全文获取类型
收费全文 | 224059篇 |
免费 | 20765篇 |
国内免费 | 15643篇 |
学科分类
医药卫生 | 260467篇 |
出版年
2024年 | 732篇 |
2023年 | 3651篇 |
2022年 | 9448篇 |
2021年 | 11893篇 |
2020年 | 8852篇 |
2019年 | 7679篇 |
2018年 | 8183篇 |
2017年 | 7247篇 |
2016年 | 6781篇 |
2015年 | 10480篇 |
2014年 | 12847篇 |
2013年 | 10968篇 |
2012年 | 16309篇 |
2011年 | 18233篇 |
2010年 | 10745篇 |
2009年 | 8344篇 |
2008年 | 11295篇 |
2007年 | 11297篇 |
2006年 | 11397篇 |
2005年 | 11476篇 |
2004年 | 7117篇 |
2003年 | 6748篇 |
2002年 | 5626篇 |
2001年 | 5004篇 |
2000年 | 5421篇 |
1999年 | 5774篇 |
1998年 | 3562篇 |
1997年 | 3552篇 |
1996年 | 2845篇 |
1995年 | 2626篇 |
1994年 | 2158篇 |
1993年 | 1385篇 |
1992年 | 1901篇 |
1991年 | 1602篇 |
1990年 | 1293篇 |
1989年 | 1098篇 |
1988年 | 1016篇 |
1987年 | 892篇 |
1986年 | 728篇 |
1985年 | 525篇 |
1984年 | 336篇 |
1983年 | 242篇 |
1982年 | 149篇 |
1981年 | 145篇 |
1980年 | 111篇 |
1979年 | 142篇 |
1978年 | 49篇 |
1977年 | 53篇 |
1975年 | 57篇 |
1974年 | 56篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
961.
酵母双杂合系统AD端阴离子交换蛋白C-末端表达质粒的构建 总被引:2,自引:0,他引:2
利用PCR方法,从阴离子交换蛋白1(AE1)全长cDNA中扩增出约350bp c末端cDNA片段,测序后将其克隆至pGADT7载体上,用醋酸锂法构建好的pADT7-AE1-c末端转染酵母菌HA109,观察其在选择性培养基上的表达情况。结果表明,获得了530bp AE1c-末端cDNA,pGADT7-AE1-c末端对酵母无毒性,不能激活检测基因,可作为酵母双杂合系统中的靶基因。 相似文献
962.
音乐疗法治疗慢性精神分裂症疗效分析 总被引:6,自引:0,他引:6
目的 观察音乐疗法对慢性精神分裂症的治疗效果。方法 住院慢性精神分裂症患者64例,随机分为实验组和对照组,各32例,观察8周,以BPRS、SANS量表评定疗效。结果 两组患者BPRS、SANS评分差异均有显著性意义。结论 音乐疗法对慢性精神分裂症病人的康复治疗有一定疗效。 相似文献
963.
Xiao Y Zhang Wing Y Chan Bruce M Whitney Dai M Fan John H S Chow Yong Liu Enders K W Ng Sheung C S Chung 《Diagnostic molecular pathology》2002,11(3):135-139
Helicobacter pylori (HP) infection induces expression of IL-8 and IL-10 in benign gastric epithelium. This study compared the expression of cytokines in CD4+ and CD8+ lymphocyte subsets of peripheral blood lymphocytes (PBL), benign mucosal lymphocytes (ML), and tumor infiltrative lymphocytes (TIL) as well as in the benign and malignant epithelial cells of the same patient, with respect to the presence of HP infection, lymph node metastases, and tumor histologic type. The mRNA of the cytokines was measured by a semiquantitative RT-PCR method. The levels were ranked and compared using the Wilcoxon sign-ranked test. Compared with CD8+ ML, the CD8+ TIL expresses higher levels of IL-6 and IL-8 but lower level of IL-4 in patients with lymph node metastases. In patients with HP infection, expression of IL-8 and IL-10 was higher in the gastric carcinoma cells than in the benign epithelial cells while expression of IL-6 and IL-8 were higher in CD8+ TIL than CD8+ ML. Overexpression of IL-8 in HP associated gastric carcinomas suggested that they might have arisen from HP-infected epithelial cells. 相似文献
964.
