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P M Williams 《Nature》1968,219(5150):152-153
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Zusammenfassung Menschliche Leukozyten, die vorher 2 resp. 4 h der Wirkung von Colcemid ausgesetzt worden waren, ergaben in Zellkulturen 45 resp. über 50% Zellen mit 45 oder weniger Chromosomen im Vergleich zu 10% in Kontrollkulturen ohne Colcemid.
This work is supported financially by Schering Chemicals Ltd., Burgess Hill, Sussex. We would like to thank Dr.A. G. Pitchford for advice and MissE. Gristwood for technical assistance. 相似文献
This work is supported financially by Schering Chemicals Ltd., Burgess Hill, Sussex. We would like to thank Dr.A. G. Pitchford for advice and MissE. Gristwood for technical assistance. 相似文献
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Zusammenfassung Grundwasserproben aus der Gort-Ebene (West-Irland) wurden auf Tritium-Gehalt analysiert und die Ergebnisse mit dem bereits bekannten Tritium-Einstrom dieser Gegend verglichen. Registrierungen des «World Precipitation Network» in Wien ergaben den Nachweis eines offenbar langsamen Durchflusses in das Grundwasser-Aquifer-System.
Acknowledgments. The authors are indebted to the Nuclear Physics Division, Atomic Energy Research Establishment, Harwell (England) for tritium analyses and to Mr.B. R. Payne, Section of Isotope Hydrology, IAEA, Wien (Austria) for providing unpublished tritium data from Valentia for the period 1966 to 1971. 相似文献
Acknowledgments. The authors are indebted to the Nuclear Physics Division, Atomic Energy Research Establishment, Harwell (England) for tritium analyses and to Mr.B. R. Payne, Section of Isotope Hydrology, IAEA, Wien (Austria) for providing unpublished tritium data from Valentia for the period 1966 to 1971. 相似文献
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Siemens J Lillo C Dumont RA Reynolds A Williams DS Gillespie PG Müller U 《Nature》2004,428(6986):950-955
Mechanoelectrical transduction, the conversion of mechanical force into electrochemical signals, underlies a range of sensory phenomena, including touch, hearing and balance. Hair cells of the vertebrate inner ear are specialized mechanosensors that transduce mechanical forces arising from sound waves and head movement to provide our senses of hearing and balance; however, the mechanotransduction channel of hair cells and the molecules that regulate channel activity have remained elusive. One molecule that might participate in mechanoelectrical transduction is cadherin 23 (CDH23), as mutations in its gene cause deafness and age-related hearing loss. Furthermore, CDH23 is large enough to be the tip link, the extracellular filament proposed to gate the mechanotransduction channel. Here we show that antibodies against CDH23 label the tip link, and that CDH23 has biochemical properties similar to those of the tip link. Moreover, CDH23 forms a complex with myosin-1c, the only known component of the mechanotransduction apparatus, suggesting that CDH23 and myosin-1c cooperate to regulate the activity of mechanically gated ion channels in hair cells. 相似文献
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Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors 总被引:5,自引:0,他引:5
Al-Tassan N Chmiel NH Maynard J Fleming N Livingston AL Williams GT Hodges AK Davies DR David SS Sampson JR Cheadle JP 《Nature genetics》2002,30(2):227-232
Inherited defects of base excision repair have not been associated with any human genetic disorder, although mutations of the genes mutM and mutY, which function in Escherichia coli base excision repair, lead to increased transversions of G:C to T:A. We have studied family N, which is affected with multiple colorectal adenomas and carcinoma but lacks an inherited mutation of the adenomatous polyposis coli gene (APC) that is associated with familial adenomatous polyposis. Here we show that 11 tumors from 3 affected siblings contain 18 somatic inactivating mutations of APC and that 15 of these mutations are G:C-->A transversions--a significantly greater proportion than is found in sporadic tumors or in tumors associated with familial adenomatous polyposis. Analysis of the human homolog of mutY, MYH, showed that the siblings were compound heterozygotes for the nonconservative missense variants Tyr165Cys and Gly382Asp. These mutations affect residues that are conserved in mutY of E. coli (Tyr82 and Gly253). Tyrosine 82 is located in the pseudo-helix-hairpin-helix (HhH) motif and is predicted to function in mismatch specificity. Assays of adenine glycosylase activity of the Tyr82Cys and Gly253Asp mutant proteins with 8-oxoG:A and G:A substrates show that their activity is reduced significantly. Our findings link the inherited variants in MYH to the pattern of somatic APC mutation in family N and implicate defective base excision repair in predisposition to tumors in humans. 相似文献
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This note reports the SHRIMP U-Pb data of zircons from the Caledonian Xiongdian eclogite, western Dabie Mountains. Zircons from the rock occur mainly in garnet and other metamorphic minerals with sharp boundaries and exhibit textures growing under metamorphic conditions. Analyses of 7 grains give 206Pb/238U ages ranging from 335 to 424 Ma, showing a certain degree of radiogenic lead loss. This suggests a minimum age of (424±5) Ma for the metamorphic zircons, as well as the high-pressure metamorphic event. The outer peripheral zone of a zircon gives 206Pb/238U age of about 300 Ma. Combined with Sm-Nd, 40Ar-39Ar, U-Pb and 207Pb/206Pb ages, the peak metamorphism of the Xiongdian eclogite is documented between 424—480 Ma. 相似文献
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