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排序方式: 共有343条查询结果,搜索用时 15 毫秒
31.
32.
Cytogenetic studies of 68 patients who developed secondary leukemia (SL)/dysmyelopoietic syndrome (DMS) after extensive chemotherapy and/or radiation therapy as well as patients who developed SL/DMS without such treatment showed that those patients who received radiation alone or with chemotherapy had more extensive numerical and structural abnormalities than those who received only chemotherapy. In terms of the specific chromosomal abnormalities, there are no differences between the various treatment groups. Hypodiploidy is the most common form of aneuploidy in these patients, with the most common numerical abnormality being the loss of chromosome 7. The most common structural abnormalities involved chromosomes 3 and 5. When compared with patients with de novo leukemia and DMS, the chromosomal abnormalities in these patients are more complex and extensive. Serial studies revealed that cytogenetic abnormalities do not precede the development of hematologic changes by significant time periods. 相似文献
33.
A microculture assay for murine granulocyte-macrophage colony- stimulating factor (GM-CSF) has been developed using fetal liver GM colony-forming cells (CFC) isolated by fluorescence-activated cell sorting. These GM-CFC are free of mature hemopoietic cells, such as granulocytes and macrophages, which may interfere with direct assays for GM-CSF. The assay procedure allows the quantitation of GM-CSF within 48 hr by measuring the number of cells produced from 50 GM-CFC in microcultures (15 microliter). The assay is particularly simple to set up and score and yet, because of the reduced volumes, this assay is still capable of detecting 0.2 pg (i.e., 0.2 U) of GM-CSF within 48 hr, i.e., 100 times less GM-CSF than the conventional soft agar assay. By allowing the microcultures to develop for 7 days, the extra proliferation allows a further tenfold increase in the sensitivity of CSF detection. The time and cost of setting up hundreds of GM-CSF assays for fractions from chromatographic columns, e.g., reverse phase high performance liquid chromatography, is reduced by at least five- fold. Enough GM-CFC can be isolated and stored frozen in one afternoon to provide sufficient cells for the daily assay of 200 samples of GM- CSF for several months. Microassay results for several sources of GM- CSF at different stages of purification are compared to the results obtained from the soft agar assay. 相似文献
34.
O Falusi AL French EC Seaberg PC Tien DH Watts H Minkoff E Piessens A Kovacs K Anastos MH Cohen 《Clinical infectious diseases》2002,35(11):1414-1417
We assessed the prevalence and predictors of latent Toxoplasma infection in a large group of human immunodeficiency virus (HIV)-infected and HIV-uninfected at-risk US women. The prevalence of latent Toxoplasma infection was 15% (380 of 2525 persons) and did not differ by HIV infection status. HIV-infected women aged > or =50 years and those born outside of the United States were more likely to have latent Toxoplasma infection, with prevalences of 32% and 41%, respectively. 相似文献
35.
36.
Percutaneous transjejunal approaches to the biliary system 总被引:2,自引:0,他引:2
37.
De Klein A; Riegman PH; Bijlsma EK; Heldoorn A; Muijtjens M; den Bakker MA; Avezaat CJ; Zwarthoff EC 《Human molecular genetics》1998,7(3):393-398
We describe a G-->A transition within intron 5 of the NF2 gene. This
mutation creates a consensus splice branch point sequence. To our knowledge
this is the first report of a mutation that creates a functional branch
point sequence in a human hereditary disorder. The new branch point
sequence is located 18 bp upstream of a consensus splice acceptor site. A
consensus splice donor site is found 106 bp 3' of the acceptor site. Asa
consequence the G-->A transition results in an alternatively spliced
mRNA containing an additional exon 5a of 106 bp derived from intron
sequences. We cloned the mutant cDNA and show that due to an in-frame stop
codon the cDNA codes for a truncated NF2 protein. The mutation was observed
in three affected members of an NF2 family. In a tumour of one of the
family members both alternatively spliced and wild-type mRNA were found,
although the wild-type allele of the gene is absent due to an interstitial
deletion on chromosome 22. We also show that immunoprecipitations reveal
the presence of full-length wild-type NF2 protein in the tumour lysate.
These data support the hypothesis that some degree of normal splicing of
the mutant precursor RNA is taking place. It is therefore likely that this
residual activity of the mutant allele explains the relatively mild
phenotype in the family. These data also indicate that complete
inactivation of the gene is not required for tumour formation.
相似文献
38.
Thurman EC; Walker J; Jayaraman S; Manjunath N; Ardman B; Green JM 《International immunology》1998,10(5):691-701
Accessory molecule interactions can be critical in determining the outcome
of a T cell's encounter with antigen. Cell adhesion proteins may augment T
cell responses by facilitating TCR engagement of the antigen-MHC complex,
while co-stimulatory molecules may deliver distinct signals that modulate T
cell responsiveness. CD43 (leukosialin, sialophorin) has been suggested to
influence cell activation by steric hindrance based upon the large size and
glycosylation of the protein, as well as the relative abundance of the
protein on the cell surface. In this paper we examine both in vitro and in
vivo T cell-dependent responses in CD43-deficient mice. We demonstrate that
T cells from CD43-deficient mice are hyper-responsive following both in
vivo and in vitro activation, and that this is observed in response to not
only TCR-CD3-mediated stimulation, but also following receptor-independent
activation. This data suggests that mechanisms other than non-specific
steric hindrance are important in the regulation of T cell activation by
CD43.
相似文献
39.
40.
Emergency room radiography of asthma: an efficacy study 总被引:2,自引:0,他引:2