201 research outputs found
IN VITRO STUDIES OF MAMMALIAN SOMATIC CELL VARIATION : I. DETECTION OF H-2 PHENOTYPE IN CULTURED MOUSE CELL LINES
The isoantigenic phenotype of the H-2 locus has been detected by isohemagglutinin absorption in a line of mouse lymphoma cells growing continuously in culture for 6 years and in two established lines of fibroblastic mouse cells growing continuously in culture for 1 year. Quantitative absorption studies suggest that the concentration of H-2 isoantigens is higher in the cultured lymphoma cells than in the other two fibroblastic cell lines
Assessing the Challenges Heads of Department Encounter in Instructional Supervision in Ghana. A Case of Selected Senior High Schools in Kwabre East District
The purpose of the study was to assess the challenges HoDs in Senior High Schools face during instructional supervision. In so doing, the study employed case study and used mixed method approach. In all a total of 92 questionnaires were administered with a response rate of 75.40%. The population consisted of School Heads /Assistant Heads, HoDs and Teachers drawn from the three study areas. 45.55% of HoDs âagreedâ or âstrongly agreedâ as against 44.82% either âdisagreeingâ or âstrongly disagreeingâ that HoDs face a myriad of challenges that are hindering their efforts. The opinion of the 45.55% was confirmed by 60% school heads/ assistants and nearly 60% teachers as against a little over 25% teachers and similar percentage of school heads /assistant heads disagreeing and apparently supporting the views of the 44.82% HoDs above. HoDs employed varied strategies to overcome some of their challenges. Majority of the respondents believed that HoDs are not adequately empowered to perform creditably and for which over 50% of them think that they are performing to some extent. Resultantly, the study recorded the satisfaction level of HoDs with their condition of service as 35% âmoderateâ, 35% to a âsmallâ extent and 30% to a âgreatâ or âvery greatâ extent. The study concludes that HoDs must be empowered enough to perform their roles successfully for better results. Keywords: Instructional leadership, Heads of department, Empowerment, Challenges, Satisfactio
Cognitive facilitation following intentional odor exposure
This paper reviews evidence that, in addition to incidental olfactory pollutants, intentional odor delivery can impact cognitive operations both positively and negatively. Evidence for cognitive facilitation/interference is reviewed alongside four potential explanations for odor-induced effects. It is concluded that the pharmacological properties of odors can induce changes in cognition. However, these effects can be accentuated/attenuated by the shift in mood following odor exposure, expectancy of cognitive effects, and cues to behavior via the contextual association with the odor. It is proposed that greater consideration is required in the intentional utilization of odors within both industrial and private locations, since differential effects are observed for odors with positive hedonic qualities
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Insights into human genetic variation and population history from 929 diverse genomes.
Genome sequences from diverse human groups are needed to understand the structure of genetic variation in our species and the history of, and relationships between, different populations. We present 929 high-coverage genome sequences from 54 diverse human populations, 26 of which are physically phased using linked-read sequencing. Analyses of these genomes reveal an excess of previously undocumented common genetic variation private to southern Africa, central Africa, Oceania, and the Americas, but an absence of such variants fixed between major geographical regions. We also find deep and gradual population separations within Africa, contrasting population size histories between hunter-gatherer and agriculturalist groups in the past 10,000 years, and a contrast between single Neanderthal but multiple Denisovan source populations contributing to present-day human populations.Wellcome grants 098051 and 206194, and S.A.M. and R.D. also by Wellcome grant 207492. A.B. and P.S. were supported by the Francis Crick Institute (FC001595) which receives its core funding from Cancer Research UK, the UK Medical Research Council and the Wellcome Trust. P.S. was also supported by the European Research Council (grant no. 852558) and the Wellcome Trust (217223/Z/19/Z). R.H. was supported by a Gates Cambridge scholarship. P.H. was supported by Estonian Research Council Grant PUT1036. D.R. is an Investigator of the Howard Hughes Medical Institute
Submersible study of an oceanic megamullion in the central North Atlantic
Author Posting. © American Geophysical Union, 2001. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 106, no. B8 (2001): 16145â16161, doi:10.1029/2001JB000373.Recently discovered megamullions on the seafloor have been interpreted to be the exhumed footwalls of long-lived detachment faults operating near the ends of spreading segments in slow spreading crust. We conducted five submersible dives on one of these features just east of the rift valley in the Mid-Atlantic Ridge at 26°35âČN and obtained visual, rock sample, gravity, and heat flow data along a transect from the breakaway zone (where the fault is interpreted to have first nucleated in âŒ2.0â2.2 Ma crust) westward to near the termination (âŒ0.7 Ma). Our observations are consistent with the detachment fault hypothesis and show the following features. In the breakaway zone, faulted and steeply backtilted basaltic blocks suggest rotation above a deeper shear zone; the