全文获取类型
收费全文 | 7527篇 |
免费 | 423篇 |
国内免费 | 39篇 |
专业分类
耳鼻咽喉 | 135篇 |
儿科学 | 250篇 |
妇产科学 | 129篇 |
基础医学 | 978篇 |
口腔科学 | 186篇 |
临床医学 | 583篇 |
内科学 | 1999篇 |
皮肤病学 | 84篇 |
神经病学 | 870篇 |
特种医学 | 325篇 |
外科学 | 1001篇 |
综合类 | 30篇 |
一般理论 | 8篇 |
预防医学 | 439篇 |
眼科学 | 149篇 |
药学 | 392篇 |
中国医学 | 14篇 |
肿瘤学 | 417篇 |
出版年
2024年 | 11篇 |
2023年 | 71篇 |
2022年 | 215篇 |
2021年 | 360篇 |
2020年 | 209篇 |
2019年 | 282篇 |
2018年 | 332篇 |
2017年 | 228篇 |
2016年 | 226篇 |
2015年 | 283篇 |
2014年 | 350篇 |
2013年 | 408篇 |
2012年 | 638篇 |
2011年 | 648篇 |
2010年 | 340篇 |
2009年 | 282篇 |
2008年 | 510篇 |
2007年 | 441篇 |
2006年 | 376篇 |
2005年 | 423篇 |
2004年 | 366篇 |
2003年 | 271篇 |
2002年 | 243篇 |
2001年 | 57篇 |
2000年 | 52篇 |
1999年 | 46篇 |
1998年 | 42篇 |
1997年 | 42篇 |
1996年 | 28篇 |
1995年 | 25篇 |
1994年 | 22篇 |
1993年 | 15篇 |
1992年 | 16篇 |
1991年 | 17篇 |
1990年 | 8篇 |
1989年 | 13篇 |
1988年 | 12篇 |
1987年 | 11篇 |
1986年 | 10篇 |
1985年 | 11篇 |
1984年 | 6篇 |
1983年 | 6篇 |
1982年 | 6篇 |
1981年 | 8篇 |
1980年 | 4篇 |
1977年 | 3篇 |
1973年 | 2篇 |
1972年 | 2篇 |
1969年 | 2篇 |
1968年 | 2篇 |
排序方式: 共有7989条查询结果,搜索用时 15 毫秒
101.
102.
Kenneth S. Brandenburg MS Diego F. Calderon DVM Patricia R. Kierski BA Amanda L. Brown BS Nihar M. Shah PhD Nicholas L. Abbott PhD Michael J. Schurr MD Christopher J. Murphy DVM PhD Jonathan F. McAnulty DVM PhD Charles J. Czuprynski PhD 《Wound repair and regeneration》2015,23(6):842-854
Chronic nonhealing skin wounds often contain bacterial biofilms that prevent normal wound healing and closure and present challenges to the use of conventional wound dressings. We investigated inhibition of Pseudomonas aeruginosa biofilm formation, a common pathogen of chronic skin wounds, on a commercially available biological wound dressing. Building on prior reports, we examined whether the amino acid tryptophan would inhibit P. aeruginosa biofilm formation on the three‐dimensional surface of the biological dressing. Bacterial biomass and biofilm polysaccharides were quantified using crystal violet staining or an enzyme linked lectin, respectively. Bacterial cells and biofilm matrix adherent to the wound dressing were visualized through scanning electron microscopy. d ‐/l ‐tryptophan inhibited P. aeruginosa biofilm formation on the wound dressing in a dose dependent manner and was not directly cytotoxic to immortalized human keratinocytes although there was some reduction in cellular metabolism or enzymatic activity. More importantly, d ‐/l ‐tryptophan did not impair wound healing in a splinted skin wound murine model. Furthermore, wound closure was improved when d ‐/l ‐tryptophan treated wound dressing with P. aeruginosa biofilms were compared with untreated dressings. These findings indicate that tryptophan may prove useful for integration into wound dressings to inhibit biofilm formation and promote wound healing. 相似文献
103.
