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排序方式: 共有1798条查询结果,搜索用时 31 毫秒
941.
Schwarzenbacher R von Delft F Abdubek P Ambing E Biorac T Brinen LS Canaves JM Cambell J Chiu HJ Dai X Deacon AM DiDonato M Elsliger MA Eshagi S Floyd R Godzik A Grittini C Grzechnik SK Hampton E Jaroszewski L Karlak C Klock HE Koesema E Kovarik JS Kreusch A Kuhn P Lesley SA Levin I McMullan D McPhillips TM Miller MD Morse A Moy K Ouyang J Page R Quijano K Robb A Spraggon G Stevens RC van den Bedem H Velasquez J Vincent J Wang X West B Wolf G Xu Q Hodgson KO Wooley J Wilson IA 《Proteins》2004,54(4):810-813
942.
Erlandsen H Canaves JM Elsliger MA von Delft F Brinen LS Dai X Deacon AM Floyd R Godzik A Grittini C Grzechnik SK Jaroszewski L Klock HE Koesema E Kovarik JS Kreusch A Kuhn P Lesley SA McMullan D McPhillips TM Miller MD Morse A Moy K Ouyang J Page R Robb A Quijano K Schwarzenbacher R Spraggon G Stevens RC van den Bedem H Velasquez J Vincent J Wang X West B Wolf G Hodgson KO Wooley J Wilson IA 《Proteins》2004,54(4):806-809
943.
Schwarzenbacher R Deacon AM Jaroszewski L Brinen LS Canaves JM Dai X Elsliger MA Floyd R Godzik A Grittini C Grzechnik SK Klock HE Koesema E Kovarik JS Kreusch A Kuhn P Lesley SA McMullan D McPhillips TM Miller MD Morse A Moy K Nelson MS Ouyang J Page R Robb A Quijano K Spraggon G Stevens RC van den Bedem H Velasquez J Vincent J von Delft F Wang X West B Wolf G Hodgson KO Wooley J Wilson IA 《Proteins》2004,54(4):801-805
944.
McMullan D Schwarzenbacher R Jaroszewski L von Delft F Klock HE Vincent J Quijano K Abdubek P Ambing E Biorac T Brinen LS Canaves JM Dai X Deacon AM DiDonato M Elsliger MA Eshaghi S Floyd R Godzik A Grittini C Grzechnik SK Hampton E Karlak C Koesema E Kreusch A Kuhn P Levin I McPhillips TM Miller MD Morse A Moy K Ouyang J Page R Reyes R Rezezadeh F Robb A Sims E Spraggon G Stevens RC van den Bedem H Velasquez J Wang X West B Wolf G Xu Q Hodgson KO Wooley J Lesley SA Wilson IA 《Proteins》2004,56(3):615-618
945.
Levin I Schwarzenbacher R McMullan D Abdubek P Ambing E Biorac T Cambell J Canaves JM Chiu HJ Dai X Deacon AM DiDonato M Elsliger MA Godzik A Grittini C Grzechnik SK Hampton E Jaroszewski L Karlak C Klock HE Koesema E Kreusch A Kuhn P Lesley SA McPhillips TM Miller MD Morse A Moy K Ouyang J Page R Quijano K Reyes R Robb A Sims E Spraggon G Stevens RC van den Bedem H Velasquez J Vincent J von Delft F Wang X West B Wolf G Xu Q Hodgson KO Wooley J Wilson IA 《Proteins》2004,56(3):629-633
946.
Described herein is a study of the reductive alkylation chemistry of mitosene antitumor agents. We employed a 13C-enriched electrophilic center to probe the fate of the iminium ion resulting from reductive activation. The 13C-labeled center permitted the identification of complex products resulting from alkylation reactions. In the case of DNA reductive alkylation, the type and number of alkylation sites were readily assessed by 13C NMR. Although there has been much excellent work done in the area of mitosene chemistry and biochemistry, the present study provides a number of new findings: (1) The major fate of the iminium ion is head-to-tail polymerization, even in dilute solutions. (2) Dithionite reductive activation results in the formation of mitosene sulfite esters as well as the previously observed sulfonate adducts. (3) The mitosene iminium ion alkylates the adenosine 6-amino group as well as the guanosine 2-amino group. The identification of the latter adduct was greatly facilitated by the 13C-label at the electrophilic center. (4) The mitosene iminium ion alkylates DNA at both nitrogen and oxygen centers without any apparent base selectivity. The complexity of mitosene reductive alkylation of DNA will require continued adduct isolation studies. 相似文献
947.
