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排序方式: 共有284条查询结果,搜索用时 93 毫秒
191.
SE?Aleshin AV?Timofeev MV?Khoretonenko LG?Zakharova GV?Pashvykina JR?Stephenson AM?Shneider AD?AltsteinEmail author 《BMC microbiology》2005,5(1):45
Background
Heterologous prime-boost immunization protocols using different gene expression systems have proven to be successful tools in protecting against various diseases in experimental animal models. The main reason for using this approach is to exploit the ability of expression cassettes to prime or boost the immune system in different ways during vaccination procedures. The purpose of the project was to study the ability of recombinant vaccinia virus (VV) and bacterial plasmid, both carrying the NS1 gene from tick-borne encephalitis (TBE) virus under the control of different promoters, to protect mice against lethal challenge using a heterologous prime-boost vaccination protocol. 相似文献192.
Maria Benitez‐Guijarro Cesar Lopez‐Ruiz Žygimantė Tarnauskaitė Olga Murina Mahwish Mian Mohammad Thomas C Williams Adeline Fluteau Laura Sanchez Raquel Vilar‐Astasio Marta Garcia‐Canadas David Cano Marie‐Jeanne HC Kempen Antonio Sanchez‐Pozo Sara R Heras Andrew P Jackson Martin AM Reijns Jose L Garcia‐Perez 《The EMBO journal》2018,37(15)
193.
A survey was done to find microorganisms useful for assaying sterigmatocystin; T-2 toxin and zearalenone.Staphylococcus aureus was found to be sensitive to T-2 toxin and zearalenone;Bacillus cereus was found to be sensitive to T-2 toxin only; andEscherichia coli was sensitive to sterigmatocystin. The response of the organisms to sterigmatocystin; T-2 toxin and zearalenone was found to be linear between 4 and 100 μg with sterigmatocystin toE. coli; between 2 and 25 μg with T-2 toxin toStaph, aureus andB. cereus; and between 4 and 100 μg with zearalenone toStaph, aureus. The lower limits of sensitivity of the test were 2 μg T-2 toxin and zearalenone, and 4 μg sterigmatocystin. The assay is rapid (15–17 hrs); simple and inexpensive; and can be used to verify the toxicity of samples and to confirm thin layer chromatographic results. 相似文献
194.
Induction and Accumulation of Heat Shock-Specific Poly(A) RNAs and Proteins in Soybean Seedlings during Arsenite and Cadmium Treatments 总被引:5,自引:2,他引:3
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Northern blot hybridization analyzes revealed that poly(A+) RNAs homologous to eight heat shock (HS)-specific cDNA clones were induced by arsenite (As) or Cd treatments. The mRNAs accumulated slower, and maximum accumulations were consistently lower than HS-induced levels. Prolonged treatment with low concentrations (50-100 micromolar) of As for 6 hours, or Cd for 12 hours, resulted in decreased accumulations of HS-specific mRNAs. This response resembled the `autoregulation' observed during continuous 40°C HS. However, no autoregulation was evident when soybean seedlings were exposed to high concentrations of As (250 micromolar) or Cd (1 millimolar) for 12 hours. The cDNA probe pCE54 detected a second higher molecular weight poly(A+) RNA following As or Cd treatments which accumulated concomitantly with the lower molecular weight HS-specific poly(A+) RNA. The patterns of low molecular weight HS polypeptides from in vitro translations induced by HS, As, and Cd, and analyzed by one-dimensional and two-dimensional SDS-PAGE, were similar but temporal differences were apparent. In addition to HS proteins, many control proteins were also detected in both in vitro and in vivo labeling patterns from As and, to a lesser extent, Cd treatments. The chemical agents used in this study apparently induced the accumulation and translation of HS messages in vivo but not in the selective manner as observed during HS treatment. 相似文献
195.
