Ciliary Hedgehog signaling regulates cell survival to build the facial midline

Craniofacial defects are among the most common phenotypes caused by ciliopathies, yet the developmental and molecular etiology of these defects is poorly understood. We investigated multiple mouse models of human ciliopathies (including Tctn2, Cc2d2a, and Tmem231 mutants) and discovered that each di...

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Auteurs principaux: Shaun R Abrams, Jeremy F Reiter
Format: article
Langue:EN
Publié: eLife Sciences Publications Ltd 2021
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R
Q
Accès en ligne:https://doaj.org/article/f11836e51aab41898f41c1a9efe6035c
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