Associated Papers
Association of Mutations in the Melanocortin-2 Receptor Accessory Protein 2 Gene (MRAP2) and Obesity: A Systematic Review and Meta-Analysis.
Ji RL et al.
International Journal of Molecular Sciences, 2026
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini A et al.
Journal of Thrombosis and Haemostasis : Jth, 2017
Regulation of the Ste20-like kinase, SLK: involvement of activation segment phosphorylation.
Luhovy AY et al.
The Journal of Biological Chemistry, 2012
Chlamydophila pneumoniae PknD exhibits dual amino acid specificity and phosphorylates Cpn0712, a putative type III secretion YscD homolog.
Johnson DL et al.
Journal of Bacteriology, 2007
Glycogen synthase kinase-3 beta mutagenesis identifies a common binding domain for GBP and Axin.
Ferkey DM et al.
The Journal of Biological Chemistry, 2002
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