Paulo Roberto Santos Diego Levi Silveira Monteiro Paulo Henrique Alexandre de Paula Vicente Lopes Monte Neto Maria Leilah Ponte Monte Coelho Cecília Costa Arcanjo Sânkia Maria Lopes Aragão Camila Barbosa Gondim Janaína Teixeira Pereira Carneiro Tapeti Hyngridd Soares Mendes Luise Vasconcelos Vieira Rita de Cássia Parente Prado 《Nephrology (Carlton, Vic.)》2015,20(8):519-522
104.
Preclinical cadaveric study of transanal robotic proctectomy with total mesorectal excision combined with laparoscopic assistance 下载免费PDF全文
105.
Arroyo Diego Gasche Yvan Banfi Carlo Stiasny Brian Bendjelid Karim Giraud Raphaël 《Journal of cardiothoracic surgery》2015,10(1):1-8
Previously designed intra-thoracic paraaortic counterpulsation device has limited stroke volume and may depress the lung to cause complications. The purpose of this study was to evaluate the hemodynamic effects of an extra-thoracic paraaortic counterpulsation device (ETPACD) in comparison to intraaortic balloon pump (IABP) in an animal model with acute heart failure. The acute heart failure model was successfully induced by snaring branch of anterior descending coronary artery in sheep (weighting, 38-50 kg, n = 8). The ETPACD is a single port, 65-ml stroke volume blood chamber designed to be connected to descending aorta through a valveless graft and placed extra-thorax. In comparison, a standard clinical 40-ml IABP was placed in the descending aorta. The hemodynamic indices of both devices were recorded during counterpulsation assistance. Two of the sheep were allowed to survive for 1 week to examine the prolonged effect. Both ETPACD and IABP increased cardiac output with higher effect of ETPACD (13.52 % vs. 8.19 % in IABP, P < 0.05) and on mean diastolic aortic pressure (26.73 % vs. 12.58 % in IABP, P < 0.01). Both ETPACD and IABP also produced a greater reduction in left ventricular end-diastolic pressure (26.77 % vs. 23.08 %, P > 0.05). The ETPACD increased left carotid artery flow more significantly the IABP (18.00 % vs. 9.19 % , P < 0.05). In two of the sheep allowed to survive for 1 week, the device worked well with no complications and there was no thrombus formation in the chamber of ETPACD. This study demonstrated that both ETPACD and IABP provided benefit of circulatory support in acute heart failure with better effect on hemodynamic parameters provided by ETPACD. Therefore, ETPACD with theoretical larger stroke volume may become a promising counterpulsation device for treatment of heart failure. 相似文献
106.
Andrés?Felipe?Duque AmayaEmail author Adalberto?Gabriel?Díaz Torres Diego?Andrés?Acosta Maya 《International Journal on Interactive Design and Manufacturing》2016,10(4):401-415
A mathematical and numerical model of flow and combustion process for spark ignition engines is developed using the principles of the first and second law of thermodynamic. Availability (exergy) analysis is applied to cylinder of a spark ignition engine during the combustion process using a two-zone combustion model. Special attention is given to identification and quantification of irreversibility of combustion process and energy available basing on the isooctane fuel explosion. To predict emissions generation (greenhouse gases) a skeletal mechanism including 32 species and 61 reactions was developed and tested for different engine operations and exergy destructions. 相似文献
107.
