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61.
Yu Nakamura Masatoshi Takeda Hideo Suzuki Hitoshi Morita Kunitoshi Tada Shiro Hariguchi Tsuyoshi Nishimura 《Mechanisms of ageing and development》1989,50(3):215-225
The age-dependent change in activities of seven lysosomal enzymes (cathepsin D, β-glucuronidase, acid phosphatase, acid/alkaline DNases and acid/alkaline RNases) was studied in four brain regions (cerebrum, hippocampus, pons and cerebellum) of Wistar rats. The activity of cathepsin D was significantly increased with aging in the four regions. The age-dependent change in activities of acid and alkaline DNases showed the characteristic regional difference, and the ratio of acid to alkaline DNases was increased with aging in all regions. Acid RNase showed the lowest activity in 18-month-old rats, and alkaline RNase activity was decreased with aging. The activity of β-glucuronidase was higher in 2-month-old rats in all of the regions studied. Acid phophatase showed no significant age-dependent change except in pons. The study demonstrated that all of the lysosomal enzyme activities do not change in parallel with aging, and that the age-dependent change showed the characteristic regional difference. 相似文献
62.
Masashi Ikeda Nakao Iwata Tatsuyo Suzuki Tsuyoshi Kitajima Yoshio Yamanouchi Yoko Kinoshita Norio Ozaki 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2005,(1):90-92
Several lines of evidence indicate that glycogen synthase kinase-3beta (GSK3beta) is one of the candidates for schizophrenia-susceptibility factor. However, it has not been reported the association analysis between GSK3beta gene (GSK3B) and Japanese schizophrenia based on linkage disequilibrium (LD). We provide an association analysis using relatively large samples (381 schizophrenia, and 352 controls) after determination of "tag single nucleotide polymorphisms (SNPs)." In this LD mapping, we selected and genotyped for eight polymorphisms (seven SNPs and one diallelic (CAA)(n) repeat), which covered the entire region of GSK3B, and determined two "tag SNPs." In the following association analysis using these two "tag SNPs," we could not find association with Japanese schizophrenia. Furthermore, we also include subgroup analysis considering age-at-onset and subtypes, neither could we find associations. Because our samples provided quite high power, these results indicate that GSK3B may not play a major role in Japanese schizophrenia. 相似文献
63.
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65.
In vivo labeling of amyloid with BF-108 总被引:3,自引:0,他引:3
Suemoto T Okamura N Shiomitsu T Suzuki M Shimadzu H Akatsu H Yamamoto T Kudo Y Sawada T 《Neuroscience research》2004,48(1):65-74
Detection of aggregated amyloid-beta (Abeta) with a non-invasive imaging modality such as positron emission tomography (PET) was suggested to be ideal for the diagnosis of Alzheimer's disease (AD) prior to the onset of clinical symptoms. We have been searching for imaging probe candidates with a high affinity for aggregated Abeta in vitro and in vivo and high lipophilicity, a characteristic that allows for the permeation of the blood-brain barrier (BBB). As analyzed by Thioflavin T (ThT) assay and octanol/water partition coefficient test (PC), 3-diethylamino-6-(2-fluoroethyl)ethylaminoacridine (BF-108) were found to have high affinity for Abeta aggregates in vitro and high lipophilicity. Intravenously administrated BF-108 labeled Abeta aggregates injected into the amygdala as observed under a fluorescence microscope, showing this compound's permeability of BBB and an ability to label Abeta in vivo. BF-108 also labeled neuritic senile plaques (SPs), neurofibrillary tangles, and amyloid-laden vessels in temporal and hippocampal sections from AD patients. Following intravenous administration of BF-108 to an APP23 transgenic (TG) mouse, in vivo labeling of endogenous plaques was seen in brain sections by fluorescence microscopy. These properties suggest the potential utility of BF-108 for in vivo imaging of AD pathology. 相似文献
66.
Kandori A Yokoe M Sakoda S Abe K Miyashita T Oe H Naritomi H Ogata K Tsukada K 《Neuroscience research》2004,49(2):253-260
To develop a new measurement tool for quantitatively detecting the finger movement of a patient with Parkinson's disease (PD), we designed a magnetic sensing system consisting of a magnetic induction coil, a sensing coil, and a circuit unit. The sensing coil detects the inducted magnetic field that varies with the distance between the two coils, and the detected signals are demodulated in the circuit unit in order to obtain the variation voltage from the oscillation frequency. To obtain a coefficient for converting voltage to distance, we measured the output voltages for seven fixed finger positions of 12 normal volunteers. The voltage differences corresponding to the finger movement in 20 PD patients, six age-matched controls, and 12 normal volunteers were then recorded for 30s. To investigate the velocity and acceleration of the finger movement, we calculated their waveforms from the measured displacement waveform. We also detected the main frequency of the tapping rhythm by using a fast Fourier transform (FFT). The averaged amplitude of each waveform decreased with the disorder in the Hoehn-Yahr (HY) stage, while the averaged tapping frequency of PD patients did not have any correlation with this stage. It can be concluded that this magnetic sensing system can assess finger movement quantitatively. 相似文献
67.
