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81.
Update on Pneumocystis carinii f. sp. hominis Typing Based on Nucleotide Sequence Variations in Internal Transcribed Spacer Regions of rRNA Genes 总被引:6,自引:0,他引:6 下载免费PDF全文
Chao-Hung Lee Jannik Helweg-Larsen Xing Tang Shaoling Jin Baozheng Li Marilyn S. Bartlett Jang-Jih Lu Bettina Lundgren Jens D. Lundgren Mats Olsson Sebastian B. Lucas Patricia Roux Antonietta Cargnel Chiara Atzori Olga Matos James W. Smith 《Journal of clinical microbiology》1998,36(3):734-741
Pneumocystis carinii f. sp. hominis isolates from 207 clinical specimens from nine countries were typed based on nucleotide sequence variations in the internal transcribed spacer regions I and II (ITS1 and ITS2, respectively) of rRNA genes. The number of ITS1 nucleotides has been revised from the previously reported 157 bp to 161 bp. Likewise, the number of ITS2 nucleotides has been changed from 177 to 192 bp. The number of ITS1 sequence types has increased from 2 to 15, and that of ITS2 has increased from 3 to 14. The 15 ITS1 sequence types are designated types A through O, and the 14 ITS2 types are named types a through n. A total of 59 types of P. carinii f. sp. hominis were found in this study. 相似文献
82.
Allele-Specific PCR Method Based on pncA and oxyR Sequences for Distinguishing Mycobacterium bovis from Mycobacterium tuberculosis: Intraspecific M. bovis pncA Sequence Polymorphism 总被引:1,自引:0,他引:1 下载免费PDF全文
Luz Elena Espinosa de los Monteros Juan Carlos Galn Montserrat Gutirrez Sofía Samper Juan F. García Marín Carlos Martín Lucas Domínguez Luis de Rafael Fernando Baquero Enrique Gmez-Mampaso Jesús Blzquez 《Journal of clinical microbiology》1998,36(1):239-242
An allele-specific amplification method based on two genetic polymorphisms to differentiate Mycobacterium tuberculosis from Mycobacterium bovis was tested. Based on the differences found at position 169 in the pncA genes from M. tuberculosis and M. bovis, a PCR system which was able to differentiate most of the 237 M. tuberculosis complex isolates tested in one of the two species was developed. All 121 M. tuberculosis strains showed the expected base (cytosine) at position 169. Most of the M. bovis isolates had a guanine at the cited position. Nevertheless, 18 of the 116 M. bovis isolates, all of them goat isolates, showed the pncA polymorphism specific to M. tuberculosis. These results suggest that goat M. bovis may be the nicotinamidase-missing link at the origin of the M. tuberculosis species. Based on the polymorphism found at position 285 in the oxyR gene, the same system was used to differentiate M. tuberculosis from M. bovis. In this case, DNAs from all 121 M. tuberculosis isolates had the expected base (guanine) at this position. In addition, all 116 M. bovis isolates, including those from goats, showed the identical polymorphism (adenine). The oxyR allele-specific amplification method can differentiate M. bovis from M. tuberculosis, is rapid (results can be obtained in less than 3 h), and is easy to perform. 相似文献
83.
Maitrot A Lucas MF Doncarli C Farina D 《Medical & biological engineering & computing》2005,43(4):487-492
In the study, an efficient method to perform supervised classification of surface electromyogram (EMG) signals is proposed.
The method is based on the choice of a relevant representation space and its optimisation with respect to a training set.
As EMG signals are the summation of compact-support waveforms (the motor unit action potentials), a natural tool for their
representation is the discrete dyadic wavelet transform. The feature space was thus built from the marginals of a discrete
wavelet decomposition. The mother wavelet was designed to minimise the probability of classification error estimated on the
learning set (supervised classification). As a representative example, the method was applied to simulate surface EMG signals
generated by motor units with different degrees of short-term synchronisation. The proposed approach was able to distinguish
surface EMG signals with degrees of synchronisation that differed by 10%, with a misclassification rate of 8%. The performance
of a spectral-based classification (error rate approximately 33%) and of the classification with Daubechies wavelet (21%)
was significantly poorer than with the proposed wavelet optimisation. The method can be used for a number of different application
fields of surface EMG classification, as the feature space is adapted to the characteristics of the signal that discriminate
between classes.
An erratum to this article is available at . 相似文献
84.
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86.
McRobert SP Tompkins L Barr NB Bradner J Lucas D Rattigan DM Tannous AF 《Behavior genetics》2003,33(3):347-356
Many aspects of the reproductive behavior of Drosophila melanogaster are modified dramatically by experience and age. Males' courtship of immature males and fertilized females decreases over time. Females' receptivity to copulation, and the behaviors that females perform and elicit, are affected by their age and sexual experience. We show that mutations in a raised stock affect all of these age- and experience-dependent aspects of male and female sexual behavior. Experience has no effect on raised males' courtship of immature males and has opposite effects on raised and wild-type males' courtship of fertilized females. In comparison to controls, raised females become sexually mature at an earlier age, and sexually mature raised virgin females copulate more quickly. Following mating, raised females elicit more courtship and remate faster and more frequently than control females. 相似文献
87.
Frei K Szuhai K Lucas T Weipoltshammer K Schöfer C Ramsebner R Baumgartner WD Raap AK Bittner R Wachtler FJ Kirschhofer K 《European journal of human genetics : EJHG》2002,10(7):427-432
Mutations in the connexin 26 (Cx26) gene (GJB2) are associated with autosomal nonsyndromic sensorineural hearing loss. This study describes mutations in the Cx26 gene in cases of familial and sporadic hearing loss (HL) by gene sequencing and identifies the allelic frequency of the most common mutation leading to HL (35delG) in the population of eastern Austria. For this purpose we have developed and applied a molecular beacon based real-time mutation detection assay. Mutation frequencies in the Cx26 gene of individuals from affected families (14 out of 46) and sporadic cases (11 out of 40) were 30.4% and 27.5%, respectively. In addition to known disease related alterations, a novel mutation 262 G-->T (A88S) was also identified. 35delG accounted for almost 77% of all Cx26 mutations detected and displayed an allelic frequency in the normal hearing population of 1.7% (2 out of 120). The high prevalence of the 35delG mutation in eastern Austria would therefore allow screening of individuals and family members with Cx26 dependent deafness by a highly specific and semi-automated method. 相似文献
88.
89.
Allen M Pratscher B Krepler C Frei K Schöfer C Pehamberger H Müller M Lucas T 《International journal of immunogenetics》2005,32(6):375-378
Two novel interleukin-24 (IL-24) splice variants were identified in normal human melanocytes by sequencing cloned polymerase chain reaction (PCR) products that are not expressed in metastatic melanoma. These gene products have been generated by differential skipping of exons 3 (IL-24 delE3) and 5 (IL-24 delE5). IL-24 delE3 has limited sequence identity to the IL-24-interacting protein mda-7s, and IL-24 delE5 is homologous to IL-24. 相似文献
90.
Aging and the Immune Response to the Haemophilus influenzae Type b Capsular Polysaccharide: Retention of the Dominant Idiotype and Antibody Function in the Elderly 下载免费PDF全文
Anti-Haemophilus influenzae b polysaccharide (Hib PS) antibodies elicited in elderly subjects following conjugate vaccination expressed a light-chain variable-region (VL)-associated idiotype and had functional activities similar to those previously observed in children and younger adults. These findings indicate that advanced age is not accompanied by shifts in the major VL component of the Hib PS-specific repertoire or by diminution of the protective function of antibodies. 相似文献