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Showing 1 to 2 of 2 for “"Syndrome of Lowe"”.
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Analisi molecolare in pazienti italiani con sindrome di Lowe
The oculocerebrorenal syndrome of Lowe (OCRL, also called OCRL1) is a rare X-linked disorder characterized by major abnormalities of eyes, nervous system, and kidneys. The gene responsible for OCRL encodes an inositol polyphosphate-5-phosphatase. We performed the molecular analysis in 20 Italian …
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High throughput RNA interference based screen for the identification of genes implicated in listeria monocytogenes infection
… monocytogenes has acquired a versatile arsenal of adaptor proteins. It uses these proteins to invade and undermine the host immune surveillance system, as well as to survive and propagate within the host cell. Our understanding of how L. monocytogenes infects cells points towards an interplay …