全文获取类型
收费全文 | 16067篇 |
免费 | 821篇 |
国内免费 | 1533篇 |
专业分类
18421篇 |
出版年
2023年 | 252篇 |
2022年 | 332篇 |
2021年 | 425篇 |
2020年 | 423篇 |
2019年 | 474篇 |
2018年 | 441篇 |
2017年 | 402篇 |
2016年 | 495篇 |
2015年 | 494篇 |
2014年 | 573篇 |
2013年 | 1279篇 |
2012年 | 451篇 |
2011年 | 588篇 |
2010年 | 479篇 |
2009年 | 630篇 |
2008年 | 618篇 |
2007年 | 671篇 |
2006年 | 656篇 |
2005年 | 533篇 |
2004年 | 559篇 |
2003年 | 532篇 |
2002年 | 492篇 |
2001年 | 377篇 |
2000年 | 338篇 |
1999年 | 321篇 |
1998年 | 306篇 |
1997年 | 315篇 |
1996年 | 283篇 |
1995年 | 308篇 |
1994年 | 337篇 |
1993年 | 291篇 |
1992年 | 275篇 |
1991年 | 235篇 |
1990年 | 216篇 |
1989年 | 215篇 |
1988年 | 199篇 |
1987年 | 184篇 |
1986年 | 154篇 |
1985年 | 287篇 |
1984年 | 348篇 |
1983年 | 255篇 |
1982年 | 333篇 |
1981年 | 215篇 |
1980年 | 200篇 |
1979年 | 182篇 |
1978年 | 106篇 |
1977年 | 69篇 |
1976年 | 89篇 |
1974年 | 47篇 |
1973年 | 45篇 |
排序方式: 共有10000条查询结果,搜索用时 10 毫秒
21.
Harjot K. Saini-Chohan Michael G. Holmes Adam J. Chicco William A. Taylor Russell L. Moore Sylvia A. McCune Diane L. Hickson-Bick Grant M. Hatch Genevieve C. Sparagna 《Journal of lipid research》2009,50(8):1600-1608
Cardiolipin (CL) is responsible for modulation of activities of various enzymes involved in oxidative phosphorylation. Although energy production decreases in heart failure (HF), regulation of cardiolipin during HF development is unknown. Enzymes involved in cardiac cardiolipin synthesis and remodeling were studied in spontaneously hypertensive HF (SHHF) rats, explanted hearts from human HF patients, and nonfailing Sprague Dawley (SD) rats. The biosynthetic enzymes cytidinediphosphatediacylglycerol synthetase (CDS), phosphatidylglycerolphosphate synthase (PGPS) and cardiolipin synthase (CLS) were investigated. Mitochondrial CDS activity and CDS-1 mRNA increased in HF whereas CDS-2 mRNA in SHHF and humans, not in SD rats, decreased. PGPS activity, but not mRNA, increased in SHHF. CLS activity and mRNA decreased in SHHF, but mRNA was not significantly altered in humans. Cardiolipin remodeling enzymes, monolysocardiolipin acyltransferase (MLCL AT) and tafazzin, showed variable changes during HF. MLCL AT activity increased in SHHF. Tafazzin mRNA decreased in SHHF and human HF, but not in SD rats. The gene expression of acyl-CoA: lysocardiolipin acyltransferase-1, an endoplasmic reticulum MLCL AT, remained unaltered in SHHF rats. The results provide mechanisms whereby both cardiolipin biosynthesis and remodeling are altered during HF. Increases in CDS-1, PGPS, and MLCL AT suggest compensatory mechanisms during the development of HF. Human and SD data imply that similar trends may occur in human HF, but not during nonpathological aging, consistent with previous cardiolipin studies. 相似文献
22.
