全文获取类型
收费全文 | 85058篇 |
免费 | 2039篇 |
国内免费 | 48篇 |
出版年
2018年 | 956篇 |
2017年 | 1132篇 |
2016年 | 2872篇 |
2015年 | 6252篇 |
2014年 | 5815篇 |
2013年 | 5635篇 |
2012年 | 4795篇 |
2011年 | 2043篇 |
2010年 | 2128篇 |
2009年 | 2063篇 |
2008年 | 588篇 |
2007年 | 565篇 |
2006年 | 587篇 |
2005年 | 6668篇 |
2004年 | 5339篇 |
2003年 | 3554篇 |
2002年 | 1119篇 |
2001年 | 1108篇 |
2000年 | 332篇 |
1999年 | 1485篇 |
1998年 | 331篇 |
1997年 | 177篇 |
1992年 | 1929篇 |
1991年 | 2025篇 |
1990年 | 2088篇 |
1989年 | 2012篇 |
1988年 | 1966篇 |
1987年 | 1824篇 |
1986年 | 1634篇 |
1985年 | 1667篇 |
1984年 | 1107篇 |
1983年 | 848篇 |
1982年 | 478篇 |
1981年 | 432篇 |
1980年 | 376篇 |
1979年 | 1087篇 |
1978年 | 765篇 |
1977年 | 619篇 |
1976年 | 642篇 |
1975年 | 887篇 |
1974年 | 1008篇 |
1973年 | 1013篇 |
1972年 | 966篇 |
1971年 | 939篇 |
1970年 | 830篇 |
1969年 | 837篇 |
1968年 | 744篇 |
1967年 | 762篇 |
1966年 | 594篇 |
1965年 | 437篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Complete amino acid sequence of human intestinal aminopeptidase N as deduced from cloned cDNA 总被引:15,自引:0,他引:15
J Olsen G M Cowell E K?nigsh?fer E M Danielsen J M?ller L Laustsen O C Hansen K G Welinder J Engberg W Hunziker 《FEBS letters》1988,238(2):307-314
The complete primary structure (967 amino acids) of an intestinal human aminopeptidase N (EC 3.4.11.2) was deduced from the sequence of a cDNA clone. Aminopeptidase N is anchored to the microvillar membrane via an uncleaved signal for membrane insertion. A domain constituting amino acid 250-555 positioned within the catalytic domain shows very clear homology to E. coli aminopeptidase N and contains Zn2+ ligands. Therefore these residues are part of the active site. However, no homology of the anchor/junctional peptide domain is found suggesting that the juxta- and intra-membraneous parts of the molecule have been added/preserved during development. It is speculated that this part carries the apical address. 相似文献
992.
A collection of Tn5 transposon Nah- mutants of the plasmid pBS286 was obtained. The insertion sites were localized and orientation of Tn5 determined. The mutants obtained were biochemically analyzed, the nah-region map of the plasmid being elaborated. Structural genes of the nah operon were shown to be organized similarly to those of the nah1 operon of the NAH7 plasmid discussed in the literature. The data obtained are in favour of the previously published information on the presence of elements operating the pBS286 plasmid. The results are given indicating a possibility of regulating the expression of catechol splitting meta-pathway genes with participation of products on early stages of naphthalene oxidation. 相似文献
993.
Summary In the search for a functional role for the polarized glycoconjugates of rat collecting duct epithelial cells, the relation between binding of various lectins and expression of cellular transport enzyme profile of the cells was studied. For this purpose, principal and intercalated cells of rat kidney collecting duct were identified by morphological criteria and by their immunocytochemically determined content of (Na++K+)-ATPase and carbonic anhydrase (CA II), respectively. VariousN-acetylgalactosamine-specific lectins such as those fromHelix pomatia andMaclura pomifera revealed heterogeneity among both principal and intercalated cells, whereas -N-acetylgalactosa nine-specific lectin fromDolichos biflorus andVicia villosa bound preferentially to principal cells. Still another lectin fromArachis hypogaea reacted with most collecting duct cells in the cortex and outer medulla, but only with a subpopulation of cells in the inner medulla. Interestingly, some lectins reacted exclusively with the apical aspect of the collecting duct epithelial cells, whereas others revealed both an apical and basolateral distribution of lectin reactive glycoconjugates. The results thus show subtle differences in the glycocalyx structure of principal and intercalated cells and differences in the intracellular polarization of glycoconjugates of these cells. Thus, lectins may be useful tools in the study of the molecular mechanisms which establish and maintain the polarized functions of principal and intercalated cells. 相似文献
994.
995.
