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171.
Gregory T. Ruggerone Beverly A. Agler Jennifer L. Nielsen 《Environmental Biology of Fishes》2012,94(1):149-163
Increasing production of hatchery salmon over the past four decades has led to concerns about possible density-dependent effects
on wild Pacific salmon populations in the North Pacific Ocean. The concern arises because salmon from distant regions overlap
in the ocean, and wild salmon populations having low productivity may compete for food with abundant hatchery populations.
We tested the hypothesis that adult length-at-age, age-at-maturation, productivity, and abundance of a Norton Sound, Alaska,
chum salmon population were influenced by Asian hatchery chum salmon, which have become exceptionally abundant and surpassed
the abundance of wild chum salmon in the North Pacific beginning in the early 1980s. We found that smaller adult length-at-age,
delayed age-at-maturation, and reduced productivity and abundance of the Norton Sound salmon population were associated with
greater production of Asian hatchery chum salmon since 1965. Modeling of the density-dependent relationship, while controlling
for other influential variables, indicated that an increase in adult hatchery chum salmon abundance from 10 million to 80
million adult fish led to a 72% reduction in the abundance of the wild chum salmon population. These findings indicate that
competition with hatchery chum salmon contributed to the low productivity and abundance of Norton Sound chum salmon, which
includes several stocks that are classified as Stocks of Concern by the State of Alaska. This study provides new evidence
indicating that large-scale hatchery production may influence body size, age-at-maturation, productivity and abundance of
a distant wild salmon population. 相似文献
172.
The Odc-rs8 locus belongs to a family of mouse DNA sequences related to the gene encoding ornithine decarboxylase (ODC). Odc-rs8 was mapped by recombinant inbred (RI) strain analysis to the region of Chromosome (Chr) 12 occupied by the variable region genes of the immunoglobulin heavy chain (Igh) complex. In the present study, alleles at Odc-rs8 were shown to cosegregate with those for Igh variable region (Igh-V or V
H) genes among 37 inbred mouse strains that had been characterized previously for their haplotypes at Igh. For a more precise definition of the location of Odc-rs8 relative to Igh-V, DNAs from 17 Abelson murine leukemia virus (A-MuLV)-transformed pre-B cell lines cultured from mice heterozygous at Igh and Odc-rs8 were analyzed for the presence of DNA restriction fragments (RFs) derived from each parental Odc-rs8 allele. These cell lines, each of which has rearranged one or both Igh genes, previously were employed in mapping members of nine V
H gene families by deletion analysis (Brodeur et al. 1988). Comparing the deletion profiles of the cell lines for Odc-rs8 with those for the V
H gene families has located Odc-rs8
b within the VHJ558/VH3609 gene cluster and Odc-rs8
c either within or upstream of the 5-most 9% of VHJ558, identifying Odc-rs8 as a potentially useful marker for the 5 end of the Igh complex. 相似文献
173.
A linkage map of mouse Chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation 总被引:6,自引:0,他引:6
Mark L. Watson Peter D'Eustachio Beverly A. Mock Alfred D. Steinberg Herbert C. Morse III Rebecca J. Oakey Thad A. Howard Julie M. Rochelle Michael F. Seldin 《Mammalian genome》1992,2(3):158-171
An interspecific backross was used to define a high resolution linkage map of mouse Chromosome (Chr) 1 and to analyze the segregation of the generalized lymphoproliferative disease (gld) mutation. Mice homozygous for gld have multiple features of autoimmune disease. Analysis of up to 428 progeny from the backcross [(C3H/HeJ-gld x Mus spretus)F1 x C3H/HeJ-gld] established a map that spans 77.6 cM and includes 56 markers distributed over 34 ordered genetic loci. The gld mutation was mapped to a less than 1 cM segment on distal mouse Chr 1 using 357 gld phenotype-positive backcross mice. A second backcross, between the laboratory strains C57BL/6J and SWR/J, was examined to compare recombination frequency between selected markers on mouse Chr 1. Significant differences in crossover frequency were demonstrated between the interspecific backcross and the inbred laboratory cross for the entire interval studied. Sex difference in meiotic crossover frequency was also significant in the laboratory mouse cross. Two linkage groups known to be conserved between segments of mouse Chr 1 and the long arm of human Chrs 1 and 2 where further defined and a new conserved linkage group was identified that includes markers of distal mouse Chr 1 and human Chr 1, bands q32 to q42. 相似文献
174.
