全文获取类型
收费全文 | 1453篇 |
免费 | 70篇 |
国内免费 | 2篇 |
专业分类
1525篇 |
出版年
2023年 | 2篇 |
2022年 | 6篇 |
2021年 | 18篇 |
2020年 | 5篇 |
2019年 | 5篇 |
2018年 | 13篇 |
2017年 | 12篇 |
2016年 | 21篇 |
2015年 | 57篇 |
2014年 | 67篇 |
2013年 | 82篇 |
2012年 | 89篇 |
2011年 | 115篇 |
2010年 | 69篇 |
2009年 | 68篇 |
2008年 | 94篇 |
2007年 | 106篇 |
2006年 | 105篇 |
2005年 | 95篇 |
2004年 | 94篇 |
2003年 | 81篇 |
2002年 | 95篇 |
2001年 | 13篇 |
2000年 | 16篇 |
1999年 | 20篇 |
1998年 | 26篇 |
1997年 | 17篇 |
1996年 | 18篇 |
1995年 | 20篇 |
1994年 | 8篇 |
1993年 | 11篇 |
1992年 | 8篇 |
1991年 | 10篇 |
1990年 | 4篇 |
1989年 | 10篇 |
1988年 | 7篇 |
1987年 | 4篇 |
1986年 | 2篇 |
1985年 | 4篇 |
1984年 | 6篇 |
1983年 | 3篇 |
1982年 | 4篇 |
1981年 | 2篇 |
1979年 | 1篇 |
1978年 | 3篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1975年 | 1篇 |
1970年 | 1篇 |
1969年 | 1篇 |
排序方式: 共有1525条查询结果,搜索用时 15 毫秒
1.
Frédéric Boccard Jean-Luc Pernodet Annick Friedmann Michel Guérineau 《Molecular & general genetics : MGG》1988,212(3):432-439
Summary
Streptomyces ambofaciens strain ATCC23877 contains the 11.1 kb plasmid pSAM2 stably integrated into its chromosome. This plasmidic sequence is able to loop out and to be transferred at high frequency to S. lividans where it is found simultaneously as both free and integrated plasmid. When a UV derivative of strain ATCC23877 (strain ATCC15154) is used, the resident copy of pSAM2 can be transferred to S. lividans, but only the integrated form is found in this strain. In both cases, the integration occurs at a unique chromosomal region through the same plasmidic integration site as that in strain ATCC23877. The resident copy of strain ATCC15154 can also be transferred at low frequency to S. ambofaciens DSM40697 (devoid of any pSAM2 sequence). In this case, as several copies of pSAM2 are integrated, the integration pattern is complicated. Integration of a complete pSAM2 sequence in this strain occurs in a region that hybridizes with the integration zones of S. lividans and of S. ambofaciens strain ATCC23877. Comparison of the cloned integration zone of S. lividans before and after the integration event showed that the restriction pattern of the resident pSAM2 in strain ATCC15154 is similar to that of the free form of pSAM2 found naturally in another UV derivative of strain ATCC23877 (strain JI3212). 相似文献
2.
Anther-specific,developmentally regulated expression of genes encoding a new class of proline-rich proteins in sunflower 总被引:6,自引:0,他引:6
Jean-Luc Evrard Colette Jako Agnès Saint-Guily Jacques-Henry Weil Marcel Kuntz 《Plant molecular biology》1991,16(2):271-281
We have used RNA gel blot analysis to demonstrate the anther-specific expression of three genes in sunflower. Expression of these genes was first detected shortly before flower opening, which occurs sequentially on the sunflower inflorescence, and continues during pollination. In contrast, these genes are not expressed (or only weakly expressed) in a male-sterile line in which anther development aborts. In situ hybridization experiments showed that these genes are only expressed in the single cell layer of the sunflower anther epidermis. In the case of one of these genes, which codes for an abundant mRNA, we report the peptide sequences deduced from the sequence of two similar but non identical cDNAs. These proteins contain a potential signal peptide and are characterized by the presence of a proline-rich region which reads KPSTPAPPPPPP(PP)K. Our results also suggest that several proline-rich proteins of unknown functions are specifically synthesized during the maturation of anthers in sunflower. 相似文献
3.
