Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 20 of 21 for “"CDG"”.
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Congenital Disorder of Glycosylation (CDG) - Ih
Congenital Disorders of Glycosylation (CDG) comprise a rapidly growing group of multisystemic inherited disorders caused by mutations in genes which are required for the biosynthesis of glycoproteins. Here the molecular defect in a new type of CDG with an unusual clinical phenotype and a difficult …
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Congenital Disorder of Glycosylation (CDG)-IIc: Eine retrovirale Expressionsklonierung identifiziert das CDG-IIc Syndrom (Leukozyten Adhäsionsdefekt II) als eine GDP-Fukose Transporter Defizienz
… "Congenital Disorders of Glykosylation (CDG)" als eine Krankheitsgruppe klassifiziert. In der vorliegenden Arbeit konnte ein weiteres Syndrom biochemisch und molekulargenetisch identifiziert werden (CDG-IIc). Bei einem Patienten, der die typischen klinischen Merkmale des "Leukozyten …
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Mini-Isoelektrofokussierung von Serum-Transferrin bei Patienten mit CDG-Syndrom
… „Congenital Disorders of Glycosylation“ (CDG). Die klassische Galaktosämie und der Fruktosemangel führen auf ähnliche Weise zu sekundären Glykosylierungsstörungen. Um Patienten mit CDG-Syndrom und anderen Stoffwechselerkrankungen auf eine Glykosylierungsstörung hin zu untersuchen, haben …
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Arnold Jacobs à luz da Proposta Musicopedagógica CDG: do ensino individual à aprendizagem coletiva de instrumentos de metal
… teóricos da Proposta Musicopedagógica CDG; 2) Pesquisa-Ação, com o desenvolvimento de uma experiência prática de formação inspirada no Modelo Teórico CDG, visando a uma Performance de Professor capaz de promover equilíbrio entre habilidades musicais e humanas dos alunos, devidamente …
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Congenital Disorders of Glycosylation IIj (CDG-IIj): Identifizierung eines Defekts der COG6-Untereinheit des Conserved Oligomeric Golgi-Komplexes
`Congenital Disorders of Glycosylation` (CDG) ist eine schnell wachsende Gruppe mit bislang 23 autosomal rezessiven, multisystemischen Erkrankungen, welche mit einem Defizit in der Glykoproteinbiosynthese einhergeht. Die Übertragung der Oligosaccharidketten auf neu synthetisierte Proteine …
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DISSECTING THE ROLE OF GOLGI TRAFFIC IN BRAIN DEVELOPMENT ACROSS HEALTH AND DISEASE: A LESSON FROM COG5-CDG STUDIES
… to as Congenital Disorders of Glycosylation (CDGs). Notably, brain development impairments, such as primary microcephaly, are described in most CDG patients. Despite the increased number of diagnosed patients, the cell biological mechanisms linking defective Golgi glycosylation and …
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Evaluation of Corn Distillers Grains and a Blend of Protein Supplements with or without Ruminally Protected Amino Acids for Lactating Cows
… were used to compare com distillers grains (CDG) versus a blend (BLEND) of other protein sources (fish meal and soybean meal) with CDG, and to determine the effectiveness of ruminally protected lysine and methionine (RPLM) in improving the utilization of CDG as a protein supplement for …
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Modeling congenital disorders of glycosylation in Caenorhabditis elegans: Genetic influences and structural consequences of N-linked glycosylation
… cause congenital disorders of glycosylation (CDG) in humans. This disease is very rare, but exceedingly life-threatening. The CDGs are inherited in an autosomal recessive manner and clinical manifestations range from severe to mild. Most commonly, the disorders begin in infancy; manifestations …
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The Type IV Pilus Assembly ATPase PilB as a Regulator of Biofilm Formation and an Antivirulence Target
… with the secondary messenger cyclic-di-GMP (cdG). Specifically we investigated how cdG binding regulates PilB functions not only as the assembly ATPase, but also as an EPS signaling molecule in Myxococcus xanthus biofilm regulation. Chapter 2 focuses on the development of a microplate-based …
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A Dynamic Application Analysis Framework
… a graph called a Compact Dataflow Graph (CDG), of the object references used intraprocedurally. The CDG is designed to be independent of the internal representation used by the runtime and general enough to facilitate a large range of dynamic interprocedural analysis and optimizations. We …
