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91.
目的 将人乳头瘤病毒16型(Human papillomavirus type 16,HPV-16)的晚期表达蛋白E7上的抗原24肽(从第38位氨基酸到第61位氨基6病毒感染防治酸)与人免疫球蛋白G的重链恒定区融合表达,并以此融合蛋白作为抗原,可能为HPV-1提供免疫治疗方法。方法 利用PCR方法分别扩增HPV-16 E7(38-61)24肽的DNA片段和人免疫球蛋白G的重链恒定区DNA片段,并构建到pEV21a表达载体上,转化入E.coli中表达,利用SDS-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹(Western-blotting)的方法对表达结果进行鉴定。结果 构建的表达载体HPV16E7e/hIgGHCCR-pET21a经酶切鉴定和测序显示序列正确;通过SDS-PAGE和Western-blotting的鉴定,重组融合蛋白Mr约40000,表达量可占菌体蛋白的20%左右。结论 成功构建HPV16-E7的抗原多肽片段和人免疫球蛋白G的重链恒定区的融合蛋白,并可在E.coli中高效表达。 相似文献
92.
93.
目的为了获得基因工程重组人胰岛素样生长因子1。方法采用Trizol试剂法,从人胎肝中提取,6-RNA,RT-PCR扩增得到人胰岛素样生长因子1基因,用EcoRⅠ和Hind Ⅲ双酶酶切后,将该基因片段插入表迭栽体pkk223—3,筛选得到了重组质粒pkk-hIGF1。结果加IPTG诱导该质粒转化的大肠杆菌JM109表达,hIGF1的表达水平约30mg/L。结论用肝素亲和层析的方法,获得了电泳纯基因工程重组人胰岛素样生长因子1样品。纯化样品的理化及生物活性分析与天然对照品完全一致。 相似文献
94.
Formation of intrachondral vessels (cartilage canals) in the proximal femoral epiphysis was studied in 13- to 22-week-old human fetuses using a corrosion casting technique and scanning electron microscopy. Several successive morphological stages of angiogenesis occurring inside the hyaline cartilage were distinguished. The process of cartilage vascularization starts with the formation of hairpin loops sent off from the perichondrial vascular network into the adjacent cartilage. A capillary glomerulus is then formed at the leading end, and the entire vascular unit grows in length, assuming a mushroom-like shape. Its further elongation is accompanied by a backward expansion of the capillary network which surrounds a pair of main vessels (arteriole and venule) like a manchette. The subsequent branching of such primary vascular units proceeds according to the same morphological patterns. The resulting tree-like vascular formations become interconnected via their lateral branches. This study clearly supports the invasion theory of cartilage canal formation. 相似文献
95.
M. M. Giraud-Guille 《Calcified tissue international》1988,42(3):167-180
Summary Ultrathin sections of decalcified human compact bone, observed by transmission electron microscopy, reveal that collagen fibrils
can be distributed in the form of a superimposed series of nested arcs. This characteristic pattern has never been interpreted
in previous works on compact bone structure. We demonstrate, by goniometric observations at the ultrastructural level, that
such series of nested arcs are a consequence of the “twisted plywood” architecture of collagen fibrils in the compact bone
matrix. In the same specimens, an “orthogonal plywood” disposition of collagen fibrils is also observed; a transition exists
between these two types of orders. We show that the “twisted plywood structure” accounts well for certain optical properties
of osteons, observed in polarizing microscopy, described as “intermediate osteons.” The particular geometry of collagen fibrils,
leading to nested arcs in oblique sections, is analogous to the distribution of molecules in certain liquid crystals (called
cholesteric liquid crystals). The principle of a liquid crystalline self-assembly of the collagen matrix in bone is therefore
discussed. 相似文献
96.
A. Jouvet E. Derrington J. Pialat C. Lapras M. Fèvre-Montange R. Besançon M. F. Belin G. Saint-Pierre 《Acta neuropathologica》1994,88(4):334-348
We have studied 20 pineal parenchymal tumors (PPT) and 4 normal or cystic pineal glands both by light and electron microscopy and immunohistochemistry with antibodies against glial markers [glial fibrillary acidic protein (GFAP) and protein S-100] or neural/neuroendocrine markers [neurofilaments (NF), synaptophysin and chromogranin A]. Light microscopy revealed the cellular organization of pinealocytes in the normal gland and in different morphological types of pineal tumors (typical pineocytomas, PPT with intermediate differentiation, mixed PPT exhibiting elements of both pineocytoma and pineoblastoma and pineoblastomas). Immunohistochemistry showed the presence of GFAP and protein S-100 in interstitial cells in nonneoplastic pineal gland. Cell processes were labeled with anti-synaptophysin and anti-NF antibodies. No immunoreactivity was found for chromogranin A in non-neoplastic pineal gland. In pineocytomas, GFAP and protein S-100 were observed in interstitial cells. Synaptophysin and NF were present in the large rosettes of pineocytomas. Synaptophysin, NF and chromogranin A were present in pineocytomas with a lobular arrangement of cells. Anti-chromogranin A immuno-reactivity was also seen in lobular areas of some PPT with intermediate differentiation. Analysis of normal human pineal gland by electron microscopy showed the presence of vesicle-crowned rodlets (VCR or synaptic ribbons), fibrous filaments (F), paired twisted filaments but few dense-core vesicles (DCV) in normal pinealocytes. Tumoral pineal cells appeared to differentiate either towards a neurosensory pathway characterized by the presence of sensory cells elements (VCR and F), or towards a neuroendocrine pathway, with the occurrence of many DCV. Immunogold labeling demonstrated the presence of chromogranin A in neurosecretory granules.Supported by grants from the Région Rhône Alpes and from INSERM (CJF 90-10) 相似文献
97.
