<?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>2026-09-22T02:02:44Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/148422" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/148422</identifier><datestamp>2026-06-16T18:17:40Z</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">Gerald N. Wogan.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Thilly, William George.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Nutrition and Food Science.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department" lang="en_US">Massachusetts Institute of Technology. Department of Nutrition and Food Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2023-03-08T20:24:54Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">1971</dim:field>
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   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1371248901</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Sc. D., Massachusetts Institute of Technology, Department of Nutrition and Food Science, 1971</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 211-215, 216a-216g).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">HeLa S3 cells have been induced to divide synchronously in suspension culture through more than ten generations. Cellular DNA and RNA have been determined at hourly intervals throughout the cell cycle defining the pattern of nucleic acid accumulation in HeLa cells. Cellular activity of the enzymes thymidine kinase, alkaline DNase, catalase, acid phosphatase and lactic dehydrogenase has been determined as a function of the division cycle. The method of synchronization developed here allows the continuous synchronous growth of mammalian cells in suspension culture. This system facilitates studies of cell cycle events since it provides a large amount of cellular material with minimal maintenance time required.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by William George Thilly.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Sc.D.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="collection" lang="en_US">Sc. D. Massachusetts Institute of Technology, Department of Nutrition and Food Science</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">xi, 261 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 may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.</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">Nutrition and Food Science.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Studies of the division cycle of human cancer cells (HELA) using a new system for continuous synchronization</dim:field>
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   	&lt;Title>Studies of the division cycle of human cancer cells (HELA) using a new system for continuous synchronization&lt;/Title>
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   	&lt;PublicationDate>1971&lt;/PublicationDate&gt;
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    &lt;Keyword>Nutrition and Food Science.&lt;/Keyword>
   	&lt;Abstract>HeLa S3 cells have been induced to divide synchronously in suspension culture through more than ten generations. Cellular DNA and RNA have been determined at hourly intervals throughout the cell cycle defining the pattern of nucleic acid accumulation in HeLa cells. Cellular activity of the enzymes thymidine kinase, alkaline DNase, catalase, acid phosphatase and lactic dehydrogenase has been determined as a function of the division cycle. The method of synchronization developed here allows the continuous synchronous growth of mammalian cells in suspension culture. This system facilitates studies of cell cycle events since it provides a large amount of cellular material with minimal maintenance time required.&lt;/Abstract>
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