Tesis sobre el tema "DYSF"
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Patel, Pryank. "Structural studies of the inner DysF domain of human myoferlin". Thesis, Birkbeck (University of London), 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479383.
Texto completoHeidt, Leonie Victoria [Verfasser]. "Proteinfehlfaltung als Ursache der Muskeldystrophie Dysferlinopathie: Das Mausmodell Dysf-MMex38 / Leonie Victoria Heidt". Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2018. http://d-nb.info/1176637223/34.
Texto completoSlaviero, André. "Konstruktionsoptimering av självrensande dysa". Thesis, Högskolan i Gävle, Avdelningen för Industriell utveckling, IT och Samhällsbyggnad, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-8064.
Texto completoLie, Gustavsson Victor. "Konstruktion av infästning till dysa". Thesis, Karlstads universitet, Fakulteten för hälsa, natur- och teknikvetenskap (from 2013), 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-33641.
Texto completoMålet med detta arbete är att konstruera en infästning mellan en dysa och en pod. En pod är vad som kan liknasen utombordsmotor för stora fartyg som sitter på utsidan av skrovet och kan rotera 360 ̊. En dysa är en stor stålring som kan sättas runt propellern, dysan ger förenklaten ökad framdrivningskraft och är lämplig för användning vid fartygstillämpningar där det handlar om låga hastigheter.Arbetet utförs på uppdrag av Rolls Royce AB i Kristinehamn.Kraven som ställdes på konstruktionen var att den skulle vara lätt att anpassa och att det skulle gå att montera och demontera dysan.Problemformuleringen för arbetet är att en ny infästning behövs för att kunna fästa dysan i poden.Resultatet av arbetet blev en övre och en nedre infästning på dysan. Den övre infästningen består av två parallella plåtar som skruvas ihop med en svetsad infästning på dysan. Den nedre infästningen består av en vinge med en strömningsvänlig profil som skruvas fast på ett stag. Båda infästningarna består av ett skruvförband, två styrpinnar och sprängskruv.Konstruktionen parametriserades i CAD så attomdysans storlekändrasså följer infästningarna med.Hela arbetet resulterade i ett konstruktionsförslag.Konstruktionen har dimensionerats med hjälp av en lastanalys och hållfasthetsberäkningarför att uppskatta infästningarnas nedböjning. Skruvförbanden har dimensionerats med enklare beräkningar och styrpinnarna har dimensioneratför att uppta skjuvspänningar.Slutsatsen som dras av arbetet är att konstruktionen är en lämplig lösning på problemet och rekommendationen är att det är värt att undersöka denna lösning vidare.Vidarearbete som behöver utföras är nogrannare dimensionering av konstruktionen, ingen hänsynhar tagits till utmattning eller vridning då det inte fanns tid inom arbetets tidsram för detta.
Storm, Josef. "Termisk utmattning : Hur termiska belastningar avgör livslängden på en Pressure seal-dysa och en bultad dysa". Thesis, Karlstads universitet, Fakulteten för hälsa, natur- och teknikvetenskap (from 2013), 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-85207.
Texto completoHuguenel, Colin John. "Ciliated Sensory Neuron Defects in Caenorhabditis elegans". Thesis, Boston College, 2008. http://hdl.handle.net/2345/573.
