全文获取类型
收费全文 | 7934篇 |
免费 | 821篇 |
出版年
2021年 | 108篇 |
2020年 | 55篇 |
2019年 | 76篇 |
2018年 | 108篇 |
2017年 | 92篇 |
2016年 | 148篇 |
2015年 | 232篇 |
2014年 | 277篇 |
2013年 | 352篇 |
2012年 | 523篇 |
2011年 | 424篇 |
2010年 | 302篇 |
2009年 | 264篇 |
2008年 | 365篇 |
2007年 | 370篇 |
2006年 | 341篇 |
2005年 | 322篇 |
2004年 | 334篇 |
2003年 | 305篇 |
2002年 | 288篇 |
2001年 | 211篇 |
2000年 | 195篇 |
1999年 | 189篇 |
1998年 | 105篇 |
1997年 | 98篇 |
1996年 | 84篇 |
1995年 | 96篇 |
1994年 | 89篇 |
1993年 | 67篇 |
1992年 | 161篇 |
1991年 | 123篇 |
1990年 | 121篇 |
1989年 | 117篇 |
1988年 | 105篇 |
1987年 | 96篇 |
1986年 | 110篇 |
1985年 | 78篇 |
1984年 | 83篇 |
1983年 | 76篇 |
1982年 | 89篇 |
1981年 | 68篇 |
1980年 | 54篇 |
1979年 | 81篇 |
1978年 | 87篇 |
1977年 | 68篇 |
1976年 | 58篇 |
1975年 | 77篇 |
1974年 | 79篇 |
1973年 | 53篇 |
1972年 | 50篇 |
排序方式: 共有8755条查询结果,搜索用时 875 毫秒
351.
R L Burger R J Schneider C S Mehlman R H Allen 《The Journal of biological chemistry》1975,250(19):7707-7713
The normal human granulocyte vitamin B12-binding protein, transcobalamin I, and transcobalamin III, have been labeled with 125I-labeled N-succinimidyl 3-(4-hydroxyphenyl)propionate and utilized for plasma clearance studies performed with rabbits. Both moieties of 125I-labeled granulocyte vitamin B12-binding protein-[57Co]vitamin B12 were cleared rapidly from the plasma (is less than 90% by 5 min) by the liver. After 30 min, the bulk of the 125I reappeared in the plasma in small molecular weight (less than 1000) form and was rapidly excreted in the urine. After 60 min the bulk of the [57Co]vitamin B12 reappeared in the plasma bound to rabbit transcobalamin II and was subsequently taken up by a variety of tissues. Approximately 15% of the 125I-labeled granulocyte vitamin B12-binding protein-[57Co-a1vitamin B12 was excreted intact into the bile during the period from 10 to 80 min after injection. The hepatic uptake of the protein-vitamin B12 complex was blocked by the prior injection of desialyzed fetuin but not by native fetuin. Similar results were obtained with 125I-labeled transcobalamin III-[57Co]vitamin B12. Approximately 90% of both moieties of 125I-labeled transcobalamin I-[57Co]vitamin B12 had prolonged plasma survivals similar to that of 125I-labeled bovine serum albumin. After treatment with neuraminadase, both moieties of the 125I-labeled transcobalamin I-[57Co]vitamin B12 complex were cleared rapidly from the plasma by the liver in a manner that was indistinguishable from that observed in the case of untreated granulocyte vitamin B12-binding protein and transcobalamin III. These observations indicate that desialyzed transcobalamin I and the native forms of the granulocyte vitamin B12-binding protein and transcobalamin III are cleared from plasma by the mechanism elucidated by Ashwell and Morell (Ashwell, G., and Morell A. G. (1974) Adv. Enzymol. 41, 99-128) that is capable of clearing a wide variety of asialoglycoproteins. These observations have implications concerning the function of the human R-type vitamin B12-binding proteins, the nature of the enterohepatic circulation of vitamin B12, the biological significance of the mechanism described by Ashwell and Morell, and the etiology of the increased plasma concentration of human R-type protein that occurs frequently in chronic myelogenous leukemia and occasionally in hepatocellular carcinoma and other solid tumors. 相似文献
352.
A technique is described for labeling mammalian chromosomes in vivo with BUdR. Rats and mice are given BUdR by tail vein infusion over a 24-h period at a concentration of 25 μg/g wt/h. Metaphase cells that have gone through two or three cycles of DNA synthesis reveal characteristic differential chromatid fluorescence after staining with Hoechst dye. Sister chromatid exchanges can then be easily detected in these cells. 相似文献
353.
Recently developed differential staining techniques based on the incorporation of bromodeoxyuridine (BUdR) into DNA permits the unequivocal identification of metaphase cells which have replicated once, twice, and three or more times. This technique has the potential of being utilized in the examination of kinetics of dividing cell populations. This potential is examined in a phytohemagglutinin-stimulated lymphocyte system. Determinations of the effect of increasing concentrations of BUdR on the distribution of metaphase cells between different generation cycles reveals no inhibition of cellular kinetics below 35 μM. The ability to distinguish third generation metaphase cells from subsequent generations is examined through the determination of “labelled” centromeric regions. The applicability of this system to current cellular kinetics is discussed. 相似文献
354.