T A Duhamel R D Stewart A R Tupling J Ouyang H J Green 《Journal of applied physiology》2007,103(4):1212-1220
The study investigated the hypothesis that three consecutive days of prolonged cycle exercise would result in a sustained reduction in the Ca(2+)-cycling properties of the vastus lateralis in the absence of changes in the sarcoplasmic (endoplasmic) reticulum Ca(2+)-ATPase (SERCA) protein. Tissue samples were obtained at preexercise (Pre) and postexercise (Post) on day 1 (E1) and day 3 (E3) and during recovery day 1 (R1), day 2 (R2), and day 3 (R3) in 12 active but untrained volunteers (age 19.2 +/- 0.27 yr; mean +/- SE) and analyzed for changes (nmol.mg protein(-1).min(-1)) in maximal Ca(2+)-ATPase activity (V(max)), Ca(2+) uptake and Ca(2+) release (phase 1 and phase 2), and SERCA isoform expression (SERCA1a and SERCA2a). At E1, reductions (P < 0.05) from Pre to Post in V(max) (150 +/- 7 vs. 121 +/- 7), Ca(2+) uptake (7.79 +/- 0.28 vs. 5.71 +/- 0.33), and both phases of Ca(2+) release (phase 1, 20.3 +/- 1.3 vs. 15.2 +/- 1.1; phase 2, 7.70 +/- 0.60 vs. 4.99 +/- 0.48) were found. In contrast to V(max), which recovered at Pre E3 and then remained stable at Post E3 and throughout recovery, Ca(2+) uptake remained depressed (P < 0.05) at E3 Pre and Post and at R1 as did phase 2 of Ca(2+) release. Exercise resulted in an increase (P < 0.05) in SERCA1a (14% at R2) but not SERCA2a. It is concluded that rapidly adapting mechanisms protect V(max) following the onset of regular exercise but not Ca(2+) uptake and Ca(2+) release. 相似文献
948.
Correlations between tissue-level stresses and strains and cellular damage within the guinea pig spinal cord white matter 总被引:1,自引:0,他引:1
Strain magnitude, strain rate, axon location, axon size, and the local tissue stress state have been proposed as the mechanisms governing primary cellular damage within the spinal cord parenchyma during slow compression injury. However, the mechanism of axon injury has yet to be fully elucidated. The objective of this study was to correlate cellular damage within the guinea pig spinal cord white matter, quantified by a horseradish peroxidase (HRP) exclusion test, with tissue-level stresses and strains using a combined experimental and computational approach. Force-deformation curves were acquired by transversely compressing strips of guinea pig spinal cord white matter at a quasi-static rate. Hyperelastic material parameters, derived from a Mooney-Rivlin constitutive law, were varied within a nonlinear, plane strain finite element model of the white matter strips until the computational force-deformation curve converged to the experimental results. In addition, white matter strips were subjected to nominal compression levels of 25%, 50%, 70%, and 90% to assess axonal damage by quantifying HRP uptake. HRP uptake density increased with tissue depth and with increased nominal compression. Using linear and nonlinear regression analyses, the strongest correlations with HRP uptake density were found for groups of tissue-level stresses and groups of log-transformed tissue-level strains. 相似文献
949.
Owing to unsuitable green space construction, abundant allergenic pollen plants are centralized in urban areas, producing allergenic pollen. A mass of airborne allergenic pollen could cause pollinosis to badly influence people's robustness. To provide scientific basis for reasonable green space construction, the research advances of allergenic plants were reviewed. Firstly, species composition, phenological characteristics and influential factors (which include unsuitable green land construction, urban heat island effect, traffic pollution, etc.) were summarized. Secondly, the strategies controlling allergenic pollen plants were proposed. Thirdly, some problems on allergenic plants worthy of more research, including allergenic mechanism and methodology, were also put forward. 相似文献
950.
Weiwei Sun Xiongjun Liu Ruiwen Wu Weikai Wang Yanli Wu Shan Ouyang Xiaoping Wu 《Ecology and evolution》2019,9(24):14142-14153
Freshwater mussels provide important functions and services for aquatic ecosystems, but populations of many species have been extirpated. Information on biodiversity plays an important role in the conservation and management of freshwater mussels. The Xin River Basin is a biodiversity hotspot for freshwater mussels in China, with more than 43 species known, but populations of which are decreasing. Here, we quantify the diversity of freshwater mussels in the middle and lower reaches of the Xin River Basin and study the correlation of habitat characteristics and freshwater mussel diversity. Compared to the historical period, the number of species, density, and biomass of freshwater mussels decreased 33%, 83%, and 82% in the current period, respectively. Fifty two percent of recorded species were empty shells, and 14 native freshwater mussels were not found in the study area. Four species are currently listed as vulnerable species using IUCN criteria and their global status. The assemblage structure of freshwater mussels exhibits significant spatial differences, and there was a correlation with substrate and physicochemical parameters. The main tributary of the Xin River with higher freshwater mussel diversity should be established as one large protected area because the nestedness component was the main pattern of beta diversity. These results indicated freshwater mussel diversity was declining rapidly, which can help focus conservation effort for freshwater mussel biodiversity. 相似文献