全文获取类型
收费全文 | 29370篇 |
免费 | 2323篇 |
国内免费 | 3篇 |
出版年
2023年 | 226篇 |
2022年 | 307篇 |
2021年 | 620篇 |
2020年 | 448篇 |
2019年 | 530篇 |
2018年 | 942篇 |
2017年 | 797篇 |
2016年 | 1032篇 |
2015年 | 1278篇 |
2014年 | 1302篇 |
2013年 | 1875篇 |
2012年 | 2445篇 |
2011年 | 2487篇 |
2010年 | 1477篇 |
2009年 | 1192篇 |
2008年 | 1809篇 |
2007年 | 1729篇 |
2006年 | 1633篇 |
2005年 | 1408篇 |
2004年 | 1400篇 |
2003年 | 1260篇 |
2002年 | 1156篇 |
2001年 | 564篇 |
2000年 | 615篇 |
1999年 | 399篇 |
1998年 | 311篇 |
1997年 | 207篇 |
1996年 | 196篇 |
1995年 | 162篇 |
1994年 | 177篇 |
1993年 | 153篇 |
1992年 | 142篇 |
1991年 | 122篇 |
1990年 | 107篇 |
1989年 | 90篇 |
1988年 | 78篇 |
1987年 | 77篇 |
1986年 | 56篇 |
1985年 | 85篇 |
1984年 | 86篇 |
1983年 | 62篇 |
1982年 | 70篇 |
1981年 | 67篇 |
1980年 | 57篇 |
1979年 | 53篇 |
1978年 | 38篇 |
1977年 | 45篇 |
1976年 | 32篇 |
1975年 | 40篇 |
1973年 | 42篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
Palmar flexion creases have been studied in schizophrenics with a family history of schizophrenia or other psychiatric disorders
and without such a background, and compared to a control population. Palmar flexion creases have been analyzed according to
the method suggested byBali & Chaube (1971). When compared to controls, differences in the DRBC and TRBC frequencies are significant in the subgroup with no family
history, supporting the existence of biological heterogeneity in schizophrenia, and of congenital factors when there is no
known genetic background. 相似文献
102.
M. Mačor 《Folia microbiologica》1988,33(6):466-473
Streptomycin and N-methyl-N’-nitro-N-nitrosoguanidine (MNNG) cause a 100% hereditary bleaching ofEuglena gracilis. In spite of the outcomes being the same, the corresponding mechanisms differ. By investigating the incorporation of the14C-labelled precursors of macromolecule synthesis we showed streptomycin to inhibit the synthesis of nucleic acids and proteins to the same extent (56%), whereas in the case of MNNG a 66% inhibition of nucleic acid synthesis and a 24% one of protein synthesis were observed. 相似文献
103.
The components of magnesium efflux in squid axons have been studied under internal dialysis and voltage clamp conditions. The present report rules out the existence of an ATP-dependent, Na0- and Mg0-independent Mg2+ efflux (ATP-dependent Mg2+ pump) leaving the Mg2+---Na+ exchange system as the only mechanism for Mg2+ extrusion. The main features of the Mg2+ efflux are: (1) The efflux is completely dependent on ATP. (2) The efflux can be activated either by external Na+ (forward Mg2+---Na+ exchange) or external Mg2+ (Mg2+---Mg2+ exchange). (3) The mobility of the Mg2+ exchanger in the Na0+-loaded form is greater than that in the Mg2+-loaded one. (4) In variance with the Na+---Ca2+ exchange mechanism, Mg2+---Mg2+ exchange is not activated by external monovalent cations. (5) ATPγS replaces ATP in activating Mg2+---Na+ exchange suggesting that a phosphorylation/dephosphorylation process regulates this transport mechanism. 相似文献
104.
Solubilization of the active vasoactive intestinal peptide receptor from human colonic adenocarcinoma cells 总被引:1,自引:0,他引:1
A el Battari J M Martin J Luis O Pouzol J Secchi J Marvaldi J Pichon 《The Journal of biological chemistry》1988,263(33):17685-17689
The non-ionic detergent n-octyl-beta-D-glucopyranoside was used to solubilize the VIP (vasoactive intestinal peptide) receptor from human colonic adenocarcinoma cell line HT29-D4. The binding of monoiodinated 125I-VIP to the solubilized receptor was specific, time-dependent, and reversible. Scatchard analysis of data obtained from competitive displacement of monoiodinated 125I-VIP by native VIP suggested the presence of two classes of VIP binding sites with Kd values of 0.32 and 46.7 nM. The binding capacities of these two classes were 1.7 x 10(10) and 30.2 x 10(10) sites/mg of proteins, respectively. The solubilized receptor retained the specificity of the human VIP receptor towards the peptides of the VIP/secretin/glucagon family. The order of potency in inhibiting monoiodinated 125I-VIP binding was VIP (IC50 = 1.0 x 10(-9) M) much greater than peptide histidine methionine amide (IC50 = 10(-7) M) greater than growth hormone-releasing factor (IC50 = 3 x 10(-7) M) greater than secretin (IC50 greater than 10(-6) M); glucagon had no effect on VIP binding. The reducing agent dithiothreitol inhibited in a dose-dependent manner the binding of 125I-VIP. Covalent cross-linking experiments between the solubilized receptor and 125I-VIP showed that after sodium dodecyl sulfate-polyacrylamide gel electrophoresis and autoradiography two major and one minor polypeptides of Mr 67,000, 72,000, and 83,000 were specifically labeled. When analyzed by gel filtration, the n-octyl-beta-D-glucopyranoside-solubilized 125I-VIP-receptor complex was resolved into two major peaks with molecular mass in the range of 60-70 and 270-300 kDa. Thus, the soluble form of the VIP receptor was probably a multimeric complex in which disulfide bonds may play an important role to hold the receptor in an active configuration. 相似文献
105.