youngest normal faults in this sequence are interpreted to have evolved into the long-lived detachment fault. In younger crust the interpreted detachment surface rises as monotonously flat seafloor in a pair of broad, gently sloping domes that formed simultaneously along isochrons and are now thinly covered by sediment. The detachment surface is locally littered with basaltic debris that may have been clipped from the hanging wall. The domes coincide with a gravity high that continues along isochrons within the spreading segment. Modeling of on-bottom gravity measurements and recovery of serpentinites imply that mantle rises steeply and is exposed within âŒ7 km west of the breakaway but that rocks with intermediate densities prevail farther west. Within âŒ5 km of the termination, small volcanic cones appear on the detachment surface, indicating melt input into the footwall. We interpret the megamullion to have developed during a phase of limited magmatism in the spreading segment, with mantle being exhumed by the detachment fault <0.5 m.y. after its initiation. Increasing magmatism may eventually have weakened the lithosphere and facilitated propagation of a rift that terminated slip on the detachment fault progressively between âŒ1.3 m.y. and 0.7 m.y. Identifiable but low-amplitude magnetic anomalies over the megamullion indicate that it incorporates a magmatic component. We infer that much of the footwall is composed of variably serpentinized peridotite intruded by plutons and dikes.B. Tucholke's research was supported by NSF grant OCE-9503561 and by an award from the Andrew W. Mellon Foundation Endowed Fund for Innovative Research and the Henry Bryant Bigelow Chair in Oceanography at Woods Hole Oceanographic Institution. G. Hirth acknowledges support by NSF grant OCE-9907244
Genotype, haplotype and copy-number variation in worldwide human populations
Genome-wide patterns of variation across individuals provide a powerful source of data for uncovering the history of migration, range expansion, and adaptation of the human species. However, high-resolution surveys of variation in genotype, haplotype and copy number have generally focused on a small number of population groups(1-3). Here we report the analysis of high-quality genotypes at 525,910 single-nucleotide polymorphisms ( SNPs) and 396 copy-number-variable loci in a worldwide sample of 29 populations. Analysis of SNP genotypes yields strongly supported fine-scale inferences about population structure. Increasing linkage disequilibrium is observed with increasing geographic distance from Africa, as expected under a serial founder effect for the out-of-Africa spread of human populations. New approaches for haplotype analysis produce inferences about population structure that complement results based on unphased SNPs. Despite a difference from SNPs in the frequency spectrum of the copy-number variants (CNVs) detected-including a comparatively large number of CNVs in previously unexamined populations from Oceania and the Americas-the global distribution of CNVs largely accords with population structure analyses for SNP data sets of similar size. Our results produce new inferences about inter-population variation, support the utility of CNVs in human population-genetic research, and serve as a genomic resource for human-genetic studies in diverse worldwide populations.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/62552/1/nature06742.pd
The complete genome sequence of a Neandertal from the Altai Mountains
We present a high-quality genome sequence of a Neandertal woman from Siberia. We show that her parents were related at the level of half siblings and that mating among close relatives was common among her recent ancestors. We also sequenced the genome of a Neandertal from the Caucasus to low coverage. An analysis of the relationships and population history of available archaic genomes and 25 present-day human genomes shows that several gene flow events occurred among Neandertals, Denisovans and early modern humans, possibly including gene flow into Denisovans from an unknown archaic group. Thus, interbreeding, albeit of low magnitude, occurred among many hominin groups in the Late Pleistocene. In addition, the high quality Neandertal genome allows us to establish a definitive list of substitutions that became fixed in modern humans after their separation from the ancestors of Neandertals and Denisovans
Treatment of Inborn Errors of Urea Synthesis â Activation of Alternative Pathways of Waste Nitrogen Synthesis and Excretion
Abstract
Children with inborn errors of urea synthesis accumulate ammonium and other nitrogenous precursors of urea, leading to episodic coma and a high mortality rate. We used alternative pathways for the excretion of waste nitrogen as substitutes for the defective ureagenic pathways in 26 infants. These pathways involve synthesis and excretion of hippurate after sodium benzoate administration, and of citrulline and argininosuccinate after arginine supplementation.
The children were treated for seven to 62 months; 22 survived. The mean plasma level of ammonium (±S.E.) was 36±2 Όmol per liter, and that of benzoate was 1.5±1.0 mg per deciliter. Alternative pathways accounted for between 28 and 59 per cent of the total effective excretion of waste nitrogen. Nineteen infants had normal height, weight, and head circumference, and 13 had normal intellectual development.
Activation of alternative pathways of waste nitrogen excretion can prolong survival and improve clinical outcome in children with inborn errors of urea synthesis. (N Engl J Med. 1982; 306:1387â92.
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