All new modifications are analyzed and experimentally verified.
Different types of chromatin associated with histone modifications were analyzed by immunolocalization in Costus spiralis.
Histone modifications were analyzed in three ICF (ICF3, ICF4, and ICF5) and three control (N9, N10, and N11) lymphoblast cell lines.
Post-translational protein modifications were analyzed and potentially deiminated peptides were found on aldolase, α-enolase, PGK1, calreticulin, HSP60 and the FUSE-BPs.
The genomic distributions of four histone modifications were analyzed in opossum fibroblasts by ChIP-seq, using antibodies against H3K4me3, H3K9me3, H3K27me3, and H3K9Ac (see Methods).
In this study, allele-specific H3K27me3 and H3K36me3 modifications were analyzed in two rice F1 hybrids, Guangluai (GL) × 93-11 and GL × Teqing (TQ), and their parents.
Additionally, mostly repressive histone H3K27m1/K27m3 and H4K20m1 together with positive-acting H3K36m3 modifications were analyzed in parental plant and derived calli (Fig. S3A ).
The laser-assisted surface modification was analyzed and described as a function of incident laser pulse intensity.
Surprisingly, data in which ChIP-qPCR for specific histone-modifications was analyzed during memory formation are sparse, and at least in the brain, there is also evidence that transient changes in gene expression do not always correlate with altered histone-modifications at differentially expressed genes (Kenney et al, 2012).
Interesting results were obtained when another type of putative post-translational modification was analyzed, sumoylation.