Kida T Nishihira Y Hatta A Wasaka T Nakata H Sakamoto M Nakajima T 《European journal of applied physiology》2003,89(3-4):326-330
We investigated the relationship between somatosensory event-related potentials (ERP) and the variation of reaction time (RT).
For this purpose, we recorded the ERPs (N250 and P300) in fast- and slow-reaction trials during a somatosensory discrimination
task. Strong, standard, and weak target electrical stimuli were randomly delivered to the left median nerve at the wrist with
a random interstimulus interval (900–1,100 ms). All the subjects were instructed to respond by pressing a button with their
right thumb as fast as possible whenever a target stimulus was presented. We divided all the trials into fast- and slow-RT
trials and averaged the data. N250 latency tended to be delayed when the RT was slow, but not significantly. P300 latency
was delayed significantly when the RT was slow, but to a much lesser extent than the RT delay, so we concluded that the change
of RT was not fully determined by the processes reflected by the somatosensory N250 or P300. Furthermore, the larger and earlier
P300 in the fast-RT trials implied that when larger amounts of attentional resources were allocated to a given task, the speed
of stimulus evaluation somewhat increased and RT was shortened to a great extent. N250 amplitude did not significantly vary
in the two RT clusters. In conclusion, the somatosensory N250 reflects active target detection, which is relatively independent
of the modulation of the response speed, whereas the somatosensory P300 could change without manipulation of either the stimulus
or the response processing demand.
Electronic Publication 相似文献
68.
Differential expression of decorin and biglycan genes during palatogenesis in normal and retinoic acid-treated mice. 总被引:1,自引:0,他引:1
Yuxiang Zhang Tetsuji Mori Ken Iseki Seita Hagino Hiromi Takaki Mayumi Takeuchi Tsuyoshi Hikake Choichiro Tase Masahiro Murakawa Sachihiko Yokoya Akio Wanaka 《Developmental dynamics》2003,226(4):618-626
Proteoglycans are involved in secondary palate formation. In the present study, we focused on two small leucine-rich proteoglycans, decorin and biglycan, because they assembled extracellular matrix molecules such as collagens and modulated signaling pathway of transforming growth factor-beta. To investigate the functions of decorin and biglycan in palatogenesis, we compared their mRNA expression patterns between normal palate and retinoic acid-induced cleft palate in mice by using in situ hybridization analysis during the period of embryonic day 13.5 (E13.5) to E15.5. On E13.5, decorin mRNA was expressed in the epithelia and mesenchyme on the nasal side of the developing secondary palate. During the period the palate shelves were fusing (E14.5), decorin mRNA was strongly expressed in the mesenchyme but its expression pattern was asymmetric; decorin mRNA expression area in the nasal side was broader than that in the oral side. The expression of decorin mRNA was hardly detected in the mesenchyme on either side of the medial edge epithelium. After fusion (E15.5), its expression converged to the mesenchyme just around the palatine bone. Biglycan mRNA was ubiquitously distributed throughout the palatal mesenchyme for the mid-gestation period. Its expression area became limited to the ossification area within the palate after the late gestation period. In the retinoic acid-treated mice, the area of the decorin gene expression expanded to the core region of the palate primordium where little signal was observed in control mice. On the other hand, biglycan in the retinoic acid-treated mice did not show remarkable change in its distribution patterns compared with that in the control mice. These findings suggest that decorin and biglycan play distinct roles in palatogenesis, and decorin was more actively involved in the process of secondary palate formation than biglycan. Up-regulation of decorin gene expression in the retinoic acid-treated mice might influence the pathogenesis of cleft palate. 相似文献
69.
Sasaki K Kato M Takahashi T Ochi S Ichinose Y Shiraki K Asano Y Iwanaga M Tsuji T 《Journal of medical virology》2003,70(2):329-335
This study was undertaken to determine whether the specific Th1- or Th2-cell response to varicella-zoster virus was induced predominantly by a mucosal adjuvant, cholera toxin, in mice. A commercially available live varicella vaccine (Oka strain) and cholera toxin or its B subunit were administered simultaneously via the nasal route. Delayed-type hypersensitivity to the Oka vaccine was induced, but the systemic neutralizing antibody response was low. The delayed-type hypersensitivity evoked after a single administration was relatively higher than that on administration three times. When spleen cells from mice immunized once with the vaccine and cholera toxin or its B subunit were restimulated with the live vaccine in vitro, there was greater thymidine uptake and production of interleukin- 2 (IL-2) than controls, but only a low level of IL-4 production. The production of IL-2 induced by the B subunit of cholera toxin was less than that by cholera toxin and a mutant of Escherichia coli enterotoxin on co-immunization with the vaccine in mice. Cholera toxin and its B subunit have been reported to induce predominantly a specific Th2-type T-cell response to various antigens. However, the Oka vaccine is an antigen that polarizes the activation of specific Th1/Th2-type T cells by cholera toxin or its B subunit to the Th1-type side. Cholera toxin and its B subunit are thus useful mucosal adjuvants for inducing cellular immunity to the Oka vaccine similar to Escherichia coli enterotoxin. 相似文献