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Development of a Quality Management System (QMS) in Conformance with International Organization for Standardization (ISO) 13485:2016 Focusing on Sections 4 and 5 by Utilizing Technical Project Management Techniques for CDG Biotech Corporation
<p>CDG Biotech Corporation, a new biotechnology startup, plans to introduce medical devices for use in immunological diagnostics and therapies. CDG seeks to develop and implement a quality manual as part of their quality management system and to gain accreditation approval domestically and …
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Mathematical Model of the Cell Cycle Control and Asymmetry Development in Caulobacter crescentus
… of vital regulatory second messengers, c-di-GMP (cdG) and guanosine pentaphosphate or tetraphosphate (pppGpp or ppGpp), under normal and stressful conditions. This research suggests that the RelA-SpoT homolog enzymes have the potential to effectively influence the cell cycle in response to …
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Spurenelementverteilungen in orogenen Granat-Peridotiten und Granat-Olivin-Websteriten als Indikator ihrer geochemischen und metamorphen Entwicklung
… von der Alpe Arami (AA) und von Cima di Gagnone (CdG), Zentralalpen (Schweiz), sowie vom Granat-Olivin-Websterit aus Kalskaret, Western Gneiss Region (SW-Norwegen), mittels Elektronenstrahlmikrosonde und Sekundärionenmassenspektrometer detailliert untersucht. Die P-T-Entwicklung des AA-Peridotites …
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Ein Knockout-Mausmodell für Congenital Disorder of Glycosylation-IIc: Defizienz des Golgi-GDP-Fucose-Transporters
… der 'Congenital Disorders of Glycosylation' (CDG) werden durch Defekte von Enzymen und Transportern verursacht, die an der Modifikation von Proteinen durch kovalente Verknüpfung mit verschiedenen Zuckerbausteinen beteiligt sind. Die große Bedeutung des Zuckers Fucose als Teil dieser …
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IS B4GALT5 DEFICIENCY A NEW CONGENITAL DISORDER OF GLYCOSYLATION?
… two human congenital disorders of glycosylation (CDG) characterized by clinical pictures not really predicted by the corresponding mouse KO models. Previous studies showed that two similar galactosyltransferases, B4GALT5 and B4GALT6, are both responsible for the synthesis of lactosylceramide …
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Animal models for investigating coronavirus heterotypic immunity
… of the immunostimulatory molecule cyclic-di-GMP (CDG) significantly increased generation of resident memory in lymphoid aggregates around lung vasculature and promoted Th1/Th17 polarization. The T cells and antibodies, with or without CDG, were specific to OC43 and did not cross-react with …
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An Assessment of Factors Affecting Financial Management of Local Government Capital Development Fund in Tanzania:the case of Songea District
… for those personnel found guilty of fraud of CDG.
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Investigating the role of UDP-<i>N</i>-acetylhexosamine pyrophosphorylases in regulating <i>O</i>-GlcNAcylation in human disease
… Congenital Disorder of Glycosylation (OGT-CDG). O-GlcNAcylation has been shown to provide beneficial effects on cells in coping with environmental stresses, such as hypoxia and glucose deprivation, and on the development of many cancers where O-GlcNAc levels are often …
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Water Quality Impacts of Pure Chlorine Dioxide Pretreatment at the Roanoke County (Virginia) Water Treatment Plant
… gas:solid ClO₂ generation system manufactured by CDG Technology, Inc. was installed at the plant and is the first full-scale use of this technology in the world. The ClO₂ generator produces a feed stream free of chlorine, chlorite ion (ClO₂⁻), and chlorate ion (ClO₃⁻), resulting in lower …
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Análisis funcional y biomecánico del baile flamenco.
… oscilaciones suaves del centro de gravedad (CDG) en los tres planos; en el f) no hubo diferencias significativas entre la extremidad izquierda y derecha en cuanto al componente vertical de la fuerza de reacción del suelo, el golpe más dinámico se realizó con el talón y el desplazamiento …
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