The main purpose of this study was to consider the effects of amplification and vocal function exercises on the perceived vocal health of elementary music educators (N = 37) from Oklahoma (n = 11) and Texas (n = 26). Participants were assigned to the use of the ChatterVoxTM amplifier or vocal function exercises based on pretest scores on the Voice Handicap Index with Music Teacher Voice Questionnaire (VHI/MVQ). Following the 4-week study period, participants completed the posttest VHI/MVQ. The results of a one-way ANCOVA that used treatment group as the independent variable, the summed posttest scores as the dependent variable, and the summed pretest scores as the covariate or control variable indicated that there was a statistically significant difference between the adjusted means for the posttest scores, favoring the exercises group. The overall group and both treatment groups reported frequent loud voice use in work settings and in public places. The overall group and the amplification group reported hoarseness after prolonged talking. The exercises group did not report as great a problem with hoarseness after prolonged talking. Secondary purposes addressed demographic variables. Women perceived greater overall vocal difficulties than men; men frequently reported specific vocal complaints that were not commonly indicated by women. The vocal problems of women may have been associated with loud voice use. The following common vocal complaints of men may have been related to the use of falsetto while teaching: need for vocal rest, worse voices in the evening, dry throats, loss of voice, obvious pitch breaks in their singing voices, pain after singing for an extended time, and limited use of their high range. VHI/MVQ scores indicated that the study participants with 21 to 39 years of teaching experience had more vocal difficulties than other participants and indicated limited use of the low range of their speaking voices, inconsistency in the sound of their voices, dry throats, throat pain after singing for a prolonged time, difficulty singing softly, and the need for vocal rest. Participants with 6 or more years of experience experienced hoarseness after speaking for an extended time.

Plasmodium is a genus well known for causing malaria, a life-threatening infection for many people where malaria is endemic. The blood-borne disease is transmitted by the female Anopheles mosquito. Till date, eight parasite species have been reported to cause malaria in humans that include P. falciparum, P. vivax, P. malariae, P. ovale curtisi, P. ovale wallikeri, P. cynomolgi, P. knowlesi and more recently P. simium. Amongst them, the most genetically understood species is P. falciparum, causing most of the deaths in children from malaria. Understanding genome variation at the population level of all malaria species is of utmost importance, including clinical cases with very low parasitemia. To achieve this purpose, we need sufficient amounts of parasite DNA material from the pool of host DNA, which always is overrepresented in clinical infections. We utilized a strategy of selective whole genome amplification (SWGA) technology on P. malariae and P. ovale curtisi (two neglected human infecting malaria parasites that often cause mild yet clinically relevant infections with low parasitemia) to efficiently enrich their genomic DNA for high-quality whole genome sequencing. Previous studies on SWGA applied on P. falciparum and P. vivax showed that SWGA could efficiently enrich the amount of starting DNA material from inadequate amounts of parasites directly from clinical samples without separating the host DNA using specifically designed primer sets. We have successfully designed multiple sets of primers and tested the efficiency of five best primer sets using polymerase chain reaction to enrich the genomes of P. malariae and P. ovale curtisi. The efficiency of primers in enriching the genome was tested on two clinical samples for each of P. malariae and P. ovale curtisi. We were able to enrich the genome of P. malariae with an average of 19-fold (19X) enrichment across both samples. For P. ovale curtisi, we could achieve an enrichment of 3 folds only. Nevertheless, we still obtained a sufficient amount of gDNA to prepare Illumina sequencing libraries and call for SNPs and Indels in a biologically reproducible manner at genome-scale.

No description available.

No description available.

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第22759号 / 工博第4758号 / 新制||工||1744(附属図書館) / 京都大学大学院工学研究科都市社会工学専攻 / (主査)教授 三村 衛, 教授 渦岡 良介, 准教授 肥後 陽介 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

[pt] Diante do crescimento do interesse pelos amplificadores Raman faz-se necessário um estudo mais detalhado destes. Uma técnica tradicionalmente já utilizada para analise de atenuação em enlaces, a reflectometria óptica no domínio do tempo, é empregada de maneira inovadora neste trabalho para a observação da amplificação Raman distribuída. O objetivo principal deste trabalho não é a analise de amplificadores Raman, mas sim a apresentação desta técnica como nova ferramenta observação do ganho Raman distribuído em fibras ópticas. / [en] Due to increased interest in Raman amplifiers, a more detailed study of them is required. A technique traditionally used for analysis of attenuation on optical links, time domain optical reflectometry, is used in an innovative way in this work for observation of distributed Raman amplification. The main objective of this work in not the analysis of Raman amplifiers, but the introduction of this technique as a new tool for the observation of distributed Raman gain in optical fibers.

Excerpt: What? You say you don't believe in prescriptive methods for programming hearing aids? Really? Then let me ask you this: Your Monday morning patient has a relatively flat 60 dB loss of cochlear origin. Would you program his hearing aids with 60 dB gain? Of course not. How about 10 dB gain? Not good either, right? Guess what—the moment you reached these conclusions, you're already using a prescriptive fitting approach.

No description available.

No description available.

