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61.
Elastin, the protein responsible for tissue elasticity, is contained in arterial walls, lungs, and skin. Given the cassette like organization of the human tropoelastin gene, giving rise to alternating exons encoding for crosslink domains and elastomeric domains, it is tempting to suggest that polypeptides encoded by different exons could adopt structures independent of the other exons. The results obtained with the polypeptide sequences encoded by exons 3, 7, and 30 of human tropoelastin are described. It is shown that these hydrophobic exons may partly assume the polyproline II (PPII) structure, as found by circular dichroism studies in aqueous solution. Classical Raman spectroscopy evidences a specific sharp band at 1314 cm(-1), which is assigned to the PPII structure adopted by these exons in the solid state. As these sequences are among those putatively responsible for elastomeric properties, these findings are of particular interest in relation to the current models of the elasticity of elastin. 相似文献
62.
J Caroff E Girin D Alix C Cann-Moisan J Sizun L Barthelemy 《Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie》1992,314(10):451-454
The study of 33 cerebrospinal fluids of infants victims of sudden death shows a very significant increase of the metabolites of dopamine and serotonin. These determinations, compared to a control group, indicate a failure, concerning these two neurotransmitters, which could induce a cardiorespiratory seizure. This failure has likely a multifactorial origin. 相似文献
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64.
Derek R. Stein Bryce M. Warner Jonathan Audet Geoff Soule Vinayakumar Siragam Patrycja Sroga Bryan D. Griffin Anders Leung Allen Grolla Kevin Tierney Alix Albietz Darwyn Kobasa Abdulmajid S. Musa Adama Ahmad Afolabi M. Akinpelu Nwando Mba Rebecca Rosenke Dana P. Scott Greg Saturday Chikwe Ihekweazu David Safronetz 《PLoS pathogens》2021,17(10)
Nigeria continues to experience ever increasing annual outbreaks of Lassa fever (LF). The World Health Organization has recently declared Lassa virus (LASV) as a priority pathogen for accelerated research leading to a renewed international effort to develop relevant animal models of disease and effective countermeasures to reduce LF morbidity and mortality in endemic West African countries. A limiting factor in evaluating medical countermeasures against LF is a lack of well characterized animal models outside of those based on infection with LASV strain Josiah originating form Sierra Leone, circa 1976. Here we genetically characterize five recent LASV isolates collected from the 2018 outbreak in Nigeria. Three isolates were further evaluated in vivo and despite being closely related and from the same spatial / geographic region of Nigeria, only one of the three isolates proved lethal in strain 13 guinea pigs and non-human primates (NHP). Additionally, this isolate exhibited atypical pathogenesis characteristics in the NHP model, most notably respiratory failure, not commonly described in hemorrhagic cases of LF. These results suggest that there is considerable phenotypic heterogeneity in LASV infections in Nigeria, which leads to a multitude of pathogenesis characteristics that could account for differences between subclinical and lethal LF infections. Most importantly, the development of disease models using currently circulating LASV strains in West Africa are critical for the evaluation of potential vaccines and medical countermeasures. 相似文献
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It has been shown that in Escherichia coli the chaperone DnaK is necessary for the late stages of 50S and 30S ribosomal subunit assembly in vivo. Here we focus on the roles of other HSPs (heat-shock proteins), including the chaperonin GroEL, in addition to DnaK, in ribosome biogenesis at high temperature. GroEL is shown to be required for the very late 45S-->50S step in the biogenesis of the large ribosome subunit, but not for 30S assembly. Interestingly, overproduction of GroES/GroEL can partially compensate for a lack of DnaK/DnaJ at 44 degrees C. 相似文献
67.
Hugo Schweke Qifang Xu Gerardo Tauriello Lorenzo Pantolini Torsten Schwede Frédéric Cazals Alix Lhéritier Juan Fernandez-Recio Luis Angel Rodríguez-Lumbreras Ora Schueler-Furman Julia K. Varga Brian Jiménez-García Manon F. Réau Alexandre M. J. J. Bonvin Castrense Savojardo Pier-Luigi Martelli Rita Casadio Jérôme Tubiana Haim J. Wolfson Romina Oliva Didier Barradas-Bautista Tiziana Ricciardelli Luigi Cavallo Česlovas Venclovas Kliment Olechnovič Raphael Guerois Jessica Andreani Juliette Martin Xiao Wang Genki Terashi Daipayan Sarkar Charles Christoffer Tunde Aderinwale Jacob Verburgt Daisuke Kihara Anthony Marchand Bruno E. Correia Rui Duan Liming Qiu Xianjin Xu Shuang Zhang Xiaoqin Zou Sucharita Dey Roland L. Dunbrack Emmanuel D. Levy Shoshana J. Wodak 《Proteomics》2023,23(17):2200323
Reliably scoring and ranking candidate models of protein complexes and assigning their oligomeric state from the structure of the crystal lattice represent outstanding challenges. A community-wide effort was launched to tackle these challenges. The latest resources on protein complexes and interfaces were exploited to derive a benchmark dataset consisting of 1677 homodimer protein crystal structures, including a balanced mix of physiological and non-physiological complexes. The non-physiological complexes in the benchmark were selected to bury a similar or larger interface area than their physiological counterparts, making it more difficult for scoring functions to differentiate between them. Next, 252 functions for scoring protein-protein interfaces previously developed by 13 groups were collected and evaluated for their ability to discriminate between physiological and non-physiological complexes. A simple consensus score generated using the best performing score of each of the 13 groups, and a cross-validated Random Forest (RF) classifier were created. Both approaches showed excellent performance, with an area under the Receiver Operating Characteristic (ROC) curve of 0.93 and 0.94, respectively, outperforming individual scores developed by different groups. Additionally, AlphaFold2 engines recalled the physiological dimers with significantly higher accuracy than the non-physiological set, lending support to the reliability of our benchmark dataset annotations. Optimizing the combined power of interface scoring functions and evaluating it on challenging benchmark datasets appears to be a promising strategy. 相似文献
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In this paper we introduce Armadillo v1.1, a novel workflow platform dedicated to designing and conducting phylogenetic studies, including comprehensive simulations. A number of important phylogenetic and general bioinformatics tools have been included in the first software release. As Armadillo is an open-source project, it allows scientists to develop their own modules as well as to integrate existing computer applications. Using our workflow platform, different complex phylogenetic tasks can be modeled and presented in a single workflow without any prior knowledge of programming techniques. The first version of Armadillo was successfully used by professors of bioinformatics at Université du Quebec à Montreal during graduate computational biology courses taught in 2010-11. The program and its source code are freely available at: . 相似文献
70.
Sabrina Ceeraz Susan K. Eszterhas Petra A. Sergent David A. Armstrong Alix Ashare Thomas Broughton Li Wang Dov Pechenick Christopher M. Burns Randolph J. Noelle Matthew P. Vincenti Roy A. Fava 《Arthritis research & therapy》2017,19(1):270