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61.
Shirai Y Hashimoto M Kato R Kawamura YI Kirikae T Yano H Takashima J Kirihara Y Saito Y Fujino MA Dohi T 《Journal of clinical immunology》2004,24(1):42-52
Despite the huge number of colonized Gram-negative bacteria in the colon, the normal colon maintains its homeostasis without any excessive immune response. To investigate the potential mechanisms involved, human colonic lamina propria mononuclear cells (LPMCs) obtained from uninflamed mucosa were cultured with lipopolysaccharide (LPS) prepared from Bacteroides vulgatus (BV-LPS) or Bacteroides fragilis (BF-LPS), as representatives of indigenous flora, or pathogenic Salmonella minnesota (SM-LPS). Colonic LPMCs failed to produce inflammatory cytokines in response to any type of LPS. Colonic macrophages barely expressed mRNA for MD-2, an essential association molecule for LPS signaling via Toll-like receptor 4. Further, BV-LPS induced CD25 and Foxp3 expression in lymphocytes and CD4(+)CD25(+) cells expressed IL-10 mRNA. Thus, the low expression of functioning LPS receptor molecules and induction of IL-10-producing CD4(+)CD25(+) lymphocytes by indigenous LPS may play a central role in the maintenance of colonic immunological homeostasis. 相似文献
62.
Model of bicarbonate secretion by resting frog stomach fundus mucosa I. Transepithelial measurements
Silvana Curci Lucantonio Debellis Rossella Caroppo Eberhard Frömter 《Pflügers Archiv : European journal of physiology》1994,428(5-6):648-654
In the present in vitro experiments on gastric fundus mucosa of Rana esculenta we try to define the mechanism of alkaline secretion that is observed in summer frogs in the resting stomach (blockage of HCl secretion by ranitidine, 10–5 mol/l). The transepithelial voltage and the rate of alkalinization (ASR) of an unbuffered gastric lumen perfusate was measured as a function of serosal (and mucosal) fluid composition. ASR was high (0.88±S.E. 0.09 Eq·cm–2·h–1, n=11) during serosal bath perfusion with HCO3
–-Ringer solution, decreased slightly to 0.50±0.07 Eq·cm–2·h–1 (n=6) in HCO3
–-free HEPES-buffered Ringer solution of the same pH, and decreased to approximately 20% when carbonic anhydrase was inhibited by acetazolamide. While replacement of mucosal or serosal Cl– did not — within 1 h — significantly alter ASR, replacement of serosal Na+ in the presence or absence of HCO3
– strongly reduced ASR, and a similar reduction was observed after serosal application of the anion transport inhibitor DIDS (4,4-diisomiocyanatostilbene-2,2-disulphonate, 2·10–4 mol/l), the metabolic poison rotenone (10–5 mol/l), the uncoupler dinitrophenol (10–4 mol/l), and the Na+ pump inhibitor ouabain (10–4 mol/l), while serosal amiloride (10–4 mol/l) had no effect. These data can be accounted for by a model of alkaline secretion that consists of basolateral HCO3
– uptake from the serosal fluid into the cell via a DIDS-inhibitable Na+(HCO3
–)n-cotransporter and HCO3
– secretion from the cell to the gastric lumen via an anionic conductance pathway. Microelectrode experiments on oxyntopeptic cells reported in the subsequent paper suggest that these cells may also be involved in the resting state alkaline secretion. 相似文献
63.
Analysis of gamma delta V region usage in normal and diseased human intestinal biopsies and peripheral blood by polymerase chain reaction (PCR) and flow cytometry. 总被引:1,自引:1,他引:1 下载免费PDF全文
64.
Oral administration of insulin conjugated to the B chain of cholera toxin (CTB-insulin) in non-obese diabetic (NOD) mice results in diabetes prevention. We investigated the respective contributions of L-selectin (CD62L) and alpha4-integrin pathways during CTB-driven tolerance. Purified CD62L+CD4+ cells from CTB-insulin fed mice significantly reduced the capacity of diabetogenic T cells to transfer diabetes in syngeneic recipients. In vivo antibody blockade of fed animals during adoptive co-transfer experiments indicated that both CD62L and alpha4-integrins pathways were necessary to develop a protective response after oral tolerance induction. In contrast, when antibodies were given to recipient mice, only CD62L was critical for the protection. In vitro stimulated CD62L+CD4+ cells from the spleen of fed animals secreted lower amounts of IL-4 and IL-10 but comparable levels of TGFbeta than CD62L-cells. A reduced IFN-gamma production between the two cell subsets was specifically observed in CTB-insulin fed mice. Furthermore, antibody treatments induced changes in T-cell migration to the spleen, mesenteric and pancreatic lymph nodes. The protective effect was also associated with migration of regulatory T cells into pancreatic islets. Taken together, our results suggest that L-selectin and alpha4-integrin have distinct but complementary roles in the generation and function of regulatory CD4+ T cells following CTB-insulin administration. 相似文献
65.
目的: 观察腹腔海水浸泡伤后大鼠胃黏膜和血浆中神经激肽A(NKA)和降钙素基因相关肽(CGRP)水平的动态变化,以探讨感觉神经肽在急性胃黏膜病变中的作用。方法:32只SD大鼠随机分成正常对照组和腹腔浸泡伤组,后者又分为1 h、2 h、3 h 3组,取大鼠胃黏膜和血浆,采用酶标法和放免法测定胃黏膜和血浆中NKA和CGRP水平。结果:随着浸泡时间的延长,腹腔浸泡伤组大鼠胃黏膜NKA和CGRP水平进行性低于正常大鼠(P<0.05),而血浆NKA和CGRP水平进行性高于正常大鼠。结论:海水浸泡伤是一损伤性因素,可引起胃黏膜中NKA和CGRP水平降低、血浆中NKA和CGRP水平升高,提示NKA和CGRP等感觉神经肽在急性胃黏膜病变发生发展过程中可能有重要作用。 相似文献
66.
