全文获取类型
收费全文 | 17601篇 |
免费 | 1301篇 |
国内免费 | 386篇 |
专业分类
19288篇 |
出版年
2023年 | 127篇 |
2022年 | 249篇 |
2021年 | 371篇 |
2020年 | 307篇 |
2019年 | 349篇 |
2018年 | 437篇 |
2017年 | 366篇 |
2016年 | 528篇 |
2015年 | 798篇 |
2014年 | 931篇 |
2013年 | 1211篇 |
2012年 | 1352篇 |
2011年 | 1218篇 |
2010年 | 794篇 |
2009年 | 651篇 |
2008年 | 952篇 |
2007年 | 887篇 |
2006年 | 840篇 |
2005年 | 760篇 |
2004年 | 715篇 |
2003年 | 739篇 |
2002年 | 635篇 |
2001年 | 379篇 |
2000年 | 372篇 |
1999年 | 319篇 |
1998年 | 179篇 |
1997年 | 141篇 |
1996年 | 122篇 |
1995年 | 100篇 |
1994年 | 139篇 |
1993年 | 99篇 |
1992年 | 193篇 |
1991年 | 172篇 |
1990年 | 149篇 |
1989年 | 165篇 |
1988年 | 137篇 |
1987年 | 124篇 |
1986年 | 115篇 |
1985年 | 113篇 |
1984年 | 79篇 |
1983年 | 92篇 |
1982年 | 59篇 |
1981年 | 63篇 |
1980年 | 55篇 |
1979年 | 65篇 |
1977年 | 90篇 |
1976年 | 53篇 |
1975年 | 52篇 |
1974年 | 65篇 |
1973年 | 45篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
32.
33.
The accessibility of DNA to dimethylsulfate in complexes with recA protein. 总被引:3,自引:1,他引:2 下载免费PDF全文
recA protein coats DNA co-operatively to form filaments approximately 100 A thick, which in the presence of ATP, and more stably so in the presence of the non-hydrolyzable analog ATP gamma S, have a helical appearance with a deep cleft in the protein coat. This protein helix follows the DNA helix, to which it imparts a new helicity of 18.5 bp per turn of 97 A pitch. Here we test the accessibility of the DNA in the complex to modification by dimethylsulfate, and find that the complexed DNA is approximately 2-fold more reactive on the major groove side than it was in B-DNA (methylation of guanine N7), while it is protected approximately 2-fold on the minor groove side (methylation of adenine N3), suggesting that the protein coats the DNA along the minor groove. Furthermore, N3 of cytosine, a residue involved in base pairing, is found exposed in complexes with single strands as it is in naked single-stranded DNA, while it remains inaccessible in complexes with double strands, suggesting that the latter is not melted at this stage of the strand exchange reaction. 相似文献
34.
G Del Boccio C Di Ilio E Casalone A Pennelli A Aceto P Sacchetta G Federici 《The Italian journal of biochemistry》1987,36(1):8-17
An anionic (pI 4.6) isoenzyme of glutathione transferase was purified to homogeneity from human thyroid by affinity chromatography followed by isoelectric focusing. The content of enzyme was calculated to constitute about 0.2% of soluble proteins. The enzyme is formed by two identical subunits of 23,000 daltons approximately. The thyroid transferase did not catalyze the reduction of peroxides. Physical, catalytic and immunological analyses demonstrated extensive similarities between the thyroid transferase and the transferase from placenta, erythrocytes and breast. On the other hand, the thyroid transferase appears catalytically different from transferase 7-7, even if both cross-react with the antibodies raised against human placenta transferase. 相似文献
35.
Increased efflux rather than oxidation is the mechanism of glutathione depletion by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) 总被引:2,自引:0,他引:2
D Di Monte M S Sandy M T Smith 《Biochemical and biophysical research communications》1987,148(1):153-160
Incubation of isolated hepatocytes in the presence of either the parkinsonian-inducing compound 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) or its putative toxic metabolite 1-methyl-4-phenylpyridinium ion (MPP+) led to a depletion of intracellular reduced glutathione (GSH), which was mostly recovered as glutathione disulfide (GSSG). However, both MPTP- and MPP+-induced glutathione perturbances were relatively unaffected by the prior inhibition of glutathione reductase with 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU), suggesting that intracellular oxidation was not the major mechanism involved in the GSH loss. Inclusion of cystine in the incubation mixtures revealed a time-dependent formation of cysteinyl glutathione (CySSG), indicating that an increased efflux was mostly responsible for the MPTP- and MPP+-induced GSH depletion. Therefore, the measurement of GSSG, which is apparently formed extracellularly, was not associated with oxidative stress. 相似文献
36.
