全文获取类型
收费全文 | 4973篇 |
免费 | 566篇 |
国内免费 | 4篇 |
出版年
2021年 | 55篇 |
2020年 | 38篇 |
2019年 | 57篇 |
2018年 | 60篇 |
2017年 | 49篇 |
2016年 | 100篇 |
2015年 | 125篇 |
2014年 | 177篇 |
2013年 | 194篇 |
2012年 | 281篇 |
2011年 | 286篇 |
2010年 | 176篇 |
2009年 | 163篇 |
2008年 | 241篇 |
2007年 | 221篇 |
2006年 | 214篇 |
2005年 | 211篇 |
2004年 | 231篇 |
2003年 | 191篇 |
2002年 | 224篇 |
2001年 | 127篇 |
2000年 | 120篇 |
1999年 | 112篇 |
1998年 | 75篇 |
1997年 | 73篇 |
1996年 | 92篇 |
1995年 | 70篇 |
1994年 | 67篇 |
1993年 | 54篇 |
1992年 | 106篇 |
1991年 | 88篇 |
1990年 | 73篇 |
1989年 | 73篇 |
1988年 | 72篇 |
1987年 | 51篇 |
1986年 | 54篇 |
1985年 | 61篇 |
1984年 | 65篇 |
1983年 | 52篇 |
1982年 | 50篇 |
1981年 | 58篇 |
1980年 | 47篇 |
1979年 | 50篇 |
1978年 | 46篇 |
1977年 | 55篇 |
1976年 | 38篇 |
1975年 | 40篇 |
1973年 | 36篇 |
1972年 | 38篇 |
1971年 | 34篇 |
排序方式: 共有5543条查询结果,搜索用时 31 毫秒
91.
pH Selectivity of N-Ethylmaleimide Reactions with Opiate Receptor Complexes in Rat Brain Membranes 总被引:1,自引:1,他引:0
N-Ethylmaleimide (NEM) decreases opiate agonist binding presumably by blocking crucial sulfhydryl (SH) groups at receptor binding sites. At physiological pH, NEM decreased GTP and manganese regulation but increased sodium effects on [3H]D-Ala2-Met5-enkephalinamide (D-Ala enk) binding to rat brain membranes. To determine the apparent pK values of putative SH groups in opiate receptors that react with NEM, rat brain membranes were incubated with 100-250 microM NEM in buffers ranging from pH 4.5 to 8.0. Results showed that lowering pH below 6.5 reduced the NEM effect on opiate receptor functions and that the apparent pK values of NEM-reacting SH groups in binding and regulatory sites ranged between 5.4 to 6.0. Most of the total SH groups in brain membranes continued to react with NEM at low pH, so that when nonspecific SH groups were blocked by incubating membranes at pH 4.5 with NEM, opiate receptors became sensitive to very low concentrations (1 microM) of NEM. 相似文献
92.
M K Jenkins R W Melvold S D Miller 《Journal of immunology (Baltimore, Md. : 1950)》1984,133(2):616-622
We have isolated a BALB/c (H-2d, Mlsb) T cell clone (JTL-G12) specific for the synthetic polypeptide antigen poly(Glu60Ala30Tyr10) (GAT) in the context of self I-A determinants and for Mlsa,d antigens in the absence of GAT. JTL-G12 proliferation in response to GAT was mapped to the Kd, I-Ad subregions by using inbred H-2 congenic and recombinant strains. In addition, monoclonal antibody directed against I-Ad but not Kd or I-As determinants blocked JTL-G12 proliferation in response to GAT presented by syngeneic splenocytes, indicating I-A restriction. The Mls cross-reactivity of this clone was verified by using a panel of inbred strains bearing the Mlsa,b,c,d alleles and by using BXD recombinant inbred strains bearing the Mlsa allele or the Mlsb allele. All of the Mlsa BXD strains of the H-2d or H-2b haplotypes stimulated JTL-G12 in the absence of GAT, whereas all of the Mlsb BXD strains were nonstimulatory. This response pattern is in complete accordance with recognition of the Mlsa determinant encoded by Mls or closely linked loci on chromosome 1. JTL-G12 proliferation in response to GAT/I-Ad and Mlsa,d determinants could be blocked with a monoclonal antibody (GK1.5) directed against L3T4, a structure involved in class II major histocompatibility complex antigen recognition. These results suggest that antigen/class II responsiveness, Mls reactivity, and expression of L3T4 can be properties of a single T cell population. 相似文献
93.