Ar+ ion beam sputtering/mixing deposition was used to produce thin calcium phosphate coatings on titanium substrate from hydroxyl-poly-calcium sodium phosphate (HPPA) and HPPA + Ti targets. Three types of coatings (one type of monolayer coating and two types of functionally graded coating) were manufactured. It was found that as-sputtered coatings were amorphous. No distinct hydroxyl band was observed in the FTIR spectra, but new absorption bands were determined for CO3(2-), which resulted during the deposition process. Compositional gradients from the surface to the interior (i.e. adjacent to the substrate) were achieved for the functionally graded coatings. Post-deposition heat treatment indicated that the bonding strength between the coating and the substrate was improved by the use of functionally graded structures. 相似文献
965.
以甲基丙烯酸羟乙酯为原料,过硫酸铵/偏重亚硫酸钠为引发体系,二甲基丙烯酸三乙二醇酯为交联剂,采用溶液聚合法制备了聚甲基丙烯酸羟乙酯水凝胶(PHEMA)人工晶状体材料。系统考察了聚合反应时间、温度及引发剂和交联剂的用量等对该水凝胶材料机械强度、平衡水含量(EWC)的影响,并对PHEMA水凝胶的结构和光学性能进行了表征。实验结果表明,PHEMA水凝胶的最佳合成条件为:引发剂0.5wt%,交联剂1.0wt%,反应温度40℃,反应时间36h。在此条件下制备的PHEMA水凝胶的拉伸强度达到0.57MPa,邵氏A硬度为23.0,平衡含水量超过40%,透光率≥97%。 相似文献
966.
Yu-Li Liu Cathy Shen-Jang Fann Chih-Min Liu Jer-Yuarn Wu Shuen-Iu Hung Hung-Yu Chan Jiahn-Jyh Chen Chin-Yu Lin Shih-Kai Liu Ming H Hsieh Tzung-Jeng Hwang Wen-Chen Ouyang Chun-Ying Chen Jin-Jia Lin Frank Huang-Chih Chou Ching-Mo Chueh Wei-Ming Liu Ming-Min Tsuang Stephen V Faraone Ming T Tsuang Wei J Chen Hai-Gwo Hwu 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2006,(4):418-420
Several studies have suggested that the regulator of G-protein signaling 4 (RGS4) may be a positional and functional candidate gene for schizophrenia. Three single nucleotide polymorphisms (SNP) located at the promoter region (SNP4 and SNP7) and the intron 1 (SNP18) of RGS4 have been verified in different ethnic groups. Positive results have been reported in these SNPs with different numbers of SNP combinatory haplotypes. In this study, these three SNP markers were genotyped in 218 schizophrenia pedigrees of Taiwan (864 individuals) for association analysis. Among these three SNPs, neither SNP4, SNP7, SNP18 has shown significant association with schizophrenia in single locus association analysis, nor any compositions of the three SNP haplotypes has shown significantly associations with the DSM-IV diagnosed schizophrenia. Our results fail to support the RGS4 as a candidate gene for schizophrenia when evaluated from these three SNP markers. 相似文献
967.
