全文获取类型
收费全文 | 11698篇 |
免费 | 1090篇 |
国内免费 | 8篇 |
专业分类
12796篇 |
出版年
2021年 | 102篇 |
2019年 | 92篇 |
2018年 | 127篇 |
2017年 | 147篇 |
2016年 | 186篇 |
2015年 | 360篇 |
2014年 | 341篇 |
2013年 | 471篇 |
2012年 | 621篇 |
2011年 | 580篇 |
2010年 | 411篇 |
2009年 | 338篇 |
2008年 | 526篇 |
2007年 | 554篇 |
2006年 | 493篇 |
2005年 | 583篇 |
2004年 | 498篇 |
2003年 | 486篇 |
2002年 | 473篇 |
2001年 | 201篇 |
2000年 | 184篇 |
1999年 | 181篇 |
1998年 | 158篇 |
1997年 | 121篇 |
1996年 | 127篇 |
1995年 | 120篇 |
1994年 | 95篇 |
1993年 | 131篇 |
1992年 | 141篇 |
1991年 | 142篇 |
1990年 | 141篇 |
1989年 | 148篇 |
1988年 | 149篇 |
1987年 | 123篇 |
1986年 | 128篇 |
1985年 | 96篇 |
1984年 | 99篇 |
1983年 | 95篇 |
1982年 | 97篇 |
1981年 | 131篇 |
1980年 | 100篇 |
1979年 | 121篇 |
1978年 | 111篇 |
1977年 | 107篇 |
1975年 | 90篇 |
1974年 | 108篇 |
1973年 | 116篇 |
1972年 | 94篇 |
1970年 | 101篇 |
1969年 | 87篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
The enzyme acetyl-CoA: 17-O-deacetylvindoline 17-O-acetyltransferase which terminates vindoline biosynthesis has been isolated from Catharanthus roseus leaves, further characterized and purified to homogeneity by three step column chromatography and subsequent preparative isoelectric focusing. Kinetic properties concerning the enzyme reaction are discussed. Five multiple forms of the acetyl-transferase could be observed, each consisting of two subunits. This enzyme is now the best characterized of the enzymes involved in vindoline biosynthesis.Abbreviations DTE
dithiothreitol
- EDTA
ethylenediamine-tetraacetic acid
- HEPES
N-(2-hydroxyethyl)-piperazine-N-2-ethanesulfonic acid
- IEF
isoelectric focusing
- KPi
potassium phosphate
- Mr
rel.molecular mass
- PEG
polyethylene glycol
- SDS-PAGE
sodium dodecylsulfate polyacrylamide gel electrophoresis
- Tris
2-amino-2-(hydroxymethyl)-1,3-propandiol 相似文献
52.
Pollination Ecology of Pedicularis punctata Decne. (Scrophulariaceae) in the Kashmir Himalaya 总被引:2,自引:0,他引:2
Abstract The pollination ecology of Pedicularis punctata was studied in the Pir Panjal Range of the Kashmir Himalaya in the summer of 1989. Its nectarless, rostrate, long-tubed flower was found to be pollinated exclusively by Bombus foragers vibrating pollen while the stigma contacted pollen in the pollinator's cervical crevice. Workers of Bombus tunicatus and B. flavothoracicus comprised 95% of its pollinators. Pollen-foraging fidelity of its pollinators was greatest where diversity of Bombus -pollinated plant species in three plant communities was least. Foragers on other plants carried virtually no Pedicularis pollen. P. punctata is a mid-season blooming species similar in its pollination syndrome to comparable species in other geographic regions. The enigmatic function of its long, nectarless corolla tube, even more exaggerated in other Asiatic species, requires further investigation. 相似文献
53.
A long-term suspension culture ofBrachycome dichromosomatica (2n = 4) was induced from a cotyledon-derived callus. Subcultures were obtained every week up to three years. The bulk of the cultures displayed a stable diploid karyotype, while one cell line evolved with 2n = 5 chromosomes in the 86th reinoculation. No further chromosomal change occurred also in that cell line. It is assumed that the fifth chromosome is the expression of a trisomy 2.The chromatin ultrastructure was of the species-specific chromomeric type in the wild-type line, while the trisomic line displayed more condensed chromatin, what probably indicates a rather inactive state of the extra-chromosome.Brachycome dichromosomatica is suggested to represent an ideal species to follow-up karyotype stability and/or variation in cell culture.As a former student W. N. dedicates this paper in gratitude and admiration to Prof. DrElisabeth Tschermak-Woess on the occasion of her 70th birthday. Prof.Woess with her scientific work has stimulated in an unique manner the study of nuclear structures in plants, of endopolyploidy and polytene chromosomes, and has thus established the basis for the rapidly increasing research in these fields. 相似文献
54.
Summary Two -glucosidase genes, designatedbglA andbglB, were isolated from a gene bank ofClostridium
thermocellum DSM 1237. The coding sequences forbglA andbglB were located on non-homologous DNA fragments of 3.2– and 3.4-kb, respectively. Both genes direct inEscherichia
coli the synthesis of cytoplasmic -glucosidases, which differ with respect to substrate specificity and temperature profile. The properties of thebglA-encoded -glucosidase A closely resemble that of a -glucosidase previously isolated fromC.
thermocellum cultures. 相似文献
55.
