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41.
Quantum Requirement for Photosynthesis in Chlorophyll-Deficient Plants with Unusual Lamellar Structures 总被引:1,自引:0,他引:1
Neither an over-all deficiency of chlorophyll, nor an increased enzymatic capacity for maximal rates, nor an unusual lamellar structure was found to change the number of quanta required for the evolution of one molecule of oxygen in healthy aurea mutants of tobacco. The average minimal quantum number remains 10 (efficiency 0.1) as in many algae and typical higher plants. Most of the time the optimal efficiency depends on the availability of some far-red radiation, particularly in the blue region of the spectrum where blue light alone is rather inefficient. These results fit an explanation offered earlier in connection with the hydrogen or acetate photometabolism of algae in far-red light. 相似文献
42.
Georg Steinbacher Otto Wettstein Josef Scholze Wolfgang Makatsch Kurt Bauer Harald Duchrow Klaus Warncke Peter Dancker E. Bezzel H. Remold und Helmut Sick 《Journal of Ornithology》1959,100(1):103-112
Ohne Zusammenfassung 相似文献
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44.
Lars Nitschke Karin Heeger Hans Bender Georg E. Schulz 《Applied microbiology and biotechnology》1990,33(5):542-546
Summary The -cyclodextrin glycosyltransferase (-CGTase) gene was isolated from a -library prepared from Bacillus circulans strain no. 8. It was subcloned into plasmid pTZ and expressed by its endogenous regulatory sequences in Escherichia coli JM 103. The structural gene was sequenced and showed an open reading frame for a polypeptide of 718 amino acid residues. The recombinant -CGTase had the same enzymatic properties as the extracellular CGTase (684 amino acid residues, corresponding to a mol. wt. of 74416) produced by B. circulans strain no. 8. The amino acid sequence showed the highest homology (74.6% identical amino acids) with the CGTase of B. circulans strain F-2, which had been erroneously described as an amylase. The homology with the enzyme from the alkalophilic Bacillus sp. strain no. 1011 was 71.4%. The amino acid sequence derived will be used for elucidating the three-dimensional structure of the enzyme.
Offprint requests to: H. Bender 相似文献
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46.
Shells of probable former living communities ofDreissena polymorpha were found within sediments of the shallow polytrophic to hypertrophic hard water Lake Breitling (Havel-Lake system, Germany).
Corresponding sediments have been deposited between approximately 1940 and 1970 and reflect increasing eutrophication and
heavy metal pollution of the Lake during this period (Schettler, 1992). Single shells from various sediment depths were analysed
by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) along a line on the outer part of the shell. The
response of these freshwater mussels to increasing heavy metal pollution is clearly reflected in the distribution of Pb, Cu,
Cd and Zn within their valves. In general, Cd, Cu, Pb and Zn contents are lower, and the distribution more even, in the outer
parts of the deepest (oldest) shells compared to shells from higher in the cored sediments. Notably higher contents of Cu,
Pb and Zn were recorded from the central (umbonal) part of the more recent shells, but this behaviour is not recorded for
Cd. Metabolic changes brought on by worsening environmental conditions are proposed to explain this phenomena. Acidity produced
during anaerobic metabolism can be neutralised by dissolution of the carbonate part of the shell. Copper, Zn and Pb, which
show an affinity for the organic component of the shell, may thus accumulate by repeated dissolution and reprecipitation of
the shell during the lifetime of an individual organism. Cadmium, which is bound mainly in the aragonite of the shells, is
released during the dissolution of carbonate and is not concentrated in the umbonal area of the shell. 相似文献
47.
Anaerobic metabolism of 2-hydroxybenzoic acid (salicylic acid) by a denitrifying bacterium 总被引:6,自引:0,他引:6
The anaerobic metabolism of 2-hydroxybenzoic acid (salicylic acid) was studied in a denitrifying bacterium. Cells grown with
2-hydroxybenzoate were simultaneously adapted to degrade benzoate. Extract of these cells formed benzoate or benzoyl-CoA when
incubated under reducing conditions with salicylate, MgATP, and coenzyme A, suggesting a degradation of 2-hydroxybenzoate
via benzoate or benzoyl-CoA. This suggestion was supported by enzyme activity measurements. In extracts of 2-hydroxybenzoate-grown
cells, the following enzyme activities were detected: two CoA ligases, one specific for 2-hydroxybenzoate, the other for benzoate,
and two different enzyme activities catalyzing the reductive transformation of 2-hydroxybenzoyl-CoA. These findings suggest
a degradation of salicylic acid by two new enzymes, 2-hydroxybenzoate-CoA ligase (AMP-forming) and 2-hydroxybenzoyl-CoA reductase
(dehydroxylating), catalyzing (1) 2-hydroxybenzoate + MgATP + CoASH → 2-hydroxybenzoyl-CoA + MgAMP + PPi (2) 2-hydroxybenzoyl-CoA + 2[H] → benzoyl-CoA + H2O Benzoyl-CoA was dearomatized by reduction of the ring. This represents another case in which benzoyl-CoA is a central intermediate
in anaerobic aromatic metabolism.
Received: 1 February 1996 / Accepted: 24 February 1996 相似文献
48.
PET1402, a nuclear gene required for proteolytic processing of cytochrome oxidase subunit 2 in yeast
Mathias Bauer Meinhardt Behrens Karlheinz Esser Georg Michaelis Elke Pratje 《Molecular & general genetics : MGG》1994,245(3):272-278
The nuclear mutation pet ts1402 prevents proteolytic processing of the precursor of cytochrome oxidase subunit 2 (cox2) in Saccharomyces cerevisiae. The structural gene PET1402 was isolated by genetic complementation of the temperature-sensitive mutation. DNA sequence analysis identified a 1206-bp open reading frame, which is located 215 by upstream of the PET122 gene. The DNA sequence of PET1402 predicts a hydrophobic, integral membrane protein with four transmembrane segments and a typical mitochondrial targeting sequence. Weak sequence similarity was found to two bacterial proteins of unknown function. Haploid cells containing a null allelle of PET1402 are respiratory deficient. 相似文献
49.
Modification of sialic acids by 9-O-acetylation is detected in human leucocytes using the lectin property of influenza C virus 总被引:1,自引:0,他引:1
Zimmer Gert; Suguri Toshiaki; Reuter Gerd; Yu Robert K.; Schauer Roland; Herrler Georg 《Glycobiology》1994,4(3):343-349
Influenza C virus spike glycoprotein HEF specifically recognizesglycoconjugates containing 9-O-acetyl-N-acetylneuraminic acid.The same protein also contains an esterase activity. Takingadvantage of these two properties, influenza C virus was usedas a very sensitive probe for the detection of traces of 9-O-acetyl-N-acetylneuraminicacid in human leucocytes. The binding of influenza C virus toleucocyte glycoproteins and gangliosides separated by sodiumdodecyl sulphatepolyacrylamide gel electrophoresis andthin-layer chromatography, respectively, was assayed using achromogenic esterase substrate. In this way, glycoproteins ofB-lymphocytes and T-lymphocytes were found to contain 9-O-acetylatedsialic acids. Of the various 9-O-acetylated gangliosides detected,one had the characteristics of 9-O-acetylated GD3. The identificationof 9-O-acetylated sialic acids on distinct glycoproteins andglycolipids should be helpful in assigning a physiological roleto this sugar. O-acetylation gangliosides influenza C virus lymphocytes sialic acids 相似文献
50.