Publication & Citation Trends
Publications
0 total
The carboxy-terminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH.
Cited by 108
Semantic Scholar
Diversity of the damage recognition step in the global genomic nucleotide excision repair in vitro.
Cited by 135
Semantic Scholar
Centrosome Protein Centrin 2/Caltractin 1 Is Part of the Xeroderma Pigmentosum Group C Complex That Initiates Global Genome Nucleotide Excision Repair* OA
Cited by 347
Semantic Scholar
ATP‐dependent chromatin remodeling facilitates nucleotide excision repair of UV‐induced DNA lesions in synthetic dinucleosomes OA
Cited by 180
Semantic Scholar
Reconstitution of damage DNA excision reaction from SV40 minichromosomes with purified nucleotide excision repair proteins.
Cited by 40
Semantic Scholar
Xeroderma pigmentosum variant: from a human genetic disorder to a novel DNA polymerase.
Cited by 24
Semantic Scholar
The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η
Cited by 1,329
Semantic Scholar
Xeroderma pigmentosum variant (XP‐V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity OA
Cited by 424
Semantic Scholar
Identification and characterization of XPC-binding domain of hHR23B OA
Cited by 113
Semantic Scholar
Research Topics
Myeloproliferative Neoplasms: Diagnosis and Treatment
(68)
Kruppel-like factors research
(27)
Chronic Myeloid Leukemia Treatments
(25)
Acute Myeloid Leukemia Research
(21)
Eosinophilic Disorders and Syndromes
(18)
Affiliations
Hudson Institute
Duke University
Juntendo University
Chugai Pharma (United States)
Nippon Soken (Japan)