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91.
Radek Litvín David Bína Pavel Siffel Frantisek Vácha 《Photochemical & photobiological sciences》2005,4(12):999-1002
Accumulation of reduced pheophytin in photosystem II under illumination at low redox potential is known to be accompanied by a pronounced decrease of a chlorophyll fluorescence yield. Simultaneous measurement of this fluorescence quenching and absorbance changes in photosystem II reaction centres, in the presence of dithionite, showed each event to have a different temperature dependence. While fluorescence quenching was suppressed more than 20 times when measured at 77 K, pheophytin accumulation decreased only 5 times. At 77 K, the fluorescence was quenched considerably, but only in those reaction centres where reduced pheophytin had been accumulated at room temperature before sample freezing. This showed that the accumulation of reduced pheophytin above 240 K was accompanied by an additional, most probably conformational, change in the reaction centre that substantially enhanced non-radiative dissipation of excitation energy. 相似文献
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Procamallanus (Spirocamallanus) chetumalensis n. sp. is described from the stomach and intestine of the Mayan sea catfish Ariopsis assimilis (Günther, 1864), from the Bay of Chetumal, Quintana Roo, México. It is characterized by bifurcate deirids; males have 3 pairs of preanal papillae, 6 pairs of postanal papillae, 2 pairs of transverse elongate adanal papillae surrounding the cloacal aperture, wide caudal alae, spicules of unequal length, and a gubernaculum, and females have a rounded tail bearing a digit-like process terminating in 2 spines. This is the seventh Procamallanus (Spirocamallanus) species reported from fishes in Mexico and the first one recorded in sea catfishes of the Ariidae. 相似文献
98.
Detailed structures and electronic properties of three tautomeric forms of the toxin citrinin were investigated using several quantum calculation methods. Energetic preference of the predominant p- and o-quinone methide tautomeric forms is dependent on the method of calculation. A previously unstudied carboxylic acid enol tautomer was calculated to be surprisingly stable in vacuo, being within 2.5 kcal mol? 1 at the B3LYP/6-311++G(2d,2p) level of theory. Despite differences in bond nature and connectivity of tautomers, the natural bond orbital analysis revealed that tautomeric forms share similar natural charges and natural electron configurations. Calculated bond lengths corresponded with experimentally observed values and assignments for the calculated infrared vibrational frequencies are reported. 相似文献
99.
L-Carnitine transport and free fatty acid oxidation have been studied in hearts of rats with 3-month-old aorto-caval fistula. For carnitine transport experiments, the hearts were perfused via the ascending aorta with a bicarbonate buffer containing 11 mM glucose and variable concentrations L-[14C]carnitine (10-200 microM). In some experiments, the active component of carnitine transport was suppressed by the adjunction of 0.05 mM mersalyl acid. The subtraction of passive from total transport allowed reconstruction of the saturation curves of the carrier-mediated transport of L-carnitine. Our data suggest that at a physiological carnitine concentration (50 microM), the rate of [14C]carnitine accumulation was significantly depressed in mechanically overloaded hearts. In addition, according to Lineweaver-Burk analysis, the affinity of the membrane carrier for L-carnitine was considerably diminished (Km carnitine 125 instead of 83 microM, Vmax unchanged). The above alterations of L-carnitine transport did not result from a decrease of the transmembrane gradient of sodium, since the intracellular Na+ content of the hypertrophied hearts was quite similar to that of control hearts. The ability of atrially perfused, working hearts to oxidize the exogenous free fatty acids was assessed from 14CO2 production obtained in the presence of [U-14C]palmitate or [1-14C]octanoate. The total 14CO2 production, expressed per min per g dry weight, was significantly diminished in hearts from rats with the aorto-caval fistula if 1.2 mM palmitate was used. On the other hand, in the presence of 2.4 mM octanoate, a substrate which circumvents the carnitine-acylcarnitine translocase, no such reduction of the 14CO2 production could be detected. Our results suggest that the decrease of L-carnitine transport, resulting in a significant depression of tissue carnitine, may impair long-chain fatty acid activation and/or translocation into mitochondria. In contrast, the oxidation of short-chain fatty acids, the activation of which takes place directly in mitochondrial matrix, is not limited in volume-overloaded hearts. 相似文献
100.
Sona Cacanyiova Andrea Berenyiova Magdalena Malekova Frantisek Kristek Ima Dovinova Peter Krenek Lenka Pivackova Ivana Pifkova 《Journal of physiology and biochemistry》2014,70(3):749-760
While the unequivocal pattern of endothelial nitric oxide synthase (eNOS) inhibition in cardiovascular control is recognized, the role of NO produced by neuronal NOS (nNOS) remains unclear. The aim of this study was to compare the effects of chronic treatment with 7-nitroindazole (7-NI, nNOS inhibitor) and NG-nitro-l-arginine methylester (l-NAME, general and predominantly eNOS inhibitor) on cardiovascular system of young normotensive rats. Wistar rats (4 weeks old) were used: controls and rats administered either 7-NI (10 mg/kg bw/day) or l-NAME (50 mg/kg bw/day) in drinking water for 6 weeks. The systolic blood pressure (sBP) was measured by plethysmographic method, and the vasoactivity of isolated arteries was recorded. 7-NI-treatment did not affect sBP; however, the sBP was increased after l-NAME-treatment. l-NAME inhibited acetylcholine-induced relaxation of thoracic aorta (TA), whereas it remained unchanged after 7-NI-treatment. The response of TA to sodium nitroprusside was increased in both experimental groups. The expression of eNOS and nNOS in TA was unchanged in both experimental groups, whereas the activity of NOS was decreased in l-NAME-treated group. Noradrenaline- and angiotensin II-induced contractions of TA were reduced in l-NAME-treated group; however, the contractions remained unchanged in 7-NI-treated group. In all groups, the endogenous angiotensin II participated in adrenergic contraction of TA; this contribution was significantly increased in l-NAME-treated group. Neurogenic contractions in mesenteric artery (MA) remained unchanged after 7-NI-treatment, but increased after l-NAME-treatment. Results show that NO deficiency induced by administration of 7-NI and l-NAME had different cardiovascular effects: eNOS and nNOS triggered distinct signaling pathways in young normotensive rats. 相似文献