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71.
BACKGROUND. The fortification of milk and infant formula with vitamin D has had an important role in eliminating rickets in children and osteomalacia in adults. A recent outbreak of vitamin D intoxication caused by drinking milk fortified with excess vitamin D has led to questions about the level of vitamin D in milk from other producers. METHODS. We used high-performance liquid chromatography to measure vitamin D in samples of 13 brands of milk with various fat contents and 5 brands of infant formula purchased at random from local supermarkets in five Eastern states. RESULTS. Only 12 (29 percent) of the 42 samples of the 13 brands of milk and none of the 10 samples of the 5 brands of infant formula contained 80 to 120 percent of the amount of vitamin D stated on the label. Twenty-six of the 42 milk samples (62 percent) contained less than 80 percent of the amount claimed on the label. No vitamin D was detected in 3 of the 14 samples of skim milk tested (lower limit of assay, 4.7 IU per quart [5.0 IU per liter]). One milk sample labeled as containing vitamin D2 (ergocalciferol) contained vitamin D3 (cholecalciferol). Seven of the 10 samples of infant formula contained more than 200 percent of the amount stated on the label; the sample with the highest concentration contained 419 percent of the stated amount. None of the samples of infant formula contained less than the amount stated. CONCLUSIONS. Milk and infant-formula preparations rarely contain the amount of vitamin D stated on the label and may be either underfortified or overfortified. Since both underfortification and overfortification are hazardous, better monitoring of the fortification process is needed. 相似文献
72.
73.
Sun Y Shao H Li Z Liu J Gao L Peng X Meng Y Li W 《International journal of molecular medicine》2004,14(6):971-975
The advancement in gene knockout and transgenesis have brought about enormous improvement in our understanding of mouse embryogenesis in the past decade or so. On the other hand, relatively little is known about human embryogenesis due largely to the lack of easy access to human embryos and tissues for biomedical studies. We have previously isolated a novel zinc finger gene, ZNF268, from a 3-week-old human embryo cDNA library in an effort to identify genes important for human embryonic development. To investigate the potential involvement of ZNF268 in human embryogenesis, we report here the spatial and temporal regulation of its expression during development. Northern blot and Western blot analyses revealed that ZNF268 is expressed in early embryos, predominantly, if not exclusively, in fetal liver with little detectable expression in other fetal organs. Interestingly, unlike most zinc finger proteins, ZNF268 protein was found to be localized mainly in the cytoplasm of embryonic hepatocytes. This subcellular localization was substantiated by the localization of EGFP-ZNF268 fusion protein overexpressed in the transfected COS7 cells. These results suggest that ZNF268 plays a role in early human liver development most likely by functioning through a cytoplasmic mechanism. 相似文献
74.
Anthony J Sharp Paul E Polak Vittoria Simonini Shao X Lin Jill C Richardson Ernesto R Bongarzone Douglas L Feinstein 《Journal of neuroinflammation》2008,5(1):33
Background
The purinergic receptor P2x7 is expressed on myeloid cells as well as on CNS glial cells, and P2x7 activation has been shown to increase both glial and T-cell activation. These properties suggest a role in the development of autoimmune disease including multiple sclerosis. 相似文献75.
Holm-Hansen C Stern B Rustad S Shao J Asjö B 《APMIS : acta pathologica, microbiologica, et immunologica Scandinavica》2000,108(9):608-616
The aim of this study was to determine HIV-1 V3 sequences, in vitro biological characteristics and co-receptor usage of virus isolates from Tanzania. Virus was isolated from 14 of 17 samples investigated. Four of the isolates induced syncytia in MT-2 cells and used the CXCR4 co-receptor, while the remaining 10 isolates used the CCR5 co-receptor characteristic of non-MT-2 tropic viruses. One of the four MT-2 tropic isolates also used the CCR5 and CCR3 co-receptors. Proviral DNA was detected in all 14 isolates and PCR products were subjected to DNA sequencing. Unambiguous V3 amino acid sequences were obtained from 11 amplificates. Phylogenetic analysis indicated that these sequences were divergent and clustered in HIV-1 subtypes A, C or D. Sequences from the viruses that induced syncytia in MT-2 cells presented characteristic V3 phenotype-associated amino acids. Results of co-receptor analysis are in concordance with the isolate phenotype as determined by replication and induction of syncytia in MT-2 cells. The considerable diversity illustrated by a limited number of isolates from Tanzania is in accordance with reports from other regions of Africa. 相似文献
76.
