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排序方式: 共有182条查询结果,搜索用时 15 毫秒
1.
Various 2-nitronaphthofuran derivatives (related to each other by simple structural modifications) were tested for 2 different effects in CV-1 monkey kidney cell cultures: the immediate inhibition of normal DNA synthesis and the capacity of pretreated cultures (40 h of contact) to support the replication of UV-damaged Herpes simplex virus (HSV). For all compounds tested, a fair correlation was found between their efficiencies to inhibit cellular DNA synthesis and to provoke an increase in UV-HSV production (virus reactivation). Virus reactivation was due to an increase in both the number of virus-producing cells and the amount of infectious particles produced per cell. The most efficient 2-nitronaphthofurans (particularly 2-nitro-7-methoxy-naphtho[2,1-b]furan-R 7000) were at least as potent as aflatoxin B1 in inducing virus reactivation. 相似文献
2.
Bernard Buisson 《Zoomorphology》1970,68(1):1-36
The morphological supports of integration, including the nervous system, are to be found.After a morphological observation, ecto and endoderms and their intercellular junctions are presented.The regionally different mesogleal synaptic nerve nets are surrounded by ecto and endodermal nervous structures.The presence of behavioural activity centers is also discussed.
Liste des abréviations des figures AS autozoïde sectionné - AU autozoïde - CAL canal longitudinal - CAV cavité gastrique - CC corps compact - CGL cellule globuleuse myo-épitheliale MESlame mésentériale MF microfilament - CGR cellule granuleuse myo-épithéliale - CLC cloison commune à deux autozoïdes - CLR cloison radiale - CLT cloison transversale - CM corps myélinique - CME cellule mesenchymateuse - CNE cellule nerveuse ectodermique - CNEN cellule nerveuse endodermique - CNM cellule nerveuse mésogléenne - COL colonne - CSP cellule spumeuse - CSPH cellule sphéruleuse - CU cellule urticante - D dépot de matériel intercellulaire (zonula adhaerens) - DS desmosome septé - ECT ectoderme - EE empilement d'ergastoplasme rappelant un corps de Nissl - FF fibres fasciculées h structure - G glycogène - GA granule aréolé - IC inclusion crênelée - M mitochondrie - MB membrane basale - ME mésoglée - MES lame mésentériale - MF microfilament - MT figure interprétée on terme de microtubule - MV microvilli - N noyau - E neurite - NO nodosité - P pédoncule - PC paroi des canaux - PE perforation - R rachis - SF siphonozoïde fendu - SIPH siphonozoïde - SM sipment musculaire d'une cellule myoépithéliale - T travé ous-siphonozoïdale - TME travée mésogléenne - VC vésicule claire - VME vésicule mésenchymateuse - ZI zône intermédiaire - I synapse polarisée - 2 synapse réciproque - 3 figure ressemblant à un desmosome septé - 4 contact par apposition Cc travail correspond à la première partie d'une thèse de Doctorat d'Etat, consacrée aux «Structures et aux mécanismes de l'intégration dans la colonie de Veretillum cynomoriurra» — Il a été effectué au sein de l'Equipe de Recherche Associée au C.N.R.S., n°183 (Directeur Al. Pavans de Ceccatty) avec le concours du Laboratoire Arago à Banyuls sur Mer (France) et la collaboration technique de Madame J. Villeneuve. 相似文献
