全文获取类型
收费全文 | 1042篇 |
免费 | 203篇 |
国内免费 | 66篇 |
专业分类
耳鼻咽喉 | 7篇 |
儿科学 | 10篇 |
基础医学 | 392篇 |
口腔科学 | 11篇 |
临床医学 | 18篇 |
内科学 | 97篇 |
皮肤病学 | 11篇 |
神经病学 | 164篇 |
特种医学 | 5篇 |
外科学 | 9篇 |
综合类 | 101篇 |
预防医学 | 33篇 |
眼科学 | 28篇 |
药学 | 321篇 |
中国医学 | 85篇 |
肿瘤学 | 19篇 |
出版年
2024年 | 8篇 |
2023年 | 40篇 |
2022年 | 62篇 |
2021年 | 84篇 |
2020年 | 71篇 |
2019年 | 63篇 |
2018年 | 54篇 |
2017年 | 68篇 |
2016年 | 80篇 |
2015年 | 73篇 |
2014年 | 76篇 |
2013年 | 107篇 |
2012年 | 70篇 |
2011年 | 89篇 |
2010年 | 79篇 |
2009年 | 80篇 |
2008年 | 71篇 |
2007年 | 54篇 |
2006年 | 13篇 |
2005年 | 11篇 |
2004年 | 16篇 |
2003年 | 13篇 |
2002年 | 9篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1999年 | 4篇 |
1998年 | 2篇 |
1997年 | 2篇 |
1996年 | 2篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1992年 | 1篇 |
排序方式: 共有1311条查询结果,搜索用时 15 毫秒
1.
An intact enteric nervous system is required for normal gastrointestinal tract function. Several human conditions result from decreased innervation by enteric neurons; however, the genetic basis of enteric nervous system development and function is incompletely understood. In an effort to increase our understanding of the mechanisms underlying enteric nervous system development, we screened mutagenized zebrafish for changes in the number or distribution of enteric neurons. We also established a motility assay and rescreened mutants to learn whether enteric neuron number is correlated with gastrointestinal motility in zebrafish. We describe mutations isolated in our screen that affect enteric neurons specifically, as well as mutations that affect other neural crest derivatives or have pleiotropic effects. We show a correlation between the severity of enteric neuron loss and gastrointestinal motility defects. This screen provides biological tools that serve as the basis for future mechanistic studies. 相似文献
2.
Isha Jain Christine Stroka Jianying Yan Wei-Min Huang M Kathryn Iovine 《Developmental dynamics》2007,236(9):2668-2674
Fin length in the zebrafish is achieved by the distal addition of bony segments of the correct length. Genetic and molecular data provided evidence that segment growth uses a single pulse of growth, followed by a period of stasis. Examination of cell proliferation during segment growth was predicted to expose a graphical model consistent with a single burst of cell division (e.g., constant, parabolic, or exponential decay) during the lengthening of the distal-most segment. Cell proliferation was detected either by labeling animals with bromodeoxyuridine (during S-phase) or monitoring histone3-phosphate (mitosis). Results from both methods revealed that the number of proliferating cells fluctuates in apparent pulses as a segment grows (i.e., during the growth phase). Thus, rather than segment size being the result of a single burst of proliferation, it appears that segment growth is the result of several pulses of cell division that occur approximately every 60 microns (average segment length approximately 250 microns). These results indicate that segment lengthening requires multiple pulses of cell proliferation. 相似文献
3.
4.
Ping Li Sitar Shah Luoxiu Huang Aprell L Carr Yan Gao Christine Thisse Bernard Thisse Lei Li 《Developmental dynamics》2007,236(5):1339-1346
Dopamine plays important roles in the regulation of central nervous system (CNS) development and functions. In vertebrates, two families of dopamine receptors, collectively known as dopamine D1 and D2 receptors, have been identified. Recently, dopamine receptors have been targeted by pharmacological and therapeutic studies of neurological disorders, such as Parkinson's disease. Here, we report a study on the molecular characterization of dopamine D1 receptor in zebrafish (Danio rerio). We cloned the full-length cDNA of a zebrafish dopamine D1 receptor, designated as drd1. The sequence of drd1 shares high homology to the sequences of dopamine D1 receptors in mammalian, amphibian, and other fish species. drd1 is expressed in the CNS. The first drd1 expression was observed at approximately 30 hours postfertilization, at which time the expression was seen in the developing diencephalon and hindbrain. In developing retinas, the expression of drd1 was detected in the inner nuclear layer with the exception of the marginal zones. In adult retinas, drd1 expression was detected in most cell types in the inner and outer nuclear layers as well as ganglion cell layer. Differential expression of drd1 in developing and adult retinas may play various roles in regulating visual system functions. 相似文献
5.