Texto completoPresented here is research investigating genes that are involved in the development and maintenance of ciliated nerve endings in the nematode Caenorhabditis elegans. C. elegans utilizes a subset of neurons, referred to as ciliated sensory neurons, to sense certain changes in its environment. There are two amphid sensilla (sense organs) that mediate exposure of these ciliated endings to the animal's external environment. Those ciliated endings that penetrate the cuticle are responsible for a myriad of behaviors that range from chemotaxis to osmotic avoidance, but in general function for the reception of environmental cues and stimuli. The intraflagellar transport (IFT) process facilitates the morphogenesis of these ciliated endings, and animals lacking intact ciliated endings may not be able to detect nourishment, hazardous environments, or other worms for mating. Mutant strains used in this study were generated by EMS mutagenesis of wild-type N2 animals and a subsequent screen of those worms displaying significant cilia dysfunction as evidenced by their dye-filling defective (Dyf) phenotype. Cilia-mediated uptake of lipophilic DiI into six pairs of amphid sensory neurons and two pairs of phasmid sensory neurons is expected in wild-type (N2) animals, but in Dyf animals, this dye-filling is disrupted, either through morphological defects, or deleterious mutations in the IFT process. To investigate the morphogenesis of cilia in C. elegans, we analyzed two specific mutant strains, WX737 dyf-3(og022)IV and PK841 dyf-15(pk841)V, that are defective in the uptake of fluorescent dye DiI and abnormal in sensory cilium structure. Through a variety of genetic mapping techniques, we were able to successfully map experimental gene dyf-15(pk841) to an interval of 2.84cM on chromosome V, and identify og022 as an allele of the gene dyf-3. It has been previously shown that dyf-3 expression is detected in 26 chemosensory neurons, including six IL2 neurons, eight pairs of amphid neurons (ASE, ADF, ASG, ASH, ASI, ASJ, ASK and ADL) and two pairs of phasmid neurons (PHA and PHB). Analysis of cilium malformation and the presence of a recognition sequence for the DAF-19 transcription factor suggest that dyf-3 is involved in the intraflagellar transport system complex B
Thesis (BS) — Boston College, 2008
Submitted to: Boston College. College of Arts and Sciences
Discipline: Biology
Discipline: College Honors Program
Vadamootoo, Kavi. "Theory of art therapy : dys-embodiment and embodiment". Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418942.
Texto completoKnapek, Olga. "Opowiadanie, błąd, dys-kurs : naruszenie reguły jako praktyka literacka". Doctoral thesis, Katowice : Uniwersytet Śląski, 2015. http://hdl.handle.net/20.500.12128/5873.
Texto completoGalli, Ursula. "Stress and pain (dys)regulation in chronic orofacial pain". Göttingen Cuvillier, 2008. http://d-nb.info/99103158X/04.
Texto completoEby, Christine A. "Pediatric Cochlear Implant Outcomes in Auditory Neuropathy/Auditory Dys-Synchrony". University of Cincinnati / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1085691784.
Texto completoKopal, Jakub. "Usage de la connectivité pour étudier les (dys)fonctions cérébrales". Thesis, Toulouse 3, 2021. http://www.theses.fr/2021TOU30020.
Texto completoWe picture the brain as a complex network of structurally connected regions that are functionally coupled. Brain functions arise from the coordinated activity of distant cortical regions. Connectivity is used to represent the cooperation of segregated and functionally specialized brain regions. Whether it is the analysis of anatomical links, statistical dependencies, or causal interactions, connectivity reveals fundamental aspects of brain (dys)function. However, estimating and applying connectivity still faces many challenges; therefore, this work is devoted to tackling them. The first challenge stems from the detrimental effect of systematic noise (such as head movements) on connectivity estimates. We proposed an index that depicts connectivity quality and can reflect various artifacts, processing errors, and brain pathology, allowing extensive use in data quality screening and methodological investigations. Furthermore, connectivity alterations play an invaluable role in understanding brain dysfunction. Investigating the mechanisms of epilepsy, we show that connectivity can track gradual changes of seizure susceptibility and identify driving factors of seizure generation. Identifying critical times of connectivity changes could help in successful seizure prediction. Finally, how the brain adapts to task demands on fast timescales is not well understood. We present a combination of intracranial EEG and state-of-art measures to investigate network dynamics during recognition memory. Understanding how the brain dynamically faces rapid changes in cognitive demands is vital to our comprehension of the neural basis of cognition. In conclusion, the modest goal of this thesis is to at least partially answer some of the many challenges that current neuroscience is facing
Blyth, Maria Del Carmen. "Chronicle of a dys-appearance: an autoethnography of a teacher in conflict". Doctoral thesis, University of Cape Town, 2015. http://hdl.handle.net/11427/16436.