The enteric nervous system has been studied thus far as an isolated unit. As researchers probe deeper into the function of this system, it is evident that the neural network stretches beyond enteric neurons. It is formed by both intrinsic and extrinsic neurons innervating the gut, enteric glia, and innervated sensory epithelial cells, such as enteroendocrine cells. This Review series summarizes recent knowledge on function and disease of nerves, glia, and sensory epithelial cells of the gut in eight distinctive articles. The timing and growing knowledge for each individual field calls for an appropriate term encompassing the entire system. We call this neuronal ensemble the “gut connectome” and summarize the work from a food sensory perspective.“Tell me what you eat, and I will tell you what you are,” wrote the French gastronome Jean Brillat-Savarin in 1826 (1).Although at the time of Brillat-Savarin the connection between well-being and ingested food was clear, only in recent years have we discovered the mechanisms by which the gut senses food. With all its folds, villi, and microvilli, the gut is arguably the largest surface in the body. It is here where food is deconstructed into nutrients, ultimately giving rise to signals that control a range of bodily functions, including the desire to eat.Because of the need to be aware of ingested food, the body has an intricate network of electrically excitable cells, carefully arranged into circuits and strategically distributed throughout the gut. These circuits convert food into electrical signals coordinating motility, secretion, food intake, and even mood and other behaviors. In the past, study of this network was limited to neurons of the enteric nervous system, but in recent years it has become clear that the neural network extends beyond enteric neurons. It is comprised of enteric glia, neurons of peripheral ganglia innervating the gut, intrinsic neurons, and specialized innervated epithelial sensors such as enteroendocrine cells. We believe it appropriate to call this network the “gut connectome.”Two characters of the gut connectome, the glia and enteric neurons, arise from neural crest cells. They are immigrants to the bowel, traveling from the neural tube. Avetisyan et al. describe the molecular instruments orchestrating the migration of neural crest–derived cells to the intestine (2). Receptors, cofactors, and ligands meticulously coordinate the migration and transformation of progenitors into enteric ganglia. Ultimately, over 20 distinct types of neurons and accompanying glia are formed (3). These neurons are then guided by chemical cues to develop axons and establish synaptic connections with sensory and motor targets (4).The gut connectome is a neural network built around food sensing. From the moment the fetus swallows amniotic fluid, the luminal contents of the digestive tract become a major factor in axonal pathfinding; after all, the network has to find the correct location to sense and utilize nutrients. Although there are reports of bacteria colonizing internal organs, including the gut, before birth (5), the gut microbiome, primarily after birth, serves as a beacon in the development of the network by priming the immune system and producing chemoattractants (6).Kabouridis and Pachnis discuss how the gut microbiota increases the density of enteric nerves (7). The mechanisms appear to involve epithelial receptors, like those of the large family of toll-like receptors. In normal conditions, microbes in the gut do not have physical access to enteric nerves; therefore, their ability to alter the development and function of the enteric neural network is probably mediated by bacterial byproducts that sieve through the epithelium into the lamina propria or, more likely, through direct activation of epithelial sensory cells such as enteroendocrine cells. Enteroendocrine cells are in direct contact with the gut lumen and express molecular receptors specifically activated by bacterial ligands (8). If the integrity of the epithelial barrier is compromised by infection, the function of the neural circuitry is affected, as discussed by Mawe (9).Enteroendocrine cells are essential for normal life. In their absence, severe diarrhea and early death occur (10). Like taste cells in the tongue or olfactory receptor cells in the nose, enteroendocrine cells are sensory epithelial cells. Recently their molecular sensing mechanisms have been uncovered, as reported by Psichas et al. (11). Enteroendocrine cells even express some of the same olfactory and taste receptors known to mediate the sense of smell and taste (12, 13). But unlike other epithelial sensors, they were thought to lack synaptic connections with nerves. Historically, enteroendocrine cells have been studied exclusively as a source of hormones. However, they have typical neural circuit features of sensory cells, including electrical excitability; functional voltage-gated channels; small, clear synaptic vesicles; nourishment from glial-derived neurotrophic factors; and a neuropod (14). It is through neuropods that enteroendocrine cells connect to nerves (15). This discovery opens up the possibility of the gut processing sensory signals in the lumen in a temporally precise, circuit-specific, and