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161.
本文用~(125)Ⅰ标记LC-1进行了一些体内外实验。实验结果表明:LC-1单抗的结合常数为4.8×10~8M~(-1),LC-1针对的SPC-A_1细胞表面抗原的位点数为7.2×10~4/细胞;LC-1与LAC-122两单抗针对的抗原决定簇没有交叉;用蛋白酶和过碘酸钠处理SPC-A_1细胞,前者对LC-1的结合抑制39%,后者抑制66%;LC- 1不但有较强的体外结合靶细胞的能力,从LC-1在荷瘤裸鼠中的组织器官分布来看,LC-1与肿瘤有较高的体内亲和性,并且是特异性的结合。 相似文献
162.
Mildred S. Seelig 《Biological trace element research》1979,1(4):273-297
Except for a few experimental models of magnesium (Mg)-deficiency-induced neoplasms, less attention has been paid in the past
quarter century in the Western world to this macromineral than to the trace elements; e.g., selenium (Se) and zinc (Zn), and
to vitamins, deficiencies of which are each considered probable factors in oncogenesis. Although early epidemiologic studies
showed an inverse correlation between the amount of Mg in soil and water and the incidence of (gastric) cancer, and several
animal studies supported the premise that Mg has a prophylactic effect against induction of cancer, other studies showed that
Mg supplementation increased the growth of established experimental tumors. Thus, enthusiasm for this approach subsided. The
early epidemiologic findings have since been confirmed, and there have been studies demonstrating the importance of Mg in
maintaining immunocompetence, and others indicating that immunodeficiencies increase susceptibility to the development of
cancer. Evidence has now accrued that indicates that Mg deficiency increases susceptibility to chemical oncogens. The abnormal
metabolism of tryptophan (yielding a carcinogenic metabolite) that indicates functional or absolute pyridoxine deficiency
is an indirect clue to Mg deficiency. Vitamin B6-activated enzymes require Mg as a cofactor. However, the early warnings against the use of Mg as part of an antineoplastic
program against established cancer were justified, since rapidly metabolizing cells (such as cancers) are dependent on Mg.
There are similarities between experiences with Mg and with Se and Zn. All three are required for normal metabolism; Se also
protects against free radicals in the environment. Mg and Zn have increased established tumor growth, and their depletion
has been applied to antineoplastic programs, with risks comparable to those of using antimetabolic agents. 相似文献
163.
George L. Wied Peter H. Bartels Marluce Bibbo May Chen Frank R. Reale Hans Schreiber Jaroslav J. Sychra 《Cell biochemistry and biophysics》1979,1(1):39-54
Cytologic preparations made from the tracheobronchial tree taken by the Schreiber catheter have been scanned by three color
microphotometry. The digitized cell images were processed by the analytical cytodiagnostic programs of the TICAS system. Cells
were sorted into two control groups and five groups of increasing atypia ranging from normal epithelium to invasive squamous
cell carcinoma. Standard statistical tests, including Wilk's Lambda, Rao's V, and the Kruskal-Wallis tests are performed on
these subsets of cell image features. This study demonstrates that discriminant analyses permit differentiation between normal
cells and those from marked atypia or carcinoma and that the classification achieves a high degree of agreement with visual
assignment. 相似文献
164.
Rajagopalan Sridhar Eric C. Stroude W. Rodger Inch 《In vitro cellular & developmental biology. Plant》1979,15(9):685-690
Summary 2-Deoxy-d-glucose (2DG) and 5-thio-d-glucose (5TG) are glucose antimetabolites that are known to be selectively toxic to hypoxic cells grown as single cells or
as monolayer cultures. These analogues were toxic to Chinese hamster V79 cells grown as multicell spheroids even under aerobic
conditions. When spheroids, 500- to 600-μm diameter, were exposed to 7.5mm of these chemicals for 3 days, the number of clonogenic cells per spheroid dropped to 50% for 5-thio-d-glucose and 20% for 2-deoxy-d-glucose, relative to control values. Survivals were reduced to less than 1% when the experiment was repeated in glucose-free
medium. Scanning electron photomicrographs of spheroids treated with 7.5mm of either analogue showed extensive damage to the outer cells. The cell killing observed was much more than could be predicted
on the basis of the hypoxic fraction known to be present in these spheroids. The crowded tumor-like environment may make the
cells vulnerable to the cytotoxic action of glucose analogues and other glycolytic inhibitors.
