全文获取类型
收费全文 | 4230篇 |
免费 | 526篇 |
国内免费 | 3篇 |
出版年
2022年 | 27篇 |
2021年 | 69篇 |
2020年 | 41篇 |
2019年 | 40篇 |
2018年 | 47篇 |
2017年 | 61篇 |
2016年 | 92篇 |
2015年 | 138篇 |
2014年 | 172篇 |
2013年 | 218篇 |
2012年 | 253篇 |
2011年 | 276篇 |
2010年 | 189篇 |
2009年 | 153篇 |
2008年 | 233篇 |
2007年 | 260篇 |
2006年 | 225篇 |
2005年 | 229篇 |
2004年 | 209篇 |
2003年 | 219篇 |
2002年 | 206篇 |
2001年 | 94篇 |
2000年 | 70篇 |
1999年 | 75篇 |
1998年 | 59篇 |
1997年 | 54篇 |
1996年 | 50篇 |
1995年 | 47篇 |
1994年 | 55篇 |
1993年 | 40篇 |
1992年 | 53篇 |
1991年 | 60篇 |
1990年 | 48篇 |
1989年 | 56篇 |
1988年 | 40篇 |
1987年 | 45篇 |
1986年 | 38篇 |
1985年 | 40篇 |
1984年 | 37篇 |
1983年 | 34篇 |
1982年 | 29篇 |
1981年 | 21篇 |
1980年 | 27篇 |
1979年 | 38篇 |
1978年 | 29篇 |
1977年 | 20篇 |
1976年 | 22篇 |
1974年 | 27篇 |
1972年 | 21篇 |
1970年 | 20篇 |
排序方式: 共有4759条查询结果,搜索用时 218 毫秒
71.
72.
73.
The alphaviruses are a genus of 26 enveloped viruses that cause disease in humans and domestic animals. Mosquitoes or other hematophagous arthropods serve as vectors for these viruses. The complete sequences of the +/- 11.7-kb plus-strand RNA genomes of eight alphaviruses have been determined, and partial sequences are known for several others; this has made possible evolutionary comparisons between different alphaviruses as well as comparisons of this group of viruses with other animal and plant viruses. Full-length cDNA clones from which infectious RNA can be recovered have been constructed for four alphaviruses; these clones have facilitated many molecular genetic studies as well as the development of these viruses as expression vectors. From these and studies involving biochemical approaches, many details of the replication cycle of the alphaviruses are known. The interactions of the viruses with host cells and host organisms have been exclusively studied, and the molecular basis of virulence and recovery from viral infection have been addressed in a large number of recent papers. The structure of the viruses has been determined to about 2.5 nm, making them the best-characterized enveloped virus to date. Because of the wealth of data that has appeared, these viruses represent a well-characterized system that tell us much about the evolution of RNA viruses, their replication, and their interactions with their hosts. This review summarizes our current knowledge of this group of viruses. 相似文献
74.
Carola Borries Volker Sommer Arun Srivastava 《International journal of primatology》1994,15(3):421-443
We studied grooming among adults of a one-male multifemale troop of free-ranging Hanuman langurs (Presbytis entellus)living near Jodhpur, India, for 9 years. The 11–13 females devoted about 6% of their day to allogrooming. Adult males, whose
tenures averaged 2.2 years, were transient figures in the troop's history, as reflected by their rather peripheral role in
the grooming network. Females groomed males 4–40 times more frequently (1006 episodes) than vice versa- (176 episodes). Adult
females received 97% of all grooming from other adult females (6655 episodes). Although females exhibited an age- inversed
dominance hierarchy, they did not compete for grooming access to particular troop mates. Dyads of all possible rank differences
occurred as frequently as expected: 51% of grooming was directed up the hierarchy and 49% down it. Young, high- ranking individuals
gave and received significantly more grooming than the oldest, low- ranking females did. The pattern seemed to be influenced
by kin selection because of the presumably high degree of female relatedness. They invested most in troopmates with the highest
reproductive value, i.e., the youngest individuals. This trend was coupled with a preference of closest kin (mothers and daughters).