Liste des abréviations des figures AS autozoïde sectionné - AU autozoïde - CAL canal longitudinal - CAV cavité gastrique - CC corps compact - CGL cellule globuleuse myo-épitheliale MESlame mésentériale MF microfilament - CGR cellule granuleuse myo-épithéliale - CLC cloison commune à deux autozoïdes - CLR cloison radiale - CLT cloison transversale - CM corps myélinique - CME cellule mesenchymateuse - CNE cellule nerveuse ectodermique - CNEN cellule nerveuse endodermique - CNM cellule nerveuse mésogléenne - COL colonne - CSP cellule spumeuse - CSPH cellule sphéruleuse - CU cellule urticante - D dépot de matériel intercellulaire (zonula adhaerens) - DS desmosome septé - ECT ectoderme - EE empilement d'ergastoplasme rappelant un corps de Nissl - FF fibres fasciculées h structure - G glycogène - GA granule aréolé - IC inclusion crênelée - M mitochondrie - MB membrane basale - ME mésoglée - MES lame mésentériale - MF microfilament - MT figure interprétée on terme de microtubule - MV microvilli - N noyau - E neurite - NO nodosité - P pédoncule - PC paroi des canaux - PE perforation - R rachis - SF siphonozoïde fendu - SIPH siphonozoïde - SM sipment musculaire d'une cellule myoépithéliale - T travé ous-siphonozoïdale - TME travée mésogléenne - VC vésicule claire - VME vésicule mésenchymateuse - ZI zône intermédiaire - I synapse polarisée - 2 synapse réciproque - 3 figure ressemblant à un desmosome septé - 4 contact par apposition Cc travail correspond à la première partie d'une thèse de Doctorat d'Etat, consacrée aux «Structures et aux mécanismes de l'intégration dans la colonie de Veretillum cynomoriurra» — Il a été effectué au sein de l'Equipe de Recherche Associée au C.N.R.S., n°183 (Directeur Al. Pavans de Ceccatty) avec le concours du Laboratoire Arago à Banyuls sur Mer (France) et la collaboration technique de Madame J. Villeneuve. 相似文献
3.
Jean-Jacques Madjar Monique Arpin Monique Buisson Jean-Paul Reboud 《Molecular & general genetics : MGG》1979,171(2):121-134
Summary Separation of the proteins from rat liver 40S and 60S ribosomal subunits and polysomes was done in four different two-dimensional polyacrylamide gel electrophoresis systems. The first dimension was run at acidic or basic pH, the second dimension either with sodium dodecyl sulphate or at acidic pH in 18% acrylamide. The position of each individual protein of both subunits and polysomes was determined in each system. This identification resulted from a new method avoiding any previous purification of individual proteins. The new proposed uniform nomenclature for mammalian ribosomal proteins (McConkey et al. in press) was used for numbering the proteins in the four systems. 相似文献
4.
tRNA binding stabilizes rat liver 60 S ribosomal subunits during treatment with LiCl 总被引:1,自引:0,他引:1
A M Reboud S Dubost M Buisson J P Reboud 《The Journal of biological chemistry》1980,255(14):6954-6961
We have shown recently that, in the absence of mRNA, 1 molecule of nonacylated tRNA binds to the large ribosomal subunit of rat liver with a high affinity constant (Buisson, M., Reboud, A.M., Dubost, S., and Reboud, J. P. (1979) Biochem. Biophys. Res. Commun. 90,634-640). In this paper, free and tRNA-bound 60 S subunits were treated with increasing concentrations of LiCl to obtain information on tRNA binding site. The rationale for using deacylated tRNA was that it is assumed to bind to the peptidyl donor site. We observed that tRNA has a strong protective effect on subunit modifications produced by LiCl: tRNA prevents subunit inactivation as measured by puromycin reaction and polyphenylalanine synthesis and it shifts the Li+/Mg2+ ratio value needed to reach 50% inactivation, from 60 to 250; it also prevents ribosomal protein and 5 S RNA release and large sedimentation changes of subunits, induced by LiCl. To explain the mechanism of 60 S subunit stabilization by tRNA, two hypotheses are considered: stabilization can be consequent on direct interaction of tRNA with specific proteins, or on maintenance on subunits of essential cations which are otherwise displaced by Li+, or both. 相似文献
5.