Ann De Mazière Leon Parker Suzanne Van Dijk Weilan Ye Judith Klumperman 《Developmental dynamics》2008,237(3):580-591
The endothelial cell (EC) -specific secreted protein EGFL7 is important for tubulogenesis in newly forming blood vessels. We studied its role in vascular tube formation by a quantitative ultrastructural analysis of Egfl7-knockdown zebrafish embryos. At 24 hours postfertilization, the endothelia of dorsal aorta (DA) and posterior cardinal vein (PCV) were correctly anchored to the hypochord and endoderm, respectively, but failed to expand into the vascular area. This resulted in vessels with reduced or split lumen and open sheets of ECs. Concomitantly, the organization of hematopoietic cells-identified by the presence of previously undescribed membrane tubules-between DA and PCV, and within the vessels, was severely disturbed. Strikingly, ectopic cell junctions occurred across the obstructed vessel lumen, on the luminal EC surfaces, which in control conditions never display junctions of any kind. These data suggest that Egfl7 provides ECs with a cue for their extension into the vascular area and in establishing EC cell polarity. 相似文献
6.
Martina Milanetto Natascia Tiso Paola Braghetta Dino Volpin Francesco Argenton Paolo Bonaldo 《Developmental dynamics》2008,237(1):222-232
Emilins are a family of extracellular matrix proteins with common structural organization and containing a characteristic N-terminal cysteine-rich domain. The prototype of this family, Emilin-1, is found in human and murine organs in association with elastic fibers, and other emilins were recently isolated in mammals. To gain insight into these proteins in lower vertebrates, we investigated the expression of emilins in the fish Danio rerio. Using sequence similarity tools, we identified eight members of this family in zebrafish. Each emilin gene has two paralogs in zebrafish, showing conserved structure with the human ortholog. In situ hybridization revealed that expression of zebrafish emilin genes is regulated in a spatiotemporal manner during embryonic development, with overlapping and site-specific patterns mostly including mesenchymal structures. Expression of certain emilin genes in peculiar areas, such as the central nervous system or the posterior notochord, suggests that they may play a role in key morphogenetic processes. 相似文献
7.
Parith Wongkittichote Tae-Ik Choi Oc-Hee Kim Kacie Riley Dwight Koeberl Vinodh Narayanan Keri Ramsey Chris Balak Charles E. Schwartz Anna Maria Cueto-Gonzalez Francina Munell Casadesus Cheol-Hee Kim Marwan S. Shinawi 《Clinical genetics》2023,103(2):167-178
ZC4H2 (MIM# 300897) is a nuclear factor involved in various cellular processes including proliferation and differentiation of neural stem cells, ventral spinal patterning and osteogenic and myogenic processes. Pathogenic variants in ZC4H2 have been associated with Wieacker-Wolff syndrome (MIM# 314580), an X-linked neurodevelopmental disorder characterized by arthrogryposis, development delay, hypotonia, feeding difficulties, poor growth, skeletal abnormalities, and dysmorphic features. Zebrafish zc4h2 null mutants recapitulated the human phenotype, showed complete loss of vsx2 expression in brain, and exhibited abnormal swimming and balance problems. Here we report 7 new patients (four males and three females) with ZC4H2-related disorder from six unrelated families. Four of the 6 ZC4H2 variants are novel: three missense variants, designated as c.142T>A (p.Tyr48Asn), c.558G>A (p.Met186Ile) and c.602C>T (p.Pro201Leu), and a nonsense variant, c.618C>A (p.Cys206*). Two variants were previously reported : a nonsense variant c.199C>T (p.Arg67*) and a splice site variant (c.225+5G>A). Five patients were on the severe spectrum of clinical findings, two of whom had early death. The male patient harboring the p.Met186Ile variant and the female patient that carries the p.Pro201Leu variant have a relatively mild phenotype. Of note, 4/7 patients had a tethered cord that required a surgical repair. We also demonstrate and discuss previously under-recognized phenotypic features including sleep apnea, arrhythmia, hypoglycemia, and unexpected early death. To study the effect of the missense variants, we performed microinjection of human ZC4H2 wild-type or variant mRNAs into zc4h2 null mutant zebrafish embryos. The p.Met186Ile mRNA variant was able to partially rescue vsx2 expression while p.Tyr48Asn and p.Pro201Leu mRNA variants were not. However, swimming and balance problems could not be rescued by any of these variants. These results suggest that the p.Met186Ile is a hypomorphic allele. Our work expands the genotypes and phenotypes associated with ZC4H2-related disorder and demonstrates that the zebrafish system is a reliable method to determine the pathogenicity of ZC4H2 variants. 相似文献
8.
