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Article

The Association Between Runx Signaling and Craniofacial Development and Disease.

Current osteoporosis reports - 1 Feb 2022

Yamashiro Takashi, Kurosaka Hiroshi, Inubush Toshihiro

Abstract excerpt

PURPOSE OF REVIEW: The Runx family genes (Runx1, Runx2, Runx3, and Cbfb) are important transcriptional regulators in the development of various tissues. We herein highlight the roles of the Runx family genes in morphogenesis in the craniofacial regions and in the pathogenesis of congenital morphological problems in these regions. RECENT FINDINGS: A recent analysis using conditional Runx mutant animals and a human...

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Identifiers

PMID: 34931296
DOI: 10.1007/s11914-021-00692-w

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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