2023 - Research.com Molecular Biology in China Leader Award
2022 - Research.com Genetics and Molecular Biology in China Leader Award
His scientific interests lie mostly in Molecular biology, DNA repair, Cell biology, DNA damage and DNA. His research in Molecular biology intersects with topics in Protein kinase A, Phosphorylation, Histone, Chromatin and Nuclear protein. His biological study spans a wide range of topics, including Autophosphorylation, Homologous recombination and Kinase activity.
His Cell biology study integrates concerns from other disciplines, such as Genetics, Cellular differentiation, Genome instability and Chromosome breakage. His Double Strand Break Repair study in the realm of DNA damage connects with subjects such as Premature aging. His study looks at the relationship between DNA and fields such as DNA-binding protein, as well as how they intersect with chemical problems.
His primary areas of study are Molecular biology, DNA repair, DNA damage, Cell biology and DNA. His Molecular biology study incorporates themes from Ku80, Protein kinase A, Homologous recombination, Ku70 and Mutant. As a member of one scientific family, David J. Chen mostly works in the field of DNA repair, focusing on Replication protein A and, on occasion, Nucleotide excision repair.
His research on DNA damage also deals with topics like
His primary scientific interests are in DNA damage, DNA repair, Cell biology, Molecular biology and DNA. As a part of the same scientific study, David J. Chen usually deals with the DNA damage, concentrating on Ataxia Telangiectasia Mutated Proteins and frequently concerns with Kinase. The study incorporates disciplines such as Cancer research, Ubiquitin, Ku80, Cell killing and DNA replication in addition to DNA repair.
His research investigates the link between Cell biology and topics such as DNA repair protein XRCC4 that cross with problems in XRCC2 and DNA Repair Pathway. David J. Chen has included themes like Chromatin, Poly ADP ribose polymerase, Mutant and Homologous recombination in his Molecular biology study. His DNA research includes elements of Biophysics and Live cell imaging.
DNA repair, DNA damage, Molecular biology, Cell biology and DNA are his primary areas of study. His studies deal with areas such as P53 binding, Cancer research, Live cell imaging, Dose fractionation and Chromatin as well as DNA repair. His DNA damage research incorporates elements of Transport protein, Cell cycle checkpoint, Cell growth and Protein–protein interaction.
Ku70, Ku80, S phase and Cell cycle is closely connected to Homologous recombination in his research, which is encompassed under the umbrella topic of Molecular biology. His Cell biology study combines topics from a wide range of disciplines, such as DNA End-Joining Repair, Ataxia Telangiectasia Mutated Proteins, Biochemistry and DNA repair protein XRCC4. His work deals with themes such as Ionizing radiation and High doses, which intersect with DNA.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
Fredrick S. Leach;Nicholas C. Nicolaides;Nickolas Papadopoulos;Bo Liu.
Cell (1993)
ATM Phosphorylates Histone H2AX in Response to DNA Double-strand Breaks
Sandeep Burma;Benjamin P. Chen;Michael Murphy;Akihiro Kurimasa.
Journal of Biological Chemistry (2001)
Telomere Shortening Triggers Senescence of Human Cells through a Pathway Involving ATM, p53, and p21CIP1, but Not p16INK4a
Utz Herbig;Wendy A Jobling;Benjamin P.C Chen;David J Chen.
Molecular Cell (2004)
XRCC2 and XRCC3, New Human Rad51-Family Members, Promote Chromosome Stability and Protect against DNA Cross-Links and Other Damages
Nan Liu;Jane E. Lamerdin;Robert S. Tebbs;David Schild.
Molecular Cell (1998)
Radiation-induced epidermal growth factor receptor nuclear import is linked to activation of DNA-dependent protein kinase
Klaus Dittmann;Claus Mayer;Birgit Fehrenbacher;Martin Schaller.
Journal of Biological Chemistry (2005)
Genomic instability in laminopathy-based premature aging
Baohua Liu;Jianming Wang;Kui Ming Chan;Wai Mui Tjia.
Nature Medicine (2005)
The oxygen-rich postnatal environment induces cardiomyocyte cell-cycle arrest through DNA damage response.
Bao N. Puente;Wataru Kimura;Shalini A. Muralidhar;Jesung Moon.
Cell (2014)
DNA double strand break repair via non-homologous end-joining
Anthony J. Davis;David J. Chen.
Translational cancer research (2013)
Autophosphorylation of the DNA-dependent protein kinase catalytic subunit is required for rejoining of DNA double-strand breaks.
Doug W. Chan;Doug W. Chan;Benjamin Ping Chi Chen;Sheela Prithivirajsingh;Akihiro Kurimasa;Akihiro Kurimasa.
Genes & Development (2002)
Differential roles for bone morphogenetic protein (BMP) receptor type IB and IA in differentiation and specification of mesenchymal precursor cells to osteoblast and adipocyte lineages.
D. Chen;X. Ji;M.A. Harris;J.Q. Feng.
Journal of Cell Biology (1998)
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