Reciprocity was the outstanding feature since all adult females groomed and were groomed by all others. Such a tight social
net might establish the necessary cohesion during frequent territorial disputes with neighboring troops. 相似文献
75.
Nucleocapsid-glycoprotein interactions required for assembly of alphaviruses. 总被引:30,自引:19,他引:11 下载免费PDF全文
We have studied interactions between nucleocapsids and glycoproteins required for budding of alphaviruses, using Ross River virus-Sindbis virus chimeras in which the nucleocapsid protein is derived from one virus and the envelope glycoproteins are derived from the second virus. A virus containing the Ross River virus genome in which the capsid protein had been replaced with that from Sindbis virus was almost nonviable. Nucleocapsids formed in normal numbers in the infected cell, but very little virus was released from the cell. There are 11 amino acid differences between Ross River virus and Sindbis virus in their 33-residue E2 cytoplasmic domains. Site-specific mutagenesis was used to change 9 of these 11 amino acids in the chimera from the Ross River virus to the Sindbis virus sequence in an attempt to adapt the E2 of the chimera to the nucleocapsid. The resulting mutant chimera grew 4 orders of magnitude better than the parental chimeric virus. This finding provides direct evidence for a sequence-specific interaction between the nucleocapsid and the E2 cytoplasmic domain during virus budding. The mutated chimeric virus readily gave rise to large-plaque variants that grew almost as well as Ross River virus, suggesting that additional single amino acid substitutions in the structural proteins can further enhance the interactions between the disparate capsid and the glycoproteins. Unexpectedly, change of E2 residue 394 from lysine (Ross River virus) to glutamic acid (Sindbis virus) was deleterious for the chimera, suggesting that in addition to its role in nucleocapsid-E2 interactions, the N-terminal part of the E2 cytoplasmic domain may be involved in glycoprotein-glycoprotein interactions required to assemble the glycoprotein spikes. The reciprocal chimera, Sindbis virus containing the Ross River virus capsid, also grew poorly. Suppressor mutations arose readily in this chimera, producing a virus that grew moderately well and that formed larger plaques. 相似文献
76.
Cytochrome-c reductase (EC 1.10.2.2.) from Solanum tuberosum L. comprises ten subunits with apparent molecular sizes of 55, 53, 51, 35, 33, 25, 14, 12, 11 and 10 kDa on 14% SDS-PAGE. The identity of the subunits was analysed by direct amino-acid sequencing via cyclic Edman degradation. A large-scale purification procedure for the enzyme complex based on affinity chromatography and gelfiltraton is described. All subunits were enzymatically fragmented and the generated peptides were separated by reverse-phase HPLC. Complete or partial sequence determination of 33 peptides comprising a total of nearly 500 amino acids showed, that cytochrome-c reductase from potato contains three respiratory proteins (cytochrome b, cytochrome c
1 and the Rieske iron-sulfur protein), four small proteins with molecular sizes below 15 kDa (so-called Q-binding, hinge, cytochrome-c
1-linked and core-linked proteins) and three proteins in the 50-kDa range which show similarity to members of the core/PEP/MPP protein family (core/processing enhancing protein/mitochondrial processing peptidase). In fact these subunits show highest sequence identity either to MPP or PEP, which is in line with earlier findings, that isolated cytochrome-c reductase from potato exhibits processing activity towards mitochondrial precursor proteins.Abbreviations MPP
mitochondrial processing peptidase
- PEP
processing enhancing protein
This research was supported by the Deutsche Forschungsgemeinschaft. 相似文献
77.
By computer simulation of experimental dynamic gas chromatographic elution profiles, the rotational energy barrier ΔG= of racemic 2,2′-diisopropylbiphenyl has been determined as 114.6–115.0 kJ/mol (75–100°C). These data are in good agreement with a value that was determined previously by measuring the racemization kinetics of an enriched sample. This indicates that there is no measurable catalytic or inhibitory effect of the stationary phase. © 1994 Wiley-Liss, Inc. 相似文献
78.
