1. Saga, Y, Hata, N, Koseki, H, Taketo, M M. . Mesp2: a novel mouse gene expressed in the presegmented mesoderm and essential for segmentation initiation. In Genes & development, 11, 1827-39. doi:. https://pubmed.ncbi.nlm.nih.gov/9242490/
2. Okada, Hajime, Saga, Yumiko. 2022. Repurposing of the enhancer-promoter communication underlies the compensation of Mesp2 by Mesp1. In PLoS genetics, 18, e1010000. doi:10.1371/journal.pgen.1010000. https://pubmed.ncbi.nlm.nih.gov/35025872/
3. Morimoto, Mitsuru, Sasaki, Nobuo, Oginuma, Masayuki, Kanno, Jun, Saga, Yumiko. 2007. The negative regulation of Mesp2 by mouse Ripply2 is required to establish the rostro-caudal patterning within a somite. In Development (Cambridge, England), 134, 1561-9. doi:. https://pubmed.ncbi.nlm.nih.gov/17360776/
4. Saga, Y. . Genetic rescue of segmentation defect in MesP2-deficient mice by MesP1 gene replacement. In Mechanisms of development, 75, 53-66. doi:. https://pubmed.ncbi.nlm.nih.gov/9739106/
5. Kageyama, Ryoichiro, Niwa, Yasutaka, Isomura, Akihiro, González, Aitor, Harima, Yukiko. 2012. Oscillatory gene expression and somitogenesis. In Wiley interdisciplinary reviews. Developmental biology, 1, 629-41. doi:10.1002/wdev.46. https://pubmed.ncbi.nlm.nih.gov/23799565/
6. Qiu, Xu-sheng, Zhou, Song, Jiang, Hua, Cheng, Jack C Y, Qiu, Yong. . Mutation analysis of MESP2, HES7 and DUSP6 gene exons in patients with congenital scoliosis. In Studies in health technology and informatics, 176, 52-5. doi:. https://pubmed.ncbi.nlm.nih.gov/22744456/
7. Zhang, Erge, Yang, Jianping, Liu, Yang, Yu, Yu, Sun, Kun. 2020. MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation. In Journal of molecular medicine (Berlin, Germany), 98, 1035-1048. doi:10.1007/s00109-020-01929-4. https://pubmed.ncbi.nlm.nih.gov/32572506/