Comparative analysis of physical stress responses in soybean seedlings using cloned heat shock cDNAs
Summary Soybean seedlings were subjected to a wide range of physical (abiotic) or environmental stresses. Cloned cDNAs to heat shock (hs)-induced mRNAs were used to assess whether these diverse stresses induced the accumulation of poly(A)RNAs in common with those induced by hs. Northern blot hybridization analyses indicated that a wide range of stress agents lead to the accumulation of detectable levels of several of the hs-induced poly(A)RNAs; the relative concentration of those RNAs induced by the wide range of stress agents (e.g. water stress, salt stress, anaerobiosis, high concentrations of hormones, etc.), was generally in the order of 100-fold lower than that induced by hs. There are two notable exceptions to that pattern of response to the stress agents. First, arsenite treatment resulted in accumulation of the hs poly(A)RNAs to levels similar to those induced by hs. Cadmium also induced a somewhat normal spectrum of the hs poly(A)RNAs, but generally lower levels accumulated than in hs- and arsenite0treated tissues. Second, one set of poly(A)RNAs which are present at low and variable levels in control (non-stressed tissue) tissue, and which are increased some 5- to 10-fold by hs, increased in relative concentration in response to a wide range of the stress agents similarly to the response to hs. The physiological significance of the accumulation of this set of poly(A)RNAs (which translate into four electrophoretically different 27 kd proteins) is not known, but they certainly seem to serve as a monitor (or barometer) of physiological stress conditions. Cadmium treatment results in the accumulation of those same poly(A)RNAs and an additional band of higher molecular weight poly(A)RNA homologous to the same hs cDNA clone (clone pCE 54). Ethylene seems to have no obvious causal relationship to the hs response, even though hs-treated seedlings display some symptoms similar to those exhibited by ethylene-treated seedlings. 相似文献
196.
Evidence for effect of random genetic drift on G+C content after lateral transfer of fucose pathway genes to Escherichia coli K-12 总被引:4,自引:0,他引:4
The cps cluster of Escherichia coli K-12 comprises genes involved in
synthesis of capsular polysaccharide colanic acid. Part of the E. coli K-12
cps region has been cloned and sequenced and compared to its Salmonella
enterica LT2 counterpart. The cps genes from the two organisms are
homologous; in the case of the LT2 genes, with G+C content of 0.61 and
codons characteristic of high G+C species, it seems clear that they have
been acquired relatively recently by lateral transfer from a high G+C
species. The K-12 form of these cps genes is closely related to those of
LT2 so must derive from the same high G+C species, but it appears to have
transferred much earlier such that random genetic drift has brought P3 (the
corrected G+C content of codon base 3) down from 0.77 to 0.64, more than
halfway to the E. coli average of 0.57. We estimate, using an equation
developed by Sueoka, that the lateral transfer to E. coli took place
approximately 45 million years ago. This is the first report we are aware
of demonstrating the expected adjustment of P3 after lateral transfer
between species with different G+C content DNA.
相似文献
197.
Studies on the binding site of the galactose-specific agglutinin PA-IL from Pseudomonas aeruginosa 总被引:1,自引:0,他引:1
The binding properties of Pseudomonas aeruginosa agglutinin-I (PA-IL) with
glycoproteins (gps) and polysaccharides were studied by both the
biotin/avidin-mediated microtiter plate lectin-binding assay and the
inhibition of agglutinin-glycan interaction with sugar ligands. Among 36
glycans tested for binding, PA-IL reacted best with two glycoproteins
containing Galalpha1-->4Gal determinants and a human blood group ABO
precursor equivalent gp, but this lectin reacted weakly or not at all with
A and H active gps or sialylated gps. Among the mammalian disaccharides
tested by the inhibition assay, the human blood group Pkactive
Galalpha1-->4Gal, was the best. It was 7.4-fold less active than
melibiose (Galalpha1-->6Glc). PA-IL has a preference for the
alpha-anomer in decreasing order as follows: Galalpha1-->6
>Galalpha1-->4 >Galalpha1-->3. Of the monosaccharides studied,
the phenylbeta derivatives of Gal were much better inhibitors than the
methylbeta derivative, while only an insignificant difference was found
between the Galalpha anomer of methyl- and p -NO2-phenyl derivatives. From
these results, it can be concluded that the combining size of the
agglutinin is as large as a disaccharide of the alpha-anomer of Gal at
nonreducing end and most complementary to Galalpha1-->6Glc. As for the
combining site of PA-IL toward the beta-anomer, the size is assumed to be
less than that of Gal; carbon-6 in the pyranose form is essential, and
hydrophobic interaction is important for binding.
相似文献
198.
