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91.
Summary Mössbauer spectroscopy was used to investigate the cellular acquisition of iron byPseudomonas aeruginosa which had been incubated with ferripyoverdine for 20, 40, 60, 120 or 360 min. Studies revealed that no ferripyoverdine accumulated in the cells at any of these times and that the amounts and kinds of iron complexes produced by cellular metabolism vary with time. At 20 and 40 min a ferric species, with isomer shift =0.38–0.42 mm/s and quadrupole splitting E
Q=0.94–0.92 mm/s, was the major iron metabolite comprising approximately 80% of the iron. At later times at least three other ferric species appeared with =0.54 0.72, E
Q = 0.84 1.07 mm/s. Ferrous species, =1.43 1.77 mm/s and E
Q = 2.69 1.82 mm/s, were also seen at times as early as 20 min and comprised as much as 17% of the total iron at 20 and 40 min. The parameters of all these species identify them as being six-coordinated high-spin complexes. In addition a low-spin species, =0.19 mm/s E
Q=0.67 0.91 mm/s, never before reported in cells, appeared at 60, 120, and 360 min as one of the major iron metabolites (50% or more). All isomer shifts are measured with respect to natural iron. 相似文献
92.
Synopsis Fishes of the genus Pardachirus (Soleidae) are reviewed. Four species are recognized and their distribution mapped: P. marmoratus (Lacépède) from the Red Sea and Indian Ocean, P. pavoninus (Lapédè) and P. poropterus (Bleeker) from the Indo-Pacific, and P. hedleyi (Ogilby) from estuarine waters of Australia. Achirus rautheri Chabanaud is placed in synonymy with P. hedleyi. The ichthyocrinotoxic effect on teleosts of the secretion from P. pavoninus is described and compared with that of P. marmoratus. The distribution of poison glands in these two species shows more glands present on the eyed side. The number of glands range from 212 to 235 in P. marmoratus and 204 to 237 in P. pavoninus and number of rays on fins associated with the poison glands are about the same for both species. P. marmoratus appears to be more toxic than P. pavoninus. 相似文献
93.
94.
The object of this review is to describe the role of the renin–angiotensin system in control of aldosterone secretion. The review focuses on the roles of the circulating renin–angiotensin (RAS) system, the activity of which is determined predominantly by control of renin secretion from the kidney and on the role of the intra-adrenal RAS. Angiotensin can bind to two types of G protein coupled receptors, the AT1 and AT2 receptors. Both receptors are found on cells from the zona glomerulosa, the site of aldosterone synthesis. Angiotensin II acting via the AT1 receptor stimulates the synthesis of aldosterone at early and late steps in the pathway. Its effect on aldosterone is influenced by a number of other factors such as plasma potassium levels, sodium status, other peptides such as ANP and adrenomedullin and proadrenomedullin N-terminal peptide. All components of the RAS are found in the adrenal gland. The activity of this intra-adrenal RAS is unmasked and amplified in nephrectomised animals. Aldosterone controls sodium transport across epithelial cells, but recently novel effects on the heart have been described. 相似文献
95.
Laura L. Worth Shu-Fang Jia Taeha An Eugenie S. Kleinerman 《Cancer immunology, immunotherapy : CII》1999,48(6):312-320
ImmTher, a liposome-encapsulated lipophilic disaccharide tripeptide derivative of muramyl dipeptide, previously showed activity
against liver and lung colorectal metastases in a phase I trial. The purpose of the current studies was to investigate whether
ImmTher could up-regulate specific cytokine gene expression and protein production, as well as activate the tumoricidal or
cytostatic activity of human monocytes. ImmTher induced the expression and production of interleukin(IL)-1α IL-1β, IL-6, IL-8,
IL-12, macrophage chemotactic and activating factor, and tumor necrosis factor α but not IL-2 or IL-10. Cytostatic or cytotoxic
monocyte activity was stimulated against human Ewing's sarcoma, osteosarcoma, and melanoma cells but not breast cancer cells.
Production and secretion of these cytokine proteins may play a role in the antitumor activity of ImmTher.
Received: 15 December 1998 / Accepted: 18 March 1999 相似文献
96.
Plant Genome Complexity May Be a Factor Limiting In Situ the Transfer of Transgenic Plant Genes to the Phytopathogen Ralstonia solanacearum 下载免费PDF全文
Franck Bertolla Regis Pepin Eugenie Passelegue-Robe Eric Paget Andrew Simkin Xavier Nesme Pascal Simonet 《Applied microbiology》2000,66(9):4161-4167
The development of natural competence by bacteria in situ is considered one of the main factors limiting transformation-mediated gene exchanges in the environment. Ralstonia solanacearum is a plant pathogen that is also a naturally transformable bacterium that can develop the competence state during infection of its host. We have attempted to determine whether this bacterium could become the recipient of plant genes. We initially demonstrated that plant DNA was released close to the infecting bacteria. We constructed and tested various combinations of transgenic plants and recipient bacteria to show that the effectiveness of such transfers was directly related to the ratio of the complexity of the plant genome to the number of copies of the transgene. 相似文献
97.
Eugenie C. Scott 《Evolution》2010,3(2):241-244
The author reflects on how much she has learned about teaching from K-12 teachers, and about the difficulties teachers encounter
when they teach about evolution. Misconceptions and preconceptions, especially those concerning the compatibility or incompatibility
of evolution with religion, are difficult to overcome, but teachers have devised many ingenious approaches to “defuse the
religion issue.” The easy way out for many teachers is to omit evolution, or compromise its teaching by either including creationism
or denigrating evolution, but the many teachers who teach with integrity are inspiring to us all. 相似文献
98.
