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 12 of 12 for “"congenital diseases"”.
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The Role of Gap Junctions in Congenital Diseases of the Heart
… subjects and 30 children with a variety of congenital heart diseases was amplified by the polymerase chain reaction and sequenced. <strong>Mutant DNA</strong> was expressed in cell culture and examined for its effect on the regulation of cell-cell communication.</p> <p><strong>Results. …
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Infant populations exposed to prolonged sedation: are they at risk for long-term sequelae?
… proportion (35%; 16/46) was diagnosed with congenital anomalies. The other diagnoses included respiratory diseases (24%; 11/46), neurological diseases (13%; 6/46), and the remaining infants had a combination of two to three of these diagnoses (28%; 13/46). Infants with congenital diseases …
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Regulation of Traffic into and out of the Yeast Endosome by the VPS9P Cue Domain and the VPS5P Domain
… lysosomal trafficking system have been linked to congenital diseases including mucolipidosis type II (I-cell disease). An analogous trafficking system functions in the fungi Saccharomyces cerevisiae to deliver biosynthetic and endocytic cargo to the yeast vacuole. Genetic and biochemical analyses …
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AMBIGUOUS BODIES: GENDER NON-CONFORMITY AND BODILY TRANSFORMATION IN EARLY MODERN ITALIAN ART
… use of medical knowledge from treatises on congenital diseases, anatomical illustrations, and surgical manuals. In combination with artists’ use of classicizing myths and religious doctrines, these medical sources enabled artists to render figures as recognizable derivations from the natural …
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The Behavioral Phenolype of Children with Velocardiofacial Syndrome
… (VCFS) is one of the most common genetic, congenital diseases to date. The clinical symptoms of patients with VCFS have included up to 180 medical and psychological features, such as velopharyngeal insufficiency, cleft palate, schizophrenia or bipolar disorder, cognitive limitations, and …
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A multi-lineage in vitro mouse embryo model derived exclusively from mouse embryonic stem cells
… model to study human embryonic development and congenital diseases. As the mouse embryo implants, it undergoes drastic morphological changes to form the egg cylinder consisting of the epiblast (EPI), extraembryonic ectoderm (ExE) and visceral endoderm (VE), which give rise to the embryo proper, …
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Parents' perspectives and experiences of having a child with hereditary hearing loss
Congenital hearing loss (HL) occurs in 1-2 per 1000 newborns globally. Of all the congenital diseases that occur worldwide, HL remains the most disabling, with the highest rate for age-standardised disability life years and is a significant public health concern particularly in the developing …
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The design, development, and validation of an accessible high flow nasal oxygen solution with patient scoring outputs
… the COVID-19 pandemic and ongoing to treat congenital diseases, to effectively treat poor patient vitals and oxygenate patients. Clinical settings such as the general ward, for which HFNO is suitable, is left to be managed with manual patient monitoring means. Continuous monitoring methods …
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Regulation of the anti-senescence factor, TBX2, by the UV stress signaling pathway and the mitotic cyclin dependent kinases
… genes are associated with a number of human congenital diseases. Several lines of evidence have also implicated members of the T-box gene family in cell cycle regulation and in cancer. Importantly, the highly related T-box factors, Tbx2 and Tbx3, can suppress senescence through repressing the …
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Regulation of the anti-senescence factor, TBX2, by the UV stress signalling pathway and the mitotic cyclin dependent kinases
… genes are associated with a number of human congenital diseases. Several lines of evidence have also implicated members of the T-box gene family in cell cycle regulation and in cancer. Importantly, the highly related T-box factors, Tbx2 and Tbx3, can suppress senescence through repressing the …
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Genetic Analysis of Drosophila Stomatogastric Nervous System
… of colon and rectum (HSCR) is a multigenic congenital disease and occurs one in five thousand live births (0.02%). Affected children require corrective surgery due to a lack of neurons in the lower intestine. The main causative mutations for HSCR are in the Ret receptor tyrosine kinase, …