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131.
Albornoz CR Bach PB Pusic AL McCarthy CM Mehrara BJ Disa JJ Cordeiro PG Matros E 《Plastic and reconstructive surgery》2012,129(5):1071-1079
132.
Hossein Soleimani-B. Caro Lucas Babak N. Araabi Lars Schwabe 《Biomedical signal processing and control》2012,7(5):456-464
Previous work has demonstrated that some dynamic properties of intracranial EEG signals are indicative of epileptic seizures and hence could be used for prediction in order to realize counter measures. However, most previous studies only investigated predictability via offline analysis of EEG signals as compared to actually predicting seizures in a setting applicable to implantable devices. Here we address this problem, which calls for simple and fast online methods, and based on previous offline analyses we hypothesize that prediction can be further improved when using multiple features to detect the preictal patterns. We propose a simple adaptive online method (an evolving neuro-fuzzy model) to adaptively learn such combined features. The classifier starts out with a simple structure and patient-independent parameters and then grows into a personal seizure predictor as recursive methods tune the model structure and parameters. We apply the adaptive classifier to a publicly available database of intracranial recordings from 21 patients and demonstrate that seizure prediction is improved with our online method as compared to offline non-adaptive techniques. We show that our method is robust with respect to those few model parameters, which are not adapted. Moreover, as we report the performance on data from a publicly available seizure database, our results can serve as a yardstick for future method developments. 相似文献
133.
Dihydropteroate synthase (DHPS) catalyzes the formation of dihydropteroate and Mg-pyrophosphate from 6-hydroxymethyl-7,8-dihydropterin diphosphate and para-aminobenzoic acid. The Bacillus anthracis DHPS is intrinsically resistant to sulfonamides. However, using a radioassay that monitors the dihydropteroate product, the enzyme was inhibited by the same sulfonamides. A continuous spectrophotometric assay for measuring the enzymatic activity of DHPS was developed and used to examine the effects of sulfonamides on the enzyme. The new assay couples the production of MgPPi to the pyrophosphate-dependent phosphofructokinase/aldolase/triose isomerase/alpha-glycerophosphate dehydrogenase reactions and monitors the disappearance of NADH at 340nm. The coupled enzyme assay demonstrates that resistance of the B. anthracis DHPS results in part from the use of the sulfonamides as alternative substrates, resulting in the formation of sulfonamide-pterin adducts, and not necessarily due to an inability to bind them. 相似文献
134.
135.
Mehrara BJ Santoro TD Arcilla E Watson JP Shaw WW Da Lio AL 《Plastic and reconstructive surgery》2006,118(5):1100-9; discussion 1110-1
136.
137.
Caveolin-1-deficient mice are lean, resistant to diet-induced obesity, and show hypertriglyceridemia with adipocyte abnormalities. 总被引:20,自引:0,他引:20
Babak Razani Terry P Combs Xiao Bo Wang Philippe G Frank David S Park Robert G Russell Maomi Li Baiyu Tang Linda A Jelicks Philipp E Scherer Michael P Lisanti 《The Journal of biological chemistry》2002,277(10):8635-8647
Caveolae organelles and caveolin-1 protein expression are most abundant in adipocytes and endothelial cells. Our initial report on mice lacking caveolin-1 (Cav-1) demonstrated a loss of caveolae and perturbations in endothelial cell function. More recently, however, observation of the Cav-1-deficient cohorts into old age revealed significantly lower body weights, as compared with wild-type controls. These results suggest that Cav-1 null mice may have problems with lipid metabolism and/or adipocyte functioning. To test this hypothesis directly, we placed a cohort of wild-type and Cav-1 null mice on a high fat diet. Interestingly, despite being hyperphagic, Cav-1 null mice show overt resistance to diet-induced obesity. As predicted, adipocytes from Cav-1 null null mice lack caveolae membranes. Early on, a lack of caveolin-1 selectively affects only the female mammary gland fat pad and results in a near complete ablation of the hypo-dermal fat layer. There are also indications of generalized adipose tissue pathology. With increasing age, a systemic decompensation in lipid accumulation occurs resulting in dramatically smaller fat pads, histologically reduced adipocyte cell diameter, and a poorly differentiated/hypercellular white adipose parenchyma. To gain mechanistic insights into this phenotype, we show that, although serum insulin, glucose, and cholesterol levels are entirely normal, Cav-1 null mice have severely elevated triglyceride and free fatty acid levels, especially in the post-prandial state. However, this build-up of triglyceride-rich chylomicrons/very low density lipoproteins is not due to perturbed lipoprotein lipase activity, a major culprit of isolated hypertriglyceridemia. The lean body phenotype and metabolic defects observed in Cav-1 null mice are consistent with the previously proposed functions of caveolin-1 and caveolae in adipocytes. Our results show for the first time a clear role for caveolins in systemic lipid homeostasis in vivo and place caveolin-1/caveolae as major factors in hyperlipidemias and obesity. 相似文献
138.
