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排序方式: 共有1186条查询结果,搜索用时 15 毫秒
1.
Characterization of nephropathy induced by immunization with high molecular weight dextran 总被引:1,自引:0,他引:1
Pasi A; Dendorfer U; Holthofer H; Nelson P; Tazzari S; Armelloni S; Fornasieri A; D'Amico G; Schlondorff D 《Nephrology, dialysis, transplantation》1997,12(9):1849-1855
Background. Injection of DEAE dextran into Lewis rats
can produce proteinuria and has been reported as a model of IgA
nephropathy. Methods. Cationic diethyl aminoethyl
(DEAE) dextran of molecular weight 500 KDa was injected into male Lewis
rats. After a pre-immunization period of 3 weeks, the animals were divided
into two groups: group 1 (n=14) received daily i.v. injections of 3.5 mg of
antigen, group 2 (n=14) was injected with 1.5 mg three times per week for a
total period of 6 weeks. I.v. treatment was initiated with gradually
increasing doses of DEAE dextran in both groups for 1 week, after which the
maintenance dose was reached. Results. We observed the
appearance of proteinuria in a nephrotic range after 5 weeks of i.v.
injections in group 1 (urinary excretion: 332±83 mg/24 h,
controls: 53±14 mg/24 h). In group 2, the proteinuria was almost
equal to protein excretion of healthy rats of the same weight
(67±20 mg/24 h). The serum and urine creatinine were normal. By
light microscopy of kidney biopsies, the presence of focal and segmental
proliferation of mesangial cells after 6 weeks of i.v. injections was
identified. Immunohistochemistry revealed no deposition of IgA, IgM, IgG,
or C3. Using anti-ED1 antibodies, there was no evidence of interstitial
infiltration of monocytes/macrophages after 6 weeks of i.v. injections.
Staining for proliferating cell nuclear antigen (PCNA) did not show the
presence of proliferating cells either in glomeruli or in the interstitium.
Staining with FITC-WGA lectin revealed focal and segmental loss of the
negative charge in the capillary wall. By electron microscopy there was
deposition of dextran in the basal membrane and segmental and focal damage
of the podocyte foot processes. As the chemokine RANTES may be involved in
glomerular injury, we examined the kidneys of proteinuric and
non-proteinuric rats for the presence of RANTES. By indirect
immunofluorescence only the proteinuric rats showed RANTES deposition in
mesangium. Conclusions. Injection of rats with DEAE
dextran leads to dose-dependent proteinuria without deposition of immune
complexes but with podocyte damage. This is associated with local
expression of the chemokine RANTES which may play a role in proteinuria of
glomerular disease. 相似文献
2.
Neill Booth Antti Jula Pasi Aronen Minna Kaila Timo Klaukka Katriina Kukkonen-Harjula Antti Reunanen Pekka Rissanen Harri Sintonen Marjukka Mäkelä 《BMC health services research》2007,7(1):172
Background
Hypertension is one of the major causes of disease burden affecting the Finnish population. Over the last decade, evidence-based care has emerged to complement other approaches to antihypertensive care, often without health economic assessment of its costs and effects. This study looks at the extent to which changes proposed by the 2002 Finnish evidence-based Current Care Guidelines concerning the prevention, diagnosis, and treatment of hypertension (the ACCG scenario) can be considered cost-effective when compared to modelled prior clinical practice (the PCP scenario). 相似文献3.
Acute IP injection of benzyl alcohol but not benzaldehyde (0.5 g/kg) caused aversion to voluntary drinking of 5% ethanol solution by male rats with preference to ethanol. Benzyl alcohol noncompetitively inhibited hepatic alcohol dehydrogenase of rats maintained for a short term on 5% ethanol compared to control. The results suggest an adverse interaction between benzyl alcohol and ethanol underlying the observed aversion to ethanol. 相似文献
4.
5.
Elomaa O Pulkkinen K Hannelius U Mikkola M Saarialho-Kere U Kere J 《Human molecular genetics》2001,10(9):953-962
Anhidrotic ectodermal dysplasia (EDA) is an X-linked disorder characterized by abnormal development of ectoderm and its appendices. The EDA gene encodes different isoforms of ectodysplasin, a transmembrane protein. The two longest isoforms, ectodysplasin-A1 and -A2, which differ by an insertion of two amino acids, are trimeric type II membrane proteins with an extracellular portion containing a short collagenous domain and a TNF ligand motif in the C-terminal region. We show that ectodysplasin is released from cells to the culture medium. Deletion constructs were used to localize the cleavage site and show that the putative recognition sequence of a furin-like enzyme is needed for the cleavage. Some EDA patients have missense mutations affecting this recognition sequence, suggesting that cleavage has biological significance in vivo. EDAR, a recently cloned member of the TNFR family and the product of the downless gene, is able to co-precipitate ectodysplasin, confirming that they form a ligand-receptor pair. In situ hybridization and immunostaining studies show that ectodysplasin and EDAR are expressed in adjacent or partially overlapping layers in the developing human skin. We conclude that as a soluble ligand, ectodysplasin is able to interact with EDAR and mediate signals needed for the development of ectodermal appendages. 相似文献
6.
7.