Supported by the Ontario Cancer Treatment and Research Foundation, London Clinic. 相似文献
165.
Injections of urine of patients with bladder cancer linked with bilharziasis, simple urinary bilharziasis, ascariasis or ancylostomiasis, induced cyst formation found in Opalina sudafricana when injected into its host Bufo regularis. It is suggested that the carcinogenic tryptophan metabolites present in the injected urine reach the parasites in the recta of the experimental toads and stimulate them to divide mitotically to form small forms which eventually encyst. This test may be of a diagnostic help in detecting any abnormality in tryptophan metabolism in some human patients. 相似文献
166.
167.
《Biomarkers》2013,18(8):639-649
AbstractContext: Freshwater cyanobacterial toxins, microcystins, may be a contributing factor to the development of hepatocellular cancer and colorectal cancer.Objectives: This review summarizes the toxicity data, exposure routes and the methodologies available to determine exposure to elucidate the relationship to liver and colorectal cancer.Methods: Literature searches were conducted using Medline, PubMed and Web of Science.Results: There is evidence of human poisonings resulting from exposure to microcystins, however current methods rely on targeted approaches only suitable for acute exposure. No methods exist for the determination of chronic exposure to microcystins.Conclusions: With the growing evidence of exposure to microcystins and the possible links to cancer, methods to measure medium to long-term human exposure are needed. The identification and validation of candidate biomarkers are key to undertaking urgently required epidemiological studies. 相似文献
168.
169.
《Bioorganic & medicinal chemistry》2014,22(21):6270-6287
Novel cationic dimethylaminopyridine derivatives of pentacyclic triterpenes were previously described to promote mitochondrial depolarization and cell death in breast and melanoma cell lines. The objective of this work was to further investigate in detail the mechanism of mitochondrial perturbations, correlating those effects with breast cancer cell responses to those same agents. Initially, a panel of tumor and non-tumor cell lines was grown in high-glucose or glucose-free glutamine-containing media, the later forcing cells to synthesize ATP by oxidative phosphorylation only. Cell proliferation, cell cycle, cell death and mitochondrial membrane polarization were evaluated. Inhibition of cell proliferation was observed, accompanied by an arrest in the G1-cell cycle phase, and importantly, by loss of mitochondrial membrane potential. On a later time-point, caspase-9 and 3 activation were observed, resulting in cell death. For the majority of test compounds, we determined that cell toxicity was augmented in the galactose media. To investigate direct evidences on mitochondria isolated rat liver mitochondria were used. The results showed that the compounds were strong inducers of the permeability transition pore. Confirming our previous results, this work shows that the novel DMAP derivatives strongly interact with mitochondria, resulting in pro-apoptotic signaling and cell death. 相似文献
170.
The association of interleukin-1β (IL-1B) -511C?>?T and IL-1 receptor antagonist (IL-1RN) VNTR, transforming growth factor-β (TGF-B1) +28C?>?T and interferon-γ (IFN-G)?+?874T>A polymorphisms with bladder cancer (CaB) susceptibility and risk of recurrence in Bacillus Calmette–Guérin (BCG)-treated patients was analyzed in 287 controls and 213 CaB patients (73 BCG treated). Increased risk was observed with the IL-1RN*2 allele (odds ratio (OR) 5.01) and the IFN-G +874 A allele (OR 1.78). TGF-B TT and IFN-G +874 A carriers were associated with reduced (hazard ratio (HR) 0.37) and enhanced (HR 2.24) risk of recurrence after BCG immunotherapy, respectively. The study suggests that cytokine gene variants may modulate CaB susceptibility and risk of recurrence after BCG immunotherapy. 相似文献