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101.
In aged mice,low surrogate light chain promotes pro‐B‐cell apoptotic resistance,compromises the PreBCR checkpoint,and favors generation of autoreactive,phosphorylcholine‐specific B cells 下载免费PDF全文
Michelle Ratliff Sarah Alter Kelly McAvoy Daniela Frasca Jacqueline A. Wright Sandra S. Zinkel Wasif N. Khan Bonnie B. Blomberg Richard L. Riley 《Aging cell》2015,14(3):382-390
In aged mice, new B‐cell development is diminished and the antibody repertoire becomes more autoreactive. Our studies suggest that (i) apoptosis contributes to reduced B lymphopoiesis in old age and preferentially eliminates those B‐cell precursors with higher levels of the surrogate light chain (SLC) proteins (λ5/VpreB) and (ii) λ5low B‐cell precursors generate new B cells which show increased reactivity to the self‐antigen/bacterial antigen phosphorylcholine (PC). Pro‐B cells in old bone marrow as well as pro‐B cells from young adult λ5‐deficient mice are resistant to cytokine‐induced apoptosis (TNFα; TGFβ), indicating that low λ5 expression in pro‐B cells is sufficient to cause increased survival. Transfer of TNFα‐producing ‘age‐associated B cells’ (ABC; CD21/35? CD23?) or follicular (FO) B cells from aged mice into RAG‐2 KO recipients led to preferential loss of λ5high pro‐B cells, but retention of λ5low, apoptosis‐resistant pro‐B cells. In old mice, there is increased reactivity to PC in both immature bone marrow B cells and mature splenic FO B cells. In young mice, absence of λ5 expression led to a similar increase in PC reactivity among bone marrow and splenic B cells. We propose that in old age, increased apoptosis, mediated in part by TNFα‐producing B cells, results in preferential loss of SLChigh pro‐B cells within the bone marrow. Further B‐cell development then occurs via an ‘SLClow’ pathway that not only impairs B‐cell generation, but promotes autoreactivity within the naïve antibody repertoires in the bone marrow and periphery. 相似文献
102.
Stefan Paula Josh Abell Joel Deye Christopher Elam Michael Lape Justin Purnell Robert Ratliff Kelly Sebastian Jodie Zultowsky Robert J. Kempton 《Bioorganic & medicinal chemistry》2009,17(18):6613-6619
Analogues of the compound 2,5-di-tert-butylhydroquinone (BHQ) are capable of inhibiting the enzyme sarco/endoplasmic reticulum ATPase (SERCA) in the low micromolar and submicromolar concentration ranges. Not only are SERCA inhibitors valuable research tools, but they also have potential medicinal value as agents against prostate cancer. This study describes the synthesis of 13 compounds representing several classes of BHQ analogues, such as hydroquinones with a single aromatic substituent, symmetrically and unsymmetrically disubstituted hydroquinones, and hydroquinones with ω-amino acid tethers attached to their hydroxyl groups. Structure–activity relationships were established by measuring the inhibitory potencies of all synthesized compounds in bioassays. The assays were complemented by computational ligand docking for an analysis of the relevant ligand/receptor interactions. 相似文献
103.
M Ozkan SG Desai Y Zhang DM Stevenson J Beane EA White ML Guerinot LR Lynd 《Journal of industrial microbiology & biotechnology》2001,27(5):275-280
Characteristics of 13 newly isolated thermophilic, anaerobic, and cellulolytic strains were compared with previously described
strains of Clostridium thermocellum: ATCC 27405 and JW20 (ATCC 31549). Colony morphology, antibiotic sensitivity, fermentation end-products, and cellulose degradation
were documented. All 13 strains were sensitive to erythromycin (5 μg/ml) and chloramphenicol (25 μg/ml), and all strains but
one were sensitive to kanamycin (20 μg/ml). Polymerase chain reaction (PCR) amplification using primers based on gene sequences
from C. thermocellum ATCC 27405 was successful for all 13 strains in the case of the hydrogenase gene and 11 strains in the case of phosphotransacetylase/acetate
kinase genes. Ten strains amplified a product of the expected size with primers developed to be specific for C. thermocellum 16SrRNA primers. Two of the 13 strains did not amplify any product with the PCR primers designed for the phosphotransacetylase/acetate
kinase and 16SrRNA primers. A MboI-like GATC- recognizing restriction activity was present in all of the five strains examined. The results of this study have
several positive implications with respect to future development of a transformation system for cellulolytic thermophiles.
Journal of Industrial Microbiology & Biotechnology (2001) 27, 275–280.
Received 12 September 2000/ Accepted in revised form 20 November 2000 相似文献
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106.
