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Zhengke Li

Researcher at East Tennessee State University James H. Quillen College of Medicine

Publications -  32
Citations -  641

Zhengke Li is an academic researcher from East Tennessee State University James H. Quillen College of Medicine. The author has contributed to research in topics: DNA damage & Nucleotide excision repair. The author has an hindex of 9, co-authored 32 publications receiving 462 citations. Previous affiliations of Zhengke Li include Children's Hospital Los Angeles & Beckman Research Institute.

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DNA-PK, ATM and ATR collaboratively regulate p53-RPA interaction to facilitate homologous recombination DNA repair.

TL;DR: The results reveal a mechanism for the crosstalk between HR repair and NHEJ through the co-regulation of p53–RPA interaction by DNA-PK, ATM and ATR.
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Checkpoint Kinase ATR Promotes Nucleotide Excision Repair of UV-induced DNA Damage via Physical Interaction with Xeroderma Pigmentosum Group A

TL;DR: The results suggest that the ATR-XPA interaction mediated by the helix-turn-helix motif of XPA plays an important role in DNA-damage responses to promote cell survival and genomic stability after UV irradiation.
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ATR Plays a Direct Antiapoptotic Role at Mitochondria, which Is Regulated by Prolyl Isomerase Pin1

TL;DR: It is reported that ATR has an antiapoptotic activity at mitochondria in response to UV damage, and this activity is independent of its hallmark checkpoint/kinase activity and partner ATRIP.
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A Selective Small Molecule DNA2 Inhibitor for Sensitization of Human Cancer Cells to Chemotherapy

TL;DR: It is shown that homozygous deletion of DNA2 sensitizes cells to ionizing radiation and camptothecin (CPT), and C5 is an even more potent inhibitor of restart of stalled DNA replication forks and over-resection of nascent DNA in cells defective in replication fork protection, including BRCA2 and BOD1L.
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hDNA2 nuclease/helicase promotes centromeric DNA replication and genome stability

TL;DR: It is shown that DNA2 binds preferentially to centromeric DNA, and the DNA2 inhibitor C5 mimics DNA2 knockout and synergistically kills cancer cells when combined with an ATR inhibitor, providing mechanistic insights into how DNA2 supports replication of centromic DNA.