Texto completoWith the growth in number of international schools from the 50 identified in 1964 to the current 5,000 international schools worldwide with an associated teaching staff of 250,000 predicted to grow to 10,000 and 500,000 respectively by 2020, the international school is an increasingly prominent sector of education. Yet despite this standing what is known about how international schools discipline and silence their dissenting teachers is negligible. Metaphorically speaking, the problem is that the "black box" of teacher control and correction remains firmly closed in the international school domain. The aim of this study is to open up the "black box" as it were, to use my experiences as an educator to shed some light on how organisational structures and the people working within them can disempower, silence and discipline a dissenting teacher. Although I have used autoethnography as methodology the study is not purely autoethnographic but rather a bricolage of methods that through conceptual enquiries of a philosophical nature (on the emotions, ethics etc.) deepen not only my narrative research but also my understanding of the issues. Engaging with these diverse philosophical analyses has taken me from questions of essence that focused on a Cartesian understanding of difference and conflict ( us/them; cause/effect ; guilt/innocence; darkness/light) to a posthumanist stance on both and questions of how conflict can be understood as emergent from intra-actions between apparatuses of material-discursive practices, conditions both social and material. For conflicts are collisions head on, to the accompaniment of squealing brakes and breaking glass. And it is important to understand not why but how such collisions occur if we are to avoid, prevent, or resolve them ethically. As such I hope that this study contributes to studies on conflict by showing how discourses, material conditions, affect, and power can converge to produce situations with serious consequences for those involved.
Tian, Min. "Dys-regulated Metabolism and Cardiac Dysfunction in A Mouse Model of Cancer Cachexia". The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1297196325.
Texto completoKelly-Blake, Karen Denise. "Sexual (dys)function and benign prostate disease implications for health care decision-making /". Diss., Connect to online resource - MSU authorized users, 2008.
Buscar texto completoEl, Fassihi Laure Jusnel Victoria. "Évaluations de rentrée de CE2 quels signes d'alerte pour dépister les enfants "DYS" ? /". Nancy : Université Henri-Poincaré, 2009. http://www.scd.uhp-nancy.fr/docnum/SCDMED_MORT_2009_EL_FASSIHI_LAURE_JUSNEL_VICTORIA.pdf.
Texto completoSaynor, Zoe Louise. "Assessment and interpretation of aerobic exercise (dys)function in paediatric patients with cystic fibrosis". Thesis, University of Exeter, 2016. http://hdl.handle.net/10871/21875.
Texto completoRehfeldt, Miriam [Verfasser]. "Pro-Enkephalin and Pro-Relaxin2 as Biomarkers for (Dys-)Function of Mammalian Kidney / Miriam Rehfeldt". Berlin : Freie Universität Berlin, 2018. http://d-nb.info/1151509744/34.
Texto completoFelgerolle, Chloé. "Anomalies sensorielle visuelle du Syndrome de l'X fragile, contribution rétinienne au phénotype de dys-sensibilité". Thesis, Orléans, 2019. http://www.theses.fr/2019ORLE2012.
Texto completoFragile X syndrome (FXS) is the leading cause of X-linked hereditary monogenic intellectual disability (1/3000 boys). In addition to mental retardation, patients present autism spectrum disorders and sensory disturbances, including impaired visual functions. The molecular origin of the FXS is the silencing of the FMR1 gene, which can no longer express the FMRP protein. At the molecular and cellular levels, the loss of FMRP results in structural and functional abnormalities of the synapses, at the brain as well as at the retinal level. This PhD thesis project aims to deepen knowledge of retinal and visual phenotypes in the absence of FMRP protein, as well as the study of the involvement of this retinal phenotype in the visual and global phenotypes of fragile X syndrome.We have revealed the precocity and stability of retinal abnormalities in the absence of the FMRP protein, which confirms the strength of the retinal phenotype under FXS conditions, and raises the question of its influence on other structures. In parallel, we have shown that the absence of FMRP protein causes significant disturbances of several visual traits in a behavioral standpoint. Finally, a strategy was developed to create an animal model "FXS-retina-specific", the study of which would provide information on the consequences of the absence of the FMRP protein only in the retina.This PhD thesis project highlights the importance of visual and retinal phenotypes of FXS, and provides new insights supporting the centrality of sensory disturbances in this pathology
Earl, Polly Jeannette. "Communication Behaviors of a Young Child with Auditory Dys-Synchrony: Seeing Cued Dutch and Cued Spanish". Cincinnati, Ohio : University of Cincinnati, 2006. http://www.ohiolink.edu/etd/view.cgi?acc%5Fnum=ucin1155582704.
