SIRT4 is essential for metabolic control and meiotic structure during mouse oocyte maturation.
Zeng, Juan; Jiang, Manxi; Wu, Xinghan; Diao, Feiyang; Qiu, Danhong; Hou, Xiaojing; Wang, Haichao; Li, Ling; Li, Chunling; Ge, Juan; Liu, Jiayin; Ou, Xianghong; Wang, Qiang.
; : e12789, 2018 May 29.
Artigo em Inglês | MEDLINE | ID: mdl-29845740
HDAC3 promotes meiotic apparatus assembly in mouse oocytes by modulating tubulin acetylation.
Differing roles of pyruvate dehydrogenase kinases during mouse oocyte maturation.
Sirt2 functions in spindle organization and chromosome alignment in mouse oocyte meiosis.
Eccentric localization of catalase to protect chromosomes from oxidative damages during meiotic maturation in mouse oocytes.
Oocyte development, meiosis and aneuploidy.
Epsin2 promotes polarity establishment and meiotic division through activating Cdc42 in mouse oocyte.
Live imaging RNAi screen reveals genes essential for meiosis in mammalian oocytes.
TCTP regulates spindle microtubule dynamics by stabilizing polar microtubules during mouse oocyte meiosis.
Melatonin protects against maternal obesity-associated oxidative stress and meiotic defects in oocytes via the SIRT3-SOD2-dependent pathway.
Meiotic maturation failure induced by DICER1 deficiency is derived from primary oocyte ooplasm.