Isolation and Genetic Analysis of Mutant Strains of CHLAMYDOMONAS REINHARDI Defective in Gametic Differentiation 总被引:1,自引:0,他引:1
Impotent mutant strains of Chlamydomonas reinhardi, mating-type (mt) plus, are described that have normal growth and motility but fail to differentiate into normal gametes. Procedures for their isolation and their genetic analysis are described. Five of the imp strains (imp-2, imp-5, imp-l, imp-7, and imp-8) exhibit no flagellar agglutination when mixed with mt- or mt+ gametes and the mutations are shown to be unlinked to the mt locus (with the possible exception of imp-7). Two of the strains (imp-3 and imp-4) carry leaky mutations that affect cell fusion; neither mutation is found by tetrad analysis to be linked to mt or to the other. Cells of the imp-1 strain agglutinate well with mt- gametes and active agglutination continues for up to 48 hours, but cell fusion occurs only very rarely. Analysis of these rare zygotes indicates that imp-1 is closely linked to the mt+ locus, and fine-structural studies reveal that imp-1 gametes produce a mutant mating structure involved in zygotic cell fusion. The development of sexuality in C. reinhardi therefore appears amenable to genetic dissection. 相似文献
355.
356.
Craig W. Schneider 《Journal of phycology》1975,11(4):391-396
Six members of the Ceramiales are added to the flora of North Carolina. Two of these, Acrosorium uncinatum (Turner) Kylin and, Rhododictyon bermudensis Taylor, are also reported from South Carolina for the first time. One species, Mesothamnion boergeseni Joly, was previously known only from Brazil and another, Dipterosiphonia reversa sp. nov., is added to the algal literature for the first time. Evidence is presented for the reassignment of R. bermudensis from the Dasyaceae to the Ceramiaceae. 相似文献
357.
Hassan-Fahmi Aly Hans Geiger Ursula Schücker Hugh Waldrum George Vander Velde Tom J. Mabry 《Phytochemistry》1975,14(7):1613-1615
Ten glycosides of kaempferol and quercetin, including the hitherto unknown kaempferol and quercetin 3-rutinoside-7-rhamnosides, have been isolated from Equisetum silvaticum L. 相似文献
358.
An abrupt concommitant increase in total cellular RNA and protein was observed as cultured human diploid fibroblasts entered the senescent phase of their in vitro lifespan. DNA content remained stable from early to final passages. Fractionation of cellular RNAs by polyacrylamide gel electrophoresis demonstrated an increase in both 28S and 18S ribosomal and 4S transfer RNAs in these senescent cells. Separation of poly(A) RNA (mRNA) by oligo(dT)-cellulose chromatography suggests an increase in this group of RNAs. However, the ratios of 28S to 18S rRNAs, tRNA to rRNA, and mRNA to total cellular RNA were not significantly different in cells before and after senescence, indicating that the overall increases in total cellular RNA was not due to an accumulation of a single RNA class. 相似文献
359.
360.
W Schepp J Schneider C Tatge V Schusdziarra M Classen 《Clinical physiology and biochemistry》1990,8(3):128-139
Parietal cells are a major source of gastric mucosal prostaglandins in various species. We examined cholinergic stimulation of prostaglandin E2 (PGE2) release from human parietal cells; using activators of the protein kinase C we attempted to get an indirect insight into cellular mechanisms which control PGE2 release. Gastric mucosal specimens were obtained at surgery and the cells were dispersed by collagenase and pronase E. Parietal cells were enriched to 65-80% by a Percoll gradient, and were incubated for 30 min. PGE2 release into the medium (radioimmunoassay) was 74-126 pg/10(6) cells/30 min under basal conditions and was 2.6-fold increased by carbachol (10(-5) and 10(-4) M). Similarly, PGE2 release was stimulated by phospholipase C (20-200 mU/ml, 364% above basal), 1-oleoyl-2-acetyl-sn-glycerol (10(-9)-10(-5) M, 229%), 12-O-tetradecanoylphorbol-13-acetate (TPA; 10(-9)-10(-5) M, 283%) and calcium ionophore A23187 (10(-7)-10(-5) M, 219%). Simultaneous presence of A23187 and TPA synergistically induced stimulation which was slightly higher than the sum of the individual responses. N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide W-7, a putative calmodulin antagonist, inhibited TPA-induced PGE2 release at concentrations regarded specific for blocking calmodulin (IC50 = 1.5 X 0(-6) M). We conclude that in human parietal cells PGE2 is released upon cholinergic stimulation and that phospholipase C and protein kinase C are involved in the control of PGE2 release. We speculate that calmodulin might interact with a protein phosphorylated by protein kinase C to cause PGE2 release. 相似文献