{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough none of the provided abstracts directly describe SNORD114-3, the collective work offers a detailed picture of the precise regulation of Src family kinases and their associated signaling molecules. Many studies demonstrate how key regulators—including C‐terminal Src kinase (Csk), its membrane adaptors (e.g., Cbp/PAG), and additional modulators—control Src activity in diverse cellular processes such as cytoskeletal remodeling, cell adhesion, migration, immune receptor signaling, and oncogenic transformation. These investigations underscore that proper tyrosine phosphorylation dynamics and the spatial recruitment of inhibitory or activating proteins are critical for maintaining cellular homeostasis and for modulating responses to physiological and pathological cues."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "14"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn light of the emerging roles of noncoding RNAs in the regulation of cellular signaling, it is conceivable that SNORD114-3—a small nucleolar RNA typically implicated in post-transcriptional modifications—might also influence these pathways indirectly. For example, SNORD114-3 may affect the processing or stability of transcripts encoding critical components of Src-mediated networks, thereby modulating cell proliferation, differentiation, or migration. 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