全文获取类型
收费全文 | 1412篇 |
免费 | 163篇 |
国内免费 | 21篇 |
专业分类
耳鼻咽喉 | 6篇 |
儿科学 | 57篇 |
妇产科学 | 62篇 |
基础医学 | 284篇 |
口腔科学 | 32篇 |
临床医学 | 143篇 |
内科学 | 191篇 |
皮肤病学 | 22篇 |
神经病学 | 31篇 |
特种医学 | 113篇 |
外科学 | 247篇 |
综合类 | 91篇 |
一般理论 | 3篇 |
预防医学 | 149篇 |
眼科学 | 10篇 |
药学 | 118篇 |
肿瘤学 | 37篇 |
出版年
2022年 | 8篇 |
2021年 | 16篇 |
2020年 | 9篇 |
2019年 | 15篇 |
2018年 | 22篇 |
2017年 | 14篇 |
2016年 | 12篇 |
2015年 | 22篇 |
2014年 | 27篇 |
2013年 | 45篇 |
2012年 | 40篇 |
2011年 | 50篇 |
2010年 | 47篇 |
2009年 | 43篇 |
2008年 | 25篇 |
2007年 | 53篇 |
2006年 | 49篇 |
2005年 | 34篇 |
2004年 | 52篇 |
2003年 | 33篇 |
2002年 | 34篇 |
2001年 | 43篇 |
2000年 | 34篇 |
1999年 | 22篇 |
1998年 | 39篇 |
1997年 | 40篇 |
1996年 | 49篇 |
1995年 | 36篇 |
1994年 | 26篇 |
1993年 | 35篇 |
1992年 | 35篇 |
1991年 | 25篇 |
1990年 | 33篇 |
1989年 | 44篇 |
1988年 | 42篇 |
1987年 | 58篇 |
1986年 | 45篇 |
1985年 | 47篇 |
1984年 | 27篇 |
1983年 | 21篇 |
1982年 | 18篇 |
1981年 | 24篇 |
1980年 | 22篇 |
1979年 | 35篇 |
1978年 | 21篇 |
1977年 | 24篇 |
1976年 | 11篇 |
1975年 | 13篇 |
1972年 | 11篇 |
1970年 | 9篇 |
排序方式: 共有1596条查询结果,搜索用时 31 毫秒
21.
22.
Localization of a gene for otosclerosis to chromosome 15q25-q26 总被引:5,自引:0,他引:5
Tomek MS; Brown MR; Mani SR; Ramesh A; Srisailapathy CR; Coucke P; Zbar RI; Bell AM; McGuirt WT; Fukushima K; Willems PJ; Van Camp G; Smith RJ 《Human molecular genetics》1998,7(2):285-290
Among white adults otosclerosis is the single most common cause of hearing
impairment. Although the genetics of this disease are controversial, the
majority of studies indicate autosomal dominant inheritance with reduced
penetrance. We studied a large multi- generational family in which
otosclerosis has been inherited in an autosomal dominant pattern. Five of16
affected persons have surgically confirmed otosclerosis; the remaining nine
have a conductive hearing loss but have not undergone corrective surgery.
To locate the disease- causing gene we completed genetic linkage analysis
using short tandem repeat polymorphisms (STRPs) distributed over the entire
genome. Multipoint linkage analysis showed that only one genomic region, on
chromosome 15q, generated a lod score >2.0. Additional STRPs were typed
in this area, resulting in a lod score of 3.4. STRPs FES (centromeric) and
D15S657 (telomeric) flank the 14. 5 cM region that contains an otosclerosis
gene.
相似文献
23.
Summary The authors report the results of 115 dissections of the base of the distal phalanx of fingers and toes. In 85% of cases including hypoplastic supernumerary digits, there is a connective ligament-like structure. It is a dorsal expansion of the lateral ligament of the distal inter-phalangeal joint arising from the intermediate phalanx and ending in the matrix and the lunula. This ligament may have a role in biomechanical strains on the nail. It can explain some dystrophic nails associated with some malpositioned joints in fingers or toes.
