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排序方式: 共有656条查询结果,搜索用时 15 毫秒
61.
Daniel Martins Bruno Menezes de Oliveira Alessandro dos Santos Farias Ricardo Shiniti Oka Horiuchi Cleyton Crepaldi Domingues Eneida de Paula Sérgio Marangoni Wagner Farid Gattaz Emmanuel Dias-Neto José Camillo Novello 《Briefings in Functional Genomics and Prot》2007,6(1):70-75
Protein extraction is the most important step to reveal a proteome by Two-Dimensional Gel Electrophoresis. Usually, the urea/thiourea based standard protein extraction buffer (SB) is combined with detergents with the aim of achieving better resolution and solubilization of different classes of proteins. In order to produce better gels and achieve the greatest spot resolution of Human Brain Proteins, comparisons using 2-DE of extracted proteins from Human Brain Frontal Cortex with SB constituents (7M Urea, 2M Thiourea and 100mM DTT) were made, using different detergent compositions in the buffer. SB preparations in combination with CHAPS and ASB-14 as well as with ASB-16 (reported for the first time in 2-DE experiments) have been tested. Our results confirm that the most efficient solubilizing solution for 2-DE analysis of cytosolic and membrane Human Brain Proteins is SB combined with 4% CHAPS and 2% ASB-14. 相似文献
62.
Farias RC Madeira-da-Silva MC Pereira-Peixoto MH Martins CF 《Neotropical Entomology》2007,36(6):863-867
Euglossina bees form a group with about 200 species known, widespread in Neotropical Region. Males collect aromatic compounds on flowers and by using synthesized analogs it is possible to accomplish faunistic inventories and study several ecological aspects of these bees. In this work we studied the activity hours and the preference of aromatic compounds by Euglossina males in forest and dunes at Environmental Protection Area of the Mamanguape River Bar, Rio Tinto, Paraíba State, between August 2002 and July 2004. Six artificial compounds were used as attractive: benzyl acetate, ionone beta, skatole, eucalyptol, eugenol and vanillin. Nine species were sampled, being two of them exclusive of the forest. Euglossa cordata (L.) and Eulaema nigrita Lepeletier were the most abundant species as in the forest as on dunes. Males were more active between 8:00 a.m. and 10:00 a.m. in both areas, with no variation throughout the year. Eucalyptol and eugenol attracted most number of species. E. cordata demonstrated preference by ionone beta and eucalyptol and E. nigrita by skatole and eucalyptol. 相似文献
63.
Piccinini Alexandre Oliveira Mariana Pacheco Silva Mariella Reinol Bett Gabriela Souza Becker Isabel Borges Mendes Talita Farias Salla Daniéle Hendler Silva Larissa Espindola Vilela Thais Ceresér Moraes Fernanda Mendes Moterle Diego Damiani Adriani Paganini Dagostin Lígia Salvan Tietbohl Lariani Tamires Bittencourt João Vitor Silvano Biehl Erica Denicol Tais Luise Bonfante Sandra Regina Andrade Vanessa Moraes Silveira Paulo Cesar Lock Prophiro Josiane Somariva Ferreira Gabriela Kozuchovski Petronilho Fabricia Kanis Luiz Alberto Rezin Gislaine Tezza 《Neurochemical research》2022,47(7):1888-1903
Neurochemical Research - This study aimed to evaluate the effect of Cynara cardunculus leaf ethanol extract on inflammatory and oxidative stress parameters in the hypothalamus, prefrontal cortex,... 相似文献
64.
Fernandes Jackellynne Fernanda Farias Freitas Jailza de Araújo Sandra Alves de Santana Thiago Campos Lobato Rafael Santos Figueiredo Marina Bezerra 《Environmental Biology of Fishes》2022,105(8):1033-1050
Environmental Biology of Fishes - To clarify the reproductive activity of lane snapper, Lutjanus synagris, a total of 359 specimens of lane snapper were collected in partnership with an artisanal... 相似文献
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Rodrigo Araújo Lima Rodrigues Ludmila Karen dos Santos Silva Fábio Pio Dornas Danilo Bretas de Oliveira Thais Furtado Ferreira Magalh?es Daniel Assis Santos Adriana Oliveira Costa Luiz de Macêdo Farias Paula Prazeres Magalh?es Cláudio Ant?nio Bonjardim Erna Geessien Kroon Bernard La Scola Juliana Reis Cortines J?natas Santos Abrah?o 《Journal of virology》2015,89(23):11812-11819
68.
Barros FW Bandeira PN Lima DJ Meira AS de Farias SS Albuquerque MR dos Santos HS Lemos TL de Morais MO Costa-Lotufo LV Pessoa Cdo Ó 《Bioorganic & medicinal chemistry》2011,19(3):1268-1276
Four derivatives of an α,β-amyrin mixture were synthesized by acylation with appropriate anhydrides. The structures of the compounds were confirmed by means of IR and (1)H and (13)C NMR. The compounds were screened for cytotoxic activity using four human tumor cell lines (HL-60, MDAMB-435, SF-295 and HCT-8) and normal peripheral blood mononuclear cells (PBMC). 3-O-Carboxymaleinate of α,β-amyrin (3a/3b) were found to be the only active compounds of the series (high cytotoxicity), showing IC(50) values ranging from 1.8 to 3μM. In PBMC, 3a/3b were not toxic, suggesting selectivity for tumor cells. To better understand the mechanism of action involved in the cytotoxicity of 3a/3b, HL-60 cells treated with 3a/3b were examined for morphological changes, DNA fragmentation, cell cycle perturbation, externalization of phosphatidylserine and activation of caspases 3/7, with doxorubicin serving as the positive control. The results indicate that the cytotoxicity of 3a/3b involves the induction of cell death by apoptosis. 相似文献
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Plasmepsin (PM) II is one of four enzymes in the food vacuole of Plasmodium falciparum. It has become an attractive target for combating malaria through research regarding its importance in the P. falciparum metabolism and life cycle, making it the target of choice for structure-based drug design. This paper reports the results of hybrid quantum mechanics / molecular mechanics (QM/MM) molecular dynamics (MD) simulations employed to study the details of the interactions established between PM II and N-(3-{(2-benzo[1, 3]dioxol-5-yl-ethyl)[3-(1-methyl-3-oxo-1,3-dihydro-isoindol-2-yl) propionyl]-amino}-1-benzyl-2-(hydroxyl-propyl)-4-benzyloxy-3,5dimethoxy-benzamide (EH58), a well-known potent inhibitor for this enzyme. Electrostatic binding free energy and energy terms decomposition have been computed for PM II complexed with the EH58 inhibitor. The results reveal that there is a strong interaction between Asp34, Val78, Ser79, Tyr192 and Asp214 residues and the EH58 inhibitor. In addition, we have computed the potential of the mean force (PMF) profile in order to assign the protonation state of the two catalytic aspartates in PM II-EH58 complex. The results indicate that the protonation of Asp214 favors a stable active site structure, which is consistent with our electrostatic binding free energy calculation and with previous published works. 相似文献