本文对19例中药雷公藤服用者精子、精浆中乳酸脱氢酶(LDH)及同功酶C_4(LDHC_4)的活性进行了测定分析。发现服药后以单位数量精子表示的LDHC_4活性在精子、精浆中均有明显升高(双侧非参数秩和检验,分别为P<0.01和P<0.02);通过酶活性与精子计数的相关分析,显示服药后精浆LDHC_4活性(mU/ml)与精子计数的正相关性(r=0.2279)较服药前(r=0.5505)弱,可能与精液中精子以外的其他LDHC_4来源贡献增大有关,诸如生精细胞的分解增多等。本文认为服药后精子LDHC_4活性上升,精液中非成熟精子比例增高是其原因之一。 相似文献
98.
In human cortex and hippocampus area, [3H]5-HT (5 nM) labels 5-HT1A, 5-HT1D and 5-HT1E sites. After masking 5-HT1A receptors by 0.1 μM 8-OH-DPAT, the binding displaced by 0.1 μM 5-CT presumably represented 5-HT1D sites and the remaining binding 5-HT1E sites. In frontal cortex, 5-HT1A receptors represented the main binding in layers II and VI and a lower fraction on other layers. 5-HT1D and 5-HT1E sites, were more homogeneously distributed in layers II to VI (21–34% of specific [3H]5-HT binding). 5-HT1E sites were of similar affinities (KD close to 6–8 nM) in the cortical layers II to VI. In CA1 field of hippocampus, (pyramidal layer, stratum radiatum, molecular layer), CA2 and dentate gyrus, 5-HT1A receptors represented the major fraction, 5-HT1D sites a significant fraction and 5-HT1E a minor fraction of the specific [3H]5-HT binding. In CA3–CA4 fields, 5-HT1A receptors were less densely present, 5-HT1D sites were predominant and 5-HT1E sites represented a significant fraction (27%). The highest densities of 5-HT1E sites have been measured in subiculum, where 5-HT1A, 5-HT1D, and 5-HT1E binding sites were equally represented and in entorhinal cortex where 5-HT1E sites represented the major binding in layer III. They were also present in layers II and IV (29 and 24%) and, to a lesser extent, in layers V and VI. 5-HT1A sites were predominant in layer VI, II and V and were less abundant in other layers. 5-HT1D were homogeneously present in layers II, III, IV and were present in low amounts in other layers. No 5-HT1E were detected in choroid plexus, where [3H]5-HT was dramatically reduced by mesulergine (5-HT2C receptors). No significant displacement of [3H]5-HT by mesulergine was measured in other structures. 相似文献
99.
以分离的细胞膜为受体制剂,对大鼠卵巢及睾丸人绒毛膜促性腺激素(HCG)受体进行比较研究,发现二者的受体结合特性有一定差异;同时将大鼠寒丸膜及睾丸匀浆作对比,友现睾丸膜制剂较睾丸匀浆更能准确地体现睾丸HCG受体的真正特性。 相似文献
100.
Jos A. Brieva Ernesto Roldn Carmen Rodríguez Gloria Navas 《European journal of immunology》1994,24(2):362-366
Human B cells capable of spontaneous IgG secretion are commonly found in circulation and in lymphoid tissues such as tonsil and bone marrow (BM). The present study compares the mechanisms that regulate tonsil, blood and BM B cells capable of spontaneous IgG secretion. The BM cell subset produced IgG during a markedly longer period of time (14 days) than did tonsil and blood cell subsets (2–3 days). Blood and BM, but not tonsil, B cell IgG secretion depended on the presence of adherent cells, as demonstrated by adherent cell depletion and re-addition experiments. Stromal BM cells supported linear IgG secretion by non-adherent BM cells for 2 weeks, but were unable to prolong the short-term IgG secretion by tonsil and blood cells. Different factors induced IgG secretion in each of the three B cell populations as optimal IgG secretion by tonsil, blood or BM cell subsets required either tumor necrosis factor-α, interleukin-6 or fibronectin + interleukin-6, respectively. Finally, these populations also showed differences in the expression of adhesion molecules; the tonsilar cell subset was PNA+/? CD44+ CD49d+ CD49e? Leu-8+/?, the blood cell subset was PNA? CD44+/? CD49d+ CD49e? Leu-8+ and the BM cell subset was PNA? CD44+/? CD49d+ CD49e? Leu-8?. These results suggest that the mechanisms controlling the final differentiation and the expression of adhesion molecules in these B lymphocytes exhibit territorial specificity. 相似文献