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141.
Xueying Liang Nathalie Schnetz-Boutaud Jackie Bartlett Melissa J. Allen Harry Gwirtsman Don E. Schmechel Regina M. Carney John R. Gilbert Margaret A. Pericak-Vance Jonathan L. Haines 《Annals of human genetics》2008,72(1):141-144
SNP rs498055 in the predicted gene LOC439999 on chromosome 10 was recently identified as being strongly associated with late-onset Alzheimer disease (LOAD). This SNP falls within a chromosomal region that has engendered continued interest generated from both preliminary genetic linkage and candidate gene studies. To independently evaluate this interesting candidate SNP we examined four independent datasets, three family-based and one case-control. All the cases were late-onset AD Caucasian patients with minimum age at onset ≥ 60 years. None of the three family samples or the combined family-based dataset showed association in either allelic or genotypic family-based association tests at p < 0.05. Both original and OSA two-point LOD scores were calculated. However, there was no evidence indicating linkage no matter what covariates were applied (the highest LOD score was 0.82). The case-control dataset did not demonstrate any association between this SNP and AD (all p-values > 0.52). Our results do not confirm the previous association, but are consistent with a more recent negative association result that used family-based association tests to examine the effect of this SNP in two family datasets. Thus we conclude that rs498055 is not associated with an increased risk of LOAD. 相似文献
142.
Under various clinical situations, it is desirable to modify the original treatment plan to better suit the clinical goals. In this work, a method to help physicians modify treatment plans based on their clinical preferences is proposed. The method uses a weighted quadratic dose objective function. The commonly used organ-/ROI-based weighting factors are expanded to a set of voxel-based weighting factors in order to obtain greater flexibility in treatment plan modification. Two different but equivalent modification schemes based on Rustem's quadratic programming algorithms--modification of a weighting matrix and modification of prescribed doses--are presented. Case studies demonstrated the effectiveness of the two methods with regard to their capability to fine-tune treatment plans. 相似文献
143.
Measurements of intrafollicular pressures in the rabbit ovary 总被引:1,自引:0,他引:1
144.
Adrian I. Katz Harry K. Genant Barbara L. Corsaw 《Pflügers Archiv : European journal of physiology》1971,330(2):136-148
Summary The role of renal Na+–K+-ATPase in the acute changes in sodium reabsorption caused by isotonic volume expansion was evaluatedin vivo andin vitro in the rat and the dog. Duringin vivo volume expansion with isotonic saline in the rat, renal medullary Na+–K+-ATPase specific activity increased, while the simultaneously determined cortical Na+–K+-ATPase specific activity and kinetics remained unchanged. Furthermore, experimentsin vitro failed to demonstrate a circulating inhibitor of renal Na+–K+-ATPase both in plasma dialysates from volume-expanded rats and in plasma dialysates concentrated 20-fold by ultrafiltration from volume-expanded dogs. These results suggest that the decreased proximal tubular reabsorption of sodium during volume expansion is not mediated by inhibition of renal cortical Na+–K+-ATPase. The acute increment in medullary Na+–K+-ATPase observed could represent an adaptive response to increased sodium reabsorption by the loops of Henle, and raises the possibility that this enzyme may participate in relatively rapid adjustments in the transport of sodium by the renal tubule. 相似文献
145.
146.
A low molecular weight (LMW) antigen of Eimeria tenella, initially identified using a murine monoclonal antibody (mAb C34F1) raised against E. tenella sporozoites, was partially characterized using enzymatic degradation, solvent extraction, and immunization into various inbred
lines of mice. The LMW antigen could be isolated using Folch extraction (methanol/chloroform/water) and the epitope recognized
by mAb C34F1 was resistant to degradation by α-amylase, pronase, and proteinase K, but was sensitive to sodium m-periodate treatment or digestion using mixed glycosidases (from Turbo cornutus). These observations suggest that the antigenic epitope recognized by mAb C34F1 is carbohydrate-dependent and, based on our ability to isolate the LMW antigen by Folch extraction, the epitope probably
resides on a polar glycolipid. The inability of sporozoite-immunized nude mice to elicit a serum antibody response to this
molecule indicates that it acts as a T-dependent antigen. Furthermore, sporozoite-immunized male CBA/N mice (with an X-linked
immunodeficiency) also failed to elicit a serum antibody response to this molecule, which is consistent with a carbohydrate
antigenic epitope. We propose that this antigenic molecule be designated ET-GL1 to reflect its origin and probable structure
(E. tenella glycolipid 1).
Received: 30 June 1999 / Accepted: 2 December 1999 相似文献
147.
Kathryn Leary Harry H. Yim Lu Bing Zhou Rose E. Sekulovich Rozanne M. Sandri-Goldin 《Virus genes》1989,3(1):57-68
To determine the role of the HSV-1 genome structure and environment on the regulation of gene expression, we constructed recombinant viruses containing a heterologous gene inserted into either the immediate early ICP0 or late glycoprotein C (gC) genes of HSV-1. The heterologous gene consisted of the SV40 early promoter (without enhancer sequences) linked to the coding sequences for the bacterial chloramphenicol acetyl transferase (CAT). The expression of CAT was examined in Vero cells infected with either virus (named ICP0-CAT and Sph 6). For both recombinants, expression of CAT was not dependent upon prior viral protein synthesis. The kinetics of expression of CAT-specific mRNA resembled that of the HSV-1 genes into which CAT was inserted. Primer extension analysis revealed that the SV40 promoter is recognized and used when placed in cis in two different HSV-1 genome locations, and Northern hybridization experiments confirmed that the heterologous gene was expressed in the absence of prior viral protein synthesis. Therefore, this gene was not regulated as strictly as an HSV-1 gene, but was influenced by the environment into which it was placed, presumably by factors that are present when the normal viral gene is on. 相似文献
148.
Treiber FA Turner JR Davis H Strong WB 《International journal of behavioral medicine》1997,4(4):278-291
Two hundred forty-six children (96 Whites, of whom 51 were mates; 150 African- Americans, of whom 69 were males) with a familial
history of essential hypertension (EH) were re-evaluated 5 years after an initial evaluation. During the initial visit, anthropometric,
demographic, and resting cardiovascular (CV) parameters (designated initial baseline levels) were assessed. These CV parameters
(systolic and diastolic blood pressure [BP], heart rate, cardiac output index [CI], and total peripheral resistance index
[TPRI]) were also measured during postural challenge, a video game challenge, and a cold pressor task. At follow-up, resting
CV parameters were again evaluated, and designated as follow-up resting levels. Moderate temporal stability (r range = .43-.56) was observed for all resting CV parameters. Mean stress responses for each CV parameter for all 3 stressors
during the initial visit were positively related to the respective CV follow-up resting level. BP stress responses to postural
change and video game challenge were found to be significant independent predictors of future resting BP after controlling
for standard EH risk factors. Follow-up resting CI was not predicted by any stress responses, whereas follow-up resting TPRI
was predicted by TPRI responses to the video game after controlling for standard EH risk Factors. These results contrast with
those from an earlier 1-year follow-up. where stress responses for neither CI nor TPRI predicted follow-up resting levels.
It appears that, as children get older. TPRI stress responses play a stronger role in vasoconstrictive function.
This research was supported by National Institutes of Health Grant HL41781. 相似文献
149.
150.