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Ahmed Jawaad Afzal Salim Ahmed Bokhari Waseem Ahmad Mohammad Hamid Rashid Mohammad Ibrahim Rajoka Khawar Sohail Siddiqui 《Biotechnology letters》2000,22(11):957-960
Two sensitive, high-resolution and exceedingly versatile methods for the detection of isoenzymes of polymer-degrading enzymes on high-resolution, alkaline, cold, in situ-native (HiRACIN)-PAGE and high-resolution in situ-inhibited, native (HiRISIN)-PAGE are described. Extracellular crude extracts containing xylanases and carboxymethylcellulases from Scopulariopsis sp. and glucoamylases from Aspergillus niger were subjected to non-denaturing PAGE containing substrates in the resolving gel. In case of HiRACIN-PAGE, the enzymes were prevented from degrading their respective substrates during run by carrying out electrophoresis at 4°C and the pH of running and resolving gel buffer systems were increased from 8.5 to 10.6. In case of HiRISIN-PAGE, adding competitive inhibitor of the enzyme, cellobiose, in the resolving gel prevents the degradation of polymer during the run. These techniques were successfully applied, for the first time, to visualize four, three and four sharp and distinct bands of xylanases, glucoamylases and CMCases, respectively. 相似文献
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Sumaira Naz Muhammad Zahoor Muhammad Naveed Umar Fatmah S. AlQahtany Yousif M. Elnahas Riaz Ullah 《Saudi Journal of Biological Sciences》2020,27(12):3267-3273
The 2-picolylamine is a simplest analogue of the alkaloid that has secondary and tertiary nitrogen function in its cyclic structure like that of alkaloids that can be derivatized to a number of biologically active compounds. In connection to our previous work, in the present work, three thiourea derivatives (I = 1,3-bis(2-benzyl-3-phenyl-1-(pyridine-2-yl) propyl) thiourea, II = 1,3-bis (pyridin-2-ylmethyl) thiourea, and III = 1-(2-benzyl-3-phenyl-1-(pyridine-2-yl) propyl)-3-phenylthiourea) were synthesized using 2-picolylamine template which is a readily available synthetic analogue of naturally occurring alkaloid. The biological effect of the synthesized derivatives were monitored on the activity of glucose-6-phosphatase in Swiss albino mice (21-days). The derivatives were also tested for their potential toxicity in a 28-days sub-chronic toxicity studies by assessing their effects on different parameters like hematological, serum biochemistry and liver histology. The therapeutic effect of the safe derivative (I) was examined in streptozotocin-induced diabetic mice as well. The derivatives showed inhibition of the enzyme activity from good to an excellent degree. Compound I had the highest inhibition with 21.42 ± 5.113 mg of the released phosphate as compared to that of the positive control group (84.55 ± 3.213 mg). Only I turned out to be safe for use in animals without exerting any toxic or lethal effects on any of the assessed parameters in the used animal model. Compound I efficiently reversed the effects like hyperglycemia, hyperlipidemia and weight loss in the test animals. Out of these three-tested compounds, I was found safe to be use as therapeutic agent in diabetes complications. However, further toxicological studies in other animal models are needed as well. 相似文献
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Christopher M. R. Bax Vijai S. Shankar A. S. M. Towhidul Alam Bridget E. Bax Baljit S. Moonga Christopher L. -H. Huang Mone Zaidi Barry R. Rifkin 《Bioscience reports》1993,13(3):169-174
We report the effects of tetracycline analogues on cytosolic Ca2+ transients resulting from application of ionic nickel (Ni2+), a potent surrogate agonist of the osteoclast Ca2+ receptor. Preincubation with minocycline (1 mg/l) or a chemically modified tetracycline, 4-dedimethyl-aminotetracycline (CMT-1) (1 or 10 mg/l), resulted in a significant attenuation of the magnitude of the cytosolic [Ca2+] response to an application of 5 mM-[Ni2+]. Preincubation with doxycycline (1 or 10 mg/l) failed to produce similar results. In addition, application of minocycline alone (0.1–100 mg/l) resulted in a 3.5-fold elevation of cytosolic [Ca2+]. The results suggest a novel action of tetracyclines on the osteoclast Ca2+ receptor. 相似文献
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Mauricio Hunsche Kathrin Bürling Amina Sirag Saied Michaela Schmitz-Eiberger Muhammad Sohail Jens Gebauer Georg Noga Andreas Buerkert 《Plant Growth Regulation》2010,61(3):253-263
Seedlings of the salt-tolerant plant grewia [Grewia tenax (Forssk.) Fiori] and the moderately salt-tolerant tamarind (Tamarindus indica L.) were grown under controlled conditions and treated daily with NaCl solutions to investigate mechanisms of tolerance to
salinity. Leaf micromorphology, cuticular wax load, chlorophyll fluorescence and light remission, as well as antioxidative
potential were evaluated. As confirmed by energy-dispersive X-ray microanalysis in both species, absorption of sodium and
chlorine increased with rising NaCl concentration in the treatment solution. In parallel, accumulation of calcium in grewia
leaves was strongly reduced, leading to less crystals of calcium oxalate in leaf tissue. In grewia the cuticular wax load,
chlorophyll content, and electron transport rate (ETR) were significantly reduced by comparatively low NaCl concentrations.
In tamarind, in contrast, wax load and ETR were not significantly affected, while the decrease of chlorophyll content was
less pronounced. Measurements of the antioxidative capacity and the imbalance between values of lipophilic and hydrophilic
extracts at different NaCl concentrations confirmed that grewia is more salt tolerant than tamarind. This higher tolerance
degree seemed to be associated with grewias’ more efficient scavenging of free radicals and the regulation of the antioxidative
potential in lipophilic and hydrophilic extracts. 相似文献