Editorial: Deciphering the etiology of rare genetic disorders associated with protein phosphatases

Frontiers in Cell and Developmental Biology

Cell and Developmental Biology

Richard E. Honkanen¹  Chenchen Li¹  Brian E. Wadzinski²  Veerle Janssens³ 

[1] Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL, United States;Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, United States;Laboratory of Protein Phosphorylation and Proteomics, Department of Cellular and Molecular Medicine, University of Leuven (KU Leuven), Leuven, Belgium;KU Leuven Brain Institute (LBI), Leuven, Belgium;KU Leuven Cancer Institute (LKI), Leuven, Belgium;

关键词: protein phosphatase (PP);    genetic disorder;    PPP2R5D;    developmental disorder;    signal transduction;    de novo;    PPP2CA;    PTPN11;   

DOI  :  10.3389/fcell.2023.1241606

 received in 2023-06-16, accepted in 2023-07-31,  发布年份 2023

来源: Frontiers

【 授权许可】

Unknown   
Copyright © 2023 Janssens, Wadzinski, Li and Honkanen.