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Journal of Plant Growth Regulation - This research was conducted to find out whether the foliar application of salicylic acid (SA) at 0.5, 1, and 1.5 mM in comparison with water spray... 相似文献
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Siddiqua Hafsa Akter Yasmin Uddin Md. Nasir Kumkum Mahadia Hossain Mohammad Afzal Aziz Md. Abdul Ahmed Mst. Sharika Chowdhury Mahmood Ahmed Islam Mohammad Safiqul Marzan Lolo Wal 《Molecular biology reports》2022,49(9):8449-8460
Molecular Biology Reports - The SHANK3 gene encodes a master synaptic scaffolding protein at the excitatory synapse’s postsynaptic density, which is predominantly responsible for constructing... 相似文献
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Jennifer Jungfleisch Ashis Chowdhury Isabel Alves-Rodrigues Sundaresan Tharun Juana Díez 《RNA (New York, N.Y.)》2015,21(8):1469-1479
The Lsm1-7-Pat1 complex binds to the 3′ end of cellular mRNAs and promotes 3′ end protection and 5′–3′ decay. Interestingly, this complex also specifically binds to cis-acting regulatory sequences of viral positive-strand RNA genomes promoting their translation and subsequent recruitment from translation to replication. Yet, how the Lsm1-7-Pat1 complex regulates these two processes remains elusive. Here, we show that Lsm1-7-Pat1 complex acts differentially in these processes. By using a collection of well-characterized lsm1 mutant alleles and a system that allows the replication of Brome mosaic virus (BMV) in yeast we show that the Lsm1-7-Pat1 complex integrity is essential for both, translation and recruitment. However, the intrinsic RNA-binding ability of the complex is only required for translation. Consistent with an RNA-binding-independent function of the Lsm1-7-Pat1 complex on BMV RNA recruitment, we show that the BMV 1a protein, the sole viral protein required for recruitment, interacts with this complex in an RNA-independent manner. Together, these results support a model wherein Lsm1-7-Pat1 complex binds consecutively to BMV RNA regulatory sequences and the 1a protein to promote viral RNA translation and later recruitment out of the host translation machinery to the viral replication complexes. 相似文献
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Bioremediation of lipid-rich model wastewater was investigated in a packed bed biofilm reactor (anaerobic filter). A detailed study was conducted about the influence of fatty acid concentration on biomethanation of the high-fat liquid effluent of edible oil refineries. The biochemical methane potential (BMP) of the liquid waste was reported and maximum cumulative methane production at the exit of the reactor is estimated to be 785 ml CH4 (STP)/(g VSS added). The effects of hydraulic retention time (HRT), organic loading rate (OLR) and bed porosity on the cold gas efficiency or energy efficiency of the bioconversion process were also investigated. Results revealed that the maximum cold gas efficiency of the process is 42% when the total organic load is 2.1 g COD/l at HRT of 3.33 days. Classical substrate uninhibited Monod model is used to generate the differential system equations which can predict the reactor behavior satisfactorily. 相似文献
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Sessions EH Chowdhury S Yin Y Pocas JR Grant W Schröter T Lin L Ruiz C Cameron MD LoGrasso P Bannister TD Feng Y 《Bioorganic & medicinal chemistry letters》2011,21(23):7113-7118
Therapeutic interventions with Rho kinase (ROCK) inhibitors may effectively treat several disorders such as hypertension, stroke, cancer, and glaucoma. Herein we disclose the optimization and biological evaluation of potent novel ROCK inhibitors based on substituted indole and 7-azaindole core scaffolds. Substitutions on the indole C3 position and on the indole NH and/or amide NH positions all yielded potent and selective ROCK inhibitors (25, 42, and 50). Improvement of aqueous solubility and tailoring of in vitro and in vivo DMPK properties could be achieved through these substitutions. 相似文献
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Fang X Chen YT Sessions EH Chowdhury S Vojkovsky T Yin Y Pocas JR Grant W Schröter T Lin L Ruiz C Cameron MD LoGrasso P Bannister TD Feng Y 《Bioorganic & medicinal chemistry letters》2011,21(6):1844-1848
Rho kinase (ROCK) is an attractive therapeutic target for various diseases including glaucoma, hypertension, and spinal cord injury. Herein, we report the development of a series of ROCK-II inhibitors based on 4-quinazolinone and quinazoline scaffolds. SAR studies at three positions of the quinazoline core led to the identification of analogs with high potency against ROCK-II and good selectivity over protein kinase A (PKA). 相似文献
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Chowdhury S Sessions EH Pocas JR Grant W Schröter T Lin L Ruiz C Cameron MD Schürer S LoGrasso P Bannister TD Feng Y 《Bioorganic & medicinal chemistry letters》2011,21(23):7107-7112
Rho kinase (ROCK) inhibitors are potential therapeutic agents to treat disorders such as hypertension, multiple sclerosis, cancers, and glaucoma. Here, we disclose the synthesis, optimization, biological evaluation of potent indole and 7-azaindole based ROCK inhibitors that have high potency on ROCK (IC(50)=1 nM) with 740-fold selectivity over PKA (47). Moreover, 47 showed very good DMPK properties making it a good candidate for further development. Finally, docking studies with a homology model of ROCK-II were performed to rationalize the binding mode of these compounds and showed the compounds bound in both orientations to take advantage to H-bonds with Lys-121 of ROCK-II. 相似文献