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101.
Judith P. Armitage R. J. Rowbury D. G. Smith 《Cellular and molecular life sciences : CMLS》1976,32(10):1266-1267
Summary The levels of cyclic AMP and adenyl cyclase in swarming and non-swarming cells ofProteus mirabilis and the effect of glucose on swarming have been investigated. The results indicate that cAMP is required for swarming, but that the flagellar derepression characteristic of swarming does not result from increased cAMP levels.One of the authors (JPA) thanks the S.R.C. for financial support. 相似文献
102.
D. G. Bamford D. E. Biggs P. Chaplen M. Davis Judith Maconochie 《Cellular and molecular life sciences : CMLS》1972,28(9):1069-1070
Résumé Le M&B 15.944 (éthiodide dep-diméthylaminophényl heptyl cétone thiosémicarbazone) est un curarisant dont la brève durée d'action est comparable à celle de la succinylcholine chez divers espèces y compris le singe. Le méchanisme du blocage neuromusculaire provoqué par le M&B 15.944 est compétitif. 相似文献
103.
Judith Polonsky Zoïa Varon H. Jacquemin G. R. Pettit 《Cellular and molecular life sciences : CMLS》1978,34(9):1122-1123
Summary An investigation of the Guyana plantSimarouba amara Aubl. (Simaroubaceae) for antineoplastic quassinoids led to isolation and structural determination of the new quassinoids 2-acetylglaucarubine (1a) and 13,18-dehydroglaucarubinone (2). The previously known 2-acetylglaucarubinone (3a) and glaucarubinone (3b) were also obtained. The new quassinoid2 was found significantly to inhibit growth of the murine lymphocytic leukemia P388.Antineoplastic agents 59. For part 58 refer to M. T. Edgar, G.R. Pettit and T.H. Smith, J. org. Chem., in preparation.Acknowledgments. We wish to thank Mr B. Septe for providing the13C-NMR-data. Dr Jean H. Schmidt and Miss Linda M. Lange for assistance with biological studies.—G.R. Pettit is grateful to the National Cancer Institute (performed pursuant to contract No. N01-67048 with the Division of Cancer Treatment, NCI, National Institutes of Health, Dept. of Health, Education and Welfare), Public Health Services Research grant No. CA 16049-03 from the National Cancer Institute, the Fannie E. Rippel Foundation, Talley Industries, and the Phoenix Coca-Cola Bottling Co., for partial support of this investigation. 相似文献
104.
105.
Adrianto I Wen F Templeton A Wiley G King JB Lessard CJ Bates JS Hu Y Kelly JA Kaufman KM Guthridge JM Alarcón-Riquelme ME;BIOLUPUS GENLES Networks Anaya JM Bae SC Bang SY Boackle SA Brown EE Petri MA Gallant C Ramsey-Goldman R Reveille JD Vila LM Criswell LA Edberg JC Freedman BI Gregersen PK Gilkeson GS Jacob CO James JA Kamen DL Kimberly RP Martin J Merrill JT Niewold TB Park SY Pons-Estel BA Scofield RH Stevens AM Tsao BP Vyse TJ Langefeld CD Harley JB Moser KL Webb CF Humphrey MB 《Nature genetics》2011,43(3):253-258
Systemic lupus erythematosus (SLE, MIM152700) is an autoimmune disease characterized by self-reactive antibodies resulting in systemic inflammation and organ failure. TNFAIP3, encoding the ubiquitin-modifying enzyme A20, is an established susceptibility locus for SLE. By fine mapping and genomic re-sequencing in ethnically diverse populations, we fully characterized the TNFAIP3 risk haplotype and identified a TT>A polymorphic dinucleotide (deletion T followed by a T to A transversion) associated with SLE in subjects of European (P = 1.58 × 10(-8), odds ratio = 1.70) and Korean (P = 8.33 × 10(-10), odds ratio = 2.54) ancestry. This variant, located in a region of high conservation and regulatory potential, bound a nuclear protein complex composed of NF-κB subunits with reduced avidity. Further, compared with the non-risk haplotype, the haplotype carrying this variant resulted in reduced TNFAIP3 mRNA and A20 protein expression. These results establish this TT>A variant as the most likely functional polymorphism responsible for the association between TNFAIP3 and SLE. 相似文献
106.