YiFeng Li ChunHong Shao Dandan Zhang Min Zhao Ling Lin Pengrong Yan Yuying Xie Kaida Jiang Li Jin 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2006,(3):269-273
Heroin dependence is resulted from the interaction between multiple genetic and environmental factors. Subjective craving is considered to be a central phenomenon, which contributes to the continuation of drug use in active abuser and the occurrence of relapse in detoxified abusers. Dopamine pathway has been implicated in the cue-elicited craving for a variety of addictive substances. The objective of this study was to test the hypothesis that heroin addicts carrying specific variants in dopamine-related genes would have higher levels of craving following exposure to a heroin-related cue. Craving induced by a series of exposure to heroin-related cue was assessed in a cohort of Chinese heroin abuser (n = 420) recruited from natural abstinence center at Shanghai. Significantly stronger cue-elicited heroin craving was found in individuals carrying D2 dopamine receptor gene (DRD2) TaqI RFLP A1 allele than the non-carriers (P < 0.001). Furthermore, we did not observed significant association of cue-elicited craving with the nine-repeat allelic variants in dopamine transporter gene (DAT) SLC6A3 and with the dinucleotide repeat polymorphism (DRP) 148bp allele in D5 dopamine receptor gene (DRD5). The results of our study suggest that human dopamine pathway be involved in cue-induced heroin craving, and indicate a potential genetic risk factor for persistent heroin behavior and relapse. 相似文献
77.
78.
Shao L Shinzawa H Zhang X Smith DB Watanabe H Mitsuhashi H Saito K Saito T Togashi H Takahashi T 《Virus genes》2000,21(3):215-221
The extent of population diversity among GB virus C (GBV-C)/hepatitis G virus (HGV) within a persistently infected individual (Iw) was investigated by sequence analysis of multiple clones generated from polymerase chain reaction (PCR)-amplified products of cDNA analogous to fragments of 5 non-coding region (5NC), envelope region 1/2 (E1/E2) and non-structural region 3 (NS3) of viral genome. Although nucleotide substitutions were more common in coding regions than in the 5NC region, there was no region corresponding to the hypervariable region of hepatitis C virus in the E1/E2 region. Transition substitution exceeded transversion by 7 to 12-fold, and 79.4% of substitutions were synonymous. This bias against substitutions producing amino acid replacements and the use of Pfu DNA polymerase with an error rate 10 times lower than the observed frequency of substitution, suggests that most substitutions were not artefactual. This data suggests that individual genomes of HGV within an infected individual may differ from each other at 0.23–0.84% nucleotide position and at 0.42–0.61% amino acid position. 相似文献
79.
本文应用放射免疫测定法,检测了单克隆抗体(λ-44-5-15,λ26-4-15,SMb,OKT10和抗B)作用于相应白血病瘤细胞后细胞内cAMP、cGMP的含量变化。结果发现:抗原、抗体比例在80∶1时经McAb作用16~24h后,瘤细胞内cAMP含量明显高于对照组,cGMP含量明显低于对照组(P<0002-0001)。从而提示:McAb可通过对细胞膜作用,调控细胞内cAMP和cGMP的水平。本文还对McAb作用浓度及作用时间进行了探讨。 相似文献
80.
目的 分析2010—2019年我国居民4类主要慢性病(恶性肿瘤、糖尿病、心血管疾病和呼吸系统疾病)的死亡率变化趋势及影响其变化的因素。方法 数据来自全国疾病监测系统死亡数据资料,运用Joinpoint模型计算死亡率的年度平均变化百分比(AAPC)和年度变化百分比(APC),并用死亡率差别分解法解释该趋势变化的影响因素。结果 2010—2019年我国居民四种慢性病的粗死亡率由456.22/10万上升至556.00/10万,标化死亡率由541.40/10万降至419.83/10万。死亡率变化是人口构成和其它危险因素共同作用的结果,其中人口构成因素促进了恶性肿瘤、糖尿病、心血管疾病和呼吸系统疾病死亡率的上升,贡献值分别48.52/10万、5.12/10万、135.28/10万、38.39/10万;其它危险因素促进糖尿病死亡率上升,而驱使另3种慢性病死亡率下降,贡献值分别- 23.11/10万、1.27/10万、- 55.87/10万、- 49.83/10万。结论 我国综合防控重大慢性病造成的死亡取得一定成效,但与此同时随着老龄化加剧,上述疾病依然是引发死亡的主要原因,卫生健康事业发展面临严峻挑战。 相似文献