<?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>2026-09-22T10:11:43Z</responseDate><request verb="GetRecord" identifier="oai:repository.rice.edu:1911/105411" metadataPrefix="dim">https://repository.rice.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:repository.rice.edu:1911/105411</identifier><datestamp>2024-01-11T20:59:18Z</datestamp><setSpec>com_1911_8299</setSpec><setSpec>col_1911_13110</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">Warmflash, Aryeh</dim:field>
   <dim:field mdschema="dc" element="creator">Mitra, Kinshuk</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2019-05-16T19:16:29Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2019-05-16T19:16:29Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="created">2019-05</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2019-04-04</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">May 2019</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="updated">2019-05-16T19:16:29Z</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="citation">Mitra, Kinshuk. &amp;quot;Barcoding tools to track development and function of stem cell constructs for biomedicine.&amp;quot; (2019) Diss.,  Rice University.  &amp;lt;a href=&amp;quot;https://hdl.handle.net/1911/105411&amp;quot;&amp;gt;https://hdl.handle.net/1911/105411&amp;lt;/a&amp;gt;.</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1911/105411</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">Biological regeneration has long been explored as a breakthrough modality for 
human therapy. Degenerative diseases, a majority of which are a related to ageing, 
manifest as a wide variety of pathologies: cardiovascular diseases, diabetes and 
Alzheimer to name a few. Consequently, the idea of a panacea in the form of a 
biological therapeutic that can grow and restore a debilitated bodily function has 
been much investigated. Outwardly, the premise has seemed remarkably simple. 
Scientists have long observed lizards growing back whole tails after decapitation and 
studied the remarkable regeneration potential of Planaria. Yet increasing work 
suggests processes including complex cellular growth dynamics, patterns of gene 
expression and clonal expansion of cells drives regeneration and analogously, 
biological tissue development. Improved understanding of developmental biology 
can thus improve the function and persistence of regenerative therapies. Our lab has 
previously developed in-vitro tools that allow the study of biological development. 
This work extends on that body by developing two distinct tool sets. Firstly, we 
develop a scheme for tracing large-scale clonal dynamics conveniently using a 
scalable lineage tracing method. We demonstrate the capacity of this system to 
accurately detect cell lineages based on a system of inheritable genetic barcoding. 
Our system can deconvolute lineage mixtures, track growth dynamics and 
consequently probe biological phenomena. Importantly, our process preserves 
spatial integrity of the sample and thus quantifies both lineage dynamics and 
captures their positional information. 
Since differential patterns of gene expression is another important component of 
regeneration and development, we develop a method to measure gene expression 
non-destructively, with the capacity to allow multiplexed monitoring of multiple 
targets even while in-vivo. As cellular and regenerative therapies move through 
primate and clinical trials, such a tool can serve the critical role of augmenting 
available biomarkers for monitoring therapy and predicting clinical outcomes 
thereby improving regulatory clearance. Taken together, our work adds to the body 
of knowledge that seeks to better understand tissue genesis and its re-engineering to 
create new therapeutic modalities.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso">eng</dim:field>
   <dim:field mdschema="dc" element="rights">Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.</dim:field>
   <dim:field mdschema="dc" element="subject">Regenerative medicine</dim:field>
   <dim:field mdschema="dc" element="subject">bioengineering</dim:field>
   <dim:field mdschema="dc" element="subject">cell therapy</dim:field>
   <dim:field mdschema="dc" element="subject">synthetic biology</dim:field>
   <dim:field mdschema="dc" element="title">Barcoding tools to track development and function of stem cell constructs for biomedicine</dim:field>
   <dim:field mdschema="dc" element="type">Thesis</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="material">Text</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="department">Bioengineering</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="discipline">Engineering</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="grantor">Rice University</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="level">Doctoral</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="name">Doctor of Philosophy</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
</dim:dim>
</metadata></record></GetRecord></OAI-PMH>