Arturo B. Ramirez Christian M. Loch Yuzheng Zhang Yan Liu Xiaohong Wang Elizabeth A. Wayner Jonathon E. Sargent Sahar Sibani Eugenie Hainsworth Eliseo A. Mendoza Ralph Eugene Joshua LaBaer Nicole D. Urban Martin W. McIntosh Paul D. Lampe 《Molecular & cellular proteomics : MCP》2010,9(7):1449-1460
The discovery of novel early detection biomarkers of disease could offer one of the best approaches to decrease the morbidity and mortality of ovarian and other cancers. We report on the use of a single-chain variable fragment antibody library for screening ovarian serum to find novel biomarkers for the detection of cancer. We alternately panned the library with ovarian cancer and disease-free control sera to make a sublibrary of antibodies that bind proteins differentially expressed in cancer. This sublibrary was printed on antibody microarrays that were incubated with labeled serum from multiple sets of cancer patients and controls. The antibodies that performed best at discriminating disease status were selected, and their cognate antigens were identified using a functional protein microarray. Overexpression of some of these antigens was observed in cancer serum, tumor proximal fluid, and cancer tissue via dot blot and immunohistochemical staining. Thus, our use of recombinant antibody microarrays for unbiased discovery found targets for ovarian cancer detection in multiple sample sets, supporting their further study for disease diagnosis.Despite many advances in the treatment of cancer, early detection and tumor removal remains the best prospect for overcoming disease. Ovarian cancer is an excellent example of the potential prognostic value of early detection because diagnosis at a localized stage has a 5-year survival rate of 93%. However, only 19% of cases are diagnosed at this stage, and by the time the disease has evolved to an advanced stage, the 5-year survival rate drops to 31% (1).Much effort has been expended to find early detection markers of ovarian cancer, and some success has been achieved. Most notable is CA125, the only approved marker for the detection of recurrence of ovarian cancer (2). Other leading targets are mesothelin and HE4, which have been examined by several groups for their efficacy as early detection markers (3–8). Nevertheless, several conditions necessitate the discovery of more specific and sensitive ovarian cancer markers: the heterogeneity of this disease, the ambiguity of its symptoms, its low incidence in the general population, and the low sensitivity and specificity of currently available markers.One of the difficulties in finding markers in blood is the complexity of the plasma/serum proteome, estimated in the tens to hundreds of thousands of proteins, as well as its large range in constituent protein concentrations, which can span 12 orders of magnitude (9). However, along with its easy accessibility, the fact that blood is in contact with virtually every tissue and contains tissue- and tumor-derived proteins makes it a preferred source for disease biomarker discovery.Our previous results (10, 11) and those of others (12–14) using high density, full-length IgG antibody microarrays to validate and discover cancer serum biomarkers demonstrated that this platform is valuable for simultaneously comparing the levels of hundreds of proteins on dozens of serum samples from cancer patients and healthy controls. We confirmed overexpression of CA125, mesothelin, and HE4 in ovarian cancer samples using this high density microarray platform, validating our array methodology for measurement of cancer serum biomarkers and yielding new putative biomarkers for this disease (10, 11).Previously reported approaches are typically limited to a few hundred antibodies. The methodology reported here allows us to exploit the specific advantages of antibodies as high affinity capture reagents to detect differential expression of thousands of tumor biomarkers using a diverse (2 × 108 binding agents) single-chain variable fragment antibody (scFv)1 library for detection of ovarian cancer markers in serum, tumor cyst fluid, and ascites fluid. Our results build on previous reports of phage display library microarrays to discover autoantibody (15–18) and other protein (12, 19, 20) cancer biomarkers. Our scFv are high affinity capture reagents consisting of the variable regions of human antibody heavy and light chains joined by a flexible linker peptide. These recombinant antibodies are able to recognize a wide variety of antigens, including many previously thought difficult, such as self-antigens and proteins that are not normally immunogenic in animals (21–24). Using a highly diverse recombinant antibody library, one has the ability to overcome the complexity of the serum proteome. It has been calculated that for an immune repertoire to be complete (at least one antibody in the repertoire has reasonable affinity for every epitope possible in nature) it requires a diversity of at least 106 antibodies (25). The reported diversity of our scFv library exceeds this value by 100-fold (21).To enrich for antibodies that differentiate disease status, we performed a selection or panning of the naïve library for proteins that are differentially expressed in cyst fluid, ascites fluid, or serum of cancer patients with respect to healthy serum. We printed this sublibrary on activated hydrogel slides that were queried with three different sets of labeled case and control sera to further select those that discriminate cancer status in a statistically significant manner. Next, we identified some of the targets that bind to the individual scFv using high density nucleic acid programmable protein arrays (NAPPAs) expressing a total of over 7000 proteins. Finally, we validated the effectiveness of the selection process by confirming overexpression of these targets in cancer serum, cyst fluid, and ascites fluid as well as in tumor sections. 相似文献
99.
Evolutionary biology owes much to Charles Darwin, whose discussions of common descent and natural selection provide the foundations
of the discipline. But evolutionary biology has expanded well beyond its foundations to encompass many theories and concepts
unknown in the 19th century. The term “Darwinism” is, therefore, ambiguous and misleading. Compounding the problem of “Darwinism”
is the hijacking of the term by creationists to portray evolution as a dangerous ideology—an “ism”—that has no place in the
science classroom. When scientists and teachers use “Darwinism” as synonymous with evolutionary biology, it reinforces such
a misleading portrayal and hinders efforts to present the scientific standing of evolution accurately. Accordingly, the term
“Darwinism” should be abandoned as a synonym for evolutionary biology. 相似文献
100.