Wolfgang H. Schwarz Silke Schimming Walter L. Staudenbauer 《Biotechnology letters》1988,10(4):225-230
Summary AClostridium
thermocellum gene directing the synthesis of a thermostable -glucanase was localized on a 1.9-kb DNA fragment by subcloning intoEscherichia
coli plasmid vectors. The enzyme was highly efficient in degrading glucans with alternating -1, 3- and -1,4-linkages such as lichenan and barley glucan. It was also active towards the -1, 3-glucan laminarin, but lacked activity on cellulosic substrates and -glucans. The enzyme was therefore classified as -1, 3-glucanase (laminarinase) and the corresponding gene was designatedlicA. With barley -glucan as substrate the enzyme had a pH optimum around pH 6.5 and a temperature optimum at 65°C. It was stable for several hours at 60°C in the absence of substrate. 相似文献
56.
Karin Bronnenmeier Walter L. Staudenbauer 《Applied microbiology and biotechnology》1988,28(4-5):380-386
Summary
Clostridium stercorarium cultures grown on cellobiose contain both an extracellular and a cell-bound -glucosidase activity. A substantial portion of the cell-bound enzyme could be extracted by osmotic shock, suggesting a periplasmic localization. The -glucosidase present in culture supernatants was purified to homogeneity. It was found to be identical in all aspects tested with the cell-bound -glucosidase. The enzyme exists as a monomer with an apparent molecular weight of 85.000 (SDS-PAGE) and a pI of 4.8. It shows optimal activity as pH 5.5 and 65° C. Thiol groups are essential for enzyme activity. In the presence of reducing agents and divalent cations the half-life of the purified enzyme was more than 5 h at 60°C. The enzyme hydrolyses at different rates a wide range of substrates including aryl--glucosides, cellobiose, and disordered cellulose. K
m
values were determined as 0.8 mM for p-nitrophenyl--glucoside (PNPG) and 33 mM for cellobiose. The cellular localization and the substrate specificity pattern are consistent with a dual role of the C. stercorarium -glucosidase in cellulose saccharification: (1) Cleavage of cellobiose formed by exoglucanase and (2) degradation of cellodextrins produced by endoglucanase action. 相似文献
57.
58.
Walter Stöcker Uta Raeder Martha M. C. Bijlholt Trijntje Wichertjes Ernst F. J. van Bruggen Jürgen Markl 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》1988,158(3):271-289
Summary Two-hexameric (2×6) hemocyanins from the brachyuran crabsCancer pagurus andCallinectes sapidus, the freshwater crayfishAstacus leptodactylus and the lobsterHomarus americanus were isolated and dissociated into native subunits.The subunits of each hemocyanin were analyzed by electrophoresis and immunology. Three immunologically distinct subunit types, which were termed, and, could be identified in each case. They were isolated preparatively, and interspecifically correlated. Subunit is subdivided into several electrophoretically distinct isoforms which are immunologically closely related (Astacus) or identical (other species). InAstacus andCancer one of these isoforms was shown to dimerize and to act as inter-hexamer bridge. It represents a fourth subunit type termed. A fifth, diffuse component, which in PAGE migrated at the position of a dimer, was identified in the crossed immunoelectrophoretic patterns as denatured hemocyanin.A common feature of the four hemocyanins is the presence of 4 copies of and 8 copies of/ within the 2×6 particles. The: ratio is 4:4 in the two Astacidea and 6:2 in the two Brachyura. exists in 2 copies inAstacus andCancer which means that a single dimer- is present in a two-hexamer. This leaves 2 monomeric copies inAstacus and 4 inCancer.Every subunit from the four species except ofAstacus
- was capable to form hexamers in reassembly experiments. If subunit combinations were tested, hetero-hexamers were formed preferentially. Two-hexamers were reconstituted only in the presence of all subunit types and the native subunit stoichiometry was required to obtain twohexamers in considerable yields. Factors limiting 2×6 reassembly are discussed.Authentic 2×6 molecules ofAstacus, Homarus andCancer hemocyanin were immunolabeled with subunit-specific antibody fragments (Fab) or IgG molecules, and the resulting immuno complexes were studied in the electron microscope. A topological model of the quaternary structure of decapod 2×6 hemocyanins is derived, showing the position of each copy of the four subunit types. In this model, the inter-hexamer bridge- is surrounded by two and two subunits forming the central core of the dodecamer. Two additional and two additional subunits form the periphery together with one subunit occupying the peripheral short edges of each hexameric half structure. The model is discussed with respect to the current literature.Abbreviations
PAGE
polyacrylamide gel electrophoresis
-
SDS
sodium dodecyl sulfate
This paper is decicated to Professor Dr. Bernt LinzenPreliminary accounts of this work have been presented in the proceedings of a symposium at Tutzing 1985. Linzen B (ed) (1986) Invertebrate oxygen carriers. Springer, Berlin Heidelberg New York. This also includes: Stöcker et al. 1986; Markl et al. 1986) and in a review article (Markl 1986) 相似文献
59.
Structural Features of Human Monoamine Oxidase A Elucidated from cDNA and Peptide Sequences 总被引:13,自引:5,他引:8
Yun-Pung P. Hsu Walter Weyler Shiuan Chen Katherine B. Sims William B. Rinehart Margot C. Utterback John F. Powell Xandra O. Breakefield 《Journal of neurochemistry》1988,51(4):1321-1324
Monoamine oxidase (MAO), an important enzyme for the degradation of amine neurotransmitters, has been implicated in neuropsychiatric illness. The amino acid sequence for one form of the enzyme, MAO-A, has been deduced from human cDNA clones and verified against proteolytic peptides. The covalent binding site for the flavin adenine dinucleotide (FAD) cofactor is near the C-terminal region. The presence of features characteristic of the ADP-binding fold suggests that the N-terminal region is also involved in the binding of FAD. These cDNAs should facilitate the study of the structure, function, and intracellular targeting of MAO, as well as the analysis of its expression in normal and pathological states. 相似文献
60.