Texto completoTitle from electronic thesis title page (viewed Jan. 26, 2007). Includes abstract. Keywords: Cued Speech, Auditory Dys-synchrony, Cued Dutch, Cued Spanish, early intervention, bilingualism, language and literacy, qualitative research, Deaf education. Includes bibliographical references.
Baumgarten, Susanne [Verfasser] y Ralph [Akademischer Betreuer] Witzgall. "miRNAs in the kidney and their role in podocyte (dys)function / Susanne Baumgarten ; Betreuer: Ralph Witzgall". Regensburg : Universitätsbibliothek Regensburg, 2017. http://d-nb.info/1124679774/34.
Texto completoTinah, Enass Nabeel. "A Population Genetic Study of Middle Eastern Populations Using DYS 458 Microvariants and Cohen Modal Haplotypes". BYU ScholarsArchive, 2008. https://scholarsarchive.byu.edu/etd/1644.
Texto completoJanukavicius, Patrick. "dyf-7 is responsible for the low levels of ivermectin resistance in Caenorhabditis elegans strains IVR6 and IVR10". Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114329.
Texto completoL'Ivermectine est un médicament qui a été très utile pour contrôler des maladies causées par les nématodes parasitiques. Cependant, le développement chez les parasites d'une résistance à ce médicament reste inquiétant. Ainsi, en reproduisant les conditions dans lesquelles les parasites développent une résistance à l'ivermectine, James et Davey (2009) ont généré deux souches de Caenorhabditis elegans, l'IVR6 et l'IVR10, en les cultivant sur une dose non-létale pour quelques générations. Afin de mieux comprendre les mécanismes impliqués dans le développement de la résistance à l'ivermectine, j'ai étudié les souches d'IVR6 et d'IVR10. J'ai découvert que celles-ci sont déficientes en absorption de teinture, soit un phénotype associé à la résistance à l'ivermectine. Les résultats obtenus présentaient le même niveau de résistance pour les deux souches. De plus, nous avons découvert une mutation dans le gène dyf-7, aussi chez les deux souches. L'usage de la cartographie génétique qui utilise les polymorphismes pour un nucléotide (SNPs), m'a permis de déterminer que le locus de résistance est en accord avec le locus de dyf-7. Le phénotype de déficience d'absorption de teinture est pénétrant à 80% chez l'IVR6 et l'IVR10. Quant à l'ivermectine, celui-ci peut sélectionner pour ce phénotype. Seulement les vers déficients en absorption de teinture peuvent survivre sur 10 ng/ml d'ivermectine. J'ai examiné quatre autres souches qui sont déficientes en absorption de teinte, incluant une souche avec un allèle différent de dyf-7; elles démontrent toutes une résistance à l'ivermectine. Des expériences préliminaires indiquent que le dyf-7 induit une résistance à un autre médicament, lévamisole. Ce qui me suggère un nouveau moyen de développer la multirésistance. Pris dans leur ensemble, mes résultats montrent que l'allèle du gène dyf-7 est la cause de la résistance à l'ivermectine chez les souches d'IVR6 et d'IVR10 et que la malformation des dendrites chez les souches Dyf est essentielle au développement de la résistance.
Pappe, Eva [Verfasser]. "Rolle der mitochondrialen (Dys-)funktion im Apoptoseprozess humaner Alveolarepithelzellen während der Infektion mit Influenza-A-Viren / Eva Pappe". Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2020. http://d-nb.info/1223927571/34.
Texto completoO'Neill, Claire Eilis. "Reversibility, dys-appearance and the telic demand : a phenomenological investigation of women's experiences of their bodies in leadership". Thesis, University of Bristol, 2017. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730865.
Texto completoReardon, Michael Joseph. "Identification and characterization of genes involved in cilia development in the nematode, Caenorhabditis elegans". Thesis, Boston College, 2008. http://hdl.handle.net/2345/30.
Texto completoThesis advisor: Stephen Wicks
Molecular biology and genetics, single nucleotide polymorphism genetic mapping, phenotypic assays including behavioral assessment, and fluorescent microscopy of GFP-tagged proteins were used to study ciliary defects in the nematode Caenorhabditis elegans. Mammalian cilia are multifunctional. Some of the physiological roles in which they are involved include sensing developmental signaling molecules and ligands as well as creating flows of mucus and cerebrospinal fluid that function as flow meters and mechanosensors. Due to the multifunctional nature of cilia, it is not surprising that many human diseases can be caused by ciliary defects. Bardet-Biedl Syndrome is a rare genetic ciliopathy characterized by retinal degeneration, polydactyly, obesity, cystic kidneys, mental retardation, and many other ailments. We have identified osm- 12/bbs-7 to be a C. elegans homologue of human BBS7, a gene known to cause Bardet-Biedl Syndrome when mutated. With the help of Michel Leroux’s group, I showed the BBS-7 protein to be localized to the base of cilia and to undergo intraflagellar transport along the ciliary axoneme. Our findings suggest that BBS- 7 plays a role in the assembly and/or functioning of the IFT complex. I also performed a mutagenesis and phenotypic screen for animals defective in the uptake of DiI into a subset of their ciliated neurons in order to identify new components involved in ciliogenesis and IFT. I describe an extended bulked segregant analysis (BSA) mapping methodology, which can save time and resources by filtering out alleles of previously known genes without performing time-consuming interval mapping. In addition, I identified one of the 11 dyefilling defective alleles from the screen to be a novel allele of dyf-3, which encodes a protein required for sensory cilia formation
Thesis (PhD) — Boston College, 2008
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Biology
Heinzel, Sebastian [Verfasser] y Andreas J. [Akademischer Betreuer] Fallgatter. "Multimodal neuroimaging of prefrontal cortex (dys)function: EEG, fNIRS, fNIRS-fMRI and Imaging Genetics approaches / Sebastian Heinzel. Betreuer: Andreas J. Fallgatter". Würzburg : Universitätsbibliothek der Universität Würzburg, 2013. http://d-nb.info/1031379746/34.
Texto completoFormentini, Lucilla. "I DSA e il mercato editoriale. Proposta di traduzione del romanzo Dys sur 10 : Dylan a un secret... Il est dyslexique". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2022.
Buscar texto completoPetersson, Anton y Alia Abdulsahib. "Sopsaltning som halkbekämpningsmetod på olika höjdnivåer i Jönköping : En studie för att utforska och undersöka kunskapsläget gällande sopsaltning i Sverige". Thesis, Tekniska Högskolan, Högskolan i Jönköping, JTH, Byggnadsteknik och belysningsvetenskap, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-46608.
Texto completoNeugebauer, Josephine [Verfasser] y Kai [Akademischer Betreuer] Sassenberg. "When social comparisons are (dys-)functional : The influence of social comparisons, knowledge awareness, and comparison motivation in collaborative learning / Josephine Neugebauer ; Betreuer: Kai Sassenberg". Tübingen : Universitätsbibliothek Tübingen, 2016. http://d-nb.info/1165309505/34.
Texto completoChartier, Angeline. "Transferts et appropriations de modèles de développement dans les pays du Sud : pour une analyse du (dys)fonctionnelment de l'aide : l'exemple de la décentralisation en Haïti et à Madagascar". Thesis, Bordeaux 3, 2016. http://www.theses.fr/2016BOR30001/document.
