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 7 of 7 for “"Situs inversus"”.
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Mutationen in DNAH5 verursachen Primäre Ziliäre Dyskinesie
… Die Hälfe der Betroffenen weist einen Situs inversus auf, der über eine Randomisation der Links-Rechts Körperasymmetrie resultiert (Kartagener Syndrom). Elektronenmikroskopisch lassen sich ultrastrukturelle Defekte in den Zilien der meisten Patienten entdecken. Darunter scheinen v.a. …
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Building capacity for diagnosis of Primary Ciliary Dyskinesia in South Africa: a descriptive study
… neonatal respiratory distress (48%, n= 16), and situs inversus (36%, n=12); 7/17 (41%) participants recorded nNO <77nl/. Ciliary beat pattern and TEM were abnormal in 55% (n=18) and 6.1% (n=2) of the participants respectively; PCD was confirmed genetically in 5/24 (21%), of which two had abnormal …
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DNALI1- und, oder DNAH5-Mislokalisation in respiratorischen Epithelzellen von PCD-Patienten
… Hälfte der PCD-Betroffenen zeigt das Bild eines Situs inversus totalis. <br>Mittels Elektronenmikroskopie können häufig ultrastrukturelle Defekte der inneren und/oder äußeren Dyneinarme, welche die Zilienbewegung vermitteln, nachgewiesen werden. Die Gene DNAI1 und DNAH5 kodieren für …
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Novel Phenotyping of the Myocardium by Diffusion Tensor Cardiovascular Magnetic Resonance
… and congenital disease, as exemplified by situs inversus totalis (SIT). Two main DT-CMR sequences, stimulated echo acquisition mode (STEAM) and second-order motion-compensated spin echo (M2-SE) were compared in a hypertrophic cardiomyopathy cohort. Volumetric analysis, strain assessment and …
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A Lightweight Defeasible Description Logic in Depth
… a human suffering from the congenital condition situs inversus - and therefore accommodate for the ability to retract defeasible conclusions in a non-monotonic fashion. Specifically tailored non-monotonic semantics have been continuously investigated for DLs in the past 30 years. A particularly …
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Mutationsanalyse des intraflagellaren Transportprotein-Gens hTg737 bei Patienten mit Situsanomalien und hereditären Nierenerkrankungen
… homozygote Mäuse sterben intrauterin und zeigen Situsanomalien, Neuralrohrdefekte, vergrößerte Extremitätenknospen und eine Aufweitung des perikardialen Sacks. <br>Im Rahmen der vorliegenden Arbeit wurden 42 Patienten mit Situsanomalien und Fehlbildungen von Niere, Herz und/oder weiteren Organen …
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Dynamics of Cilia and Flagella
Cilia and flagella are hair-like appendages of eukaryotic cells. They are actively bending structures that exhibit regular beat patterns and thereby play an important role in many different circumstances where motion on a cellular level is required. Most dramatic is the effect of nodal cilia whose …