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Domingo-Espín J Vazquez E Ganz J Conchillo O García-Fruitós E Cedano J Unzueta U Petegnief V Gonzalez-Montalbán N Planas AM Daura X Peluffo H Ferrer-Miralles N Villaverde A 《Nanomedicine (London, England)》2011,6(6):1047-1061
AIM & METHODS: We have produced two chimerical peptides of 10.2 kDa, each contain four biologically active domains, which act as building blocks of protein-based nonviral vehicles for gene therapy. In solution, these peptides tend to aggregate as amorphous clusters of more than 1000 nm, while the presence of DNA promotes their architectonic reorganization as mechanically stable nanometric spherical entities of approximately 80 nm that penetrate mammalian cells through arginine-glycine-aspartic acid cell-binding domains and promote significant transgene expression levels. RESULTS & CONCLUSION: The structural analysis of the protein in these hybrid nanoparticles indicates a molecular conformation with predominance of α-helix and the absence of cross-molecular, β-sheet-supported protein interactions. The nanoscale organizing forces generated by DNA-protein interactions can then be observed as a potentially tunable, critical factor in the design of protein-only based artificial viruses for gene therapy. 相似文献
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The Wisconsin Schizotypy Scales (WSS) have been widely used in the study of clinical and non-clinical samples. However, researchers often find the length of the scales prohibitive. The present study examined the reliability and validity of recently developed 15-item short forms of the Perceptual Aberration, Magical Ideation, Physical Anhedonia, and Revised Social Anhedonia Scales in two large samples of non-clinically ascertained young adults. The scales demonstrated good reliability and correlated highly with the original scales. The validity of the scales was assessed by comparing the association of the original and shortened WSS with interview measures of psychotic-like and schizophrenia-spectrum symptoms and impaired functioning, as well as with questionnaire measures of personality and social impairment. The associations of the shortened WSS with the interview and questionnaire measures were comparable in terms of statistical significance and effect size with the associations of the original scales. The present findings provide the first demonstration of the validity of the shortened WSS and support their use in the study of schizotypy. 相似文献
75.
Anthropogenic sources of nitrogen that pollute bodies of water can have toxic and sub-lethal effects on amphibians. It has
been hypothesized that such exposure may promote local adaptation, that is, selection for higher tolerance in individuals
in populations exposed to pollutants. We tested this hypothesis with respect to the Natterjack toad (Bufo calamita Laurenti, 1768), by comparing the nitrate dose response of tadpoles from eight populations (doses: 0, 50, 100, 500 and 1000 mg/l
nitrate) from relatively unpolluted and intensively farmed environments. We evaluated the effect of nitrate exposure by observing
the behavior (movements) of tadpoles exposed to different concentrations of nitrates. Exposure to high nitrate levels did
not cause tadpole mortality in the populations used in our experiments; however, we did observe changes in activity for all
populations, with these changes being either dose-related responses (decreased activity after exposure to 500 or 1000 mg/l),
or more complex responses (increased activity when exposed to 50 or 100 mg/l nitrate, followed by decreased activity at higher
concentrations). Natterjack toad tadpoles exhibited variable behavioural responses among the tested populations. Although
these populations were selected on the basis of their potential agrochemical contamination, the observed variation in population
tolerance was not related to the parameters used to estimate this contamination in these breeding sites. Possible explanations
for this apparent lack of local adaptation in B. calamita tadpoles include inadequate estimates of the toads’ actual nitrate exposure in the field, and the biological characteristics
of B. calamita, which may limit the effects of exposure or favor phenotypic plasticity. 相似文献
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Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: Different genetic mechanisms but equivalent poorer clinical outcome 下载免费PDF全文