M. Zamirul Hussain John C. Belton Rajendra S. Bhatnagar 《In vitro cellular & developmental biology. Plant》1978,14(9):740-745
Organ cultures of newborn rat lungs synthesize and accumulate DNA, RNA, collagen and noncollagenous proteins almost at a linear
rate for at least 5 days. During this period the synthesis of collagen consistently exceeds the synthesis of noncollagenous
proteins in a pattern similar to neonatal lung growth in vivo. Although some morphological characteristics of lung architecture
are distorted after culture, fundamental structural similarities to lungs growing in intact animals are retained. When these
cultures are maintained in atmospheres rich in oxygen, increased collagen synthesis is observed, a response similar to that
of lungs in intact animals exposed to high oxygen concentrations in vivo. Our studies suggest that lung organ cultures may
be a suitable system for investigating the biochemical aspects of lung tissue-environmental interaction.
These studies were supported in parts by NIH Grant HL-19668, a contract (68-03-2005) from the U.S. Environmental Protection
Agency, and grants from the California Lung Association. 相似文献
23.
24.
David G. Reid David M. Doddrell Dudley H. Williams Keith R. Fox 《Biochimica et Biophysica Acta (BBA)/General Subjects》1984,798(1):111-114
Uniformly 15N-labelled triostin A and echinomycin have been prepared by growing the producing organisms on enriched media and their 15N nuclear magnetic resonance spectra partially assigned by a combination of nuclear Overhauser effect and scalar coupling constant measurements. Selective feeding experiments using unlabelled L-tryptophan-supplemented media have shown that N-1 and N-4 of the quinoxaline rings have their origins in the indole and amino groups of tryptophan, respectively. 相似文献
25.
The inhibition of lipid synthesis in vitro in the locust, Schistocerca gregaria, by factors from the corpora cardiaca 总被引:1,自引:0,他引:1
ABSTRACT. The rate of lipid synthesis from [14 C]acetate in fat body from Schistocerca americana gregaria has been studied in vitro. Maximum incorporation is found on days 6–10 in adults and day 4 of the fifth stadium. The label appeared in the fatty acid components of triacyl-glycerol, diacylglycerol and phospholipid.
Lipid synthesis in vitro was inhibited by extracts of corpora cardiaca, and such inhibition was most marked (up to 85%) in fat bodies from insects at stages where fatty acid synthesis was greatest. HPLC separation of corpora cardiaca extracts gave several active fractions of which the most active was adipokinetic hormone 1 (AKH-1). 相似文献
Lipid synthesis in vitro was inhibited by extracts of corpora cardiaca, and such inhibition was most marked (up to 85%) in fat bodies from insects at stages where fatty acid synthesis was greatest. HPLC separation of corpora cardiaca extracts gave several active fractions of which the most active was adipokinetic hormone 1 (AKH-1). 相似文献
26.
Ronald J.A. Wanders Carlo Van Roermund Cor Lof Alfred J. Meijer 《Analytical biochemistry》1983,129(1):80-87
A simple fluorimetric assay for the determination of carbamoyl phosphate in tissue extracts is described. In the assay, production of ATP from carbamoyl phosphate and ADP by carbamate kinase is coupled to the formation of NADPH, using glucose, hexokinase, NADP+, and glucose-6-phosphate dehydrogenase. Production of NADPH in this system proved to be equal to the amount of carbamoyl phosphate present. 相似文献
27.
In this paper, we describe an efficient procedure for the purification of yeast phosphofructokinase. This procedure eliminates any time delay and enables to obtain an enzyme with minimum proteolytic alterations. The molecular weights of the oligomeric enzyme and of its constitutive subunits were both evaluated by means of several independent methods. However, the accuracy of each measurement was not sufficient to discriminate between an hexameric and an octameric structure of the enzyme oligomer. On the other hand, crosslinking experiments demonstrated the octameric structure of yeast phosphofructokinase. Obviously, some methods of molecular weight determination have led to erroneous results. In particular, our experiments show that the reliability of molecular weight determinations performed by gel filtration of native proteins must be considered with caution. 相似文献
28.
