机译:De Novo突变在遗传骨髓衰竭综合征中激活种系TP53
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Department of Clinical Application Center for iPS Cell Research and Application Kyoto University;
Department of General Pediatric and Interdisciplinary Medicine National Center for Child Health;
Department of Pediatrics Faculty of Medicine University of Yamanashi;
Department of Anatomy and Embryology Faculty of Medicine University of Tsukuba;
Laboratory Animal Resource Center Faculty of Medicine University of Tsukuba;
Laboratory Animal Resource Center Faculty of Medicine University of Tsukuba;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Frontier Science Research Center University of Miyazaki;
Frontier Science Research Center University of Miyazaki;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Department of Pathology and Tumor Biology Graduate School of Medicine Kyoto University;
Department of Pathology and Tumor Biology Graduate School of Medicine Kyoto University;
Laboratory of DNA Information Analysis Human Genome Center Institute of Medical Science the;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Laboratory of DNA Information Analysis Human Genome Center Institute of Medical Science the;
Laboratory of Sequence Analysis Human Genome Center Institute of Medical Science the University;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
Department of Pediatrics Nagoya University Graduate School of Medicine;
Department of Pediatrics Graduate School of Medical Sciences Kyushu University;
Department of Safety Research on Blood and Biological Products National Institute of Infectious;
Department of Safety Research on Blood and Biological Products National Institute of Infectious;
Department of Pediatrics Omori Medical Center Toho University;
Department of Transfusion Medicine and Cell Processing Tokyo Women’s Medical University;
Laboratory of DNA Information Analysis Human Genome Center Institute of Medical Science the;
Department of Pediatrics Nagoya University Graduate School of Medicine;
Division of Hematology National Center for Child Health and Development;
Department of Pediatrics Faculty of Medicine University of Yamanashi;
Frontier Science Research Center University of Miyazaki;
Department of Anatomy and Embryology Faculty of Medicine University of Tsukuba;
Department of Clinical Application Center for iPS Cell Research and Application Kyoto University;
Cancer Genomics Project Graduate School of Medicine the University of Tokyo;
Department of Pediatrics Hirosaki University Graduate School of Medicine;
TP53; p53; the C-terminal domain; inherited bone marrow failure syndrome; Diamond-Blackfan anemia; dyskeratosis congenita; zebrafish; human-induced pluripotent stem cell; iPSC; gene editing;
机译:De Novo突变在遗传骨髓衰竭综合征中激活种系TP53
机译:TP53基因启动子未在暗示Li-Fraumeni综合征且没有种系TP53突变的家族中被甲基化。
机译:小儿肾上腺皮质肿瘤中遗传的种系TP53突变编码具有异常C端基序的蛋白质
机译:通过来自体外活化B细胞慢性淋巴细胞白血病细胞超深序的De Novo IghV突变检测:活化诱导的脱氨酶功能的证据
机译:患有新型巨脑综合征的患者的MYCN de novo功能获得性突变
机译:从头突变激活遗传性骨髓衰竭综合征的生殖细胞TP53
机译:成年型肉瘤的遗传和新生命线TP53突变