TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,Molecular Biology
Reference48 articles.
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2. The mesenchymal architecture of the cranial mesoderm of mouse embryos is disrupted by the loss of Twist1 function;Bildsoe;Dev. Biol.,2013
3. Transcriptional targets of TWIST1 in the cranial mesoderm regulate cell-matrix interactions and mesenchyme maintenance;Bildsoe;Dev. Biol.,2016
4. Oculomotor nerve guidance and terminal branching requires interactions with differentiating extraocular muscles;Bjorke;Dev. Biol.,2021
5. Bone ridge patterning during musculoskeletal assembly is mediated through SCX regulation of Bmp4 at the tendon-skeleton junction;Blitz;Dev. Cell,2009
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