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Mitochondrion|January 24, 2015
Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) geneHao Liu, Ronghua Li, Weixing Li, et al.Science China. Life Sciences|February 20, 2025
Low-dose exposure to microplastics retards meiotic maturation via HDAC3 insufficiencyQi Zhao, Ming Zong, Entong Song, et al.Scientific Reports|February 27, 2025
Chlorogenic acid promotes fatty acid beta-oxidation to increase hESCs proliferation and lipid synthesisMing Zong, Jingzhang Ji, Qinglai Wang, et al.Cell Reports|February 11, 2025
Acetylation at lysine 27 on maternal H3.3 regulates minor zygotic genome activationJiaming Zhang, Xuanwen Li, Qi Zhao, et al.Gene|March 8, 2007
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutationXiaowen Tang, Li Yang, Yi Zhu, et al.Gene|August 19, 2007
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigreesJianfu Chen, Li Yang, Aifen Yang, et al.Pageof 2