全文获取类型
收费全文 | 4640篇 |
免费 | 191篇 |
国内免费 | 52篇 |
专业分类
耳鼻咽喉 | 79篇 |
儿科学 | 61篇 |
妇产科学 | 96篇 |
基础医学 | 803篇 |
口腔科学 | 78篇 |
临床医学 | 369篇 |
内科学 | 976篇 |
皮肤病学 | 86篇 |
神经病学 | 247篇 |
特种医学 | 375篇 |
外科学 | 473篇 |
综合类 | 141篇 |
一般理论 | 4篇 |
预防医学 | 193篇 |
眼科学 | 19篇 |
药学 | 497篇 |
1篇 | |
中国医学 | 64篇 |
肿瘤学 | 321篇 |
出版年
2023年 | 37篇 |
2022年 | 84篇 |
2021年 | 136篇 |
2020年 | 72篇 |
2019年 | 82篇 |
2018年 | 109篇 |
2017年 | 77篇 |
2016年 | 122篇 |
2015年 | 185篇 |
2014年 | 204篇 |
2013年 | 251篇 |
2012年 | 386篇 |
2011年 | 350篇 |
2010年 | 236篇 |
2009年 | 210篇 |
2008年 | 266篇 |
2007年 | 291篇 |
2006年 | 247篇 |
2005年 | 227篇 |
2004年 | 159篇 |
2003年 | 142篇 |
2002年 | 103篇 |
2001年 | 109篇 |
2000年 | 80篇 |
1999年 | 81篇 |
1998年 | 68篇 |
1997年 | 52篇 |
1996年 | 64篇 |
1995年 | 39篇 |
1994年 | 31篇 |
1993年 | 30篇 |
1992年 | 30篇 |
1991年 | 18篇 |
1990年 | 14篇 |
1989年 | 30篇 |
1988年 | 24篇 |
1987年 | 20篇 |
1986年 | 30篇 |
1985年 | 27篇 |
1984年 | 15篇 |
1983年 | 7篇 |
1982年 | 18篇 |
1981年 | 12篇 |
1980年 | 15篇 |
1979年 | 5篇 |
1978年 | 14篇 |
1977年 | 11篇 |
1976年 | 11篇 |
1975年 | 9篇 |
1971年 | 6篇 |
排序方式: 共有4883条查询结果,搜索用时 10 毫秒
81.
82.
83.
Correction: Self-assembled fibrillar networks comprised of a naturally-occurring cyclic peptide—LOB3
M. A. Rogers Q. Feng V. Ladizhansky D. B. Good A. K. Smith M. Corridini D. A. S. Grahame B. C. Bryksa P. D. Jadhav S. Sammynaiken L.-T. Lim B. Guild Y. Y. Shim P.-G. Burnett M. J. T. Reaney 《RSC advances》2020,10(24):13991
Correction for ‘Self-assembled fibrillar networks comprised of a naturally-occurring cyclic peptide—LOB3’ by M. A. Rogers et al., RSC Adv., 2016, 6, 40765–40776.The authors regret the omission of the following conflict of interest statement.Dr Martin J. T. Reaney is the founder of, and has an equity interest in, Prairie Tide Diversified Inc. (PTD, Saskatoon, SK, Canada: previous company name is Prairie Tide Chemicals Inc.). Dr Youn Young Shim is a Market Consultant for PTD in Korea. The terms of this arrangement have been reviewed and approved by the University of Saskatchewan in accordance with its conflict of interest policies.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers. 相似文献
84.
85.
86.
87.
Poly-γ-glutamic acid (PGA), a major component of the bacterial capsule, is known to confer hydrophilicity to bacterial surfaces and protect bacteria from interactions with blood cells. We tested whether applying a bacteriomimetic surface coating of PGA modulates interactions of nanomaterials with blood cells or affects their safety and photothermal antitumor efficacy. Amphiphilic PGA (APGA), prepared by grafting phenylalanine residues to PGA, was used to anchor PGA to reduced graphene oxide (rGO) nanosheets, a model of hydrophobic nanomaterials. Surface coating of rGO with bacterial capsule-like APGA yielded APGA-tethered rGO nanosheets (ArGO). ArGO nanosheets remained stable in serum over 4?weeks, whereas rGO in plain form precipitated in serum within 5?minutes. Moreover, ArGO did not interact with blood cells, whereas rGO in plain form or as a physical mixture with PGA formed aggregates with blood cells. Mice administered ArGO at a dose of 50?mg/kg showed 100% survival and no hepatic or renal toxicity. No mice survived exposure at the same dose of rGO or a PGA/rGO mixture. Following intravenous administration, ArGO showed a greater distribution to tumors and prolonged tumor retention compared with other nanosheet formulations. Irradiation with near-infrared light completely ablated tumors in mice treated with ArGO. Our results indicate that a bacteriomimetic surface modification of nanomaterials with bacterial capsule-like APGA improves the stability in blood, biocompatibility, tumor distribution, and photothermal antitumor efficacy of rGO. Although APGA was used here to coat the surfaces of rGO, it could be applicable to coat surfaces of other hydrophobic nanomaterials. 相似文献
88.
Akiko Suzuki Kenichi Ogata Hiroki Yoshioka Junbo Shim Christopher AWassif Forbes DPorter Junichi Iwata 《骨研究(英文版)》2020,(1):39-52
Human linkage studies suggest that craniofacial deformities result from either genetic mutations related to cholesterol metabolism or high-cholesterol maternal diets. However, little is known about the precise roles of intracellular cholesterol metabolism in the development of craniofacial bones, the majority of which are formed through intramembranous ossification. Here, we show that an altered cholesterol metabolic status results in abnormal osteogenesis through dysregulation of primary cilium formation during bone formation. We found that cholesterol metabolic aberrations, induced through disruption of either Dhcr7(which encodes an enzyme involved in cholesterol synthesis) or Insig1 and Insig2(which provide a negative feedback mechanism for cholesterol biosynthesis), result in osteoblast differentiation abnormalities. Notably, the primary cilia responsible for sensing extracellular cues were altered in number and length through dysregulated ciliary vesicle fusion in Dhcr7 and Insig1/2 mutant osteoblasts. As a consequence, WNT/β-catenin and hedgehog signaling activities were altered through dysregulated primary cilium formation.Strikingly, the normalization of defective cholesterol metabolism by simvastatin, a drug used in the treatment of cholesterol metabolic aberrations, rescued the abnormalities in both ciliogenesis and osteogenesis in vitro and in vivo. Thus, our results indicate that proper intracellular cholesterol status is crucial for primary cilium formation during skull formation and homeostasis. 相似文献
89.
Bombi Lee Bongjun Sur Insop Shim Hyejung Lee Dae-Hyun Hahm 《Journal of natural medicines》2014,68(1):132-143
90.