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91.
Structure and mechanism of copper, zinc superoxide dismutase 总被引:26,自引:0,他引:26
Copper, zinc superoxide dismutase (SOD) catalyses the very rapid two-step dismutation of the toxic superoxide radical (O-2) to molecular oxygen and hydrogen peroxide through the alternate reduction and oxidation of the active-site copper. We report here that after refitting and further refinement of the previous 2 A structure of SOD2, analysis of the new model and its calculated molecular surface shows an extensive surface topography of sequence-conserved residues stabilized by underlying tight packing and H-bonding. There is a single, highly complementary position for O-2 to bind to both the Cu(II) and activity-important Arg 141 with correct geometry; two water molecules form a ghost of the superoxide in this position. The geometry and molecular surface of the active site, together with biochemical data, suggest a specific model for the enzyme mechanism. 相似文献
92.
Jong Sik Yoon R. H. Richardson M. R. Wheeler 《Cellular and molecular life sciences : CMLS》1973,29(5):639-641
Zusammenfassung Es wird eine verbesserte Methode zur Herstellung von Quetschpräparaten von Speicheldrüsenchromosomen beschrieben. Die Methode gibt scharfe Bilder der feinsten Chromosomenbänder auf klarem Hintergrund.
Research supported by U.S. Public Health Service Research Grants No. GM-11609 and GM-19616 from the National Institute of General Medical Sciences. 相似文献
Research supported by U.S. Public Health Service Research Grants No. GM-11609 and GM-19616 from the National Institute of General Medical Sciences. 相似文献
93.
94.
DNA methylation and the regulation of gene transcription 总被引:28,自引:0,他引:28
95.
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes 总被引:25,自引:0,他引:25
Kondo S Schutte BC Richardson RJ Bjork BC Knight AS Watanabe Y Howard E de Lima RL Daack-Hirsch S Sander A McDonald-McGinn DM Zackai EH Lammer EJ Aylsworth AS Ardinger HH Lidral AC Pober BR Moreno L Arcos-Burgos M Valencia C Houdayer C Bahuau M Moretti-Ferreira D Richieri-Costa A Dixon MJ Murray JC 《Nature genetics》2002,32(2):285-289
96.
A rho-recognition site on phage lambda cro-gene mRNA 总被引:1,自引:0,他引:1
97.
Th. Cooper M. Jellinek Teresa Pinakatt A. W. Richardson 《Cellular and molecular life sciences : CMLS》1965,21(1):28-29
Résumé L'administration intraveineuse de pyridoxine et pyridoxal (10 mg/kg) à des rats anesthésiés inhibe l'augmentation du rendement du cocur. En même temps, une hyperthermie est provoquée par l'irradiation du corps entier avec des ondes de longueur minime (2,450 Mc. c.w. 0.08/w/cm2). Cet effet peut être attribué à l'interaction de ces composés d'amines vasoactifs libérés pendant l'irradiation. 相似文献
98.
M. Zacco E. M. Richardson J. O. Crittenden F. C. Dohan J. L. Hollander 《Cellular and molecular life sciences : CMLS》1955,11(7):279-280
Riassunto In pazienti affetti da artrite reumatoide viene iniettato cortisone acetato, idrocortisone acetato, o idrocortisone, nel cavo sinoviale artritico.La durata del riassorbimento di questi 17-idrossicorticoidi; la loro distribuzione nelle cellule e nel fluido articolare e nelle cellule del rivestimento sinoviale; le andamento del processo idrolitico dei composti acetati, studiati con mezzi chimici e cromatografici, si prestano a commenti utili ad interpretare la maggiore efficacia locale dell'idrocortisone.
Supported by a grant from the Helen Augusta Parkhill Foundation.—Communication at the 8th International Congress of Rheumatic Diseases, Geneva, August 1953. 相似文献
Supported by a grant from the Helen Augusta Parkhill Foundation.—Communication at the 8th International Congress of Rheumatic Diseases, Geneva, August 1953. 相似文献
99.
100.
Frequent chromosomal translocations induced by DNA double-strand breaks 总被引:40,自引:0,他引:40
The faithful repair of DNA damage such as chromosomal double-strand breaks (DSBs) is crucial for genomic integrity. Aberrant repair of these lesions can result in chromosomal rearrangements, including translocations, which are associated with numerous tumours. Models predict that some translocations arise from DSB-induced recombination in differentiating lymphoid cell types or from aberrant repair of DNA damage induced by irradiation or other agents; however, a genetic system to study the aetiology of these events has been lacking. Here we use a mouse embryonic stem cell system to examine the role of DNA damage on the formation of translocations. We find that two DSBs, each on different chromosomes, are sufficient to promote frequent reciprocal translocations. The results are in striking contrast with interchromosomal repair of a single DSB in an analogous system in which translocations are not recovered. Thus, while interchromosomal DNA repair does not result in genome instability per se, the presence of two DSBs in a single cell can alter the spectrum of repair products that are recovered. 相似文献