1971年 | 43篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
Barbara A. Brennessel Kathleen J. Keyes 《In vitro cellular & developmental biology. Plant》1985,21(7):402-408
Summary The artificial sweetener saccharin inhibits binding of epidermal growth factor (EGF) to cultured rat pituitary tumor cells
(GH4C1 cells). Saccharin also causes morphological alterations in these cells, resulting in pronounced elongation, stretching, and
firmer attachment of cells to the culture dishes. These alterations in cell shape are similar to those observed after treatment
of GH4C1 cells with EGF and with thyrotropin-releasing hormone (TRH), both of which enhance prolactin (PRL) production in these cells.
After assaying for PRL in saccharin-treated cultures, it was observed that this sweetener is also capable of stimulating PRL
production two-to sixfold in a dose-dependent manner. Enhancement of PRL production can be observed at 0.5 mM saccharin, yet this is 10 times less than the saccharin concentration required to alter cell shape. These effects of saccharin
on cell morphology and on PRL production are reversible in GH4C1 cell cultures. When added to cultures along with maximal concentrations of EGF or TRH, the effects of saccharin on PRL production
are additive, suggesting that the actions of saccharin are mediated by a somewhat different pathway from that of the peptide
hormones. Pulse labeling studies indicate that the enhancement of PRL production is highly specific inasmuch as saccharin
was found to decrease the overall rate of protein synthesis in these cells. Saccharin also causes a decrease in the rate of
DNA synthesis under these treatment conditions. Mitomycin C, which similarly inhibited DNA synthesis, had no effect on cell
morphology or PRL production.
This investigation was supported by a Faculty Research Grant from Wheaton College 相似文献
52.
A method is described for the extraction of enkephalin-like peptides from peripheral nerve using chloroform and acidic methanol to facilitate a differential extraction of peptides and lipid. Porcine splanchnic nerve contains enkephalin-like peptides in low amounts compared to porcine adrenal medulla and striatum. Gel filtration chromatography reveals the presence of enkephalin-like peptides in both processed and cryptic forms. This is the first reported isolation and partial characterization of these peptides in splanchnic nerve. The presence of these peptides in this nerve provides support for the contention that the splanchnic nerve can modulate catecholamine release from the adrenal medulla through an effect on opiate receptors located on chromaffin cells. 相似文献
53.
Dynamics of orange peel fermentation during ensilage 总被引:2,自引:0,他引:2
G. Ashbell G. Pahlow Barbara Dinter Z. G. Weinberg 《Journal of applied microbiology》1987,63(4):275-279
The dynamics of fermentation during ensilage were studied on orange peel (variety Shamouti) ensiled in 50 plastic containers, 10 kg in each, with an outlet for seepage. At predetermined intervals the containers were weighed and samples were taken from three of them for chemical and microbial analysis. Fermentation losses amounted to up to ca one-third of the fresh peel dry matter (DM) content. Most losses occurred within 10 d of commencement of fermentation, and were attributable to gas release. The major fermentation products were ethanol, lactic and acetic acids (16, 3 and 3% of DM, respectively). The dominant microbial populations were lactobacilli and yeasts. Tests are in progress to inhibit the yeasts and thereby reduce fermentation losses. 相似文献
54.
Barbara A. Israel Warren I. Schaeffer 《In vitro cellular & developmental biology. Plant》1987,23(9):627-632
Summary Using both normal and transformed rat liver epithelial cells to prepare cytoplasmic hybrids (cybrids) we have found evidence
to support the theory that the cytoplasm from a normal cell can suppress tumorigenicity. A unique aspect of this study is
that all of the cells utilized, both normal and malignantly transformed, were derived from an original cloned cell. We found
that fusing cytoplasts from normal cells to malignantly transformed whole cells resulted in cybrid clones which, when injected
into newborn rat pups, isogenic with those from which the cell culture was initiated, yielted tumors in 51% of the animals
injected compared to 92% of the animals injected with the tumorigenic parent. Those animals that did develop tumors from the
cybrid cells survived longer than those injected with cells from the tumorigenic parent. Thus, the cybrid, formed of cytoplasm
from both parents, was less tumorigenic than the malignantly transformed parent cell. When reconstituted cells were prepared
by fusing cytoplasts from normal cells with karyoplasts from malignantly transformed cells, a situation in which essentially
all of the cytoplasm of the reconstituted cell is derived from normal cells, the tumorigenic phenotype was extinguished.
This work was supported in part by United States Public Health Service grant CA12056, and grant CA09100 from the National
Cancer Institute, Bethesda, MD. This work is partial fulfillment for the degree of Doctor of Philosophy for B.A.I. 相似文献
55.
