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Pooja Khatkar

Researcher at Georgetown University

Publications -  5
Citations -  75

Pooja Khatkar is an academic researcher from Georgetown University. The author has contributed to research in topics: Nucleotide excision repair & DNA repair. The author has an hindex of 3, co-authored 3 publications receiving 46 citations.

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A new sub‐pathway of long‐patch base excision repair involving 5′ gap formation

TL;DR: A major sub‐pathway of conventional long‐patch BER that involves formation of a 9‐nucleotide gap 5′ to the lesion is discovered and is mediated by RECQ1 DNA helicase and ERCC1‐XPF endonuclease in cooperation with PARP1 poly(ADP‐ribose) polymerase and RPA.
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Slow repair of lipid peroxidation-induced DNA damage at p53 mutation hotspots in human cells caused by low turnover of a DNA glycosylase

TL;DR: In-cell and in vitro mechanism studies revealed that this delay in repair was due to inefficient turnover of N-methylpurine-DNA glycosylase (MPG), which initiates BER of εA, suggesting a previously unknown mechanism for slower repair at mutation hotspots and implicating sequence-related variability of DNA repair efficiency to be responsible for mutation hotspot signatures.
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Cannabinoids Reduce Extracellular Vesicle Release from HIV-1 Infected Myeloid Cells and Inhibit Viral Transcription

TL;DR: The data suggest that CBD significantly reduces the number of EVs released from infected cells and that this may be mediated by reducing viral transcription and autophagy activation, which may exert a protective effect by alleviating the pathogenic effects of EVs in HIV-1 and CNS-related infections.
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Retroviral infection of human neurospheres and use of stem Cell EVs to repair cellular damage

TL;DR: In this paper , the authors reported the generation of neurospheres from iPSC-derived neural progenitor cells (NPCs) and showed that these cultures are permissive to retroviral (e.g. HIV-1, HTLV-1) replication.
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A novel method for monitoring functional lesion-specific recruitment of repair proteins in live cells.

TL;DR: This microscopy-based methodology is reliable in detecting the recruitment of proteins to specific DNA substrates and can be extended to study other in vivo DNA-protein relationships in any DNA sequence and in the context of any DNA structure in transfectable proliferating or quiescent cells.