2026-09-23T04:58:02Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/80732026-06-06T01:06:25Zcom_1721.1_7582com_1721.1_7581col_1721.1_131023
William G. Thilly.
Banava, Helen.
Massachusetts Institute of Technology. Biological Engineering Division.
Massachusetts Institute of Technology. Department of Biological Engineering
2005-08-24T20:07:11Z
2005-08-24T20:07:11Z
2002
2002
http://hdl.handle.net/1721.1/8073
51165964
Thesis (S.M. in Toxicology)--Massachusetts Institute of Technology, Biological Engineering Division, 2002.
Includes bibliographical references (leaf 23, 1st group).
A formal series of conditions of lifetime genetic risk of cancer is explored, and algebra is provided for applications in human population genetics. Risks are considered in terms of alleles necessary and/or sufficient for carcinogenesis. Alleles are first classified with respect to their effects on reproductive fitness, and then in terms of their potential effects on carcinogenic pathways. The algebraic formulations for a series of genetic possibilities: monogenic, multigenic, and polygenic, are provided. It is expected that technology will be developed to identify and enumerate rare inherited alleles in large general and cancer proband populations.
by Helen Banava.
S.M. in Toxicology
25, [37] leaves
3034378 bytes
3034137 bytes
application/pdf
application/pdf
eng
Massachusetts Institute of Technology
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.
http://dspace.mit.edu/handle/1721.1/7582
Biological Engineering Division.
Monogenic, multigenic, and polygenic determinants of cancer risk
Thesis
application/pdf
false
Publication
unknown
unknown
<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="d06c09dc-de51-4ac7-bb8b-6490121b3519">
<Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type>
<Language>eng</Language>
<Title>Monogenic, multigenic, and polygenic determinants of cancer risk</Title>
<PublishedIn>
<Publication>
</Publication>
</PublishedIn>
<PublicationDate>2002</PublicationDate>
<Authors>
<Author>
<DisplayName>Banava, Helen.</DisplayName>
<Affiliation>
<OrgUnit>
</OrgUnit>
</Affiliation>
</Author>
</Authors>
<Editors>
</Editors>
<Publishers>
<Publisher>
<DisplayName>Massachusetts Institute of Technology</DisplayName>
<OrgUnit />
</Publisher>
</Publishers>
<License>http://dspace.mit.edu/handle/1721.1/7582</License>
<Keyword>Biological Engineering Division.</Keyword>
<Abstract>A formal series of conditions of lifetime genetic risk of cancer is explored, and algebra is provided for applications in human population genetics. Risks are considered in terms of alleles necessary and/or sufficient for carcinogenesis. Alleles are first classified with respect to their effects on reproductive fitness, and then in terms of their potential effects on carcinogenic pathways. The algebraic formulations for a series of genetic possibilities: monogenic, multigenic, and polygenic, are provided. It is expected that technology will be developed to identify and enumerate rare inherited alleles in large general and cancer proband populations.</Abstract>
<Access xmlns="http://purl.org/coar/access_right"
>
</Access>
</Publication>