9.
TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) is a reproductive toxicant and endocrine disruptor in nearly all vertebrates; however, the mechanisms by which TCDD alters the reproductive system is not well understood. The zebrafish provides a powerful vertebrate model system to investigate molecular mechanisms by which TCDD affects the reproductive system, but little is known regarding reproductive toxic response of zebrafish following chronic, sublethal exposure to TCDD. Here we investigate the accumulation of TCDD in selected tissues of adult female zebrafish and maternal transfer to offspring following dietary exposure to TCDD (0.08-2.16 ng TCDD/fish/day). TCDD accumulated in tissues of zebrafish in a dose- and time-dependent manner, except for brain. Chronic dietary exposure resulting in the accumulation of 1.1-36 ng/g fish did not induce an overt toxic response or suppress spawning activity. The ovosomatic index was impacted with an accumulation of as little as 0.6 ng/g fish, and 10% of the females showed signs of ovarian necrosis following accumulation of approximately 3 ng/g TCDD. Offspring health was impacted with an accumulation of as little as 1.1 ng/g female; thus the lowest observed effect level (LOEL) for reproductive toxicity in female zebrafish is approximately 0.6-1.1 ng/g fish. Maternal transfer resulted in the accumulation of 0.094-1.2 ng/g, TCDD, which was sufficient to induce the typical endpoints of larval TCDD toxicity, commonly referred to as blue sac syndrome. This study provides the necessary framework to utilize the zebrafish model system for further investigations into the molecular mechanisms by which TCDD exerts its reproductive toxic responses. 相似文献
10.
目的 基于模式生物斑马鱼结合网络药理学,研究枳壳的活性成分水合橙皮内酯增强免疫作用及作用机制。方法 建立2种斑马鱼免疫低下模型:以雷帕霉素建立尾部中性粒细胞数目减少模型,以酒石酸长春瑞滨建立静脉血管中巨噬细胞荧光强度减弱模型,检测水合橙皮内酯(10、20、50、100、200 μg·mL-1)各给药组斑马鱼尾部中性粒细胞数目、斑马鱼尾部静脉血管中巨噬细胞荧光强度,计算中性粒细胞增长率和巨噬细胞改善率。基于网络药理学预测水合橙皮内酯增强免疫作用的机制,使用 Pharm Mapper、中药系统药理学数据库与分析平台(TCMSP)进行水合橙皮内酯靶点筛选,运用Gene Cards数据库和 OMIM数据库检索增强免疫相关靶点,运用 Venny2.1将上述两组靶点取交集后导入 String数据库进行蛋白质-蛋白质相互作用(PPI)分析,进行基因本体(GO)功能富集分析和京都基因与基因组百科全书(KEGG)通路富集分析,在 Cytoscape3.9.1软件中构建水合橙皮内酯的增强靶点 PPI网络,并以节点度值的中位数筛选关键靶点。结果 与模型组相比,水合橙皮内酯可显著增加斑马鱼尾部中性粒细胞数目(P<0.01、0.001)、静脉血管中巨噬细胞荧光强度(P<0.05),证明水合橙皮内酯具有抗雷帕霉素、酒石酸长春瑞滨引起的免疫力低下作用,呈剂量相关性。水合橙皮内酯增强免疫的作用机制可能与 AKT1、EGFR、SRC、MMP9、ESR1等关键靶点及 PI3K-Akt、Rap1、AGE-RAGE等信号通路有关。结论 水合橙皮内酯具有增强免疫作用,可能通过调控PI3K-Akt、Rap1、AGE-RAGE等信号通路发挥作用。 相似文献