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71.
The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations 总被引:1,自引:0,他引:1
Mueller EE Eder W Ebner S Schwaiger E Santic D Kreindl T Stanger O Paulweber B Iglseder B Oberkofler H Maier R Mayr JA Krempler F Weitgasser R Patsch W Sperl W Kofler B 《PloS one》2011,6(1):e16455
Background
The pivotal role of mitochondria in energy production and free radical generation suggests that the mitochondrial genome could have an important influence on the expression of multifactorial age related diseases. Substitution of T to C at nucleotide position 16189 in the hypervariable D-loop of the control region (CR) of mitochondrial DNA (mtDNA) has attracted research interest because of its suspected association with various multifactorial diseases. The aim of the present study was to compare the frequency of this polymorphism in the CR of mtDNA in patients with coronary artery disease (CAD, n = 482) and type 2 diabetes mellitus (T2DM, n = 505) from two study centers, with healthy individuals (n = 1481) of Middle European descent in Austria.Methodology and Principal Findings
CR polymorphisms and the nine major European haplogroups were identified by DNA sequencing and primer extension analysis, respectively. Frequencies and Odds Ratios for the association between cases and controls were calculated. Compared to healthy controls, the prevalence of T16189C was significantly higher in patients with CAD (11.8% vs 21.6%), as well as in patients with T2DM (11.8% vs 19.4%). The association of CAD, but not the one of T2DM, with T16189C remained highly significant after correction for age, sex and body mass index (BMI) and was independent of the two study centers.Conclusions and Significance
Our results show for the first time a significant association of T16189C with CAD in a Middle European population. As reported in other studies, in patients with T2DM an association with T16189C in individuals of European decent remains questionable. 相似文献72.
73.
Gerfried?JungmeierEmail author Fred?McDarby Anders?Evald Catharina?Hohenthal Ann-Kristin?Petersen Hannes-Peter?Schwaiger Bernhard?Zimmer 《The International Journal of Life Cycle Assessment》2003,8(2):99-105
Intention and Background.
This paper outlines guidelines for the treatment of energy in LCAs of forest products. The paper is a result of the Cost Action E 9 ‘Life cycle assessment of forestry and forest products’ and reflects the experience of Cost E9 delegates, contributing to Working Group ‘End of life — recycling, disposal and energy generation’. 相似文献74.
The F-actin crosslinker filamin from Dictyostelium discoideum (ddFLN) has a rod domain consisting of six structurally similar immunoglobulin domains. When subjected to a stretching force, domain 4 unfolds at a lower force than all the other domains in the chain. Moreover, this domain shows a stable intermediate along its mechanical unfolding pathway. We have developed a mechanical single-molecule analogue to a double-jump stopped-flow experiment to investigate the folding kinetics and pathway of this domain. We show that an obligatory and productive intermediate also occurs on the folding pathway of the domain. Identical mechanical properties suggest that the unfolding and refolding intermediates are closely related. The folding process can be divided into two consecutive steps: in the first step 60 C-terminal amino acids form an intermediate at the rate of 55 s(-1); and in the second step the remaining 40 amino acids are packed on this core at the rate of 179 s(-1). This division increases the overall folding rate of this domain by a factor of ten compared with all other homologous domains of ddFLN that lack the folding intermediate. 相似文献
75.
Degradation of a short-lived glycoprotein from the lumen of the endoplasmic reticulum: the role of N-linked glycans and the unfolded protein response 下载免费PDF全文
de Virgilio M Kitzmüller C Schwaiger E Klein M Kreibich G Ivessa NE 《Molecular biology of the cell》1999,10(12):4059-4073
We are studying endoplasmic reticulum-associated degradation (ERAD) with the use of a truncated variant of the type I ER transmembrane glycoprotein ribophorin I (RI). The mutant protein, RI(332), containing only the N-terminal 332 amino acids of the luminal domain of RI, has been shown to interact with calnexin and to be a substrate for the ubiquitin-proteasome pathway. When RI(332) was expressed in HeLa cells, it was degraded with biphasic kinetics; an initial, slow phase of approximately 45 min was followed by a second phase of threefold accelerated degradation. On the other hand, the kinetics of degradation of a form of RI(332) in which the single used N-glycosylation consensus site had been removed (RI(332)-Thr) was monophasic and rapid, implying a role of the N-linked glycan in the first proteolytic phase. RI(332) degradation was enhanced when the binding of glycoproteins to calnexin was prevented. Moreover, the truncated glycoprotein interacted with calnexin preferentially during the first proteolytic phase, which strongly suggests that binding of RI(332) to the lectin-like protein may result in the slow, initial phase of degradation. Additionally, mannose trimming appears to be required for efficient proteolysis of RI(332). After treatment of cells with the inhibitor of N-glycosylation, tunicamycin, destruction of the truncated RI variants was severely inhibited; likewise, in cells preincubated with the calcium ionophore A23187, both RI(332) and RI(332)-Thr were stabilized, despite the presence or absence of the N-linked glycan. On the other hand, both drugs are known to trigger the unfolded protein response (UPR), resulting in the induction of BiP and other ER-resident proteins. Indeed, only in drug-treated cells could an interaction between BiP and RI(332) and RI(332)-Thr be detected. Induction of BiP was also evident after overexpression of murine Ire1, an ER transmembrane kinase known to play a central role in the UPR pathway; at the same time, stabilization of RI(332) was observed. Together, these results suggest that binding of the substrate proteins to UPR-induced chaperones affects their half lives. 相似文献
76.
