<?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>2026-09-21T01:18:59Z</responseDate><request verb="GetRecord" identifier="oai:drum.lib.umd.edu:1903/32720" metadataPrefix="dim">https://api.drum.lib.umd.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:drum.lib.umd.edu:1903/32720</identifier><datestamp>2024-11-13T08:02:09Z</datestamp><setSpec>com_1903_6626</setSpec><setSpec>com_1903_1654</setSpec><setSpec>com_1903_2</setSpec><setSpec>col_1903_6628</setSpec><setSpec>col_1903_3</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">He, Xiaoming</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Stewart, Samantha</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="publisher" lang="en_US">Digital Repository at the University of Maryland</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="publisher" lang="en_US">University of Maryland (College Park, Md.)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department" lang="en_US">Bioengineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2024-06-26T05:43:33Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2024-06-26T05:43:33Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2023</dim:field>
   <dim:field mdschema="dc" element="identifier">https://doi.org/10.13016/tjpz-tukw</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1903/32720</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">An estimated 9.8 million reproductive-age people with ovaries in the United States are impactedby fertility issues, oftentimes caused by the dysregulation of the tightly controlled process of
ovarian follicle development. Impaired fertility can arise from disorders like polycystic ovarian
syndrome (PCOS) or premature ovarian insufficiency (POI), which affect the function of the
ovary, an integral reproductive organ that houses the ovarian follicles. POI can also negatively
impact endocrine function, decreasing estrogen and leading to increased risk of osteoporosis,
cardiovascular disease, and neurological disorders. Novel fertility preservation and restoration
strategies, like ovarian tissue engineering, have emerged to address these effects of ovarian
dysregulation and offer alternatives for those who wish to delay childbearing. Human induced
pluripotent stem cells (hiPSCs) hold tremendous potential for tissue engineering and cell-based
medicine, as they have the capacity of differentiating into ectodermal, mesodermal, endodermal,
and germ cell lineages. In recent years, research into differentiating hiPSCs into cells like those
that make up the ovary has garnered much interest, highlighting these cells as a promising source
for ovarian tissue engineering and other types of cell-based medicine and research. This work
addresses critical challenges associated with engineering ovarian tissue for reproductive and cellbased
medicine: (1) engineering the microenvironment for the cell/microtissue and (2)
cryopreservation of the cells/microtissues. To understand the microenvironment of the ovary for
informed tissue engineering system design, we spatially characterize the micromechanical
properties of ovarian tissue from domestic cats to reveal both elastic and viscoelastic property
heterogeneities, correlating these findings with the distribution of key extracellular matrix
(ECM) molecules. We then developed a novel cryopreservation technology to enhance
cryopreservation of ovarian follicles and hiPSCs, using sand to seed ice in the extracellular
solution at high subzero temperatures during cooling. Together, this work investigates multiscale
strategies for advancing ovarian tissue engineering, contributing to the advancement of
reproductive medicine approaches for treating infertility and related endocrine dysfunction.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">MULTISCALE TECHNOLOGIES FOR ENGINEERING AND CRYOPRESERVING OVARIAN TISSUES AND HUMAN IPSCs</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Dissertation</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="pqcontrolled" lang="en_US">Bioengineering</dim:field>
   <dim:field mdschema="others" element="access-status">embargo</dim:field>
</dim:dim>
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