Anna Puiggros Marta Venturas Marta Salido Gonzalo Blanco Concepcin Fernandez‐Rodriguez Rosa Collado Alberto Valiente Neus Ruiz‐Xivill Ana Carri Francisco Jos Ortuo Elisa Luo María Jos Calasanz María Teresa Ardanaz María ngeles Pin Elisabet Talavera María Teresa Gonzlez Margarita Ortega Isabel Marugn Ana Ferrer Eva Gimeno Beatriz Bellosillo Julio Delgado Jos ngel Hernndez Jesús María Hernndez‐Rivas Blanca Espinet 《Genes, chromosomes & cancer》2014,53(9):788-797
Deletion of 13q14 as the sole abnormality is a good prognostic marker in chronic lymphocytic leukemia (CLL). Nonetheless, the prognostic value of reciprocal 13q14 translocations [t(13q)] with related 13q losses has not been fully elucidated. We described clinical and biological characteristics of 25 CLL patients with t(13q), and compared with 62 patients carrying interstitial del(13q) by conventional G‐banding cytogenetics (CGC) [i‐del(13q)] and 295 patients with del(13q) only detected by fluorescence in situ hybridization (FISH) [F‐del(13q)]. Besides from the CLL FISH panel (D13S319, CEP12, ATM, TP53), we studied RB1 deletions in all t(13q) cases and a representative group of i‐del(13q) and F‐del(13q). We analyzed NOTCH1, SF3B1, and MYD88 mutations in t(13q) cases by Sanger sequencing. In all, 25 distinct t(13q) were described. All these cases showed D13S319 deletion while 32% also lost RB1. The median percentage of 13q‐deleted nuclei did not differ from i‐del(13q) patients (73% vs. 64%), but both were significantly higher than F‐del(13q) (52%, P < 0.001). Moreover, t(13q) patients showed an increased incidence of biallelic del(13q) (52% vs. 11.3% and 14.9%, P < 0.001) and higher rates of concomitant 17p deletion (37.5% vs. 8.6% and 7.2%, P < 0.001). RB1 involvement was significantly higher in the i‐del(13q) group (79%, P < 0.001). Two t(13q) patients (11.8%) carried NOTCH1 mutations. Time to first treatment in t(13q) and i‐del(13q) was shorter than F‐del(13q) (67, 44, and 137 months, P = 0.029), and preserved significance in the multivariate analysis. In conclusion, t(13q) and del(13q) patients detected by CGC constitute a subgroup within the 13q‐deleted CLL patients associated with a worse clinical outcome. © 2014 Wiley Periodicals, Inc. 相似文献
79.
Antón A Marcos MA Codoñer FM de Molina P Martínez A Cardeñosa N Godoy P Torner N Martínez MJ Ramón S Tudó G Isanta R Gonzalo V de Anta MT Pumarola T 《Diagnostic microbiology and infectious disease》2011,69(4):419-427
Although particular attention is paid to influenza A and B virus isolates during influenza surveillance, influenza C virus (FLUCV) coexisted during the first influenza A (H1N1) 2009 pandemic wave during the 2009-2010 season. From 27 April 2009 to 9 May 2010, 12 strains of FLUCV were detected in specimens collected from 1713 nonhospitalized patients with upper respiratory tract illness using a molecular method. Half of the patients with FLUCV infection were older than 14 years. The most frequent symptoms were cough and fever, similar to other viral respiratory infections. Phylogenetic analysis of the hemagglutinin-esterase gene revealed that the strains belonged to the C/Kanagawa/1/76-related and C/Sao Paulo/378/82-related lineages, demonstrating their co-circulation in Catalonia. In addition to regular virological surveillance that provides information about the incidence and the exact role of FLUCV in acute viral respiratory infections in the general population, the genetic lineage identification offers additional data for epidemiological purposes. 相似文献
80.
Orland Diez Sara Gutiérrez-Enríquez Carmen Mediano Miriam Masas Cristina Saura Neus Gadea Judith Balma?a 《Breast cancer research and treatment》2010,121(1):221-225
Germ line mutations in either of the two major breast cancer predisposition genes, BRCA1 and BRCA2, account for a significant proportion of hereditary breast/ovarian cancer. Identification of breast cancer patients carrying
mutations in any of these genes is primarily based on a positive family history of breast/ovarian cancer or early onset of
the disease. In the course of mutation screening of the BRCA1 and BRCA2 genes in a hospital based series of patients with risk factors for hereditary breast/ovarian cancer, we identified a novel
germ line mutation in the BRCA2 gene (c.51dupA) in a patient with early onset bilateral breast cancer and no family history of the disease. None of her parents
carried the mutation, and paternity was confirmed. Subsequent molecular analysis demonstrated that the mutation was a novel
de novo germ line mutation located in the paternal allele of the BRCA2 gene. 相似文献