Comprehensive analysis of ferroptosis-related genes reveals potential therapeutic targets in osteoporosis patients: a computational analysis and in vitro experiments by Sihui Chen, Sihui Chen, Yi Jiang, Yi Jiang, Guoqin Xie, Guoqin Xie, Peng Wu, Peng Wu, Jinyu Zhu, Jinyu Zhu

Subjects: “…KMT2D…”
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The significance of follow-up in patients with dysmorphic features: a case from clinical practice by Mariya Levkova, Milena Stoyanova, Mari Hachmeriyan

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TP53 and KMT2D mutations associated with worse prognosis in peripheral T‐cell lymphomas by Lingling Wang, Lei Yang, Fangshu Guan, Jing Chen, Yuexin Cheng, Yuqing Miao, Jingsong He, Zhen Cai, He Huang, Yi Zhao

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Mapping in silico genetic networks of the KMT2D tumour suppressor gene to uncover novel functional associations and cancer cell vulnerabilities by Yuka Takemon, Erin D. Pleasance, Alessia Gagliardi, Christopher S. Hughes, Veronika Csizmok, Kathleen Wee, Diane L. Trinh, Ryan D. Huff, Andrew J. Mungall, Richard A. Moore, Eric Chuah, Karen L. Mungall, Eleanor Lewis, Jessica Nelson, Howard J. Lim, Daniel J. Renouf, Steven JM. Jones, Janessa Laskin, Marco A. Marra

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Role of histone methyltransferase KMT2D in BMSC osteogenesis via AKT signaling by Zhichun Zhang, Yanyan Guo, Xuejun Gao, Xiaoyan Wang, Chanyuan Jin

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Mutational Analysis of Extranodal NK/T-Cell Lymphoma Using Targeted Sequencing with a Comprehensive Cancer Panel by Seungkyu Choi, Jai Hyang Go, Eun Kyung Kim, Hojung Lee, Won Mi Lee, Chun-Sung Cho, Kyudong Han

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Case report of kabuki syndrome in a newborn caused by KMT2D gene mutation by Xuejiao Ba, Xiyao Yang, Yizhi Zhang, Fang Guo, Lihong Zhu, Rui Tong, Yanbin Yang, Yuan Qian, Hongqing Zhang

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