Summary The differentiation capacity of the rat epididymis after depletion of androgen was studied in organ culture and in castrated rats. The differentiation of narrow cells in 5- and 10-day-old explants and in 10-day-old castrated rats suggests that: (i) the testicular androgens are not essential for their differentiation, (ii) a differential androgen dependence exists among the epididymal cell types, (iii) the undifferentiated epithelial cells are the precursors of the narrow cells. 相似文献
4.
5.
6.
Jacques Ricard Jacques Vergne Jean-Luc Decout Marie-Christine Maurell 《Journal of molecular evolution》1996,43(4):315-325
A polyallylamine carrying long hydrophobic dodecyl groups and adenine residues as side chains (PALAD C12) may be able to catalyze the hydrolysis ofN-carbobenzoxy-l-alaninep-nitrophenyl ester (N-Cbz-Ala) as well asp-nitrophenyl acetate (pNPA). The progress curve of hydrolysis of the former displays a long lag and apparently no steady state.
After this transient the rate falls off due to the accumulation of the products. Conversely, the hydrolysis ofp-nitrophenyl acetate displays classical burst kinetics followed by a slow decline of the reaction rate.
Theoretical considerations show that a steady state may be expected to occur only if the concentration of the free catalyst
is very small during the reaction. This condition is sufficient to allow the rate of disappearance of the substrate to be
equal to the rate of appearance of the products, which is precisely a condition for the existence of a steady state. If the
catalyst is poorly active and has a loose affinity for its substrate and product, the measurement of a significant reaction
rate will require a much larger concentration of the catalyst. Therefore, under these conditions, one cannot expect a steady
state to occur. The mathematical expression of the error made in the steady-state assumption has been derived. This error
increases with the catalyst concentration and decreases if the affinity of the substrate for the catalyst is high. Therefore
the lack of steady state is associated with the affinity (or the dissociation) of the substrate and the product for the catalyst.
When this affinity is low, the free concentration of the catalyst during the reaction is high and one cannot expect a steady
state to occur. This is precisely what takes place with N-Cbz-Ala.
A mathematical expression of the rate of hydrolysis of N-Cbz-Ala and of any reactant that displays this type of kinetics may
be derived at the end of the transient when the rate is close to its maximum value. Under these conditions the rate cannot
follow classical Michaelis-Menten kinetics and displays positive cooperativity.
It may therefore be speculated that primordial template-like catalysts that were displaying a poor affinity for their substrates
and products were already exhibiting apparent positive cooperativity in the kinetic reactions they were able to catalyze.
Correspondence to: J. Ricard 相似文献
7.
In Vivo and In Vitro Evidence for the Biosynthesis of Testosterone in the Telencephalon of the Female Frog 总被引:5,自引:2,他引:3
Ayikoe G. Mensah-Nyagan Jean-Luc Do-Rego Marc Feuilloley Albert Marcual Catherine Lange †Georges Pelletier Hubert Vaudry 《Journal of neurochemistry》1996,67(1):413-422
Abstract: Neurons and glial cells are capable of synthesizing various steroid hormones, but biosynthesis of testosterone in the CNS has never been reported. The aim of the present study was to demonstrate the synthesis of testosterone in the frog brain. The presence of 17β-hydroxysteroid dehydrogenase (17β-HSD)-like immunoreactivity was detected in a population of glial cells located in the telencephalon. Reversed-phase HPLC analysis of brain tissue extracts combined with radioimmunoassay detection revealed the presence of substantial amounts of testosterone and 5α-dihydrotestosterone (5α-DHT) in the telencephalon where 17β-HSD-positive cells were visualized. In male frogs, castration totally suppressed testosterone and 5α-DHT in the blood and in the rhombencephalon but did not affect the concentration of these two steroids in the telencephalon. Chemical characterization of testosterone in female frog telencephalon extracts was performed by coupling HPLC analysis with gas chromatography-mass spectrometry. Using the pulse-chase technique with [3 H]pregnenolone as a precursor, the formation of a series of metabolites was observed, including dehydroepiandrosterone, androstenedione, testosterone, 5α-DHT, and estradiol. These data demonstrate the existence of an active form of 17β-HSD in the frog telencephalon, which is likely involved in testosterone biosynthesis within the brain. 相似文献
8.