94.
Norma L. Trolinder Jerry D. Berlin Joe R. Goodin 《In vitro cellular & developmental biology. Plant》1987,23(11):789-794
Summary A cotton cell suspension culture has been developed that provides unique opportunities for plant biologists to investigate
early developmental events regulating cotton fiber properties, plant cell elongation, and cell wall biogenesis. The suspension
culture was derived from cells of cotton (Gossypium hirsutum L.) ovule callus. These cells undergo the stages of fiber development
previously described for in vivo fiber development. Fibers range in length up to 11 mm and have secondary walls.
Supported by the U.S. Department of Agriculture, Agricultural Research Service, Southern Regional Research Laboratory, New
Orleans, Louisiana, and Cotton Incorporated, Raleigh, North Carolina. 相似文献
95.
The mechanisms underlying Ir gene control of CMI were addressed by examining the DTH and Tprlf responses specific for the synthetic polymers GT, GAT, and GA. We show that BALB/c mice (GAT/GA responders, GT nonresponders) primed with GT fail to develop DTH and Tprlf responses specific for GT, GAT, or GA. GAT immunization resulted in DTH responses that could be elicited not only with GAT and GA but also with GT, demonstrating that GT-specific TDH are present in nonresponder mice. GT-specific DTH was transferred with Thy-1+ Lyt-1+2–, H-2 Irestricted, nylon wool nonadherent cells. GA-primed BALB/c mice developed GAT- and GA-, but not GT-apecific DTH responses, indicating that GA and GT do not cross-react at the T-cell level. The ability of GAT [but not a mixture of GA plus GT, or GT electrostatically complexed to the immunogenic carrier MBSA (GT-MBSA)] to induce GT-specific DTH suggested a requirement for covalent linkage of stimulatory GA and nonstimulatory GT determinants present on the GAT molecule. Similarly, GT-specific in vitro Tprlf responses could be demonstrated in GAT-primed mice exhibiting significant levels of GT-specific DTH but not in GT- or GT-MBSA-primed mice. Tolerization experiments also suggested that GT-specific Th were involved in the development of GT-specific DTH in GAT-primed mice. The GT nonresponsiveness of BALB/c mice for DTH and Tprlf responses could not be reversed by treatments designed to abrogate Ts activity (priming with GT-MBSA and CY injection), nor could GT-primed cells be shown to inhibit the development or elicitation of GT-specific CMI in GAT-primed mice during the afferent and/or efferent stages of DTH. Our results suggest that GT nonresponsiveness does not result from the absence of GT-specific T cells or preferential induction of Ts. The results are discussed in the context of hole-in-the-repertoire and antigen presentation (determinant selection) models of Ir gene control.Abbreviations used in this paper APC
antigen-presenting cells
- BSA
bovine serum albumin
- BSS
Mishell-Dutton balanced salt solution
- CFA
complete Freund's adjuvant
- CMI
cell-mediated immunity
- CY
cyclophosphamide
- DTH
delayed-type hypersensitivity
- GA
poly(Glu60Ala40)
- GAT
poly (Glu60Ala30Tyr10)
- GT
poly(Glu50Tyr50)
- GT-MBSA
GT complexed to methylated bovine serum albumin
- It
immune response
- LN
lymph node
- PPD
purified protein derivative of tuberculin
- TDH
DTH T cells
- Th
helper T cells
- Tprlf
T-cell proliferation
- Ts
suppressor T cells
- TsF
T-cell suppressor factor(s) 相似文献
96.
