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Selected AbstractsDo conflict management styles affect group decision making?HUMAN COMMUNICATION RESEARCH, Issue 4 2000Evidence from a longitudinal field study This study examined the relationship between group conflict management styles and effectiveness of group decision making in 11 ongoing, naturally occurring workgroups from 2 large U.S. organizations. The major postulate of the study was that groups develop norms regarding how they will manage conflicts that carry over to affect other activities, such as decision making, even when these activities do not involve open conflict. To determine the impact of conflict management style on decision effectiveness, a longitudinal design was used that identified conflict management styles in the initial portion of each team's series of meetings and then analyzed a group decision taken in a meeting near the end of that series. Group conflict management styles were determined using observational methods, and decision effectiveness was measured using multiple indices that tapped member, facilitator, and external observer viewpoints. Task complexity also was considered as a possible moderating variable. The findings suggest that groups that developed integrative conflict management styles made more effective decisions than groups that utilized confrontation and avoidance styles. Groups that never developed a stable style were also less effective than groups with integrative styles. [source] An efficient use of the WATERGATE W5 sequence for observing a ligand binding with a protein receptorMAGNETIC RESONANCE IN CHEMISTRY, Issue 9 2008Kazuo Furihata Abstract An efficient pulse sequence for observing a ligand binding with a receptor has been developed by incorporating the WATERGATE W5 sequence. In the conventional water ligand observed via gradient spectroscopy (WaterLOGSY) techniques, the water resonance is selectively excited using,e.g. the double-pulsed field gradient spin,echo (DPFGSE) sequence at the initial portion of pulse sequence. In the current version, the modified WATERGATE W5 sequence is incorporated at the initial portion of the pulse sequence, and the resonance at the water frequency can be selectively reserved by the modified WATERGATE W5 sequence. The efficiency of ligand-observed NMR screening techniques has been demonstrated using the human serum albumin (HSA),tryptophan complex. Copyright © 2008 John Wiley & Sons, Ltd. [source] Practical aspects of ROESY experiments for identification of bound waters in the cyclic tetrasaccharideMAGNETIC RESONANCE IN CHEMISTRY, Issue 12 2005Kazuo Furihata Abstract ROESY pulse sequences are presented and evaluated to identify bound waters in the cyclic tetrasaccharide. The first experiment incorporated the double-pulsed field gradient spin-echo (DPFGSE) for selective water excitation at the initial portion of the pulse sequence. Although long, shaped pulses were used in DPFGSE to achieve the highly selective excitation of water resonance that is very close to resonances of the cyclic tetrasaccharide, the approach was not effective because of the loss of sensitivity. Concomitant use of long delays and moderate length of shaped pulses in the portion of DPFGSE gained more sensitivity. A simple approach incorporating spin-echo with long delays instead of DPFGSE also afforded a sensitive spectrum. Practical aspects of these ROESY experiments are illustrated using the cyclic tetrasaccharide cyclo -{,6}-,- D -Glcp -(1,3)-,- D -Glcp -(1,6)-,- D -Glcp -(1,3)-,- D -Glcp -(1,). Copyright © 2005 John Wiley & Sons, Ltd. [source] Nonsyndromic mental retardation and cryptogenic epilepsy in women with Doublecortin gene mutationsANNALS OF NEUROLOGY, Issue 1 2003Renzo Guerrini MD DCX mutations cause mental retardation in male subjects with lissencephalypachygyria and in female subjects with subcortical band heterotopia (SBH). We observed four families in which carrier women had normal brain magnetic resonance imaging (MRI) and mild mental retardation, with or without epilepsy. Affected male subjects had SBH or pachygyria-SBH. In two families, the phenotype was mild in both genders. In the first family, we found a tyr138his mutation that is predicted to result in abnormal folding in the small hinge region. In the second family, we found an arg178cys mutation at the initial portion of R2, in the putative ,-sheet structure. Carrier female subjects with normal MRI showed no somatic mosaicism or altered X-inactivation in lymphocytes, suggesting a correlation between mild mutations and phenotypes. In the two other families, with severely affected boys, we found arg76ser and arg56gly mutations within the R1 region that are predicted to affect DCX folding, severely modifying its activity. Both carrier mothers showed skewed X-inactivation, possibly explaining their mild phenotypes. Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and SBH in boys. Mutation analysis in mothers of affected children is mandatory, even when brain MRI is normal. Ann Neurol 2003 [source] CT evaluation of the vidian canal localizationCLINICAL ANATOMY, Issue 7 2007Fatih Yazar Abstract The primary purpose of our work is to show that the vidian canal can be determined on CT imaging. The secondary goal is to establish the position and configuration of the vidian canal visualization. The CT imaging of vidian canals of 150 patients were examined in axial and coronal sections in 3 mm thickness made at 3 mm intervals. The varying course of the canal inside the bone, bone structure and diameter of the canal were investigated. In all cases, the canal was seen, and in 4 of the cases (1.3%) the canal was separated into two parts by a septum on its initial portion. In 36% of the cases it was embedded in the sphenoid corpus, partially protruded in 54% of the cases, and was connected to the bone with a stalk inside the sinus in 10% of the cases. The bony structure of the canal showed continuation in 68%, with 32% showing dehisans. The incidence of dehisans was 77% in the stalked cases and 45% in the protruded cases. It was determined that it is possible to evaluate the position and configuration of the vidian canal with CT imaging. This may be useful for diagnosing vidian nerve pathology and performing surgical intervention such as vidian neuroectomy and sinus surgery. Clin. Anat. 20:751,754, 2007. © 2007 Wiley-Liss, Inc. [source] Disabled-1 mRNA and protein expression in developing human cortexEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 3 2003Gundela Meyer Abstract Disabled-1 (Dab1) forms part of the Reelin,Dab1 signalling pathway that controls neuronal positioning during brain development; Dab1 deficiency gives rise to a reeler-like inversion of cortical layers. To establish a timetable of Dab1 expression in developing human brain, Dab1 mRNA and protein expression were studied in prenatal human cortex. The earliest Dab1 signal was detected at 7 gestational weeks (GW), the stage of transition from preplate to cortical plate, suggesting a role of the Reelin,Dab1 signalling pathway in preplate partition. From 12 to 20 GW, the period of maximum cortical migration, Dab1 expression was prominent in the upper tiers of the cortical plate, to decline after midgestation. Radially orientated apical dendrites of Dab1-expressing neurons indicated a predominant pyramidal phenotype. Pyramidal cells in hippocampus and entorhinal cortex displayed a more protracted time of Dab1 expression compared to neocortex. In addition, at later stages (18,25 GW), Dab1 was also expressed in large neurons scattered throughout intermediate zone and subplate. From 14 to 22 GW, particularly high levels of Dab1 mRNA and protein were observed in cells of the ventricular/subventricular zone displaying the morphology of radial glia. The partial colocalization of vimentin and Dab1 in cells of the ventricular zone supported a radial glia phenotype. The concentration of Dab1 protein in ventricular endfeet and initial portions of radial processes of ventricular-zone cells points to a possible involvement of Dab1 in neurogenesis. Furthermore, a subset of Cajal,Retzius cells in the marginal zone colocalized Dab1 and Reelin, and may thus represent a novel target of the Reelin,Dab1 signalling pathway. [source] | ||||||||||