Please use this identifier to cite or link to this item: http://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/10283
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dc.contributor.authorPrasher, Gargi-
dc.contributor.authorSingh, Tiratha Raj [Guided by]-
dc.date.accessioned2023-10-30T06:49:57Z-
dc.date.available2023-10-30T06:49:57Z-
dc.date.issued2023-
dc.identifier.urihttp://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/10283-
dc.descriptionEnrollment No. 217811en_US
dc.description.abstractIn Alzheimer's disease (AD), amyloid-beta(Aβ)-induced neuronal damage is characterised by mitochondrial dysfunction. Researchers are now considering the potential which are related to mitochondria and intramitochondrial. Given the new emphasis on the intracellular biology of Amyloid beta and its precursor protein (APP), Amyloid beta could trigger which cause neurotoxicity. In order to promote new perspectives on the development of AD, we study the crucial part that mitochondrial dysfunction plays in AD with Codon usage analysis and with SNPs detection (CUB) is the term describing the phenomena of inconsistent use of similar codons, where a particular codon is preferred over another.en_US
dc.language.isoen_USen_US
dc.publisherJaypee University of Information Technology, Solan, H.P.en_US
dc.subjectGenomeen_US
dc.subjectAlzheimer’s Diseaseen_US
dc.titleGenomic and Evolutionary Investigations on MT-ND Gene Family for Its Regulatory Role in Alzheimer`S Diseaseen_US
dc.typeDissertationen_US
Appears in Collections:Dissertations (M.Sc.)



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