Nobox-flox 基因敲除小鼠

1. Jordan, Pénélope, Verebi, Camille, Perol, Sandrine, El Khattabi, Laila, Bienvenu, Thierry. 2023. NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights. In Journal of assisted reproduction and genetics, 41, 135-146. doi:10.1007/s10815-023-02981-y. https://pubmed.ncbi.nlm.nih.gov/37921973/

2. Rajkovic, Aleksandar, Pangas, Stephanie A, Ballow, Daniel, Suzumori, Nobuhiro, Matzuk, Martin M. . NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression. In Science (New York, N.Y.), 305, 1157-9. doi:. https://pubmed.ncbi.nlm.nih.gov/15326356/

3. Yao, Changfang, Lu, Likui, Ji, Yiting, Sun, Miao, Xia, Fei. 2022. Hypo-Hydroxymethylation of Nobox is Associated with Ovarian Dysfunction in Rat Offspring Exposed to Prenatal Hypoxia. In Reproductive sciences (Thousand Oaks, Calif.), 29, 1424-1436. doi:10.1007/s43032-022-00866-6. https://pubmed.ncbi.nlm.nih.gov/35257353/