Missense mutation in selenocysteine synthase causes cardio-respiratory failure and perinatal death in mice which can be compensated by selenium-independent GPX4
Selenoproteins are a small family of proteins containing the trace element selenium in form of the rare amino acid selenocysteine (Sec), which is decoded by the UGA codon. In humans, a number of pathogenic variants in genes encoding distinct selenoproteins or selenoprotein biosynthesis factors have...
Saved in:
Main Authors: | Noelia Fradejas-Villar, Wenchao Zhao, Uschi Reuter, Michael Doengi, Irina Ingold, Simon Bohleber, Marcus Conrad, Ulrich Schweizer |
---|---|
Format: | article |
Language: | EN |
Published: |
Elsevier
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/f6302178548c423e8a2aad1b6790908b |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Pathogenic Variants in Selenoproteins and Selenocysteine Biosynthesis Machinery
by: Didac Santesmasses, et al.
Published: (2021) -
Naringenin alleviates myocardial ischemia/reperfusion injury by regulating the nuclear factor-erythroid factor 2-related factor 2 (Nrf2) /System xc-/ glutathione peroxidase 4 (GPX4) axis to inhibit ferroptosis
by: Shujun Xu, et al.
Published: (2021) -
The Effect of tRNA<sup>[Ser]Sec</sup> Isopentenylation on Selenoprotein Expression
by: Noelia Fradejas-Villar, et al.
Published: (2021) -
Going Forward and Back: The Complex Evolutionary History of the GPx
by: Thomaz Stumpf Trenz, et al.
Published: (2021) -
MnSOD and GPx1 polymorphism relationship with coronary heart disease risk and severity
by: Souiden,Yosra, et al.
Published: (2016)