V N Krutsiak G I Kokoshchuk V A Kalugin V I Proniaev Iu T Akhtemi?chuk 《Arkhiv anatomii, gistologii i émbriologii》1988,94(2):77-81
The investigation has been performed on 107 renal preparations obtained from persons of various age (from 5-month-old fetuses up to 45 years of age), certain representatives of other classes of the Vertebrata are also included: fish, amphibia, reptile and mammalia at various stages of pre- and postnatal periods of ontogenesis by means of preparing graphic and plastic reconstructive models, histological investigation and microdissection. The complexity of the intrarenal branching of derivatives of the mesonephric duct diverticulum, development and structure of the canalicular part in nephrons directly depend on the phylogenetic position of the animal. Complexity of the nephron architectonics occurs along the progressive line of taxonomic groups of higher Vertebrata. The nephron loop becomes longer, thin segment of the nephron canalicular part increases in its length and, at last, in mammalia a cone-shaped fasciculus appears as a structural-functional unit of the osmoregulating apparatus of the constant kidney. In the comparative anatomical and comparative embryological aspects recapitulation is observed concerning certain morphological signs of derivatives of the metanephric duct and nephron. 相似文献
996.
P S Collado M E Mu?oz A Esteller J Gonzalez 《Archives internationales de physiologie et de biochimie》1988,96(1):17-23
The effect of phenobarbital and 3-methylcholanthrene pretreatment on the biliary excretion of phenolsulphonphthalein (PSP) was investigated in male Wistar rats. The dye was injected at a single dose of 200 mumol/kg body wt. About 20% of the compound was excreted as a glucuronide in the controls, the liver UDP-glucuronyltransferase activity toward PSP being 0.064 +/- 0.005 nmol.min-1.mg protein-1. Treatment for two weeks with phenobarbital (354 mumol.kg body wt-1.day-1) caused a transient increase in conjugated and unconjugated PSP excretion, but glucuronyltransferase activity was not modified. 3-Methylcholanthrene pretreatment for 4 days (75 mumol.kg body wt-1.day-1) also enhanced biliary excretion of the dye, but the increase corresponded only to the glucuronide and glucuronyltransferase activity was significantly enhanced by 20%. Our data indicate that not only the rate of biotransformation but also other factors could be responsible for increased PSP biliary excretion following administration of microsomal enzyme inducers. 相似文献
997.
998.
Molecular and catalytic properties of a butyrylesterase from human red cells and brain 总被引:2,自引:0,他引:2
A butyrylesterase from human red cells was prepared to homogeneity using DEAE-cellulose, Ultrogel ACA-34, DEAE-Sephacel, and precipitation with 1.5 M (NH4)2SO4. The yield was 25-35% relative to the enzyme activity of the hemolysate. Because of its preference for butyric acid esters the enzyme was designated a butyrylesterase. With alpha-naphthyl butyrate the Km was 7.6 microM and the kcat, 48 s-1. The molecular weight was 340,000 and the subunit weight 85,000, indicating a tetrameric structure. The isoelectric pH was 4.0. The enzyme preparation did not contain cystine. Sialic acid or other carbohydrate components could not be detected. The enzyme was irreversibly inhibited by organophosphate esters and the second-order rate constant was 192 M-1 s-1 for diethyl p-nitrophenyl phosphate. For the brain enzyme the constant was 206 M-1 s-1. The enzyme was irreversibly inhibited by sulfhydryl reagents, indicating that the enzyme is a sulfhydryl-dependent serine esterase. The enzyme was identical to the butyrylesterase from human brain, and the two enzymes were immunochemically identical. An amino acid ester has been shown to be split at a higher rate than butyric acid esters; however, the specificity constant (kcat/Km) was lower for the amino acid ester than for the butyric acid ester. The enzyme did not exhibit amidase activity. 相似文献
999.
T Ratajczak M J Brockway R H?hnel R L Moritz R J Simpson 《Biochemical and biophysical research communications》1988,156(1):116-124
Tryptic peptides generated from bovine estrogen receptor have been fractionated and purified using microbore column high performance liquid chromatography. Sequence analysis performed on six of these peptides, derived from diverse structural regions of the receptor protein, yielded 73 unique assignments corresponding to approximately 12% of the molecule. The amino acid sequences of these peptides displayed a high degree of similarity with corresponding sequences from estrogen receptors of mammalian origin, but were only moderately conserved in receptors from non-mammalian species. The sequenced residues of one tryptic peptide, positioned in the estrogen binding domain, were fully conserved in all estrogen receptors. 相似文献
1000.
R A Skidgel C D Bennett J W Schilling F L Tan D K Weerasinghe E G Erd?s 《Biochemical and biophysical research communications》1988,154(3):1323-1329
Human plasma carboxypeptidase N was purified to homogeneity and its active and inactive subunits were separated. By introducing a novel technique, both forms of the active subunit (Mr = 55,000 and Mr = 48,000) were isolated. N-terminal sequencing of the active subunit of human carboxypeptidase N revealed significant homology with the N-terminal sequence of bovine carboxypeptidase H (43% identity) and to a lesser extent with carboxypeptidase A (29% identity) or carboxypeptidase B (18% identity). The active subunit of carboxypeptidase N was hydrolyzed with trypsin and 4 of the tryptic peptides were isolated by HPLC and sequenced. The sequences of the four peptides were homologous (39-64% identity) with regions of carboxypeptidase H corresponding to the middle (residues 148-175) and C-terminal portion (residues 321-408). These regions had essentially no homology with carboxypeptidase A or B. These data indicate that carboxypeptidase H and the active subunit of carboxypeptidase N may have diverged from a common ancestral gene. 相似文献