Texto completoOriginally a western political model, decentralization became a development model and a tool in the fight against poverty between 1990 and 2000. The model has since been massively financed and transferred to developing countries, as it was expected to be a lever of good governance and social peace. However, despite 25 years of efforts to establish the model in Haiti and Madagascar, decentralization is still not efficient. More generally, the two countries are characterized by chronic instability, a false pretence of democracy, an aggravation of poverty and maintained or increased inequalities. How can we explain this paradox? Decentralization continues to be transferred and received despite consistently missing the mark because it serves unofficial interests of actors from the South…and the North. Moreover, we consider that the model’s transfer itself is at the source of its malfunctioning. As it facilitates access to power for new stakeholders, it multiplies the sources of conflicts and foments local power games. We offer a profile of Southern stakeholders, visible and invisible, who appropriate the model and aim to decode theirs strategies of power capture. Who are they? How can they maintain the system and simultaneously sabotage it? How do they turn the model into their own tool? What are their goals? What are their strategies in terms of alliances and conflicts? More broadly, we would like to show how these power games relate to Northern realities and lead to the persistent transfer of a dysfunctional model, the preservation of a small hegemony, and the (re)creation of tensions which can lead to crises. This system is ongoing: the crises justify external aid intervention and the input of a new model. In this vicious circle something does functions, but at the expense of the target population. This paradox offers an opportunity to question the aid approach based on the transfer of a standardized model
Clare, Jillian. "Becoming Leaders : An Investigation Into Women's Leadership In Male-Defined And Male-Dominated Professions". Thesis, Queensland University of Technology, 2004. https://eprints.qut.edu.au/15947/1/Jiillian_Clare_Thesis.pdf.
Texto completoClare, Jillian. "Becoming Leaders : An Investigation Into Women's Leadership In Male-Defined And Male-Dominated Professions". Queensland University of Technology, 2004. http://eprints.qut.edu.au/15947/.
Texto completoDelatour, Thierry. "Mise en évidence par spectrométries optiques de formes tautomères caractéristiques d'un pyridylazo diethylaminophénol". Nancy 1, 1987. http://www.theses.fr/1987NAN10159.
Texto completoCheng, Hsien-Wen y 鄭獻文. "Mutation analysis of the DYSF gene in LGMD2B patients using DHPLC". Thesis, 2007. http://ndltd.ncl.edu.tw/handle/11749899776360155422.
Texto completo高雄醫學大學
醫學研究所碩士班
95
Dysferlin(DYSF) gene encoding dysferlin is mutated in Miyoshi myopathy and Limb-Girdle Muscular Dystrophy type 2B(LGMD 2B), the two main phenotypes recognized in dysferlinopathies. Dysferlin deficiency in muscle is the most relevant feature for the diagnosis of dysferlinopathy and prompts the search for mutations in DYSF gene. DYSF, located on chromosome 2p13, contains 55 coding exons and spans 150 kb of genomic DNA. We performed a genomic analysis of the DYSF coding sequence in 11 unrelated LGMD 2B patients, including 7 suspected LGMD 2B Taiwanese patients, and 4 Japanese patients with 6 confirmed mutations in DYSF gene. All patients showed an absence or drastic decrease of dysferlin expression in muscle. A primary screening of DYSF using denaturing high performance liquid chromatography(DHPLC)of PCR products of each of 55 exons of the gene was followed by sequencing whenever a variation was detected. In 7 Taiwanese patients, 17 sequence variations were identified in DYSF, 3 of which predict single amino-acid substitution and are novel, while the other 14 changes are known SNPs (Single nucleotide polymorphisms). The three novel sequence variations, G486、A3472G、C334T, was not detected in 150 normal individuals and was identified as potential pathogenic mutation (SNP<1%). These three mutations were widely spread in the coding sequence of the gene.
AGUTI, SARA. "The functional consequence of TGS1 mutations and the interaction with Survival of Motor Neuron protein Molecular diagnosis of the most common forms of Limb Girdle Muscular Dystrophy with autosomal recessive inheritance". Doctoral thesis, 2018. http://hdl.handle.net/2158/1119125.
Texto completoWu, Feng-Ling y 吳鳳玲. "Di-anchoring organic dyse for dye-sensitized solar cells". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/02860114685226575550.
