Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/275526
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dc.date.accessioned2020-02-10T09:40:32Z-
dc.date.available2020-02-10T09:40:32Z-
dc.identifier.urihttp://hdl.handle.net/10603/275526-
dc.description.abstractIntroduction: newlineZidovudine (ZDV) is a thymidine analogue which has a potent activity both against HIV-1 and HIV-2 virus. It acts by inhibiting reverse transcriptase enzyme and by inhibiting viral DNA chain elongation. Efavirenz (EFV) is a non nucleoside reverse transciptase inhibitor which binds to reverse transciptase enzyme resulting in its allosteric inhibition. Both are constituent of highly active anti retroviral therapy (HAART) used for preventing maternal to child transmission of HIV virus. Zidovudine is classified as class C drug which means that although safe in animals it is yet to be tested in humans for reproductive toxicity. Efavirenz has been classified as class D drug which means that there has been reports of reproductive toxicity induced by it and should be used only when potential benefits outweigh the risk. As the teratology profile of both these drug has not yet been established so we have taken this study to ascertain the toxicity caused by both these drugs individually as well as in combination on structural, biochemical as well as on behavioural aspects of fetal mice. newline
dc.titleZidovudine and efavirenz induced teratogenicity in mice
dc.title.alternative
dc.creator.researcherMishra, Anand
dc.subject.keywordTeratogenicity in Mice
dc.description.note
dc.contributor.guidePandey, Shashi Kant
dc.publisher.placeVaranasi
dc.publisher.universityBanaras Hindu University
dc.publisher.institutionDepartment of Anatomy
dc.date.registered1-9-2011
dc.date.completed2017
dc.date.awarded
dc.type.degreePh.D.
Appears in Departments:Department of Physics

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01_title.pdfAttached File103.9 kBAdobe PDFView/Open
02_abstract.pdf179.92 kBAdobe PDFView/Open
03_certificate.pdf58.42 kBAdobe PDFView/Open
04_acknowledgement.pdf55.47 kBAdobe PDFView/Open
05_content.pdf242.73 kBAdobe PDFView/Open
06_preface.pdf161.3 kBAdobe PDFView/Open
07_chapter 1.pdf571.56 kBAdobe PDFView/Open
08_chapter 2.pdf500 kBAdobe PDFView/Open
09_chapter 3.pdf737.87 kBAdobe PDFView/Open
10_chapter 4.pdf365.5 kBAdobe PDFView/Open
11_chapter 5.pdf689.57 kBAdobe PDFView/Open
12_chapter 6.pdf187.44 kBAdobe PDFView/Open
13_chapter 7.pdf220.32 kBAdobe PDFView/Open
14_bibliography.pdf97.15 kBAdobe PDFView/Open


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