In this study a biosensor based on real time quartz crystal microbalance (QCM) monitoring is optimized and characterized for the application in the Norosensor. This biosensor is aimed to recognise, capture and amplify Norovirus (NoV). In an initial step a simplified bioassay was developed that focuses on the latter parts of the assay which consists of DNA-guided probing and amplification of the captured virus and includes the development of an amplification model assay directly to the functionalised crystal surface. A padlock probe with matching sequence to the conjugated oligonucleotide on the quartz crystal surface is used as target in the model assay. Although a number of studies have been carried out based on padlock probe ligation and rolling circle amplification (RCA) based QCM sensing, these studies utilize the entire crystal surface to capture and amplify the biomolecule. In this research work the QCM monitoring is explored on a centrally functionalised electrode surface through conjugation only at the centre of the electrode for increased mass sensitivity. Thus, allowing capture and amplification of the padlock probe only at the centre of the quartz crystal. A 14mm diameter, thermoncompensated AT-cut, nonpolished quartz crystal with a 10mm diameter gold surface coating acting as electrode was utilized for QCM measurements. The detection system is based on mass binding and amplification on the QCM to produce a negative frequency shift in the fundamental frequency of the vibrating quartz crystal. The amplification products were additionally fluorescently labelled and fluorescent microscopy images were also obtained at the end of every experiment to verify the presence or absence of DNA capture and amplification. Experimental findings show that the current flow chamber with a 15ul capacity is able to detect a specific padlock probe concentration of 1nM on a conjugated region of ~2.5mm diameter. RCA amplified the mass with an average frequency shift of -80Hz in 60mins RCA incubation time. Further, the specificity and sensitivity of the QCM system was explored. However, the system has limitations where sensor binding of reaction proteins, such as DNA ligase and BSA, to some extent is observed. The storage stability of the functionalized self-assembled monolayer (SAM) on the QCM is also observed to deteriorate and thus, is of concern. Nevertheless the combination of RCA based amplification with QCM real-time monitoring has the potential for rapid and simple, low cost detection of the Norovirus. / I det här arbetet har vi optimerat och karateriserat en biosensor för detektion av Norovirus som orsakar häftiga utbrott av kräksjuka under vinterhalvåret vilket leder till både försämrad vård samt stora ekonomiska förluster för samhället. Målet inom EU projektet “Norosensor” är att utveckla ett snabbtest som kan tillämpas efter ett utbrott på till exempel en vårdavdelning och som ska mäta mängden virus i luften vilket kan fungera som riktlinje för om en avdelning är säker att användas eller ej. Tekniskt är målet med testet att fånga in viruspartiklar från luften som specifikt binds till sensorytan. Därefter ökar vi känsligheten från bundna partiklar genom en DNA-baserad amplifiering. Detta genererar specifik, viruskorrelerad massa som mäts med en kvartskristall mikrovågs sensor. När massan ökar minskar frekvenser vid vilken kristallen vibrerar och detta mäts i realtid. Det här arbetet har inte behandlat infångande eller inbindning av virus utan har fokuserat på den senare delen av protokollet som omfattar amplifieringen på sensorytan. En modell-assay har därför utvecklats där viruspartikeln istället representeras av en så kallad “padlock probe” (hänglås probe). Då sensorn är mycket känslig har först olika protokoll testats för effektiv rengöring av ytan med hjälp av ultraljud. I nästa steg har ytan funktionaliserats med thiol-modifierade syntetiska DNA molekyler som används för infångningen av målmolekylen på sensorytan (virus eller i detta fall padlock proben). Det har tidigare uppskattats att för att få maximal känslighet i massmätningen så är det fördelaktigt att binda viruset endast i mitten på en mycket liten yta av kristallen. Den här avhandlingen har därför fokuserat på att utveckla protokoll för detta där ytan först funtionaliserats i mitten innan resten av ytan blockats för att undvika ospecific inbindning. Resultaten visar att vi kan generera en centrerad funtionalisering och att vi får låg ospecifik binding. Protokollet består av flera biokemiska reakionssteg såsom (i) inbindning och lingering av padlock probe och (ii) amplifiering av den ligerade proben genom “rolling circle amplification”. För att kunna verifiera att vi fått amplifieringsprodukter på ytan har vi dels mätt frekvensändringen på grund av ökad massa men också märkt in dem med fluorescerande molekyler och detekterat dem i microskop. Under arbetets gång har ett flertal olika typer av kristaller testats. Det visade sig att om en polerad yta används (1μm grovhet) så migrerade molekylerna iväg från mitten när vi oscillerade kristallen medan vi fick bättre resultat om något grövre (3μm) ytor användes. Vi testade även ett flertal olika flödesceller av olika material och med olika reaktionsvolymer. Eftersom kristallen är mycket känslig så påverkar faktorer som flödeshastigheter och eventuella luftbubblor frekvensen. Vi optimerade därför detta och körde mätningarna vi6konstant flöde men med alternerande, låga hastigheter när vi tillsatte nya reagens eller inkuberade reaktionerna. Vi förvärmde även reaktionsmixarna för att minska ospeficika effekter och konstaterade att den funktionaliserade ytan påverkades av lagring över tid. I våra försök såg vi att protein såsom ligeringsenzymet och albumin, vilka har förhållandevis stor massa, hade effekter på frekvensen redan i sig genom att binda till ytan. Ytterligare optimeringar måste därför göras framöver för att minska denna inbinding bland annat genom bättre tvättsteg. Vi kunde dock påvisa linjär massökning med ökad amplifieringstid och har bevisad hög specificitet. Slutligen utvecklades ett litet mjukvaruprogram för att automatisera analysen och minska bruset. Sammanfattingsvis har vi lyckats utveckla ett enkelt och snabbt system för specifik massamplifering av Norovirus.