Texto completo國立臺灣科技大學
化學工程系
101
A series of metal free organic dyes (DA) with two anchoring groups were synthesized for DSSCs application. Different arylamines and 2-cyanoacrylic acid were used as the electron donor and the electron acceptor, respectively. The dyes absorb intensely (ε = 41900−54600 M-1cm-1) in the range of 350−450 nm. The HOMO (0.97 to 1.24 V vs NHE) and LUMO (-0.99 V to -1.64 vs NHE) levels calculated from electrochemical and optical data assure favorable electron injection and regeneration of the dye after electron injection. The power conversion efficiencies of DSSCs based on these dyes are in the range of 2.60-7.28 %, which are 1.2−1.7 times heigher than that of S1 dye with only one anachoring group. The power conversion efficiency of DSSC based on DA5 has the best power conversion efficiency (7.28%) among all. The efficiency reaches 88 % of the standaed cell based on N719 fabricated and measured under the same condicitions. The presence of two anchoring groups in DA dyes increases electron injection efficiency and results in higher short circuit currents. Compared the S1 congener, DA1−DA3 can more effectively suppress charge recombination, leading to higher open circuit voltage.
Piróg, Michał. "Masa centralna a krzywa rotacji dysków akrecyjnych w układach samograwitujących". Praca doktorska, 2015. https://ruj.uj.edu.pl/xmlui/handle/item/45036.
Texto completoAlmeida, Joana Patrícia Rodrigues Félix Peixoto de. "Thyroid (dys)function: a burning issue in pregnancy". Master's thesis, 2012. https://repositorio-aberto.up.pt/handle/10216/72103.
Texto completoAlmeida, Joana Patrícia Rodrigues Félix Peixoto de. "Thyroid (dys)function: a burning issue in pregnancy". Dissertação, 2012. https://repositorio-aberto.up.pt/handle/10216/72103.
Texto completoVeiga, Ana Rita da Silva. "The effects of psoriasis on diastolic (Dys) Function - A pilot echocardiographic". Master's thesis, 2017. https://repositorio-aberto.up.pt/handle/10216/109785.
Texto completoVeiga, Ana Rita da Silva. "The effects of psoriasis on diastolic (Dys) Function - A pilot echocardiographic". Dissertação, 2017. https://repositorio-aberto.up.pt/handle/10216/109785.
Texto completoМороз, М. О. "Теоретичні та методичні основи формування професійної компетентності майбутніх учителів музики в процесі фахової підготовки у педагогічному коледжі". Thesis, 2021. http://eprints.zu.edu.ua/32076/1/dys-Moroz.pdf.
Texto completoМирончук, Н. М. "Теоретичні і методичні основи контекстної підготовки майбутніх викладачів вищої школи до самоорганізації у професійній діяльності". Thesis, 2021. http://eprints.zu.edu.ua/32095/1/dys-Myronchuk.pdf.
Texto completoПідскальна, О. М. "Ґенеза дискурсу мультикультуралізму: соціально-філософський аналіз". Thesis, 2021. http://eprints.zu.edu.ua/32456/1/dys-Pidskalna.pdf.
Texto completoРоманюк, Р. К. "Теоретичні і методичні засади професійної підготовки вчителів біології до профільного навчання учнів". Thesis, 2021. http://eprints.zu.edu.ua/32569/1/dys-Romanjuk.pdf.
Texto completoМарченков, С. М. "Формування інформаційно-аналітичної компетентності майбутніх офіцерів у процесі фахової підготовки". Thesis, 2021. http://eprints.zu.edu.ua/32576/1/dys-Marchenkov.pdf.
Texto completoБірук, Н. П. "Професійно-творчий розвиток особистості педагога-дослідника в умовах діяльності науково-педагогічної школи". Thesis, 2021. http://eprints.zu.edu.ua/32583/1/dys-Biruk.pdf.
Texto completoКучинська, Л. Ф. "Рекреалогічні засади збереження професійного здоров'я педагогічних працівників у системі методичної роботи закладів дошкільної освіти". Thesis, 2021. http://eprints.zu.edu.ua/32589/1/dys-Kuchynska.pdf.
Texto completoРудик, А. В. "Професійна підготовка майбутніх учителів математики до технологізації освітнього процесу в умовах профільної школи". Thesis, 2021. http://eprints.zu.edu.ua/32601/1/dys-Rudyk.pdf.
Texto completoБілокопитова, Н. І. "Феномен соціальності в тюркському світі: соціально-філософський аналіз". Thesis, 2021. http://eprints.zu.edu.ua/32603/1/dys-Bilokopytova.pdf.
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