The Okur-Chung neurodevelopment syndrome is a rare disease caused by mutations of the CSNK2A1 gene, which encodes for the catalytic subunit of protein kinase CK2. in this study, we analyzed the most c
Variability of proteins at the sequence level creates an enormous potential for proteome complexity. Exploring this complexity is an ongoing goal in biology. Here, we survey human and plant bottom-up
To obtain more information about human proteome, especially about proteoforms (protein species) coded by 18th chromosome, we separated proteins from human cancer cell line (HepG2) by two-dimensional g