Dipl. Geol. Jens Hefter Dipl. Geol. Volker Thiel Dr. Angela Jenisch Dr. Ursula Galling Dr. Stephan Kempe Dr. habil. Walter Michaelis 《Facies》1993,29(1):93-105
Summary Biomarker investigations were applied to the hydrocarbon fractions of three Recent (cyanobacterial mat, Lake Van microbialite
and Lake Satonda microbialite) and two Late Jurassic carbonate samples obtained from sponge bioherms. The relative concentrations
ofn-alkanes, monomethyl alkanes, acyclic isoprenoids, steroids and hopanoids in these samples are studied and their probable
biological precursors are discussed. Normal alkanes with carbon chain lengths ranging from C15 to C34 and monomethyl alkanes ranging from C17 to C21 with a varying methyl branching pattern are found. The major hydrocarbons are low molecular weight (LMW)n-alkanes (C15–C21) with a slight to strong predominance ofn-heptadecane (C17). High molecular weight (HMW)n-alkanes occur in low to moderate relative concentrations showing a preference of odd-carbon numbered compounds with a maximum
at C29. Within the acyclic isoprenoids, pristane, phytane/phytene, pentamethyl-eicosane, squalane and lycopane could be identified.
Polycyclic terpenoids of the sterane and/or hopane type are present in all carbonate samples. The carbon numbers of these
components range from 27 to 29 and 27 to 32, respectively. These organic compounds identified can be attributed to various
source organisms such as cyanobacteria, archaebacteria, algae and vascular plants. All hydrocarbon fractions of the samples
are characterized by moderate to high relative concentrations of compounds derived from cyanobacteria, signifying the role
of these organisms as contributors to the Recent as well as to the Late Jurassic carbonate deposits. 相似文献
79.
Thomas Diefenthal Harald Dargatz Volker Witte Gernot Reipen Ib Svendsen 《Applied microbiology and biotechnology》1993,40(1):90-97
Proline-specific endopeptidase (PSE) (EC 3.4.21.26) from Flavobacterium meningosepticum was subjected to partial amino acid sequencing. According to the peptide sequences obtained, oligonucleotides were used to amplify a PSE-specific DNA fragment of 930 bp from F. meningosepticum genomic DNA, employing the polymerase chain reaction technique. This fragment served as a molecular probe to isolate the respective gene. DNA sequencing revealed that the PSE gene consists of 2118 bp coding for a 78,634 Da protein of 705 amino acids. The coding region was cloned in different expression vectors of Escherichia coli. Transformed E. coli cells overproduce an active prolyl endopeptidase of 75,000 relative molecular mass, which is delivered to the bacterial periplasmic space. Up to 1.6 units of active prolyl endopeptidase were obtained from 1 mg E. coli cells. Furthermore, the efficient purification of active prolyl endopeptidase from the periplasm of recombinant E. coli cells is described.
Correspondence to: G. Reipen 相似文献
80.
Sieghart Sopper Susanne Hemm Jürgen Meixensberger Cheik Coulibaly Christiane Stahl-Hennig Gerhard Hunsmann Bernhard Fleckenstein Volker ter Meulen Rüdiger Drries 《Journal of medical primatology》1993,22(2-3):138-146
Paired sera and CSF samples were collected from SIVmac-infected macaques. Animals infected with SIVmac251 maintained low gag and high env-specific antibody levels in plasma. Increasing env-specific antibody titers in CSF were associated in one animal with strong intrathecal synthesis. SIVmac239-infected monkeys revealed high antibody titers of gag and env-specificity, in one animal accompanied by weak intrathecal synthesis of virus-specific antibodies. In all animals, the CD4/CD8 ratio in CSF decreased faster compared to blood. 相似文献