Structure ligamentaire de la base de l'ongle
Résumé Les auteurs rapportent les résultats de 115 dissections portant sur la base de la phalange distale des doigts ou des orteils. Ils retrouvent dans 85 % des cas, y compris sur des doigts hypoplasiques surnuméraires, une formation conjonctive de type ligamentaire. Il s'agit d'une expansion dorsale du ligament latéral de l'articulation interphalangienne distale, naissant de l'extrémité distale de la phalange intermédiaire et se terminant au sein de la matrice et sur la lunule. Ce ligament ostéomatriciel peut jouer un rôle dans la transmission des contraintes biomécaniques sur l'ongle et expliquer les dystrophies unguéales stéréotypées associées à certaines malpositions articulaires des doigts ou des orteils.相似文献
24.
A study of the degree of progesterone support required for the maintenance
of various stages of pregnancy was undertaken in mice. Mated females were
ovariectomized at various stages of pregnancy and progesterone and
oestradiol support provided by s.c. Silastic implants with known release
characteristics. In the earliest stages of pregnancy (days 1-5), very low
concentrations of progesterone (<25% of normal physiological values)
were sufficient to maintain pre-implantation stages and allow implantation.
In the immediate post-implantation period (days 5-9), the development of
implantation sites and decidualization required considerably higher
progesterone support. In mid-pregnancy (days 11-14), progesterone alone
could not maintain pregnancy unless present in very high amounts; however,
the presence of oestradiol during this period lowered the progesterone
requirements to well within the physiological range. This effect of
oestradiol started on day 11 but required the level of oestradiol support
to be kept within strictly defined limits, with high concentrations
inducing abortion. Progesterone alone was able to maintain pregnancy from
day 15. These results indicate that the minimal progesterone support
required for pregnancy in mice varies considerably at different stages of
pregnancy and is at least partly modulated by oestradiol.
相似文献
25.
C Morland J Michael D Adu T Kizaki A J Howie A Morgan N A Staines 《Clinical and experimental immunology》1991,83(1):126-132
The effect of the administration of a xenogeneic anti-idiotype antibody (anti-Id33) to a cross-reactive idiotype (Id33) present on anti-dsDNA antibody was examined in 6-week-old (NZB/NZW) F1 (BWF1) female mice. The administration of anti-Id33 led to a transient reduction in immunoglobulins expressing Id33, followed by a rise at 30 and 34 weeks that was significantly higher than in untreated mice (P less than 0.05). Likewise, anti-dsDNA antibody levels were significantly higher at 10 and 18 weeks than in untreated mice (P less than 0.01). No differences were seen in survival to 40 weeks, proteinuria or the severity of glomerulonephritis. Concurrent administration of cyclosporin A (CyA) with anti-Id33 markedly ameliorated glomerular injury and proteinuria and improved survival. By contrast, glomerular injury, proteinuria and survival were worse in mice treated with cyclophosphamide plus anti-Id33, compared with untreated mice. Neither CyA nor cyclophosphamide treatment, when given with anti-Id33 altered serum levels of anti-dsDNA, anti-ssDNA or Id33+ immunoglobin, compared with untreated mice. The different effects of CyA and cyclophosphamide on T lymphocytes and their discrepant effects on glomerular injury when given with anti-Id33 in this model lead us to postulate a role for T lymphocytes in the glomerular injury of BWF1 lupus. 相似文献
26.
Balding CE Howie AJ Drake-Lee AB Savage CO 《Clinical and experimental immunology》2001,125(2):332-339
Wegener's granulomatosis initially affects upper respiratory tract organs including the nasal mucosa in more than 90% of patients. The inflammation is typically granulomatous with associated vasculitis. T lymphocytes are usually a prominent component of the leucocyte infiltrate. Previous studies using peripheral blood T cells have implicated IFN-gamma rich Th1-type responses. This study addressed the cytokine milieu in nasal mucosa from 10 patients with active Wegener's granulomatosis using immunohistochemistry. Increased levels of CD3+ T cells and eosinophils were present compared with normal and disease controls. There was increased expression of IL-4, down-regulation of IL-2 and no detectable IFN-gamma. There was increased expression of the chemokine receptor CCR3 by infiltrating cells, consistent with an IL-4 dominant, Th2-biased response. In contrast, renal biopsy tissue from 10 patients with active Wegener's granulomatosis showed expression of IL-2 and IL-4. The Th2-type environment within nasal mucosa, often the initial site of disease activity in Wegener's, is consistent with a local allergic response in these patients. 相似文献
27.
Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome 总被引:3,自引:4,他引:3
Sirotkin H; Morrow B; DasGupta R; Goldberg R; Patanjali SR; Shi G; Cannizzaro L; Shprintzen R; Weissman SM; Kucherlapati R 《Human molecular genetics》1996,5(5):617-624
Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome (DGS) are
developmental disorders characterized by a spectrum of phenotypes including
velopharyngeal insufficiency, conotruncal heart defects and facial
dysmorphology among others. Eighty to eighty-five percent of VCFS/DGS
patients are hemizygous for a portion of chromosome 22. It is likely that
the genes encoded by this region play a role in the etiology of the
phenotypes associated with the disorders. Using a cDNA selection protocol,
we isolated a novel clathrin heavy chain cDNA (CLTD) from the VCFS/DGS
minimally deleted interval. The cDNA encodes a protein of 1638 amino acids.
CLTD shares significant homology, but is not identical to the ubiquitously
expressed clathrin heavy chain gene. The CLTD gene also shows a unique
pattern of expression, having its maximal level of expression in skeletal
muscle. Velopharyngeal insufficiency and muscle weakness are common
features of VCFS patients. Based on the location and expression pattern of
CLTD, we suggest hemizygosity at this locus may play a role in the etiology
of one of the VCFS-associated phenotypes.
相似文献
28.
29.
R. J. Birtwistle J. Michael A. J. Howie D. Adu 《International journal of experimental pathology》1989,70(2):207-213
The effect of ''scavengers'' of reactive oxygen products (ROPs) was studied in the heterologous phase of anti-glomerular basement (anti-GBM) nephritis induced in rats. Glomerulonephritis was induced by the intravenous administration of sheep anti-GBM antibody (5 mg/100 g) to rats on day 0. The intraperitoneal administration of superoxide dismutase (SOD) 30 mg/kg/day or 150 mg/kg/day leads to a significant reduction in proteinuria on day 1 and also on day 3 in animals given SOD 30 mg/kg/day. Proteinuria was not significantly reduced by the intraperitoneal administration of inactivated SOD (150 mg/kg/day). In rats given polyethylene glycol coupled catalase (PEG-catalase) intraperitoneally at a dose of 10,000 iu/kg/day and 100,000 iu/kg/day proteinuria was lower than in rats with unmodified anti-GBM nephritis. These differences were significant on day 1 (P less than 0.05) in rats given PEG-catalase 100,000 iu/kg/day and on days 3 and 5 in rats treated with either dose of PEG-catalase (P less than 0.01). These data suggest a role for superoxide anion and hydrogen peroxide, or a product of their interaction such as hydroxyl radical, in glomerular injury induced by anti-GBM antibody. 相似文献
30.
Changes at the glomerular tip: a feature of membranous nephropathy and other disorders associated with proteinuria 总被引:1,自引:0,他引:1
A J Howie 《The Journal of pathology》1986,150(1):13-20
Renal biopsies and post-mortem kidneys were examined for segmental lesions at glomerular tips, consisting of adhesion of the tuft to Bowman's capsule with an area of intra-capillary foam cells or hyaline material or sclerosed material. Of 72 consecutive renal biopsies showing membranous nephropathy, 46 (64 per cent) had tip changes. Such changes were correlated with the presence of acute tubular damage and with later stages of the nephropathy, but otherwise seemed unrelated to any particular clinical or pathological feature. Fourteen other patients were identified whose renal biopsies showed tip changes in glomeruli that had segmental or global mesangial hypercellularity not of a well-recognized type such as IgA nephropathy. These patients had persistent proteinuria unresponsive to steroids. Tip changes were also seen in several miscellaneous conditions including IgA nephropathy and diabetic glomerulosclerosis. These findings demonstrate that tip changes are seen in many disorders of the kidney associated with proteinuria and represent a previously unrecognized common response of the glomerulus to some insult, the glomerular tip lesion, as originally defined, is distinguished by the apparent normality of tufts except for the tip changes and can be regarded as presumed minimal change nephropathy plus tip changes and when tip changes are seen, the most important factor determining the prognosis is the condition of the rest of the glomerular tuft. 相似文献