Di(1‐naphthyl) methanol ester of carboxylic acids for absolute stereochemical determination 下载免费PDF全文
The absolute stereochemistry of chiral carboxylic acids is determined as a di(1‐naphthyl)methanol ester derivative. Computational scoring of conformations favoring either P or M helicity of the naphthyl groups, capable of exciton‐coupled circular dichroic coupling, leads to a predicted stereochemistry for the derivatized carboxylic acids. 相似文献
139.
A new class of bradykinin 1 receptor antagonists containing the piperidine acetic acid tetralin core
Fotsch C Biddlecome G Biswas K Chen JJ D'Amico DC Groneberg RD Han NB Hsieh FY Kamassah A Kumar G Lester-Zeiner D Liu Q Mareska DA Riahi BB Wang YJ Yang K Zhan J Zhu J Johnson E Ng G Askew BC 《Bioorganic & medicinal chemistry letters》2006,16(8):2071-2075
The bradykinin 1 (B1) receptor is upregulated during times of inflammation and is important for maintaining inflamed and chronic pain states. Blocking this receptor has been shown to reverse and/or ameliorate pain and inflammation in animal models. In this report, we describe a new class of B1 receptor antagonists that contain the piperidine acetic acid tetralin core. A structure-activity relationship for these analogs is described in this paper. The most potent compounds from this class have IC50s<20 nM in a B1 receptor functional assay. One of these compounds, 13g, shows modest oral bioavailability in rats. 相似文献
140.
Caveolin-2-deficient mice show evidence of severe pulmonary dysfunction without disruption of caveolae 总被引:21,自引:0,他引:21 下载免费PDF全文
Razani B Wang XB Engelman JA Battista M Lagaud G Zhang XL Kneitz B Hou H Christ GJ Edelmann W Lisanti MP 《Molecular and cellular biology》2002,22(7):2329-2344
Caveolin-2 is a member of the caveolin gene family with no known function. Although caveolin-2 is coexpressed and heterooligomerizes with caveolin-1 in many cell types (most notably adipocytes and endothelial cells), caveolin-2 has traditionally been considered the dispensable structural partner of the widely studied caveolin-1. We now directly address the functional significance of caveolin-2 by genetically targeting the caveolin-2 locus (Cav-2) in mice. In the absence of caveolin-2 protein expression, caveolae still form and caveolin-1 maintains its localization in plasma membrane caveolae, although in certain tissues caveolin-1 is partially destabilized and shows modestly diminished protein levels. Despite an intact caveolar membrane system, the Cav-2-null lung parenchyma shows hypercellularity, with thickened alveolar septa and an increase in the number of endothelial cells. As a result of these pathological changes, these Cav-2-null mice are markedly exercise intolerant. Interestingly, these Cav-2-null phenotypes are identical to the ones we and others have recently reported for Cav-1-null mice. As caveolin-2 expression is also severely reduced in Cav-1-null mice, we conclude that caveolin-2 deficiency is the clear culprit in this lung disorder. Our analysis of several different phenotypes observed in caveolin-1-deficient mice (i.e., abnormal vascular responses and altered lipid homeostasis) reveals that Cav-2-null mice do not show any of these other phenotypes, indicating a selective role for caveolin-2 in lung function. Taken together, our data show for the first time a specific role for caveolin-2 in mammalian physiology independent of caveolin-1. 相似文献