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dc.contributor.advisorRaghavan, Sathees C
dc.contributor.authorGhosh, Dipayan
dc.date.accessioned2022-09-06T11:14:21Z
dc.date.available2022-09-06T11:14:21Z
dc.date.submitted2022
dc.identifier.urihttps://etd.iisc.ac.in/handle/2005/5847
dc.description.abstractThis study has provided new insights into the mechanistic details of NHEJ and showed that DNA sequence around the break site can be a factor in determining which proteins involved in NHEJ might be recruited with a higher efficiency. We have also generated a KU70-mutant Nalm6 cell line (N6-Ku70-2) using CRISPR-Cas9 genome editing technology and explored the differences between these cells and WT Nalm6 cells in terms of cell proliferation and DNA repair potential. Finally, we have investigated the importance of RNASEH2A/RNASEH2B expression in the maintenance of proper DSB repair and cellular viability in T-ALL cells.en_US
dc.language.isoen_USen_US
dc.rightsI grant Indian Institute of Science the right to archive and to make available my thesis or dissertation in whole or in part in all forms of media, now hereafter known. I retain all proprietary rights, such as patent rights. I also retain the right to use in future works (such as articles or books) all or part of this thesis or dissertationen_US
dc.subjectDNA sequenceen_US
dc.subjectnonhomologous end joiningen_US
dc.subjectDNA double-strand breaksen_US
dc.subjectDSB substratesen_US
dc.subjectKU70 geneen_US
dc.subjectNalm6 cellsen_US
dc.subject.classificationResearch Subject Categories::NATURAL SCIENCES::Chemistry::Biochemistryen_US
dc.titleUnderstanding Nonhomologous DNA End Joining: Novel Insights Into Mechanism and Regulationen_US
dc.typeThesisen_US
dc.degree.namePhDen_US
dc.degree.levelDoctoralen_US
dc.degree.grantorIndian Institute of Scienceen_US
dc.degree.disciplineFaculty of Scienceen_US


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