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AS Aktürk† N Bilen† D Bayrämgürler† EO Demirsoy† S Erdogan‡ R Kiran† 《Journal of the European Academy of Dermatology and Venereology》2007,21(8):1086-1090
BACKGROUND: It is a common opinion that expansion and darkening in melanocytic nevi may occur during pregnancy. The main problem is that whether it is a usual finding, or it is a condition that requires suspicion about melanoma. OBJECTIVES: It was aimed to find the changes that might occur in the sizes and structures of melanocytic nevi during pregnancy. METHODS: Ninety-seven nevi of the 56 pregnant women in the first trimester were evaluated in the study. The localization and size of the nevi were recorded on a standard body diagram. After clinical examination, dermoscopic analyses were applied. Pattern analyses were done, and total dermoscopy scores (TDS) were calculated by applying ABCD scoring system. All subjects were seen again during the third trimester. RESULTS: There was a statistically significant difference between the mean diameters of nevi in the first and third trimester (P = 0.001). Of nevi whose diameters increased, 10 (50.00%) were localized on the front of body, 6 (30.00%) on the face and neck, 3 (15.00%) on the legs, and 1 (5.00%) on the back. The enlargement in diameters was more significant on the front of the body, but there was no statistically significant difference. Compared according to the pattern analysis, new dot formation was observed only on the structure of six nevi during the last trimester. Four of them were localized on the front of the body. There was statistically significant increase in mean TDS in comparison between the first and third trimesters (P = 0008). CONCLUSIONS: During the pregnancy, widening in diameters and structure changes of nevi may be seen especially on the front of the body. We also think that these findings might be connected with expansion of the skin during pregnancy. Dermoscopic controls are the first choice of method to analyse the nevi since the patient may not recognize these changes. 相似文献
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Expression of mutated glucocerebrosidase alleles in human cells 总被引:1,自引:1,他引:1
Pasmanik-Chor M; Madar-Shapiro L; Stein EO; Aerts H; Gatt S; Horowitz M 《Human molecular genetics》1997,6(6):887-895
Gaucher disease is a heterogeneous disease characterized by impaired
activity of the lysosomal enzyme glucocerebrosidase. This heterogeneity is
attributed to a large number of mutations in the corresponding gene. In
order to test the biochemical properties of some mutations prevalent among
Israeli populations, the normal human glucocerebrosidase cDNA and cDNAs
carrying mutations N370S, L444P, D409H, recTL, recNcil, P415R and 84GG were
coupled to the T7 RNA polymerase promoter in a vaccinia virus- derived
expression vector (pTM-1). Recombinant viruses were produced and used to
infect human tissue culture cells. RNA and protein stability, recognition
by anti-glucocerebrosidase monoclonal antibodies and intracellular
enzymatic activity were measured. The results demonstrated that the D409H
allele directed synthesis of cytoplasmic RNA with decreased stability
compared with its normal counterpart or other mutated forms. The D409H and
L444P mutated proteins had lower stability than that of their normal
counterpart, while the recNcil- mutated protein was more stable. Only
glucocerebrosidase forms harboring leucine at position 444 were recognized
by the anti- glucocerebrosidase monoclonal antibodies used (8E4 and 2C7).
Measurements of enzymatic activity of the recombinant proteins in cells
loaded with a fluorescent glucosylceramide demonstrated that the N370S
mutated enzyme had activity similar to that of the normal enzyme. The other
mutated enzymes exhibited varying degrees of activities, generally
corresponding to the phenotypes with which they are associated. The results
presented demonstrate the use of the vaccinia virus-derived expression
system and of loading living cells with fluorescent substrate as efficient
tools for studying mutants in Gaucher disease and in other lysosomal
diseases.
相似文献
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全复配食用菌提取物对C26荷瘤小鼠的抑瘤作用和免疫功能影响 总被引:1,自引:0,他引:1
背景与目的:食用真菌在医疗保健领域的研究展现出强大的应用潜力.该课题探讨全复配食用菌提取物的抗肿瘤作用及对荷瘤小鼠免疫功能的影响.方法:小鼠随机编号分组,其中预防组预先给予全复配食用菌提取物灌胃2周,每天1次,之后各组均接种C26细胞建立荷瘤小鼠模型,接种后第2天给小鼠予以不同制剂灌胃(空白组灌0.9%氯化钠溶液,治疗组、预防阻灌复配食用菌提取物,CTX阳性组腹腔注射CTX)每天1次,观察记录小鼠一般状态,2周后处死小鼠无菌取脾脏、取瘤称重.MTT法检测小鼠脾淋巴细胞转化功能,乳酸脱氢酶(LDH)法检测NK细胞杀伤活性.结果:复配食用菌提取物预防组对小鼠C26肿瘤有30.4%的抑制率;小鼠脾淋巴细胞在ConA刺激下的增殖能力和NK细胞杀伤功能均显著高于空白组.结论:复配食用菌提取物预防性摄入对再接种C26小鼠有抑瘤和免疫增强作用. 相似文献
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Background
Development of “combination” assays detecting in parallel, within a single test, Hepatitis C Virus (HCV) antigens and antibodies, not only reduces the window period in HCV-infection but also costs. Reduction of costs is important for developing countries where money and personal resources are limited.Methods
We compared the Monolisa® HCV Antigen-Antibody Ultra (Bio-Rad Laboratories Limited, Marnes La Coquette, France) with the AXSYM HCV version 3.0 (Abbot Diagnostics, Germany)-the latter assay detecting only antibodies to HCV. Seventy three HCV-PCR positive and negative samples were tested.Results
Although the two assays showed comparable results, two samples from a bone marrow transplant (BMT) patient of viral loads 7.8 × 105 and 8.9 × 106 IU/mL could not be detected by the Monolisa® HCV Antigen-Antibody Ultra assay. Failure to detect the two samples with viral loads considered above threshold of detection for antigen proteins suggested a lack of sensitivity by this assay to discover viral capsid protein in patient samples. Genotyping of these samples revealed genotype 1b, a HCV-subtype which is widespread and should thus be easily detected.Conclusion
We conclude that although this assay depicts high sensitivity and specificity in detecting antibodies to HCV, it seems not to add further benefit in our study population to detect HCV infections by enhanced sensitivity due the potential contingency to trace viral capsid antigens. 相似文献28.
Oral rehydration mixtures are readily available in rural Kenya, but the instructions that accompany them are not always clear. Mothers will understand such instructions more readily if they explain the principles of oral rehydration and describe in a logical way the sequence of procedures to be followed. 相似文献
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Lithium has been recognized as a stimulator of granulopoiesis both in vivo and in vitro. The mechanism by which lithium provokes this stimulation is unclear, with previous data focusing on such divergent causes as direct effects on progenitor cells v elevations in granulocyte macrophage colony-stimulating activity (GM-CSA) production. In the present study, we used a model system of granulopoiesis in diffusion chambers to study this stimulation of granulopoiesis. Lithium pretreatment of mice followed by a rest period to allow for excretion of the lithium (confirmed by serum assays) revealed a stimulation of progenitor cell growth within the diffusion chambers. No changes in the serum and chamber fluid GM-CSA levels were discernible between the control host mice and the lithium-pretreated mice. These data indicate that lithium stimulates granulopoiesis by an indirect mechanism that does not appear to involve GM-CSA. 相似文献