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Spliceosomal GTPase Eftud2 deficiency-triggered ferroptosis leads to Purkinje cell degeneration
Furlanis E. Scheiffele P. Regulation of neuronal differentiation, function, and plasticity by alternative splicing. Annu. Rev. Cell Dev. Biol. 2018; 34: 451-469https://doi.org/10.1146/annurev-cellbio-100617-062826 Alternative splicing in the mammalian nervous system: recent insights into mechanisms and functional roles. Neuron. 2015; 87: 14-27https://doi.org/10.1016/j.neuron.2015.05.004 Hentze M.W. Castello A. Schwarzl T. Preiss T. A brave new world of RNA-binding proteins. Nat. Rev. Mol. Cell Biol.
The Cocrystal of Ubiquinol: Improved Stability and Bioavailability
1. Introduction Coenzyme Q10 (CoQ10) is a vitamin-like, fat-soluble organic compound and it was identified for the first time by Frederick Crane of Wisconsin (USA) in 1957 [1,2]. It comprises a quinone group and a side-chain of 10 units of isoprene (). It can be synthesized by human cells and is ubiquitously present in cell membranes [3,4].
UCHL1-PKM2 axis dysregulation is associated with promoted proliferation and invasiveness of urothelial bladder cancer cells
Background: Bladder cancer is one of the most common type of cancers globally, and the majority of cases belong to urothelial bladder carcinoma (UBC) type. Current researches have demonstrated that multiple genomic abnormalities are related to the sensitivity of cisplatin-based chemotherapy in bladder cancer patients. Previous findings have indicated a controversial role of Ubiquitin Carboxy-Terminal Hydrolase L1 (UCHL1) in malignancy, so we aimed to further explore the role of UCHL1 in UBC.
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