Esmail K. Shubber David Jacobson-Kram Dr. Jerry R. Williams 《Cell biology and toxicology》1986,2(3):379-399
Seven antischistosomal drugs, two antimalarial drugs, and one antiamoebic drug were tested in all five Ames strains for induction of mutation, as well as for induction of cytotoxicity, inhibition of cellular progression, and the induction of sister chromatid exchanges in two cultured mammalian cell lines. We found that two agents shown to be negative in the Ames test were positive for sister chromatid exchange induction. Based on qualitative and quantitative evaluation, we find that all but three of the pharmaceuticals should be considered to be potential human carcinogens.Abbreviations AA
2-aminoanthracene
- 9AACC
9-aminoacridine
- AM
amoscanate
- BrdUU
bromodeoxyuridine
- CA
chloroquine diphosphate
- CHO
Chinese hamster ovary
- CQ
chloroquine
- DAPI
46-diamidino-2-phenylindole
- DHY
dehydroemetine
- DMSO
dimethyl sulfoxide
- EB
ethidium bromide
- FCS
fetal calf serum
- FN
4-fluoro-3-nitrophenyl azide
- HY
hycanthone
- ICP
inhibiting cell progression
- LU
lucanthone
- MEM
minimal essential medium
- 2NF
2-nitrofurantoin
- 4NPD
4-nitro-O-phenylenediamine
- NZ
niridazole
- OL
oltipraz
- OX
oxaminiquine
- PBS
phosphate buffered saline
- PQ
primaquine
- PZ
praziquantel
- SA
sodium azide
- SCE
sister chromatid exchange 相似文献
97.
Detection of Sendai virus fusion with human erythrocytes by fluorescence photobleaching recovery 总被引:1,自引:0,他引:1
The subunit stoichiometry of the ATP synthetase (CF1-CF0) immunoprecipitated from Triton X-100 extracts of chloroplast thylakoid membranes was determined to be α3, β3, γ, δ, ? (CF1) and I0.3, II0.6–0.9, III4(6) (CF0). Antibodies against the polypeptides α, β, γ, δ, I, II and ? combined specifically with the isolated subunits as analysed by the protein blotting method. Applying this technique, antibodies against the CF1 subunits were found to form complexes with the corresponding polypeptides of thylakoids, whereas those against I (Mr 20 000) and II (Mr 17 000) combined with Mr 26 000 and Mr 24 500 membrane polypeptides, respectively. The Mr 26 000 polypeptide was identified as the major subunits of the light-harvesting chlorophyll a/b-protein (LHCP) complex and the Mr 24 500 component seems to be functionally connected with this complex. From the results it is concluded that the chloroplast ATP synthetase consists of the subunit of the α, β, γ, δ, ? and III (proteolipid only and that proteolytically altered LHCP polypeptides bind artifically to the protein complex during isolation. 相似文献
98.
99.
Jerry R. Colca Nirmala Kotagal Paul E. Lacy Michael L. McDaniel 《生物化学与生物物理学报:生物膜》1983,729(2):176-184
The properties of active or ATP-dependent calcium transport by islet-cell endoplasmic reticulum and plasma membrane-enriched subcellular fractions were directly compared. These studies indicate that the active calcium transport systems of the two membranes are fundamentally distinct. In contrast to calcium uptake by the endoplasmic reticulum-enriched fraction, calcium uptake by islet-cell plasma membrane-enriched vesicles exhibited a different pH optimum, was not sustained by oxalate, and showed an approximate 30-fold greater affinity for ionized calcium. A similar difference in affinity for calcium was exhibited by the Ca2+-stimulated ATPase activities which are associated with these islet-cell subcellular fractions. Consistent with the effects of calmodulin on calcium transport, calmodulin stimulated Ca2+-ATPase in the plasma membranes, but did not increase calcium-stimulated ATPase activity in the endoplasmic reticulum membranes. The physiological significance of the differences observed in calcium transport by the endoplasmic reticulum and plasma membrane fractions relative to the regulation of insulin secretion by the islets of Langerhans is discussed. 相似文献
100.
Constantin Cojocel Keizo Maita Dale A. Pasino Chao-Hen Kuo Jerry B. Hook 《Life sciences》1983,33(9):855-861
Proximal and distal tubule suspensions were prepared from kidneys of Sprague-Dawley rats by an isolation procedure on a PercollR gradient. The marker enzymes alkaline phosphatase (brush border) and hexokinase (cytoplasmic) as well as p-aminohippurate transport capacity, gluconeogenic activity and electron microscopy were used to characterize the two kidney tubule suspensions. The results of this study indicate that cytochrome P-450 is localized to the proximal tubular cells and that the O-deethylation of 7- ethoxycoumarin was higher in the proximal than distal fraction. Both proximal and distal tubules showed glucuronidation and deacetylation capacities and a relatively equal distribution of non-protein sulfhydryls. These studies demonstrate metabolic heterogeneity of the nephron, the proximal tubule being the main site of renal xenobiotic metabolism. Understanding of metabolic heterogeneity of proximal and distal kidney tubules should provide important information regarding cell specific mechanisms of nephrotoxicity. 相似文献