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D J Bowen 《Journal of clinical pathology》2002,55(1):1-18
This review focuses on selected areas that should interest both the scientist and the clinician alike: polymorphisms within the factor VIII and factor IX genes, their linkage, and their ethnic variation; a general assessment of mutations within both genes and a detailed inspection of the molecular pathology of certain mutations to illustrate the diverse cause–effect relations that exist; a summary of current knowledge on molecular aspects of inhibitor production; and an introduction to the new areas of factor VIII and factor IX catabolism. An appendix defining various terms encountered in the molecular genetics of the haemophilias is included, together with an appendix providing accession numbers and locus identification links for accessing gene and sequence information in the international nucleic acid databases. 相似文献
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Mohammad Diab Jiann-Jiu Wu Frederic Shapiro David Eyre 《American journal of medical genetics. Part A》1994,49(4):402-409
There is growing evidence that a spectrum of chondrodysplasias are caused by mutations in the gene coding for type II collagen. The basic molecular defect in diastrophic dysplasia has not been defined, but it appears not to be in collagen type II. Cartilage contains other tissue-specific collagens, types IX, X, and XI, but no mutations have yet been found in their genes in clinical disease. Type IX collagen is hypothesized to play a role in the regulation of type II collagen fibril organization and structure in cartilage extracellular matrix. In this study, we have examined iliac crest growth cartilage from a patient with diastrophic dysplasia. Although collagen fibrils were markedly increased in diameter on transmission electron microscopy, type II collagen appeared to be normal biochemically. Type XI collagen was also normal. However, type IX collagen appeared abnormal on sodium dodecyl sulfate polyacrylamide gel electrophoresis with a pronounced excess of the COL1 domain of the molecule in pepsin extracts. The findings point to an abnormality in structure or metabolism of type IX collagen in diastrophic dysplasia. © 1994 Wiley-Liss, Inc. 相似文献
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We report an 18-year-old boy with occipital horn syndrome and we review the 20 cases previously published with this syndrome. The distinctive features common to all patients were unusual facial appearance, skeletal abnormalities, chronic diarrhea and genitourinary abnormalities. The skeletal abnormalities included occipital horns, short, broad clavicles, deformed radii, ulnae, and humeri, narrowing of the rib cage, undercalci-fied long bones with thin cortical walls and coxa valga. Occipital horn syndrome is inherited in an X-linked recessive fashion. Our analysis indicates that occipital horn syndrome is associated with a recognizable characteristic phenotype. 相似文献
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Type IX collagen (CIX), a cartilage-specific glycoprotein, constitutes ≤ 10% of cartilage collagen. To ascertain whether CIX can induce arthritis as shown for type II and XI collagen (CII and CXI), outbred rats were sensitized with bovine, chick and human CIX; inbred rats, mice, and guinea pigs were sensitized with bovine CIX. Mice and guinea pigs proved resistant to arthritis, as did rats sensitized with CIX/Freund's incomplete adjuvant (FIA). Arthritis was seen in rats when 100 μg of Mycobacterium tuberculosis (Mtb) were added to FIA, but seldom with smaller doses of Mtb, suggesting the arthritis was adjuvant-induced. High levels of antibodies to rat CIX, containing complement-fixing subclasses, were detected in rat sera in addition to DTH and lymphocyte proliferation responses to rat CIX. Given the potential for CIX-induced disease, CIX-sensitized rats were injected intraperitoneally with lipopolysaccharide (LPS) to stimulate proinflammatory cytokine release, and intra-articularly with rat CIX to stimulate arthritis. LPS stimulation was ineffective; however, intra-articularly injected CIX produced transient synovitis. When rats with stable adjuvant arthritis were sensitized with CIX/FIA, significant increases in paw volume were measured compared with controls given CI/FIA. Immunohistochemical studies of actively and passively sensitized rats revealed deposits of CIX antibody, but not C3, at the joint margins where proteoglycan staining was weak. Together, these findings suggest that autoimmunity to CIX, in contrast to CII and CXI, is not directly pathogenic but may contribute to joint injury provided arthritis is initiated by an independent disease process. 相似文献
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Co-localization of calcitonin gene-related peptide-like immunoreactivity with substance P in cutaneous, vascular and visceral sensory neurons of guinea pigs 总被引:19,自引:0,他引:19
I L Gibbins J B Furness M Costa I MacIntyre C J Hillyard S Girgis 《Neuroscience letters》1985,57(2):125-130
Calcitonin gene-related peptide (CGRP) has been immunohistochemically co-localized with substance P (SP) in capsaicin-sensitive, varicose axons supplying the skin, viscera and cardiovascular system of the guinea pig. After treatment with colchicine in vitro, 82% of SP neurons in the dorsal root ganglia contained CGRP-like immunoreactivity while 96% of CGRP neurons were immunoreactive for SP. Both CGRP- and SP-like immunoreactive material are transported peripherally and centrally from dorsal root ganglia. Thus, in tissues such as the gut where there are intrinsic nerves containing SP but lacking CGRP, CGRP-like immunoreactivity is a useful means of specifically labelling axons of most sensory neurons containing SP. 相似文献
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δ-氨基乙酰丙酸脱水酶基因多态性对职业铅接触工人血铅和锌原卟啉的影响 总被引:5,自引:1,他引:5
[目的 ]研究δ 氨基乙酰丙酸脱水酶 (ALAD)基因多态性对职业铅接触工人血铅 (PbB)和锌原卟啉 (ZPP)的影响。 [方法 ]采集 170名上海市某蓄电池厂职业铅接触工人外周静脉血样 ,多聚酶链式反应 (PCR)和限制性内切酶 (MspⅠ )限制性片段长度多态性 (RFLP)方法进行ALAD基因分型分析 ,用PE 80 0型原子吸收分光光度计和ZPP 3 80 0型血液锌原卟啉测定仪分别测定PbB和ZPP含量 ,并分析其与基因型的关系。 [结果 ]①ALAD11纯合子基因型者有 15 4名 ,占90 5 9% ;ALAD12杂合子基因型者有 16名 ,占 9.41% ;未检出ALAD2 2纯合子基因型者 ;②ALAD1和ALAD2等位基因分布频率分别是 95 .2 9%和 4.71% ;③在同等外暴露条件下 ,ALAD12杂合子基因型组工人血铅水平 ( 1.0 4± 0 .48μmol/L)明显高于ALAD11纯合子基因型组工人血铅水平 ( 0 .78± 0 .3 4μmol/L) ,且差异有统计学意义 ;④ALAD12基因型工人锌原卟啉(ZPP)含量比ALAD11基因型者稍低 ,但差异没有统计学意义 ,前者为 ( 0 .42± 0 .2 4) μmol/L ,后者为 ( 0 .46± 0 .41) μmol/L。[结论 ]ALAD2等位基因频率与文献报道的亚洲人群的结果相近 ,符合Hardy Weinberg平衡 ,在同样职业铅暴露环境下 ,具有ALAD2等位基因的工人血铅水平增高 ,ALAD2等位基因可加重工人体内的铅 相似文献