Rat liver 60-S ribosomal subunits were submitted to increasing doses of radiation (253.7 nm), at 4 degrees C and 25 degrees C, as previously reported fro 40-S subunits. The existence of protein-RNA cross-linking was demonstrated by two methods. The first consisted in the separation of protein-RNA complex; the second was indirect, and took into account alteration either in the electrophoretic mobility of cross-linked proteins or the separability of 28-S RNA in a 4 M urea/3 M LiCl buffer. The peptide synthetase activity and the sedimentation characteristics of the particles irradiated at 4 degrees C were well preserved, but at 25 degrees C the large subunits were progressively inactivated and unfolded for doses higher than 2 x 10(18) quanta. The dose-dependent variations of protein cross-linkage determined by two-dimensional gel electrophoresis allowed us to distinguish those proteins which reacted at the lowest doses with a first-order reaction from those which cross-linked to RNA after a subtle modification of the subunit structure. At 25 degrees C, all proteins became low-dose reactive. The curve obtained for 28-S RNA cross-linkage was similar to that of the total protein moiety, while those obtained fro the 5-S and 5.8-S RNA (which were parallel) suggest a lower reactivity of these RNAs. As a general rule, proteins from the large subunits were more reactive to RNA than those from the small subunits. This could indicate differences in the organisation of the two subunits. 相似文献
6.
Robert A. Volkmann Christopher M. Fanger David R. Anderson Venkata Ramana Sirivolu Kathy Paschetto Earl Gordon Caterina Virginio Melanie Gleyzes Bruno Buisson Esther Steidl Susanna B. Mierau Michela Fagiolini Frank S. Menniti 《PloS one》2016,11(2)
GluN2A is the most abundant of the GluN2 NMDA receptor subunits in the mammalian CNS. Physiological and genetic evidence implicate GluN2A-containing receptors in susceptibility to autism, schizophrenia, childhood epilepsy and neurodevelopmental disorders such as Rett Syndrome. However, GluN2A-selective pharmacological probes to explore the therapeutic potential of targeting these receptors have been lacking. Here we disclose a novel series of pyrazine-containing GluN2A antagonists exemplified by MPX-004 (5-(((3-chloro-4-fluorophenyl)sulfonamido)methyl)-N-((2-methylthiazol-5-yl)methyl)pyrazine-2-carboxamide) and MPX-007 (5-(((3-fluoro-4-fluorophenyl)sulfonamido)methyl)-N-((2-methylthiazol-5-yl)methyl)methylpyrazine-2-carboxamide). MPX-004 and MPX-007 inhibit GluN2A-containing NMDA receptors expressed in HEK cells with IC50s of 79 nM and 27 nM, respectively. In contrast, at concentrations that completely inhibited GluN2A activity these compounds have no inhibitory effect on GluN2B or GluN2D receptor-mediated responses in similar HEK cell-based assays. Potency and selectivity were confirmed in electrophysiology assays in Xenopus oocytes expressing GluN2A-D receptor subtypes. Maximal concentrations of MPX-004 and MPX-007 inhibited ~30% of the whole-cell current in rat pyramidal neurons in primary culture and MPX-004 inhibited ~60% of the total NMDA receptor-mediated EPSP in rat hippocampal slices. GluN2A-selectivity at native receptors was confirmed by the finding that MPX-004 had no inhibitory effect on NMDA receptor mediated synaptic currents in cortical slices from GRIN2A knock out mice. Thus, MPX-004 and MPX-007 offer highly selective pharmacological tools to probe GluN2A physiology and involvement in neuropsychiatric and developmental disorders. 相似文献
7.
Clinical,genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation
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Caroline Alby Valérie Malan Lucile Boutaud Maria Angela Marangoni Bettina Bessières Maryse Bonniere Amale Ichkou Nadia Elkhartoufi Nadia Bahi‐Buisson Pascale Sonigo Anne‐Elodie Millischer Sophie Thomas Yves Ville Michel Vekemans Férechté Encha‐Razavi Tania Attié‐Bitach 《Birth defects research. Part A, Clinical and molecular teratology》2016,106(1):36-46
8.
Overcoming challenges on using native seeds for restoration of megadiverse resource‐poor environments: a reply to Madsen et al.
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Roberta L. C. Dayrell André J. Arruda Elise Buisson Fernando A. O. Silveira 《Restoration Ecology》2016,24(6):710-713
Madsen et al. (2016) reviewed several major limiting factors to establishment of seedlings in nonforest ecosystems (NFE), and proposed seed enhancement technologies to overcome these restoration barriers. However, biodiverse nutrient‐poor NFE present additional hurdles that preclude landscape‐scale seed‐based restoration and were not mentioned in their review. Here, we discuss issues related to native seed availability and provenance, and shortfalls in knowledge on seed quality testing and dormancy release that severely hamper restoration of degraded nutrient‐impoverished NFE. We present alternatives for overcoming these challenges and highlight the need for investments to find more practical and cost‐effective options for broad‐scale restoration. 相似文献
9.
