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   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Alan J. Grodzinsky.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Lee, Gary C. (Gary Chiaray), 1980-</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2005-09-26T20:30:34Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2004</dim:field>
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   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2004.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 61-62).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Extended mechanical stimulation of articular cartilage in an in vitro model explant system promotes growth and repair. An alternating day mechanical loading protocol consisting of dynamic sinusoidal compression results in long term extracelluar matrix macromolecule biosynthesis and increased biosynthetic rates in the cartilage system. The protocol uses total glycosaminoglycan and DNA content assays to measure matrix macromolecule biosynthesis and uses L-³H-proline and ³⁵S-sulfate radiolabel incorporation rates to measure rates of biosynthesis. The results also demonstrate the feasibility of replacing the fetal bovine serum and L-ascorbic acid components of the typical explant feeding medium with ITS (insulin-transferrin-selenium solution) and acorbyl-2-phosphate in anticipation of future long term studies of the synergistic pathways of dynamic compression and IGF-I stimulation for cartilage growth and repair.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Gary C. Lee.</dim:field>
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   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
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   <dim:field mdschema="dc" element="title" lang="en_US">Extended mechanical stimulations of cartilage for growth and repair</dim:field>
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   	&lt;Title>Extended mechanical stimulations of cartilage for growth and repair&lt;/Title>
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   	&lt;PublicationDate>2004&lt;/PublicationDate>
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   	&lt;Abstract>Extended mechanical stimulation of articular cartilage in an in vitro model explant system promotes growth and repair. An alternating day mechanical loading protocol consisting of dynamic sinusoidal compression results in long term extracelluar matrix macromolecule biosynthesis and increased biosynthetic rates in the cartilage system. The protocol uses total glycosaminoglycan and DNA content assays to measure matrix macromolecule biosynthesis and uses L-³H-proline and ³⁵S-sulfate radiolabel incorporation rates to measure rates of biosynthesis. The results also demonstrate the feasibility of replacing the fetal bovine serum and L-ascorbic acid components of the typical explant feeding medium with ITS (insulin-transferrin-selenium solution) and acorbyl-2-phosphate in anticipation of future long term studies of the synergistic pathways of dynamic compression and IGF-I stimulation for cartilage growth and repair.&lt;/Abstract>
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