finely tuned manner.Although enteroendocrine cells have a wide array of molecular receptors for chemicals in the lumen of the gut, the sensing of dietary fats has received much attention because of the obesity epidemic. The perception of fats differs between the mouth and small intestine. In the mouth, the taste of unsaturated fatty acids triggers signals to increase hunger, whereas in the small intestine, fatty acids trigger signals of satiety (16). The difference is in the epithelial sensory cells that transduce the chemical signal from a digested lipid into an electrical impulse in nerves. Some dietary fatty acids in the small intestine exert potent anorectic actions via a mechanism in which lipids bind and activate cell surface receptors such as GPR40, GPR41, or ILDR1 (17, 18). DiPatrizio and Piomelli discuss how endogenous lipids produced in the gut modulate appetitive behaviors (19). Sensory signals from fats and other nutrients are ultimately relayed via the vagus nerve to the brain, where fat ingestion is perceived.An important character of the gut connectome is the enteric glia. Discovered by Russian physiologist Dogiel in the late 1800s (20), enteric glia were first recognized as essential for normal gut function in 1998 (21). They are distributed throughout the mucosa and neuronal plexus of the gut and form a syncytium that is functionally coupled through gap junctions made of hemichannels such as connexin 43 (22). In this issue, Sharkey describes the role of enteric glia in barrier and defense functions of the gut and gastrointestinal motility disorders (23). Enteric glial cells also form neuro-glial junctions with neurons and, at least in the myenteric plexus, are known to receive cholinergic innervation (24). We have documented a physical association of enteric glia with enteroendocrine cells, highlighting how the enteric glial cell is a critical character in the gut connectome (Figure 1 and ref. 14).Open in a separate windowFigure 1The gut connectome: built for sensing food.Top left: A sensory enteroendocrine cell (EEC) in the gut epithelium can be seen extending a neuropod to connect with an underlying nerve. Bottom left: Enteric glia underneath the epithelium extend processes to contact the neuropod of an enteroendocrine cell. Right: The innervation of enteroendocrine cells brings the possibility of afferent (gut-to-brain) signaling and possible efferent (brain-to-gut; not shown) signaling, which would allow the gut to compute sensory information from food to modulate whole-body metabolism and behaviors such as hunger and satiety. Figures adapted from PLoS One (14) and J Clin Invest (15).Besides modulating the transmission of sensory information, enteric glia appear to be an important defense against pathogenic invasion. Pathogens like the JC virus and misfolded prion proteins are harbored by enteric glia. Both JC virus and prion proteins gain entry through the gut but affect the brain (25). This is an important observation because enteroendocrine cells are exposed to the gut lumen, where external viruses and prions first arrive. In an effort to unveil a gut-brain neural circuit, we recently used a modified rabies virus. This neurotropic virus infects enteroendocrine cells, and given the right conditions, the rabies virus spreads into the nervous system (15). This uncovered a conduit through which pathogens that are able to infect enteroendocrine cells could access first the peripheral then the central nervous systems. And, like astrocytes in the brain, enteric glia may also clear infections of the gut connectome.The neuronal ensemble of sensory cells, neurons, and glia is modulated and shaped by the gut microbiome. Gut microbes can have mind-altering effects as discussed by Mayer et al. and, although the mechanisms remain unknown, it is clear that the ability of the gut connectome to process sensory information is involved (26).Alterations in the gut connectome have also been observed in patients undergoing gastric bypass surgery. The procedure dates back to 1966, when Dr. Edward Mason first implemented it to treat obese patients (27). The procedure has since been refined, and there are several variations of it, the most popular being Roux-en-y (RY) gastric bypass. Manning et al. explain that RY gastric bypass forces food to bypass the stomach and enter directly into the distal small intestine (28). The effects on diabetes and body weight are remarkable. Three years after surgery almost seven of ten patients experience diabetes remission, and remarkably only six months after the surgery, an average patient loses over one-quarter of his initial body weight (29). The effects were thought to be due to the altered anatomy, but more recently it has become clear that neuroendocrine mechanisms are involved: in simple terms, the bodyweight set-point is reset.Perhaps the most remarkable observation learned from RY gastric bypass surgery is the alteration of food perception. RY gastric bypass reduces the preference for sugars and even the cravings for sweets and fatty foods (30). Rewiring of the gut connectome indeed alters where nutrients are sensed, how nutrients are sensed, and our perception of food. Jean Brillat-Savarin was right after all; we truly are what we eat. 相似文献
108.
109.
110.