Abdominal dermolipectomies: early postoperative complications and long-term unfavorable results 总被引:6,自引:0,他引:6
Chaouat M Levan P Lalanne B Buisson T Nicolau P Mimoun M 《Plastic and reconstructive surgery》2000,106(7):1614-8; discussion 1619-23
A retrospective study was done on a population of 258 women who had undergone surgery for abdominal dermolipectomy between January of 1991 and May of 1996. The postoperative complications and flaws seen at long-term follow-up are discussed. The surgical techniques used, with or without lipoaspiration, were the infraumbilical plasty and full plasties with horizontal or inverted T scars. Six types of postoperative complications were noted: hemorrhage in 1.2 percent, lymphorrhea in 10.9 percent, infection in 7 percent, skin necrosis in 6.6 percent, secondary dehiscence of the scar in 2.3 percent, and thromboembolic accidents in 1.2 percent. No significant difference was found in the rate of necrosis development between patients who did and did not undergo lipoaspiration. However, a statistically significant difference was seen in the rate of skin necrosis between the T-type plasty (35.5 percent) and the other two procedures (1.43 percent for infraumbilical plasties and 4.60 percent for full plasties with horizontal scar). With regard to the flaws found at long-term follow-up, the rate of above-scar fat folds and/or dog-ears was 27.9 percent, and the rate of defective scars was 26 percent. No significant difference was found with regard to the rate of flaws. The rate of all secondary surgical procedures was 29.1 percent, but performance of secondary procedures depended on the willingness of the patient and on the surgeon's judgment. Abdominoplasty procedures involve a high risk of early complications. The rate of skin necrosis is clearly augmented in cases of T-type plasty. The need for secondary surgical correction is frequent, and the patient should be reminded of this possibility during preoperative consultation. 相似文献
10.
Denis Vivien Myriam Bernaudin Alain Buisson Didier Divoux Eric T. MacKenzie André Nouvelot 《Journal of neurochemistry》1998,70(6):2296-2304
Abstract: The peptides of the transforming growth factor-β (TGF-β) family transduce their signal through ligand-induced heteromeric complexes that consist of type I and type II serine/threonine kinases. Both TGF-β receptors are abundant in many peripheral tissues, but clear evidence of their expression in cortical astrocytes and neurons has not been published so far. In this study, we investigated the expression of type I and type II TGF-β receptors and their potential ligands (TGF-β1, TGF-β2, and TGF-β3) in the CNS by using RT-PCR and immunohistochemistry. Moreover, to further the study of those cell types that exhibit TGF-β isoforms and related receptors, we examined through the use of RT-PCR whether cortical neurons and astrocytes in culture express the mRNAs for TGF-βs and their receptors. We show that the three TGF-β isoform mRNAs are present in the CNS. However, although astrocytes in culture display all three isoforms, neurons in culture express only TGF-β2. We have demonstrated that both type I and type II TGF-β receptor mRNAs and proteins are present in the CNS and in cultures of cortical neurons and astrocytes. Thus, TGF-βs may act as autocrine and paracrine signals in the CNS between both neurons and astrocytes via the same receptor systems as those found in peripheral tissues. TGF-β1 has been shown to be induced following hypoxic-ischemic brain injury and may play a critical role in the pathophysiology of degenerative processes in the CNS. In the present investigation, we confirmed that the expression of TGF-β1 was increased markedly up until 24 h and thereafter was stable over the first 3 days following permanent occlusion of the middle cerebral artery in mice. However, whereas the expression of the type I TGF-β receptor was not altered by the ischemic insult, the pattern of the type II TGF-β receptors was modified dramatically in the ischemic area 3 days after the occlusion. These data show that, even if ligands are present, they may not be able to transduce their signal. Finally, the present study clearly demonstrates that a knowledge of the expression of ligand-specific receptors following brain injury is a fundamental step in clarifying the involvement of cytokines in neurodegenerative diseases. 相似文献