<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-24T13:07:46Z</responseDate><request verb="GetRecord" identifier="oai:ruor.uottawa.ca:10393/27477" metadataPrefix="oai_dc">https://ruor.uottawa.ca/server/oai/request</request><GetRecord><record><header><identifier>oai:ruor.uottawa.ca:10393/27477</identifier><datestamp>2024-02-23T09:11:51Z</datestamp><setSpec>com_10393_242</setSpec><setSpec>col_10393_244</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Hypoxia-inducible factor-1 alpha (HIF-1alpha) and its role in the hypoxic preconditioning and gene expression patterns in zebrafish ( Danio rerio) embryos</dc:title>
   <dc:creator>Mohamed, Amira F</dc:creator>
   <dc:subject>Biology, General.</dc:subject>
   <dc:description>Preconditioning to lowered oxygen levels (hypoxia) may occur when an animal is subjected to non-lethal levels of hypoxia and then returned to normoxic conditions. During a subsequent exposure to hypoxia, the pre-exposed animals may exhibit increased tolerance compared to naive animals. I have demonstrated, by analysis of critical PO2&amp;apos;s (Pcrit), that zebrafish embryos can be preconditioned to hypoxia. Preconditioned embryos display a lower Pcrit than controls, indicating a heightened ability to endure hypoxic conditions. The role of the hypoxia inducible factor-1 (HIF-1) in promoting hypoxic preconditioning was examined. To determine the role of HIF-1 in preconditioning, embryos deficient in HIF-1alpha (using antisense oligonucleotide morpholinos) were assessed under hypoxic conditions. No significant difference between preconditioning capacities of control- and HIF-1alpha deficient embryos was observed. In addition to assessing Pcrit, a suite of hypoxia responsive genes were analysed by real time PCR. IGFBP-2 showed a significant decrease in expression in the HIF-1alpha deficient embryos, and EPO showed a significant increase in HIF-1alpha deficient embryos. All other genes examined showed no significant change between treated and control embryos.</dc:description>
   <dc:date>2013-11-07T18:14:19Z</dc:date>
   <dc:date>2013-11-07T18:14:19Z</dc:date>
   <dc:date>2007</dc:date>
   <dc:date>2007</dc:date>
   <dc:type>Thesis</dc:type>
   <dc:identifier>Source: Masters Abstracts International, Volume: 46-03, page: 1367.</dc:identifier>
   <dc:identifier>http://hdl.handle.net/10393/27477</dc:identifier>
   <dc:identifier>http://dx.doi.org/10.20381/ruor-18728</dc:identifier>
   <dc:language>en</dc:language>
   <dc:format>90 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>University of Ottawa (Canada)</dc:publisher>
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