Chang-Zhi Dong Jean-Luc Montillet Christian Triantaphylidès 《Physiologia plantarum》1994,90(2):307-312
The effects of ionizing radiation, used in post-harvest treatment of fruit and vegetables. were investigated on cultured apple cells ( Pyrus malus L. cv. Royal Red) on a short-term period. Irradiation (2 kGy) induced an increase of passive ion effluxes from cells and a decrease of cell capacity to regulate external pH. These alterations are likely due to effects on plasma membrane structure and function and were further investigated by studying the effects of irradiation on plasma membrane H+ -ATPase activity. Plasma membrane-enriched vesicles were prepared and the H+ -ATPase activity was characterized. Irradiation of the vesicles induced a dose dependent inhibition of H+ -ATPase activity. The loss of enzyme activity was immediate, even at low doses (0.5 kGy), and was not reversed by the addition of 2m M dithiothreitol. This inhibition may be the result of an irreversible oxidation of enzyme sulfhydryl moieties and/or the result of changes induced within the lipid bilayer affecting the membrane-enzyme interactions. Further analysis of the H+ -ATPase activity was carried out on vesicles obtained from irradiated cells confirming the previous results. In vivo recovery of activity was not observed within 5 h following the treatment, thus explaining the decrease of cell capacity to regulate external pH.
This rapid irreversible inhibition of the plasma membrane H+ -ATPase must be considered as one of the most important primary biochemical events occurring in irradiated plant material. 相似文献
This rapid irreversible inhibition of the plasma membrane H
9.
Jean-Luc J. Pellegrin Eduardo Ortega-Barria Reginaldo P. Prioli Mary Buerger Richard G. Strout Joseph Alroy Miercio E. A. Pereira 《Glycoconjugate journal》1993,10(1):57-63
Sporozoites and merozoites of three species ofEimeria, E. tenella, E. maxima, andE. necatrix, that cause diarrhea in chickens worldwide, were examined for their expression of sialidase (SA) activity. The enzyme was found in three species, and the activity of merozoites was 10–20 times higher than that of sporozoites. The enzyme was resistant to degradation by proteases that are normally present in the intestine, a site inhabited by theEimeria parasites, and it was relatively resistant to heat, with optimum activity being at 40°C, which is within the range of temperature in the chicken intestine (40–43°C).E. tenella SA was immuniprecipitated by monoclonal and polyclonal antibodies raised against theTrypanosoma cruzi SA (TCSA), and enzyme activity was neutralized by these antibodies.E. tenella SA was identified by immunoblots as a doublet of molecular weight 190 000 and 180 000 using, as a probe, anti-TCSA antibodies and antibodies against a synthetic peptide (TR) derived from the long tandem repeat domain of TCSA. Binding of the monoclonal and polyclonal antibodies toE. tenella was completely blocked by TR, but not by an irrelevant peptide (BR). Therefore,E. tenella expresses a developmentally regulated SA that is structurally related to theT. cruzi counterpart. Because of the high SA activity in merozoites, and by analogy with other SA-producing microbes that inhabit mucin-rich epithelia, we suggest that theEimeria SA plays a role in desialylating intestinal mucins to reduce viscosity of the local environment and thereby facilitate parasite migration. The enzyme could also play a role in host cell-parasite interaction.Abbreviations SA
sialidase (neuraminidase)
- Neu5Ac
N-acetylneuraminic acid
- 4-MU-Neu5Ac
2-(4-methylumbelliferyl)--N-acetyl-d-neuraminic acid
- BSA
bovine serum albumin
- PBS
phosphate buffered saline
- PMSF
phenylmethylsulfonyl fluoride
- PNA
peanut agglutinin
- Ab
antibody
- TCN-2
monoclonal antibody toT. cruzi sialidase, anti-Ars, monoclonal antibody top-azophenylarsonate
- TCSA
Trypanosoma cruzi sialidase 相似文献
10.
Rachel Baltz Jean-Luc Evrard Val/'erie Bourdon Andr/'e Steinmetz 《Sexual plant reproduction》1996,9(5):264-268
The protein PLIM-1 (formerly SF3) from sunflower is expressed exclusively in mature, free pollen. It contains two LIM domains associated with an acidic C-terminus comprising six copies of the pentapeptide motif (A,T,S) (E,D) TQN. We have expressed the pollen protein as well as some of its mutant forms inEscherichia coli and have used the bacterially produced proteins to study interactions with nucleic acids. Our studies show that the protein binds DNA and RNA in vitro to form large complexes, while mutant polypeptides containing either a single LIM domain or a destabilized first or second LIM domain do not. Although these data suggest that the biological function of PLIM-1 involves interactions with nucleic acids, its role in pollen development remains unclear. 相似文献