Analyses for phytate by an indirect precipitation method and for the minerals calcium (Ca), zinc (Zn), iron (Fe), copper (Cu),
and manganese (Mn) by atomic absorption spectrophotometry were carried out on 100 foods available in New Zealand. Foods with
1% phytate (dry weight basis) included untoasted muesli, rolled oats, wheat germ, wheat bran, soybean, and some soy products.
Most breads contained between 0.35 and 0.60% phytate; legumes on average had 0.62% phytate, as did snack bars. There was a
wide variation in Ca and Zn contents: There was a tenfold variation in Ca content among the legume products, whereas there
was a seventyfold variation in Zn content among the cereals. The phytate: Zn molar ratio, which is presumed to indicate the
biovailability of Zn, was above 20∶1 for two-thirds of the cereals and almost all of the snack bars; it was above 15∶1 for
one-third of the breads, almost all of the legumes, and half of the legume products. These high phytate: Zn molar ratios,
as well as some Ca: phytate molar ratios above 6∶1, indicate that there might be a reduced biovailability of Zn in many of
the foods analyzed in this study. 相似文献
56.
Jan Lindgren Magdalena Blaszczyk Barbara Atkinson Zenon Steplewski Hilary Koprowski 《Cancer immunology, immunotherapy : CII》1986,22(1):1-7
Summary Over 600 hybridomas were derived from the immunization of mice with live cells and aqueous extracts of the human prostatic carcinoma cell line PC3. A total of 26 hybridomas with restricted reactivities were selected, subcloned and antibodies tested on a variety of tumor and normal cells. Seven monoclonal antibodies showed reactivity for prostate cancer and other tumor cell lines, including breast carcinomas. Three of the antibodies obtained after immunization with live cells reacted with live cells only and three of the four antibodies obtained after immunization with cell extract reacted with cell extracts and spent culture media. The fourth antibody in the latter group was reactive only in the immunoperoxidase staining assay. Antibody PrS5 recognized a 90,000 molecular weight molecule from 125I-surface-labeled cells in immunoprecipitation analysis. Antibodies PrE3 and PrD8 detected a nonacid glycolipid pentasaccharide from PC3 cells and meconium, and a glycoprotein of 115,000 molecular weight from 125I-surface-labeled red blood cells. The similar patterns of reactivity in RIAs and antigen analysis suggest that antibodies PrE3 and PrD8 recognize the same molecule. The results emphasize the usefulness of immunohistochemistry in the testing of monoclonal antibodies and the impact of the form in which the antigen is presented on the resultant antibody specificity 相似文献
57.
58.
Rodney F. Boyer Barbara E. Schori 《Biochemical and biophysical research communications》1983,116(1):244-250
Ceruloplasmin, a copper ferroxidase, promotes the incorporation of Fe(III) into the iron storage protein, apoferritin. The product formed is identical to ferritin as judged by polyacrylamide electrophoresis and iron/protein measurements. Of several proteins examined, only apoferritin accumulates the Fe(III) produced by ceruloplasmin. When ceruloplasmin was replaced by tyrosinase, which we have shown to have ferroxidase activity, no iron incorporation into apoferritin was observed. It is proposed that Fe(III) is transferred directly and specifically to apoferritin. These data support a more specific role for ceruloplasmin in iron metabolism than has previously been proposed. 相似文献
59.
L1210 leukemic cells injected in vivo are eliminated from the blood and disintegrated in organs such as the lungs and liver. We present a compartmental model which reproduces one type of in vivo experiment, based on the so-called perfusion curves. Although the data are not complete and some are only approximated, modeling gives a consistent picture of the process. 相似文献
60.
Eric R. Dabbs Renate Hasenbank Berthold Kastner Karl-Heinz Rak Barbara Wartusch Georg Stöffler 《Molecular & general genetics : MGG》1983,192(3):301-308
Summary A battery of immunological tests were used to investigate mutants which had been determined as lacking one or two ribosomal proteins on the basis of two-dimensional polyacrylamide gels. Proteins which were confirmed as missing from the ribosome in one or more mutants were large subunit proteins L1, L15, L19, L24, L27, L28, L30 and L33 and small subunit proteins S1, S9, S17 and S20. Cross-reacting material (CRM) was also absent from the post-ribosomal supernatant except in the case of protein S1. Since mutants lacking protein L11 have been previously described, any one of 13 of the 52 ribosomal proteins can be missing. None of these 13 proteins, except S1, can therefore have an indispensable role in ribosome function or assembly. In several mutants in which a protein was not missing but altered, it was present as several moieties of differing charge and size. 相似文献