A R Migliaccio G Migliaccio J W Adamson B Torok-Storb 《Journal of cellular physiology》1992,152(1):199-206
We have studied stromal cell function in naive or interleukin-1 (IL-1)-stimulated (100 pg/ml) long-term marrow cultures (LTC) from 12 normal donors and 21 patients with severe aplastic anemia (AA). Conditioned media (CM) from normal LTC contained levels of erythroid burst-promoting activity (BPA) and granulocyte/macrophage (GM) colony-stimulating activity (CSA) comparable to those previously described (Migliaccio et al., [1990] Blood, 75:305-312). The addition of IL-1 to these cultures increased the level of CSA and, specifically, of granulocyte colony-stimulating factor (G-CSF) released. Anti-GM-CSF antibody neutralized BPA and CSA in normal naive LTC CM but only the CSA in the CM from IL-1-stimulated LTC. Since the concentrations of GM-CSF, as detected with a specific immunoassay, did not increase after IL-1 treatment, these data suggest that IL-1-stimulated cultures contain an unidentified growth factor having BPA. CM from AA stromal cells contained levels of CSA comparable to those observed in normal stromal cell CM but had significantly lower levels of BPA. Neither anti-GM-CSF nor anti-IL-3 antibodies neutralized the BPA in AA stromal cell CM. This activity may be related to that found in the CM of IL-1-treated normal stromal cells. In nearly 50% of stromal cell cultures of AA patients, addition of IL-1 failed to increase the BPA, CSA, or G-CSF. The presence of an inhibitor in naive or IL-1-treated AA stromal cell CM was excluded by adding the CM to IL-3-stimulated cultures. These findings suggest that G-CSF and GM-CSF genes are differentially regulated in the marrow microenvironment. Furthermore, a marrow microenvironment, deficient in BPA production and, in some cases, unresponsive to IL-1 could contribute to marrow failure in some patients with AA. 相似文献
175.
Expression of CD7 on normal human myeloid progenitors. 总被引:3,自引:0,他引:3
C Chabannon P Wood B Torok-Storb 《Journal of immunology (Baltimore, Md. : 1950)》1992,149(6):2110-2113
Existence of biphenotypic leukemias co-expressing CD7 and CD34 has prompted the question of whether a similar population of cells is present in normal human bone marrow. As CD7 is considered to be a T cell-restricted Ag, the co-expression of CD7 with the "human stem cell Ag" CD34 may identify a bipotent stage within hemopoietic differentiation. Cells with this phenotype have previously been isolated from human thymus. In this report we provide evidence that human marrow mononuclear cells also contain a minor subpopulation of cells co-expressing CD7 and CD34. The CD7+/CD34+ cells were found to contain committed myeloid progenitors assayed both as CFU in semi-solid media and by their ability to produce granulocytes in long term marrow cultures. Expression of CD7 on myeloid committed progenitors was further confirmed in a C-mediated cytotoxic assay. We conclude that CD7 expression is not restricted to T cells but is also expressed during early stages of myeloid differentiation. 相似文献
176.
177.
Ross C. Hoffman Franklin J. Moy Virginia Price Jane Richardson Dennis Kaubisch Eric A. Frieden Jonathan D. Krakover Beverly J. Castner Julie King Carl J. March Robert Powers 《Journal of biomolecular NMR》1996,7(4):273-282
Summary Oncostatin M (OM) is a cytokine that shares a structural and functional relationship with interleukin-6, leukemia inhibitory factor, and granulocyte-colony stimulating factor, which regulate the proliferation and differentiation of a variety of cell types. A mutant version of human OM in which two N-linked glycosylation sites and an unpaired cysteine have been mutated to alanine (N76A/C81A/N193A) has been expressed and shown to be active. The triple mutant has been doubly isotope-labeled with 13C and 15N in order to utilize heteronuclear multidimensional NMR techniques for structure determination. Approximately 90% of the backbone resonances were assigned from a combination of triple-resonance data (HNCA, HNCO, CBCACONH, HBHACONH, HNHA and HCACO), intraresidue and sequential NOEs (3D 15N-NOESY-HMQC and 13C-HSQC-NOESY) and side-chain information obtained from the CCONH and HCCONH experiments. Preliminary analysis of the NOE pattern in the 15N-NOESY-HMQC spectrum and the 13C secondary chemical shifts predicts a secondary structure for OM consisting of four -helices with three intervening helical regions, consistent with the four-helix-bundle motif found for this cytokine family. As a 203-residue protein with a molecular weight of 24 kDa, Oncostatin M is the largest -helical protein yet assigned.To whom correspondence should be addressed. 相似文献
178.
179.
180.
William G. Pitt Mahsa Alizadeh Ghaleb A. Husseini Daniel S. McClellan Clara M. Buchanan Colin G. Bledsoe Richard A. Robison Rae Blanco Beverly L. Roeder Madison Melville Alex K. Hunter 《Biotechnology progress》2016,32(4):823-839
The high morbidity and mortality rate of bloodstream infections involving antibiotic‐resistant bacteria necessitate a rapid identification of the infectious organism and its resistance profile. Traditional methods based on culturing the blood typically require at least 24 h, and genetic amplification by PCR in the presence of blood components has been problematic. The rapid separation of bacteria from blood would facilitate their genetic identification by PCR or other methods so that the proper antibiotic regimen can quickly be selected for the septic patient. Microfluidic systems that separate bacteria from whole blood have been developed, but these are designed to process only microliter quantities of whole blood or only highly diluted blood. However, symptoms of clinical blood infections can be manifest with bacterial burdens perhaps as low as 10 CFU/mL, and thus milliliter quantities of blood must be processed to collect enough bacteria for reliable genetic analysis. This review considers the advantages and shortcomings of various methods to separate bacteria from blood, with emphasis on techniques that can be done in less than 10 min on milliliter‐quantities of whole blood. These techniques include filtration, screening, centrifugation, sedimentation, hydrodynamic focusing, chemical capture on surfaces or beads, field‐flow fractionation, and dielectrophoresis. Techniques with the most promise include screening, sedimentation, and magnetic bead capture, as they allow large quantities of blood to be processed quickly. Some microfluidic techniques can be scaled up. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:823–839, 2016 相似文献