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排序方式: 共有139条查询结果,搜索用时 93 毫秒
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Chellaganesh Duraipandi Adam Khan M Winowlin Jappes J.T. Nouby M.Ghazaly Peter Madindwa Mashinini 《矿物冶金与材料学报》2021,28(7):1186-1193
Thermal barrier coatings are widely used as surface modifications to enhance the surface properties of the material and protect from surface degradations such as erosion and corrosion. Ceramic-based coatings are highly recommended to increase wear resistance in the industrial sector. In this paper, an alumina–titania ceramic powder was deposited on an aluminum alloy using an atmospheric plasma spray technique. Experimental investigations were performed to study the behavior and erosion rate of the material. Solid particle erosion studies were performed by varying the particle velocity and particle flow rate. The angle impingement and stand-off distance were constant for comparison. The base metal has a clinging effect and the mass change was negative at a maximum particle flow rate of 4 g·min?1. Under the same process conditions, the coated sample had a reduced lifetime and reached a maximum erosion rate of 0.052 (Δg/g). The solid particle erosion studies confirmed that the base metal aluminum alloy had severe surface damage with erodent reinforcement when compared to the coated samples. The influence of the particle velocity, particle flow rate, and input process parameters were also identified. 相似文献
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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function 总被引:15,自引:0,他引:15
Kurima K Peters LM Yang Y Riazuddin S Ahmed ZM Naz S Arnaud D Drury S Mo J Makishima T Ghosh M Menon PS Deshmukh D Oddoux C Ostrer H Khan S Riazuddin S Deininger PL Hampton LL Sullivan SL Battey JF Keats BJ Wilcox ER Friedman TB Griffith AJ 《Nature genetics》2002,30(3):277-284
Positional cloning of hereditary deafness genes is a direct approach to identify molecules and mechanisms underlying auditory function. Here we report a locus for dominant deafness, DFNA36, which maps to human chromosome 9q13-21 in a region overlapping the DFNB7/B11 locus for recessive deafness. We identified eight mutations in a new gene, transmembrane cochlear-expressed gene 1 (TMC1), in a DFNA36 family and eleven DFNB7/B11 families. We detected a 1.6-kb genomic deletion encompassing exon 14 of Tmc1 in the recessive deafness (dn) mouse mutant, which lacks auditory responses and has hair-cell degeneration. TMC1 and TMC2 on chromosome 20p13 are members of a gene family predicted to encode transmembrane proteins. Tmc1 mRNA is expressed in hair cells of the postnatal mouse cochlea and vestibular end organs and is required for normal function of cochlear hair cells. 相似文献
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M. A. Khan 《Cellular and molecular life sciences : CMLS》1978,34(6):784-785
Summary Red fibres of the pigeon pectoralis muscle showed high ATPase reaction at pH 9.4. Veronal-acetate pretreatment completely inhibited the ATPase reaction in these red fibres but not in type I fibres of the gastrocnemius. The former are type II red muscle fibres and hence are unlike type I red, the so-called slow-twitch muscle fibres. 相似文献
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R. A. A. Khan 《Cellular and molecular life sciences : CMLS》1980,36(10):1193-1194
Summary The bone mineral extraction of technetium-99m-methylene diphosphonate (99mTc-MDP), and blood supply of Krypton-81m (81mKr) have been compared in normal and osteotomy regions of the canine tibia. A partial osteotomy was carried out under aseptic conditions, and isotopic measurements made over a period of 123 days. Both blood flow and bone mineral extraction increase after a partial osteotomy.Acknowledgments. I wish to thank D. Zbrzeznj and C. Stoltenberg for their assistance. 相似文献
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Sönnichsen B Koski LB Walsh A Marschall P Neumann B Brehm M Alleaume AM Artelt J Bettencourt P Cassin E Hewitson M Holz C Khan M Lazik S Martin C Nitzsche B Ruer M Stamford J Winzi M Heinkel R Röder M Finell J Häntsch H Jones SJ Jones M Piano F Gunsalus KC Oegema K Gönczy P Coulson A Hyman AA Echeverri CJ 《Nature》2005,434(7032):462-469
A key challenge of functional genomics today is to generate well-annotated data sets that can be interpreted across different platforms and technologies. Large-scale functional genomics data often fail to connect to standard experimental approaches of gene characterization in individual laboratories. Furthermore, a lack of universal annotation standards for phenotypic data sets makes it difficult to compare different screening approaches. Here we address this problem in a screen designed to identify all genes required for the first two rounds of cell division in the Caenorhabditis elegans embryo. We used RNA-mediated interference to target 98% of all genes predicted in the C. elegans genome in combination with differential interference contrast time-lapse microscopy. Through systematic annotation of the resulting movies, we developed a phenotypic profiling system, which shows high correlation with cellular processes and biochemical pathways, thus enabling us to predict new functions for previously uncharacterized genes. 相似文献