Presentation Information
[BP-05]Establishment of a Runx2 missense mouse model of cleidocranial dysplasia and identification of a novel dental phenotype
Saki Ogawa1,2, Shinnosuke Higuchi1, Yuki Yoshimoto1,3, Shigenori Miura1, Atsuko Hamada4, Tetsushi Sakuma5, Ryo Kunimatsu2, Kotaro Tanimoto2, Toshihisa Komori6, Chisa Shukunami1 (1. Department of Molecular Biology and Biochemistry, Graduate School of Biomedical & Health Sciences, Hiroshima University, 2. Department of Orthodontics and Craniofacial Developmental Biology, Graduate School of Biomedical and Health Sciences, Hiroshima University, 3. Department of Molecular Craniofacial Embryology and Oral Histology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, 4. Department of Oral Oncology, Graduate School of Biomedical & Health Sciences, Hiroshima University, 5. Laboratory of Genome Editing Breeding, Graduate School of Agriculture, Kyoto University, 6. Department of Molecular Bone Biology, Graduate School of Biomedical Sciences, Nagasaki University)
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