Gurumurthy S Xie SZ Alagesan B Kim J Yusuf RZ Saez B Tzatsos A Ozsolak F Milos P Ferrari F Park PJ Shirihai OS Scadden DT Bardeesy N 《Nature》2010,468(7324):659-663
Haematopoietic stem cells (HSCs) can convert between growth states that have marked differences in bioenergetic needs. Although often quiescent in adults, these cells become proliferative upon physiological demand. Balancing HSC energetics in response to nutrient availability and growth state is poorly understood, yet essential for the dynamism of the haematopoietic system. Here we show that the Lkb1 tumour suppressor is critical for the maintenance of energy homeostasis in haematopoietic cells. Lkb1 inactivation in adult mice causes loss of HSC quiescence followed by rapid depletion of all haematopoietic subpopulations. Lkb1-deficient bone marrow cells exhibit mitochondrial defects, alterations in lipid and nucleotide metabolism, and depletion of cellular ATP. The haematopoietic effects are largely independent of Lkb1 regulation of AMP-activated protein kinase (AMPK) and mammalian target of rapamycin (mTOR) signalling. Instead, these data define a central role for Lkb1 in restricting HSC entry into cell cycle and in broadly maintaining energy homeostasis in haematopoietic cells through a novel metabolic checkpoint. 相似文献
107.
Calmodulin interacts with MLO protein to regulate defence against mildew in barley 总被引:29,自引:0,他引:29
Kim MC Panstruga R Elliott C Müller J Devoto A Yoon HW Park HC Cho MJ Schulze-Lefert P 《Nature》2002,416(6879):447-451
In plants, defence against specific isolates of a pathogen can be triggered by the presence of a corresponding race-specific resistance gene, whereas resistance of a more broad-spectrum nature can result from recessive, presumably loss-of-regulatory-function, mutations. An example of the latter are mlo mutations in barley, which have been successful in agriculture for the control of powdery mildew fungus (Blumeria graminis f. sp. hordei; Bgh). MLO protein resides in the plasma membrane, has seven transmembrane domains, and is the prototype of a sequence-diversified family unique to plants, reminiscent of the seven-transmembrane receptors in fungi and animals. In animals, these are known as G-protein-coupled receptors and exist in three main families, lacking sequence similarity, that are thought to be an example of molecular convergence. MLO seems to function independently of heterotrimeric G proteins. We have identified a domain in MLO that mediates a Ca2+-dependent interaction with calmodulin in vitro. Loss of calmodulin binding halves the ability of MLO to negatively regulate defence against powdery mildew in vivo. We propose a sensor role for MLO in the modulation of defence reactions. 相似文献
108.
Judith S. Weis 《Cellular and molecular life sciences : CMLS》1970,26(2):155-156
Résumé Des injections d'un sérum spécifique contre le facteur de croissance nerveuse (anti-NGF) provoquent une réduction de la taille des ganglions rachidiens de la salamandreAmbystoma par suite de la réduction de la masse cellulaire du ganglion. Il y a aussi un plus grand nombre de «petites» cellules (d'un diamètre nucléaire de moins de 6,25 ) dans les ganglions des animaux utilisés.
I should like to express my thanks to Dr.Isaac Schenkein for supplying the antiserum preparation, and to Mr.Edward Kalmar for technical assistance. This research was supported by a grant from the Rutgers University Research Council. 相似文献
I should like to express my thanks to Dr.Isaac Schenkein for supplying the antiserum preparation, and to Mr.Edward Kalmar for technical assistance. This research was supported by a grant from the Rutgers University Research Council. 相似文献
109.
Résumé Le contenu protéique des cellules glandulaires circulaires des larves de 2 races deDrosophila melanogaster est examiné en détail. Les résultats de cette étude montrent que la production et l'activité hormonale de ces 2 races diffère. 相似文献
110.
Martin J Han C Gordon LA Terry A Prabhakar S She X Xie G Hellsten U Chan YM Altherr M Couronne O Aerts A Bajorek E Black S Blumer H Branscomb E Brown NC Bruno WJ Buckingham JM Callen DF Campbell CS Campbell ML Campbell EW Caoile C Challacombe JF Chasteen LA Chertkov O Chi HC Christensen M Clark LM Cohn JD Denys M Detter JC Dickson M Dimitrijevic-Bussod M Escobar J Fawcett JJ Flowers D Fotopulos D Glavina T Gomez M Gonzales E Goodstein D Goodwin LA Grady DL Grigoriev I Groza M Hammon N Hawkins T 《Nature》2004,432(7020):988-994