77.
Moran L. B. Kösel S. Spitzer C. Schwaiger F. W. Riess O. Kreutzberg G. W. Graeber M. B. 《Brain Cell Biology》2001,30(6):515-521
The discovery that missense mutations in the alpha-synuclein gene represent a rare genetic cause of Parkinson's disease (PD) has had significant impact on the development of research into neurodegenerative disorders. It is becoming increasingly clear that alpha-synuclein plays a central role in the pathological process, which causes Lewy body formation and neurodegeneration in PD. Importantly, there is evidence to suggest that mutated alpha-synuclein is toxic to both nerve cells and glia. However, the regulation and function of wild-type alpha-synuclein are as yet ill defined. Using the facial nerve axotomy model, we have addressed the question whether the expression of alpha-synuclein in nerve cells may change in response to injury. We were particularly interested in testing the hypothesis that the severity of neuronal injury had an effect on alpha-synuclein metabolism. Facial nerve cut and crush, respectively, were performed in adult rats where normal facial motoneurones do not express alpha-synuclein. Following axotomy, a subset of facial motoneurones newly expressed high levels of alpha-synuclein immunoreactivity in their cell body and, occasionally, their nucleus. Significantly more nerve cells were labelled following facial nerve transection than following facial nerve crush. Confocal microscopy revealed a granular pattern of alpha-synuclein aggregation in degenerating nerve cells. Interestingly, the observed cell death phenotype was clearly non-apoptotic and developed over days or weeks rather than hours. Thus, axotomy of adult rat facial motoneurones triggers de novo expression of alpha-synuclein and this expression is associated with a non-apoptotic, slow form a neurodegeneration. In addition, the extent of alpha-synuclein expression is related to the severity of neuronal injury. 相似文献
78.
Uwe Dietze Thomas Braunbeck Wolfgang Honnen Heinz-R. Köhler Julia Schwaiger Helmut Segner Rita Triebskorn Gerrit Schüürmann 《Journal of Aquatic Ecosystem Stress and Recovery (Formerly Journal of Aquatic Ecosystem Health)》2001,8(3-4):319-336
The VALIMAR project aims at identifyingbiomarkers in fish that are suitable to detectand predict environmental stress from chemicalpollution or from limnological parameters inthe field. For two small streams in SouthernGermany, concentration values of 31contaminants in water and sediment and 12 limnological parameters as well as 27 biomarkersmeasured in brown trout and stone loach werecollected. All these physicochemical andbiological parameters have been analysed forpatterns that discriminate between the streams,using discriminant analysis (DA), analysis ofvariance (ANOVA) and of covariance (ANCOVA), and principal component analysis (PCA) asmultivariate statistical techniques. Moreover,the biological data were analyzed with respectto species-specific patterns, and the partialleast-squares regression method (PLS) was usedto study the impact of chemical and limnological data on the health status of the targetspecies as characterized by the biomarker data.Abiotic as well as biotic data yielded goodseparations between the streams, with theultrastructure of gill (US-gill) being thestrongest discriminator variable among all 27biomarkers tested. With regard to the two fishspecies, the biomarker data from brown troutshow significantly greater differences betweenthe two streams than the biological responsesin stone loach. Application of PLS yieldssignificant regression models for only fewbiomarkers including US-Gill, which can bepartly traced back to significant noise levelsin the data set as quantified by permutationtests. 相似文献
79.
Christine S. Schwaiger Sara I. B?rjesson Berk Hess Bj?rn Wallner Fredrik Elinder Erik Lindahl 《PloS one》2012,7(10)
The gating of voltage-gated ion channels is controlled by the arginine-rich S4 helix of the voltage-sensor domain moving in response to an external potential. Recent studies have suggested that S4 moves in three to four steps to open the conducting pore, thus visiting several intermediate conformations during gating. However, the exact conformational changes are not known in detail. For instance, it has been suggested that there is a local rotation in the helix corresponding to short segments of a 3-helix moving along S4 during opening and closing. Here, we have explored the energetics of the transition between the fully open state (based on the X-ray structure) and the first intermediate state towards channel closing (C), modeled from experimental constraints. We show that conformations within 3 Å of the X-ray structure are obtained in simulations starting from the C model, and directly observe the previously suggested sliding 3-helix region in S4. Through systematic free energy calculations, we show that the C state is a stable intermediate conformation and determine free energy profiles for moving between the states without constraints. Mutations indicate several residues in a narrow hydrophobic band in the voltage sensor contribute to the barrier between the open and C states, with F233 in the S2 helix having the largest influence. Substitution for smaller amino acids reduces the transition cost, while introduction of a larger ring increases it, largely confirming experimental activation shift results. There is a systematic correlation between the local aromatic ring rotation, the arginine barrier crossing, and the corresponding relative free energy. In particular, it appears to be more advantageous for the F233 side chain to rotate towards the extracellular side when arginines cross the hydrophobic region. 相似文献
80.