Vendelin J Pulkkinen V Rehn M Pirskanen A Räisänen-Sokolowski A Laitinen A Laitinen LA Kere J Laitinen T 《American journal of respiratory cell and molecular biology》2005,33(3):262-270
We recently identified a novel positional asthma susceptibility gene, GPRA, which belongs to the G protein-coupled receptor family. In the present studies, we show that isoform specific activation of GPRA-A with its agonist, Neuropeptide S (NPS) resulted in significant inhibition of cell growth. GPRA has several variants due to extensive alternative splicing. We observed that only the full-length variants, GPRA-A and GPRA-B, with 7 transmembrane topology are transported into the plasma membrane, while the truncated proteins retain intracellular compartments. To clarify disease mechanism, we studied co-expression of the variants without finding any indication that truncated variants would inhibit the receptor transport into the plasma membrane. By using in situ hybridization and immunohistochemistry, we detected ubiquitous expression of GPRA-B, and frequent expression of GPRA-A in the epithelia of several organs including bronchi and gastrointestinal tract. Furthermore, we observed aberrant mRNA and protein expression levels of GPRA in the asthmatic bronchi. Finally, we demonstrate that GPRA and NPS are co-expressed in bronchial epithelium. In summary, this study provides evidence that GPRA might have functional relevance in modulating asthma by increased expression levels in the relevant tissues under diseased state and by potential inhibitory effect of GPRA-A activation on cell growth. 相似文献
8.
Serological evidence that dry heating of clotting factor concentrates prevents transmission of non-A, non-B hepatitis 总被引:1,自引:0,他引:1
S J Skidmore K J Pasi S J Mawson M D Williams F G Hill 《Journal of medical virology》1990,30(1):50-52
A new test for antibodies specific for an agent causing non-A, non-B hepatitis (NANBH) was used to screen 45 children with coagulation disorders who received factor concentrates. It was found that the test results correlated with clinical evidence of NANBH and that heat treatment of concentrates (80 degrees C for 72 hours) appears to have prevented transmission of NANBH. 相似文献
9.
Apolipoprotein B gene DNA polymorphisms are associated with macro- and microangiopathy in non-insulin-dependent diabetes mellitus 总被引:2,自引:0,他引:2
Olavi Ukkola Markku J. Savolainen Pasi I. Salmela Kai von Dickhoff Y. Antero Kesäniemi 《Clinical genetics》1993,44(4):177-184
Ukkola O, Savolainen MJ, Salmela PI, von Dickhoff K, Kesäniemi YA. Apolipoprotein B gene DNA polymorphisms are associated with macro-and microangiopathy in non-insulin-dependent diabetes mellitus. Clin Genet 1993: 44: 177–184. © Munksgaard, 1993 The relationship between diabetic macroangiopathy or microangiopathy and apolipoprotein B (apoB) polymorphism was studied in 139 male and 129 female patients with non-insulin-dependent diabetes (NIDDM) mellitus, comprising consecutive patients with poor diabetic control (HBA1 13.2%\pm2.7 (SD)) referred to our hospital. Plasma cholesterol and triglyceride concentrations were higher in the patients who were homozygous for the X2 allele (presence of Xba I cleavage site). Patients with the X1 allele (absence of Xba I cleavage site) tended to have a higher frequency of macroangiopathy, although the differences were not statistically significant. There was no difference in the prevalence of microangiopathy between the groups. In subjects with only an R1 allele (= R +; homozygous for the presence of EcoR I cleavage site) the prevalence of coronary heart disease (CHD) was observed to be high (61.9%) as compared to the subjects possessing an R2 allele (= R —; homozygous or heterozygous for the absence of the EcoR I cleavage site) (46.7%; p<0.02). When the polymorphisms Xba I (subjects homozygous for the absence of the cutting site = X +; subjects homozygous or heterozygous for the presence of the cutting site = X —) and EcoR I were combined, the prevalence of macroangiopathy was observed to be high in X + R + (80.0%) as compared with X + R- (44.2%), X-R+ (56.8%) and X-R- (50.0%) (p<0.03). The prevalence of macroangiopathy tended to be particularly high in patients with the apoprotein E4 allele (phenotype E4\4 or E4/3), combined with either X+ or R +. Our findings suggest that variation at the apoB locus is one of the factors involved in predisposing diabetic patients to the development of arterial disease. As in previous studies the effect of the variation at the apoB gene on circulating lipid levels was observed. The data also support a role for the e4 allele of the apolipoprotein E gene as an important determinant of macroangiopathy in NIDDM. 相似文献
10.
A Pasi P Kulling D Voellmy C Gramsch P Mehraein M H?ni F S Messiha 《Physiology & behavior》1989,46(1):13-16
The regional levels' profile of human beta-endorphin (beta h-EP) was studied in the brainstem and the cerebellum of 16 infant victims of "Sudden Infant Death Syndrome" and other death causes. An immunoaffinity chromatography procedure based on a monoclonal antibody directed specifically against the N-terminus of beta-EP was used to extract this peptide from the tissue samples. Beta-EP was then assessed quantitatively by means of a very sensitive solid phase radioimmunoassay (using a polyclonal antibody specific for the C-terminus of beta-EP) developed especially for the study presented here. 相似文献