Please use this identifier to cite or link to this item: http://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/10294
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dc.contributor.authorSingh, Raj Laxmi-
dc.contributor.authorMittal, Shikha [Guided by]-
dc.date.accessioned2023-10-30T09:01:08Z-
dc.date.available2023-10-30T09:01:08Z-
dc.date.issued2023-
dc.identifier.urihttp://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/10294-
dc.descriptionEnrollment No. 217806en_US
dc.description.abstractThe brand-new coronavirus SARS-CoV-2 is what caused the COVID-19 pandemic. SARS-CoV-2 accesses host cells via the Angiotensin-converting enzyme 2 (ACE2), which is also a functional receptor on cell surfaces. ACE2 is abundantly expressed in the heart, kidneys, and lungs and is released into the plasma. The rennin angiotensin aldosterone system's main regulator is ACE2 (RAAS). Specifically in individuals with comorbidities such hypertension, Diabetes mellitus, and cardiovascular illness, SARS-CoV-2 promotes ACE/ACE2 balance disturbance and RAAS activation, which ultimately leads to COVID-19 development. As a Result, ACE2 expression may have contradictory effects, promoting SARS-CoV-2 pathogenicity while inhibiting viral infection.en_US
dc.language.isoen_USen_US
dc.publisherJaypee University of Information Technology, Solan, H.P.en_US
dc.subjectSARSen_US
dc.subjectHuman Corona Virusen_US
dc.subjectGenetic materialsen_US
dc.subjectVirus genomeen_US
dc.titleSequence Analysis for SNP Detection and Phylogenetic Reconstruction of SARS-CoV-2 Sequences Isolated from Different COVID-19 Sequencesen_US
dc.typeDissertationen_US
Appears in Collections:Dissertations (M.Sc.)



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