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doi: 10.3389/fphar.2021.701487 28 AhnH-SYeomJYuJKwonY-IKimJ-HKimK
doi: 10.3390/ijms251810151, 35 SongC.HeD.YangZ.FuY.ZhengH.XingZ.et al
Surprisingly, mice with specific genetic deletion of Gpx1 appear phenotypically normal and with normal life span (Ho et al., 1997), suggesting that there are alternative compensatory mechanisms for H 2 O 2 scavenging in Gpx1 deficiency
T-cell therapy for chronic viral hepatitis
Xu LX, Xuan HW, He W, Zhang L, Huang MY, Li K, et al
