<?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>2026-09-19T10:36:13Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/111262" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/111262</identifier><datestamp>2026-06-17T14:47:00Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</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">Kwanghun Chung.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Cho, Jae H. (Jae Hun)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Chemical Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Chemical Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2017-09-15T14:21:50Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2017-09-15T14:21:50Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2017</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2017</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/111262</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1003292047</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2017.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">This electronic version was submitted by the student author.  The certified thesis is available in the Institute Archives and Special Collections.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from student-submitted PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 143-158).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Understanding the brain requires integrative knowledge of its cellular-, network-, and system-level architectures. Existing volume imaging techniques have proven the potential to provide such information, but the lack of technology to label large volumes for visualization has limited their utility. Here, we address this challenge by developing technologies -- stochastic electrotransport and SWITCH -- to extend multiplexed labeling methods to larger volumes. Stochastic electrotransport selectively expedites transport of molecular probes into the tissue without damaging it. SWITCH synchronizes the labeling reaction to achieve consistent and uniform labeling. These technologies are demonstrated by successfully visualizing several molecular markers in adult mouse brain tissues, which have been previously infeasible in time and cost. Although our focus is on neuroscience, the concepts and methods described in this thesis are quite general. Stochastic electrotransport will be applicable to any nonlinear transport problems, and SWITCH will be applicable to any problem requiring synchronization of reaction kinetics across long distances..</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Jae H. Cho.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">158 pages</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Chemical Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Integrated and scalable molecular brain mapping</dim:field>
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   	&lt;Title>Integrated and scalable molecular brain mapping&lt;/Title>
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   	&lt;PublicationDate>2017&lt;/PublicationDate>
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        	&lt;DisplayName>Cho, Jae H. (Jae Hun)&lt;/DisplayName>
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    &lt;Keyword>Chemical Engineering.&lt;/Keyword>
   	&lt;Abstract>Understanding the brain requires integrative knowledge of its cellular-, network-, and system-level architectures. Existing volume imaging techniques have proven the potential to provide such information, but the lack of technology to label large volumes for visualization has limited their utility. Here, we address this challenge by developing technologies -- stochastic electrotransport and SWITCH -- to extend multiplexed labeling methods to larger volumes. Stochastic electrotransport selectively expedites transport of molecular probes into the tissue without damaging it. SWITCH synchronizes the labeling reaction to achieve consistent and uniform labeling. These technologies are demonstrated by successfully visualizing several molecular markers in adult mouse brain tissues, which have been previously infeasible in time and cost. Although our focus is on neuroscience, the concepts and methods described in this thesis are quite general. Stochastic electrotransport will be applicable to any nonlinear transport problems, and SWITCH will be applicable to any problem requiring synchronization of reaction kinetics across long distances..&lt;/Abstract>
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