李和泉 《中国病理生理杂志》1986,(2)
用反射光谱法,研究了组胺H_2受体阻断剂Famotidine对急性失血大鼠胃粘膜血液量及血氧饱和度的影响。同时观察了胃液量和酸排出量的变化,并计量了溃疡指数。Famotidine(3mg/kg及8mg/kg,iv)对失血前大鼠胃粘膜血液量和血氧饱和度均未见有影响;对失血后胃粘膜血液量和血氧饱和度的降低有明显保护作用,对胃液量和酸排出量均有显著抑制作用,溃疡指数减小。 相似文献
67.
H. F. Helander S. S. Sanders L. L. Shanbour W. S. Rehm 《Acta physiologica (Oxford, England)》1975,95(4):353-363
Functional and morphological properties of the in vitro frog gastric mucosa were studied during and after exposure to very hypotonic (? 25 mOsM) solutions. Within 20 min the acid secretory rate decreased to zero, but it returned to normal levels after isotonic fluids had been restored. The potential difference (PD) dropped within the first minutes after the exposure to hypotonic solutions, and became inverted. Following the return of isotonic conditions the PD increased to levels higher than in the controls. The electrical resistance increased about 10–fold during the hypotonic period, but decreased to near normal values when isotonic conditions were restored. By light and electron microscopy the cells of the hypotonic mucosae appeared greatly swollen, and the alterations were assessed by morphometric methods. The gland lumina were almost obliterated, and the lamina propria was reduced to about 60% of its former volume. After the return to isotonic conditions normal morphology was restored. It is conceivable that the great increase in resistance during the hypotonic period was caused by the occlusion of the gland lumina. Quantitative analyses of the Na, K, and C1 tissue concentrations indicated a large loss of these ions during the hypotonic state. Presumably the epithelial cells in the hypotonic mucosae avoid bursting by rapidly letting large numbers of ions exit, which results in a cellular osmolarity close to that of the bathing fluids. 相似文献
68.
Harrath R Bourlet T Delézay O Douche-Aourik F Omar S Aouni M Pozzetto B 《Journal of medical virology》2004,74(2):283-290
Although the transmission of coxsackievirus B3 occurs mainly via the oral route, little is known about the primary replication and persistence of this agent in the intestine. To address this question, BALB/c mice were inoculated by gavage with coxsackievirus B3, Nancy strain. The mice were killed from 1 hr to 90 days after infection. The viral markers were detected in the small intestine using RT-PCR, cell culture and detection of VP1 protein. Coxsackievirus B3 was detected positive by the three methods from hr 2 to day 45 after infection. By using monoclonal antibodies directed towards VP1, CD40 and CD26, the virus was shown to be present in the lymphocytes of the mucosa as soon as 2 hr after infection; in contrast, no virus was detected in the epithelial cells lining the intestinal lumen. Further experiments were performed to evaluate the capacity of coxsackievirus B3 to establish a persistent infection in two intestinal cell lines. In contrast to HT29 cells, the CaCo-2 cells were shown to develop a persistent infection for up to 20 passages, as demonstrated by the detection of viral RNA and VP1 protein. This study provides further evidence that, after infection by the oral route, the viral particles are concentrated in the lymphocytes of the mucosal layer. In addition, the results suggest that coxsackievirus B3 is capable of establishing a persistent infection in the small intestine that may act as a reservoir of viral particles for the delayed spread of the virus to other target organs. 相似文献
69.
The formation of the nasal lining with its sensory and its nonsensitive respiratory epithelium requires a spatially ordered
pattern of cellular differentiation. Aiming at identifying cell recognition molecules that may be involved in cellular differentiation
steps, we applied a panel of antibodies to terminal carbohydrate sequences of the lactoseries on the developing chick olfactory
epithelium. This approach is based on the idea that these terminal sugar residues may be involved in certain steps of maturation.
Restricted expression of three epitopes NALA, HNK-1, and CD15 was observed in olfactory receptor neurons. The first immature
olfactory receptor neurons were observed by day 3 of incubation, expressing the HNK-1 epitope, whereas a total epithelial
staining was observed for NALA. By day 9 of incubation high numbers of HNK-1 positive immature olfactory receptor neurons
were observed. At the same time mature olfactory receptor neurons showed immunoreactivity for CD15, whereas NALA was still
expressed throughout the whole epithelial cell population. However, there was a pronounced staining in the population of mature
olfactory receptor neurons. Around hatching only CD15 was detectable in (mature) olfactory receptor neurons, whereas HNK-1
and NALA immunoreactivity have switched to glandular and sustentacular cells respectively. The differentiation-dependent expression
patterns of these three cell surface molecules suggest them as suitable markers to explore mechanisms that determine embryonic
olfactory receptor neurogenesis.
Accepted: 15 October 1997 相似文献
70.
Laboratory of Experimental Surgery, A. V. Vishnevskii Institute of Surgery, Academy of Medical Sciences of the USSR, Moscow. (Presented by Academician of the Academy of Medical Sciences of the USSR M. I. Kuzin.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 111, No. 6, pp. 617–619, June, 1991. 相似文献