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Proceedings of the National Academy of Sciences of the United States of America|June 10, 2020
Topoisomerase I-driven repair of UV-induced damage in NER-deficient cellsLiton Kumar Saha, Mitsuo Wakasugi, Salma Akter, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2015
XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiencyChaowan Guo, Yuka Nakazawa, Lisa Woodbine, et al.
Clinical Immunology (Orlando, Fla.)|July 15, 2015
Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiencyShinobu Tamura, Kohei Higuchi, Masaharu Tamaki, et al.
Plos One|November 18, 2017
ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repairMasataka Tsuda, Kosai Cho, Masato Ooka, et al.
Scientific Reports|August 18, 2017
Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cellsRyoichiro Doi, Tomoshi Tsuchiya, Norisato Mitsutake, et al.
Cell|March 7, 2020
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled RepairYuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, et al.
Journal of Human Genetics|February 7, 2018
Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutationsHiroshi Doi, Shigeru Koyano, Satoko Miyatake, et al.
American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.
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