Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/31181
Full metadata record
DC FieldValueLanguage
dc.coverage.spatial--en_US
dc.date.accessioned2014-12-19T09:46:48Z-
dc.date.available2014-12-19T09:46:48Z-
dc.date.issued2014-12-19-
dc.identifier.urihttp://hdl.handle.net/10603/31181-
dc.description.abstractIntroduction: Dose evaluation of exposed humans to radiation becomes necessary newlineafter exposure. Such a dose evaluation can be done by biological dosimetric methods newlineof which increased somatic cell mutant frequencies in exposed individuals can be a newlinereliable index [1]. Biological dosimetry has an important role to play in assessing the newlinecumulative radiation exposure of persons working with radiation and also in estimating the true dose received during accidents involving external and internal newlineexposure. Biodosimetric methods include cytogenetic, immunological and newlinemutational assays [2]. newlineThe need for biodosimetry is essential for caliberating the actual dose received to a newlinebiological system where other conventional forms of dosimetry are unavailable. newlineEven in the presence of other dosimetric tools such as Thermo Luminescent Devices newline(TLDs) etc, biological dosimetry gives actual doses apart from an indication of the newlineextent of damage caused by such damages. This becomes all the more important newlinewith the current situations such as space programmes and dirty bombs. newlineThere are currently many advancing methods for measuring somatic mutations and newlinenew opportunities for biological dosimetry of high-risk groups. An evaluation of newlinesuch mutations becomes all the more important, as such mutations can be possible newlinepredictors of cancer risk [3]. Somatic mutations can now be measured in several newlinehuman genes. The genes currently used include the hemoglobin (Hb) genes on newlinechromosome 11 and 16, the glycophorin A (GPA) gene on chromosome 4, the newlinehypoxanthine-guanine phosphoribosyltransferase (HPRT) gene on the Xchromosome, newlinethe HLA genes on the chromosome 6 and the T-cell receptor (TCR) newlinegenes on chromosomes 7 and 14. Of the various assays for somatic mutations, only newlineGPA and HPRT have been studied sufficiently to have reliable databases.en_US
dc.format.extent130p.en_US
dc.languageEnglishen_US
dc.relationReferences 1-16en_US
dc.rightsuniversityen_US
dc.titleANALYSIS OF SOMATIC CELL MUTATIONS AT THE GLYCOPHORIN GLYCOPHORINA LOCUS IN HUMAN ERYTHROCYTESen_US
dc.title.alternativeen_US
dc.creator.researcherMaddaly Ravien_US
dc.subject.keywordNoneen_US
dc.description.notePages 1-130,Referencesen_US
dc.contributor.guidePaul Solomon F Den_US
dc.publisher.placeChennaien_US
dc.publisher.universitySri Ramachandra Universityen_US
dc.publisher.institutionDepartment of Human Geneticsen_US
dc.date.registered2001en_US
dc.date.completed2005en_US
dc.date.awarded23/02/2006en_US
dc.format.dimensions--en_US
dc.format.accompanyingmaterialNoneen_US
dc.source.universityUniversityen_US
dc.type.degreePh.D.en_US
Appears in Departments:Department of Human Genetics

Files in This Item:
File Description SizeFormat 
abstract.pdfAttached File125.67 kBAdobe PDFView/Open
acknoledgements.pdf9.58 kBAdobe PDFView/Open
certificate & declaration.pdf359.99 kBAdobe PDFView/Open
chapter_1.pdf1.64 MBAdobe PDFView/Open
chapter_2.pdf167.02 kBAdobe PDFView/Open
chapter_3.pdf147.34 kBAdobe PDFView/Open
chapter_4.pdf266.54 kBAdobe PDFView/Open
chapter_5.pdf992.65 kBAdobe PDFView/Open
chapter_6.pdf268.27 kBAdobe PDFView/Open
chapter_7.pdf366.22 kBAdobe PDFView/Open
chapter_8.pdf73.46 kBAdobe PDFView/Open
chapter_9.pdf288.19 kBAdobe PDFView/Open
conclusion.pdf92.43 kBAdobe PDFView/Open
contents.pdf310.72 kBAdobe PDFView/Open
publications.pdf62.84 kBAdobe PDFView/Open
references.pdf383.94 kBAdobe PDFView/Open
title.pdf87.19 kBAdobe PDFView/Open


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: