Kdm3b-flox 基因敲除小鼠

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3. Diets, Illja J, van der Donk, Roos, Baltrunaite, Kristina, Kuiper, Roland P, Jongmans, Marjolijn C J. 2019. De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism. In American journal of human genetics, 104, 758-766. doi:10.1016/j.ajhg.2019.02.023. https://pubmed.ncbi.nlm.nih.gov/30929739/

4. Benslimane, Zaineb, Yavuz, Sinan, Francis, Nader. 2023. A rare presentation of childhood interstitial lung disease attributed to KDM3B gene mutation: a case report. In The Pan African medical journal, 46, 84. doi:10.11604/pamj.2023.46.84.41457. https://pubmed.ncbi.nlm.nih.gov/38314229/

5. Zhu, Zhenshuo, Wu, Xiaolong, Li, Qun, Liao, Mingzhi, Hua, Jinlian. . Histone demethylase complexes KDM3A and KDM3B cooperate with OCT4/SOX2 to define a pluripotency gene regulatory network. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 35, e21664. doi:10.1096/fj.202100230R. https://pubmed.ncbi.nlm.nih.gov/34042215/