APC stimulated by CpG oligodeoxynucleotide enhance activation of MHC class I-restricted T cells 总被引:6,自引:0,他引:6
Warren TL Bhatia SK Acosta AM Dahle CE Ratliff TL Krieg AM Weiner GJ 《Journal of immunology (Baltimore, Md. : 1950)》2000,165(11):6244-6251
Oligonucleotides containing unmethylated CpG motifs (cytosine-phosphorothioate-guanine oligodeoxynucleotide (CpG ODN)) are potent immunostimulatory agents capable of enhancing the Ag-specific Th1 response when used as immune adjuvants. We evaluated the cellular mechanisms responsible for this effect. Development of a CTL response was enhanced when mice were immunized with peptide-pulsed dendritic cells (DCs) treated with CpG ODN. However, in vitro, CpG ODN had no direct effect on highly purified T cells. In vitro, CpG ODN treatment of peptide- or protein-pulsed DCs enhanced the ability of the DCs to activate class I-restricted T cells. The presence of helper T cells enhanced this effect, indicating that treatment with CpG ODN does not obviate the role of T cell help. The enhanced ability of CpG ODN-treated DCs to activate T cells was present but blunted when DCs derived from IL-12 knockout mice were used. Fixation of Ag-pulsed, CpG ODN-treated DCs limited their ability to activate T cells. In contrast, fixation had little effect on DC activation of T cells when DCs were not exposed to CpG ODN. This indicates that production of soluble factors by DCs stimulated with CpG ODN plays a particularly important role in their ability to activate class I-restricted T cells. We conclude that CpG ODN enhances the development of a cellular immune response by stimulating APCs such as DCs, to produce IL-12 and other soluble factors. 相似文献
107.
Three liquid insecticide formulations were evaluated as barrier treatments against perimeter-invading ants at a multifamily housing complex in West Lafayette, IN. Several ant species were present at the study site, including (in order of abundance) pavement ant, Tetramorium caespitum (L.); honey ant, Prenolepis imparis (Say); odorous house ant, Tapinoma sessile (Say); thief ant, Solenopsis molesta (Say); acrobat ant, Crematogaster ashmeadi (Mayr); crazy ant, Paratrechina longicornis (Latrielle), field ants, Formica spp.; and carpenter ant Camponotus pennsylvanicus (DeGeer). Studies began in May 2001 and concluded 8 wk later in July. Individual replicate treatments were placed 0.61 in (2 feet) up and 0.92 m (3 feet) out from the ends of 46.1 by 10.1-m (151 by 33-foot) apartment buildings. Ant sampling was performed with 10 placements of moist cat food for 1 h within treatment zones, followed by capture and removal of recruited ants for later counting. All treatments led to substantial reductions in ant numbers relative to untreated controls. The most effective treatment was fipronil, where 2% of before-treatment ant numbers were present at 8 wk after treatment. Both imidacloprid and cyfluthrin barrier treatments had efficacy comparative with fipronil, but to 4 and 2 wk, respectively. Odorous house ants were not sampled before treatment. Comparisons of ant species composition between treatments and controls revealed an increase in odorous house ant frequencies at 1-8 wk after treatment in treated locations only. These results demonstrate efficacy for both nonrepellent and repellent liquid insecticides as perimeter treatments for pest ants. In addition, our findings with odorous house ant highlight an apparent invasive-like characteristic of this species that may contribute to its dramatic increase in structural infestation rates in many areas of the United States. 相似文献
108.
M.?E.?ScharfEmail author C.?R.?Ratliff J.?T.?Hoteling B.?R.?Pittendrigh G.?W.?Bennett 《Insectes Sociaux》2003,50(4):346-354
Summary We report on our investigations comparing three juvenile hormone (JH) homologs and two synthetic juvenoids to induce caste differentiation in laboratory colonies of Reticulitermes flavipes and R. tibialis. Two laboratory assays were evaluated as model systems for inducing caste differentiation: (1) shorter-term dish assays on groups of 20 individuals and (2) longer-term feeding assays on groups of 500 individuals. Each assay possessed attributes that can be considered advantageous under certain conditions. Specifically, dish assays were most suitable for presoldier and soldier induction, while jar assays provided for the induction of nymphs, presoldiers, soldiers, neotenic reproductives, and intercastes. Differences in response to the JH homologs and synthetic juvenoids were noted between species, suggesting differences in JH physiology may exist between R. flavipes and R. tibialis. Substantial morpholo-gical impacts were noted in association with some treatments, including (1) juvenoid-induced mandibular mal-formation in presoldiers, (2) JH II-induced abdominal elongation in R. flavipes soldiers and workers (associated with a presence of internal reproductive anatomy that is consistent with what would be expected to occur in pseudergates), and (3) JH II-induced soldier-nymph intercastes in R. tibialis that were able to further molt into soldier-alate intercastes. Findings are discussed in relation to the potential differences in JH-related physiology between R. flavipes and R. tibialis, and the use of model systems to induce rare castes and intercastes for molecular investigations of caste differentiation. 相似文献
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110.
Prakash S Tian L Ratliff KS Lehotzky RE Matouschek A 《Nature structural & molecular biology》2004,11(9):830-837
The proteasome is the main ATP-dependent protease in eukaryotic cells and controls the concentration of many regulatory proteins in the cytosol and nucleus. Proteins are targeted to the proteasome by the covalent attachment of polyubiquitin chains. The ubiquitin modification serves as the proteasome recognition element but by itself is not sufficient for efficient degradation of folded proteins. We report that proteolysis of tightly folded proteins is accelerated greatly when an unstructured region is attached to the substrate. The unstructured region serves as the initiation site for degradation and is hydrolyzed first, after which the rest of the protein is digested sequentially. These results identify the initiation site as a novel component of the targeting signal, which is required to engage the proteasome unfolding machinery efficiently. The proteasome degrades a substrate by first binding to its ubiquitin modification and then initiating unfolding at an unstructured region. 相似文献