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291.
Delaying senescence as a response to tissue losses has been reported in some studies, but there is no information about its
influence in growth compensation. We performed a first test of the relative contribution of delaying senescence after defoliation
to growth compensation in Dactylis glomerata L. by means of an iterative growth analysis modified to estimate tissue losses to senescent leaves. We show that Dactylis glomerata overcompensated for relative growth rate after defoliation, mainly by slowing down senescence, and to a lesser extent by
increasing the newly assimilated mass allocated to leaves. 相似文献
292.
Galber Rodrigues Araujo Emília Rezende Vaz Patricia Tiemi Fujimura Jo?o Eurico Fonseca Lucélia Maria de Lima Helena Canh?o Gabriela Venturini Karina Helena Morais Cardozo Valdemir Melechco Carvalho Marcelo Henrique Napimoga Luiz Ricardo Goulart Jo?o Gon?alves Carlos Ueira-Vieira 《Arthritis research & therapy》2015,17(1)
IntroductionRheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease that affects around 1 % of the human population worldwide. RA diagnosis can be difficult as there is no definitive test for its detection. Therefore, the aim of this study was to identify biomarkers that could be used for RA diagnosis.MethodsSera from a collagen-induced arthritis mouse model were used to select potential biomarkers for RA diagnosis by phage display technology. In silico and in vitro analyses were performed to characterize and validate the selected peptides. Samples were classified into three groups: RA; two other immune-mediated rheumatic diseases (systemic lupus erythematosus (SLE) and ankylosing spondylitis (AS)); and healthy controls (HC). Enzyme-linked immunosorbent assay (ELISA) was carried out to determine antibody levels, and diagnostic parameters were determined by constructing receiver operating characteristic curves. Mass spectrometry and Western blot were performed to identify the putative autoantigen that was mimicked by a highly reactive mimotope.ResultsAfter three rounds of selection, 14 clones were obtained and tested for immunoreactivity analysis against sera from RA and HC groups. The phage-fused peptide with the highest immunoreactivity (M12) was synthesized, and was able to efficiently discriminate RA patients from SLE, AS and HCs (p < 0.0001) by ELISA. The specificity and sensitivity of anti-M12 antibodies for RA diagnosis were 91 % and 84.3 %, respectively. The M12 peptide was identified as one that mimics a predicted antigenic site of the carbonic anhydrase III (CAIII) protein, a ubiquitous biomarker that has been identified in patients with other diseases.ConclusionM12 is the first peptide associated with the CAIII protein that may be used as an antigen for antibody detection to aid in RA diagnosis with high sensitivity and specificity. 相似文献
293.
Janaína Kolling Emilene B. S. Scherer Cassiana Siebert Fernanda Hansen Felipe V. Torres Giselli Scaini Gabriela Ferreira Rodrigo B. de Andrade Carlos A. S. Gonçalves Emílio L. Streck Clovis M. D. Wannmacher Angela T. S. Wyse 《Cell biochemistry and function》2013,31(7):575-584
Homocystinuria is a neurometabolic disease caused by a severe deficiency of cystathionine beta‐synthase activity, resulting in severe hyperhomocysteinemia. Affected patients present several symptoms including a variable degree of motor dysfunction. In this study, we investigated the effect of chronic hyperhomocysteinemia on the cell viability of the mitochondrion, as well as on some parameters of energy metabolism, such as glucose oxidation and activities of pyruvate kinase, citrate synthase, isocitrate dehydrogenase, malate dehydrogenase, respiratory chain complexes and creatine kinase in gastrocnemius rat skeletal muscle. We also evaluated the effect of creatine on biochemical alterations elicited by hyperhomocysteinemia. Wistar rats received daily subcutaneous injections of homocysteine (0.3–0.6 µmol/g body weight) and/or creatine (50 mg/kg body weight) from the 6th to the 28th days of age. The animals were decapitated 12 h after the last injection. Homocysteine decreased the cell viability of the mitochondrion and the activities of pyruvate kinase and creatine kinase. Succinate dehydrogenase was increased other evaluated parameters were not changed by this amino acid. Creatine, when combined with homocysteine, prevented or caused a synergistic effect on some changes provoked by this amino acid. Creatine per se or creatine plus homocysteine altered glucose oxidation. These findings provide insights into the mechanisms by which homocysteine exerts its effects on skeletal muscle function, more studies are needed to elucidate them. Although creatine prevents some alterations caused by homocysteine, it should be used with caution, mainly in healthy individuals because it could change the homeostasis of normal physiological functions. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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Ohne ZusammenfassungMit 5 Textabbildungen 相似文献
296.