Maria Jose Gil Quilez 《Hydrobiologia》1986,143(1):209-212
Siliceous remains from Miocene lacustrine sediments near Libros (Teruel, Spain) are studied. Most of them are sponge spicules and may be assigned to Ephydatia fluviatilis. Some chrysophycean cysts and several diatom genera (Melosira, Cyclotella, Fragilaria, Navicula, Pinnularia, and Cymbella) have also been found. 相似文献
106.
Isolation and Characterization of an Fe(III)-Chelating Compound Produced by Pseudomonas syringae 总被引:2,自引:2,他引:0
下载免费PDF全文
![点击此处可从《Applied microbiology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Luis Torres Jos E. Prez-Ortín Vicente Tordera Jos P. Beltrn 《Applied microbiology》1986,52(1):157-160
The phytopathogenic bacterium Pseudomonas syringae produces a fluorescent pigment when it is grown in iron-deficient media. This pigment forms a very stable Fe(III) complex that was purified in this form by using a novel procedure based on ultrafiltration and column chromatography. The Fe(III) complex has a molecular weight of 1,100 and contains 1 mol of Fe(III). The pigment is composed of an amino acid moiety with three threonines, three serines, one lysine, δ-N-hydroxyornithine, and a quinoline-type fluorescent chromophore. These features and its stability constant (in the range of 1032) suggest that the fluorescent pigment of P. syringae is related to the siderophores produced by another Pseudomonas species. 相似文献
107.
Jose M. Martinez-Zapater Mark A. Estelle Chris R. Somerville 《Molecular & general genetics : MGG》1986,204(3):417-423
Summary Three members of a family of highly repeated DNA sequences from Arabidopsis thaliana have been cloned and characterized. The repeat unit has an average length of 180 bp and is tandemly repeated in arrays longer than 50 kb. This family represents more than one percent of the Arabidopsis genome. Sequence comparisons with tandemly repeated DNA sequences from other Cruciferae species show several regions of homology and a similar length of the repeat unit. Homologies are also found to highly repeated sequences from other plant species. When the sequence CCGG occurs in the repeated DNA, the inner cytosine is generally methylated. 相似文献
108.
109.
General recombination mechanisms in extracts of meiotic cells 总被引:9,自引:0,他引:9
Yasuo Hotta Satoshi Tabata Robert A. Bouchard Ramon Piñon Herbert Stern 《Chromosoma》1985,93(2):140-151
RecA-like proteins have been purified from somatic and meiotic cells of mouse and lily. The rec proteins have been designated s-rec and m-rec to indicate their respective tissues of origin. The two proteins differ in molecular weight and in their response to temperature, the latter being consistent with the optimal temperature for physiological function of their tissues of origin. There is a major increase in m-rec protein with the entry of cells into meiosis, the peak of activity being early pachytene. Extracts of the cells and also those of yeast (Saccharomyces cerevisiae) have been prepared that have the capacity to catalyze homologous recombination. These extracts behave similarly to the m-rec proteins upon entry of cells into meiosis. Yeast transferred to sporulation medium displays a 100-fold increase in the recombination activity of the extract at about the time of entry into meiosis. The occurrence of peak levels of m-rec and recombination activity in extracts from cells in early pachytene points strongly to that stage as the time at which the enzymatic phase of recombination occurs. 相似文献
110.
Covalent cross-linking of vasoactive intestinal peptide (VIP) to its receptor in intact colonic adenocarcinoma cells in culture (HT 29) 总被引:1,自引:0,他引:1
J M Muller J Luis J Fantini B Abadie F Giannellini J Marvaldi J Pichon 《European journal of biochemistry》1985,151(2):411-417
[125I]Monoiodinated vasoactive intestinal peptide (125I-VIP) was cross-linked with human colonic adenocarcinoma cells (HT29 cells) grown as a monolayer using dithiobis(succinimidylpropionate) as cross-linking reagent. The cross-linked polypeptides were separated by polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. A major polypeptide of Mr = 67 000 was characterized and it behaved like a high-affinity binding site for VIP according to the following data. The concentration of native VIP (0.5 nM) giving half-maximum inhibition of 125I-VIP covalent cross-linking with this polypeptide was very similar to that giving half-maximum displacement of 125I-VIP on HT 29 cells (0.6 nM). Glucagon or insulin was unable to inhibit the labelling of the Mr-67 000 component. In our experimental conditions neither specific 125I-VIP binding nor covalent labelling was observed with monolayers of Madin Darby canine kidney epithelial cells (MDCK cells) or African green monkey kidney fibroblasts (Vero cells) while the Mr-67 000 polypeptide was also characterized with human rectal adenocarcinoma cells (HRT 18 cells), known to possess the VIP receptor. Preincubation of HT 29 cells with native VIP at 37 degrees C, before 125I-VIP binding and subsequent cross-linking reaction, decreased the labelling of the Mr-67 000 polypeptide up to 80%. Assuming one molecule of 125I-VIP cross-linked per polypeptide, we have characterized, for the first time, a major polypeptide of Mr = 64 000, which belongs to the high-affinity VIP binding site of an intestinal human cell line. 相似文献