Xiao Liu Xiaohong Meng Lizhu Yang Yanling Long Yu Fujinami‐Yokokawa Jiayun Ren Toshihide Kurihara Kazuo Tsubota Kazushige Tsunoda Kaoru Fujinami Shiying Li East Asia Inherited Retinal Disease Society Study Group 《American journal of medical genetics. Part C, Seminars in medical genetics》2020,184(3):694-707
Stargardt disease 1 (STGD1) is the most prevalent retinal dystrophy caused by pathogenic biallelic ABCA4 variants. Forty‐two unrelated patients mostly originating from Western China were recruited. Comprehensive ophthalmological examinations, including visual acuity measurements (subjective function), fundus autofluorescence (retinal imaging), and full‐field electroretinography (objective function), were performed. Next‐generation sequencing (target/whole exome) and direct sequencing were conducted. Genotype grouping was performed based on the presence of deleterious variants. The median age of onset/age was 10.0 (5–52)/29.5 (12–72) years, and the median visual acuity in the right/left eye was 1.30 (0.15–2.28)/1.30 (0.15–2.28) in the logarithm of the minimum angle of resolution unit. Ten patients (10/38, 27.0%) showed confined macular dysfunction, and 27 (27/37, 73.7%) had generalized retinal dysfunction. Fifty‐eight pathogenic/likely pathogenic ABCA4 variants, including 14 novel variants, were identified. Eight patients (8/35, 22.8%) harbored multiple deleterious variants, and 17 (17/35, 48.6%) had a single deleterious variant. Significant associations were revealed between subjective functional, retinal imaging, and objective functional groups, identifying a significant genotype–phenotype association. This study illustrates a large phenotypic/genotypic spectrum in a large well‐characterized STGD1 cohort. A distinct genetic background of the Chinese population from the Caucasian population was identified; meanwhile, a genotype–phenotype association was similarly represented. 相似文献
968.
Jihai Xu Jing Wu Xiaofeng Teng Libing Cai Huizong Yuan Xiaokun Chen Mu Hu Xin Wang Ning Jiang Hong Chen 《American journal of medical genetics. Part A》2020,182(9):2117-2123
Polydactyly and syndactyly are digital abnormalities in limb‐associated birth defects usually caused by genetic disorders. In this study, a five‐generation Chinese pedigree was found with triphalangeal thumb polysyndactyly syndrome (TPTPS), showing an autosomal dominant pattern of inheritance. We utilized linkage analysis and whole genome sequencing (WGS) for the genetic diagnosis of this pedigree. Linkage analysis was performed using a genome‐wide single nucleotide polymorphism (SNP) chip and three genomic regions were identified in chromosomes 2, 6, and 7 with significant linkage signals. WGS discovered a copy number variation (CNV) mutation caused by a large duplication region at the tail of chromosome 7 located in exons 1–5 of the LMBR1 gene, including the zone of polarizing activity regulatory sequence (ZRS), with a length of approximately 180 kb. A real‐time polymerase chain reaction (PCR) assay confirmed the duplication. The findings of our study supported the notion that large duplications including the ZRS caused TPTPS. Our study showed that linkage analysis in combination with WGS could successfully identify the disease locus and causative mutation in TPTPS, which could help elucidate the molecular mechanisms and genotype–phenotype correlations in polydactyly. 相似文献
969.
970.
S.-H. Kung S.-F. Wang C.-W. Huang C.-C. Hsu H.-F. Liu J.-Y. Yang 《Clinical microbiology and infection》2007,13(8):782-787
Enterovirus 71 (EV71) infections can lead to devastating clinical outcomes in children, with an increasing number of severe cases worldwide. The genetic and antigenic variability of EV71 strains isolated in Taiwan in 1998-2005 was evaluated using partial nucleotide sequence analysis of the VP1 gene and the neutralisation assay. Phylogenetic analyses revealed that most EV71 isolates from the 1998 epidemic belonged to sub-genogroup C2, with a minority belonging to sub-genogroup B4. Between 1999 and 2003, isolates belonging to sub-genogroup B4 predominated, followed by a change to sub-genogroup C4 in 2004 and 2005. Antibodies raised in rabbits or collected from infected patients were able to neutralise EV71 virus stocks at high dilutions, regardless of the sub-genogroup of the virus being challenged. The presence of phylogenetically distinct yet antigenically similar populations of EV71 in Taiwan is of concern in the context of herd immunity and vaccine development. 相似文献