Properties of carboxymethylated cross-linked hemoglobin A 总被引:2,自引:0,他引:2
The selective carboxymethylation of the N-terminal amino groups of hemoglobin A with glyoxylic acid and sodium cyanoborohydride has been studied as a function of the state of ligation of hemoglobin. The N-terminal residues have been established as the primary sites of reaction by peptide mapping of the tryptic digest of each chain and subsequent amino acid analysis of the modified peptides. With oxyhemoglobin, the desired derivatives with a carboxymethyl group at the N-terminal of either or both chains amounted to 55% [Di Donato, A., Fantl, W. J., Acharya, A. S., & Manning, J. M. (1983) J. Biol. Chem. 258, 11890-11895]. In the present study it is shown that with deoxyhemoglobin the amount of the desired derivative is increased to 75%. The oxygen equilibrium curve of hemoglobin A carboxymethylated on its four N-terminal residues [0.5 mM as tetramer in 50 mM [bis(2-hydroxyethyl)amino]tris(hydroxymethyl)methane (Bis-Tris), pH 7.5, 37 degrees C] had a P50 value of 30 mmHg (Hill coefficient n = 2.8, alkaline Bohr value = 0.4) compared to a P50 of 9 mmHg for unmodified hemoglobin under the same conditions (n = 2.5, alkaline Bohr value = 0.5). In carboxymethylated oxyhemoglobin A, cross-linked with the mild agent glycolaldehyde for 3.5 h, there was 85% of Mr 64,000 species and 15% of Mr 128,000 or higher species. For the former, the extent of cross-linking between two subunits was 19%. For the latter, there was 29% of two cross-linked subunits and 13% of three cross-linked subunits. Termination of cross-linking, which may be desirable in some circumstances, can be successfully achieved with isonicotinic acid hydrazide.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
37.
Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second case 总被引:1,自引:0,他引:1
A syndrome of marked fetal wastage is associated with congenital factor XIII deficiency in adult women. A previously unreported case of a woman with factor XIII deficiency is described, in which substitutive treatment with normal plasma or placental factor XIII concentrate permitted two normal pregnancies. Factor XIII activity was maintained above 1-2% with intermittent infusion of 300 ml to 450 ml of plasma every 14 days or of 500 units of concentrate every 21 days. This case confirms the only other case so far reported in which factor XIII substitutive therapy was able to permit a normal pregnancy in a woman with factor XIII deficiency and seems to suggest factor XIII to be involved in the process of annidation. 相似文献
38.
39.
B Porcelli M Pizzichini A Di Stefano R Leoncini A Taddeo E Marinello 《Bollettino della Società italiana di biologia sperimentale》1989,65(12):1201-1205
The behavior of plasma and urine oxypurines (hypoxanthine and xanthine) and of uric acid has been studied in normal subjects and in gout patients. Oxypurines and uric acid were increased in the plasma of gout patients but only the urinary excretion of hypoxanthine was higher in this group. The interpretation of the observed variations is discussed. 相似文献
40.
A Tabucchi L Terzuoli A Di Stefano M Pizzichini R Leoncini E Dispensa E Marinello 《Bollettino della Società italiana di biologia sperimentale》1989,65(11):1097-1103
Phosphoribosyl-1-pyrophosphate (PRPP) amidotransferase is the "key anabolic enzyme" of purine nucleotide synthesis; PRPP synthetase connects the pentose cycle with the same pathway. We have studied their behavior in 5 control subjects and in 8 affected by CLL. Determination of PRPP amidotransferase was carried out through the evaluation of 14C-glutamic acid (released by 14C-glutamine) in the incubation mixture. PRPP synthetase was followed by adding ATP and ribose 5-phosphate to the incubation mixtures, and by evaluating the PRPP formed through the release of CO2 in a coupled reaction. In the case of PRPP-amidotransferase, our values are in the range reported in the literature: in patients affected by CLL, the enzyme activity is much higher and the increase is more evident when values referred to the patients, than when to the cells. Our values of PRPP synthetase are consistent with those of Peters and Veerkamp, but no definite conclusion is possible in the case of leukemic patients. 相似文献