Moreno E; Lanne B; Vazquez AM; Kawashima I; Tai T; Fernandez LE; Karlsson KA; Angstrom J; Perez R 《Glycobiology》1998,8(7):695-705
P3 is a mouse monoclonal antibody (mAb) that binds to several NeuGc-
containing gangliosides. It also reacts with antigens expressed in human
breast tumors (Vazquez et al. (1995) Hybridoma , 14, 551-556). In this
work, the binding specificity of P3 has been characterized in more detail
using a panel of glycolipids that included several disialylated
gangliosides and several chemical derivatives of NeuGc-GM3. The carboxyl
group and the nitrogen function of sialic acid were found to play important
roles in the antibody binding, whereas the glycerol tail appears to be
nonrelevant. Molecular modeling was used to analyze the binding data,
including the finding that P3 selectively recognizes the internal NeuGc in
GD3. For this purpose, conformational studies of GD3 were performed using
molecular dynamics. It was concluded that sialic acid binds the P3 antibody
through its upper face (the one on which the carboxyl group is exposed) and
the C4-C5 side of the sugar ring, whereas none or very little contact
between the galactose residue and the protein is evident. Conformational
analysis of GD3 revealed that, despite the large flexibility of the
NeuGcalpha8NeuGc linkage, the P3 binding epitope on the external sialic
acid is not well exposed for any of the possible conformations this linkage
can adopt, whereas the internal sialic acid presents the epitope in a
proper way for several of these conformations. As a final result, a
coherent picture of the epitope that fits the wide binding data was
obtained.
相似文献
199.
The structural basis of molecular adaptation 总被引:31,自引:21,他引:10
The study of molecular adaptation has long been fraught with difficulties,
not the least of which is identifying out of hundreds of amino acid
replacements those few directly responsible for major adaptations. Six
studies are used to illustrate how phylogenies, site- directed mutagenesis,
and a knowledge of protein structure combine to provide much deeper
insights into the adaptive process than has hitherto been possible. Ancient
genes can be reconstructed, and the phenotypes can be compared to modern
proteins. Out of hundreds of amino acid replacements accumulated over
billions of years those few responsible for discriminating between
alternative substrates are identified. An amino acid replacement of modest
effect at the molecular level causes a dramatic expansion in an ecological
niche. These and other topics are creating the emerging field of
"paleomolecular biochemistry."
相似文献
200.
Marie-Elisabeth Samson-Bouma Nicole Verthier Leo A Ginsel Grard Feldmann Jack AM Fransen Lawrence P Aggerbeck 《Biology of the cell / under the auspices of the European Cell Biology Organization》1996,87(3):189-196
Summary— Intestinal biopsies from patients having genetic disorders of lipoprotein assembly and secretion, such as abetalipoproteinemia (ABL) or Anderson's disease (AD), contain large amounts of lipids which are accumulated in the enterocytes. Determination of the intracellular sites in which the lipids accumulate and to which apolipoproteins the lipids are bound would help to identify the defects in these diseases and further elucidate the mechanisms by which lipoprotein assembly and secretion occur normally. Ultrastructural immunogold labeling, however, is hampered by the poor preservation of the lipids accumulated in the enterocytes of these patients. We have used routine electron microscopy (fixation and ultra-thin sectioning) along with three methods for immunogold labeling of lipid-laden enterocytes; ultrathin cryosectioning, low temperature freeze substitution with embedding in Lowicryl K4M, and ultra-low temperature freeze substitution with embedding in Lowicryl HM20, to establish a protocol for investigating the intestinal tissue from these patients. Ultracryosectioning, while preserving the overall morphology of the lipid laden enterocytes, did not preserve the lipid content and the immunogold labeling of apolipoprotein B (ApoB) appeared dislocated. Freeze substitution and low temperature embedding in Lowicryl K4M, in contrast, appeared to better preserve the lipid and lipoprotein structures; however, the antigenicity of both apoAI and apoB appeared to be lost and no specific labeling could be obtained. Freeze substitution and embedding in Lowicryl HM20 best preserved the lipid and lipoprotein structures while maintaining apoprotein antigenicity. In conclusion, immunogold labeling of apolipoproteins on lipid structures in the lipid-laden enterocytes of patients with ABL and AD is best obtained by freeze substitution and embedding in Lowicryl HM20. 相似文献