Hana Votavová Vladimír Gut Karel Bláha Jaroslav Šponar 《International journal of biological macromolecules》1982,4(6):341-346
DNA complexes with polypeptides (Lys-Ala-Ala)1)] and (Lys-Ala-Ala)34 have been studied using the methods of thermal melting and circular dichroism. Derivative melting curves of (Lys-Ala-Ala)10 DNA differed substantially from those of (Lys-Ala-Ala)34 prepared either by salt gradient dialysis or by direct mixing. Melting curves of the former complex were unimodal or bimodal with Tm increasing continuously withn input lysin-to-DNA phosphate ratio (r); those of the latter complex consisted of three separate transitions with Tm values almost independent of r. Complete reversibility of binding in the (Lys-Ala-Ala)10-DNA system but a slow redistribution of (Lys-Ala-Ala)34 on DNA at low temperature were found in the redistribution experiments Much faster redistribution from denatured to native DNA occurs at the temperature of melting, contributing to the unusual trimodal melting pattern. Circular dichroism curves are very similar for both complexes and indicate little change of DNA conformation upon polypeptide binding. 相似文献
29.
A. Kotyk J. Horák A. Knotková 《Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression》1982,698(3):243-251
Addition of a metabolizable substrate (glucose, ethanol and, to a degree, trehalose) to non-growing baker's yeast cells causes a boost of protein synthesis, reaching maximum rate 20 min after addition of glucose and 40–50 min after ethanol or trehalose addition. The synthesis involves that of transport proteins for various solutes which appear in the following sequence: H+, l-proline, sulfate, l-leucine, phosphate, α-methyl-d-glucoside, 2-aminoisobutyrate. With the exception of the phosphate transport system, the Kt of the synthesized systems is the same as before stimulation. Glucose is usually the best stimulant, but ethanol matches it in the case of sulfate and exceeds it in the case of proline. This may be connected with ethanol's stimulating the synthesis of transport proteins both in mitochondria and in the cytosol while glucose acts on cytosolic synthesis alone. The stimulation is often repressed by ammonium ions (leucine, proline, sulfate, H+), by antimycin (proline, trehalose, sulfate, H+), by iodoacetamide (all systems tested), and by anaerobic preincubation (leucine, proline, trehalose, sulfate). It is practically absent in a respiration-deficient petite mutant, only little depressed in the op1 mutant lacking ADP/ATP exchange in mitochondria, but totally suppressed (with the exception of transport of phosphate) in a low-phosphorus strain. The addition of glucose causes a drop in intracellular inorganic monophosphate by 30%, diphosphate by 45%, ATP by 70%, in total amino acids by nearly 50%, in transmembrane potential (absolute value) by about 50%, an increase of high-molecular-weight polyphosphate by 65%, of total cAMP by more than 100%, in the endogenous respiration rate by more than 100%, and a change of intracellular pH from 6.80 to 7.05. Ethanol caused practically no change in ATP, total amino acids, endogenous respiration, intracellular pH or transmembrane potential; a slight decrease in inorganic monophosphate and diphosphate and a sizeable increase in high-molecular-weight polyphosphate. The synthesis of the various transport proteins thus appears to draw its energy from different sources and with different susceptibility to inhibitors. It is much more stimulated in facultatively aerobic species (Saccharomyces cerevisiae, Endomyces magnusii) than in strictly aerobic ones (Rhodotorula glutinis, Candida parapsilosis) where an inhibition of transport activity is often observed after preincubation with metabolizable substrates. 相似文献
30.
Kaeko Tozawa Eiji Arakawa Toshiyuki Chikuma Yoshihiro Oh-hashi Ryuichi Yajima Katsumichi Takeda Hiroshi Shinozaki† Takeshi Kato† 《Journal of neurochemistry》1990,55(3):745-749
Axonal transport of peptidylglycine alpha-amidating monooxygenase (PAM) activity was studied in rat sciatic nerves from 12 to 120 h after double ligations. The anterograde axonal transport increased and reached a plateau between 48 and 72 h and then decreased. The flow rate was 100 mm/day, and the molecular mass of the active entity was 70 kDa, which was determined by gel filtration. In contrast, there was no evidence for significant retrograde axonal transport. Anterograde axonal transport of immunoreactive cholecystokinin, a carboxy-terminal-amidated putative neuropeptide, was also found. These results suggest that PAM is transported by a rapid axonal flow and may play a role as a processing enzyme during transport or in the terminals of rat sciatic nerves. 相似文献