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1.
A pigment made up of a protein able to bind retinal as well as retinol is described. The molecule consists of a dimer with a molecular weight of 50,000 which binds one molecule of retinal. The binding site for retinal is a Schiff base buried in the interior of the protein. Retinol is probably bound to the protein in the same site as for retinal, although not covalently, as suggested by the absorbance spectra. The protein, extracted from honeybee retina, is involved in visual pigment metabolism, and its structure may elucidate the mechanism of the stereospecific photoisomerization of all trans-retinal to 11-cis-retinal. 相似文献
2.
Effect of light and calcium on cyclic GMP synthesis in rod outer segments of toad retina 总被引:4,自引:0,他引:4
The rod outer segments of toad retina contain a guanylate cyclase activity of about 3 +/- 1 nmol of cGMP formed/min per mg protein. In darkness this value is largely independent of the Ca2+ concentration, although it is enhanced by light upon lowering the Ca2+ concentration from 10(-5) to 10(-8) M. The activating effect of light on cyclase at low Ca2+ concentrations is enlarged upon increasing the light intensity. With a flash of light bleaching 7 X 10(-2) percent of rhodopsin, cyclase activity increased by a factor of 30 when Ca2+ levels dropped from 10(-5) to 10(-8) M. In view of recent observations that shortly after a flash of light the calcium activity inside the photoreceptor cell decreases, it seems likely that Ca2+ plays a regulatory role on cGMP metabolism in visual excitation. 相似文献
3.
C Labrid G Dureng C Boero 《Comptes rendus des séances de la Société de biologie et de ses filiales》1975,169(3):566-573
The "gastric chamber" technique, performed in the anaesthetised rat, enables the study of gastric mucosal fragility induced by doses of phenylbutazone, which do not themselves cause ulceration or exulceration. The perfusion of buffered solution at pH 2-8 into the gastric chamber shows that prior oral administration of phenylbutazone 50 mg/kg increases the fragility of the mucosa. The optimal delay separating this administration from the time of experimentation is 6 hours. The effects seen are essentially vascular disorders. 相似文献
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Bella S. Galil Ferdinando Boero Marnie L. Campbell James T. Carlton Elizabeth Cook Simonetta Fraschetti Stephan Gollasch Chad L. Hewitt Anders Jelmert Enrique Macpherson Agnese Marchini Cynthia McKenzie Dan Minchin Anna Occhipinti-Ambrogi Henn Ojaveer Sergej Olenin Stefano Piraino Gregory M. Ruiz 《Biological invasions》2015,17(4):973-976
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Daniela Lenti Boero 《Ethology : formerly Zeitschrift fur Tierpsychologie》1995,100(1):26-38
Scent-deposition was investigated in Marmota marmota L. at Gran Paradiso National Park. 448 h of focal and scan sampling were performed on 22 marmots in four subsequent years. Results show that: (1) 97.4 % of the scent-deposition is done within 25 m of the edge of the territories or of the main burrows (X2 = 100.4, df 9, p < 0.001); (2) being a reproducing adult is the most prominent factor in scent-deposition (X2 = 32.4, df = 18, p < 0.002). The role of factors affecting scent-deposition in territorial defence and social communication is discussed. 相似文献
10.
R Boero F Quarello C Guarena G Piccoli 《Bollettino della Società italiana di biologia sperimentale》1985,61(2):243-248
The authors present the results of a simultaneous assay of: intracellular Na+ and K+ concentrations, Na+ and K+ outward bumetanide-sensitive effluxes (Na+, K+ cotransport), Na+ efflux stimulated by extracellular Li+ (Na+, Li+ countertransport), and ouabain- and bumetanide-resistant Na+ and K+ effluxes (passive membrane permeability) performed in red blood cells from 15 uremic patients an regular hemodialysis and from 12 normal subjects, with an established flux assay. Na+ and K+ effluxes by the Na+, K+ cotransport system were significantly (p less than 0.01) lower in uremic patients then in normals (219 +/- 37 vs 82 +/- 17 mumol/l RBC/h and 251 +/- 29 vs 139 +/- 14 mumol/l RBC/h respectively). In normal subjects the bumetanide sensitive Na+ and K+ effluxes were strongly (r = 0.89; p less than 0.01) intercorrelated; and the intracellular Na+ concentration was related to the outward Na+ cotransport flux (r = 0.53; p approximately 0.05). Among uremic patients these correlations were not found. Na+ and K+ intracellular concentrations, passive Na+ and K+ permeability, and Na+, Li+ countertransport activity were not different among uremic patients and normal controls. In conclusion, in uremic dialyzed patients, red blood cell Na+, K+ cotransport activity is quite uniformly suppressed. The possible pathogenesis of this disfunction is still speculative and deserves further studies. 相似文献