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Literature for DOID 5768: Nager acrofacial dysostosis
Xenbase Articles
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Denotes literature images)
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome.,
Devotta A,Juraver-Geslin H,Gonzalez JA,Hong CS,Saint-Jeannet JP,
Dev Biol. July 15, 2016; 415(2):1095-564X.
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| Modeling human craniofacial disorders in Xenopus., Dubey A,Saint-Jeannet JP, Curr Pathobiol Rep. March 1, 2017; 5(1):2167-485X. |
Mouth development.,
Chen J,Jacox LA,Saldanha F,Sive H,
Wiley Interdiscip Rev Dev Biol. September 1, 2017; 6(5):1759-7692.
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Molecular mechanisms of hearing loss in Nager syndrome.,
Maharana SK,Saint-Jeannet JP,
Dev Biol. August 1, 2021; 476:1095-564X.
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Function of chromatin modifier Hmgn1 during neural crest and craniofacial development.,
Ihewulezi C,Saint-Jeannet JP,
Genesis. October 1, 2021; 59(10):1526-968X.
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Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.,
Griffin C,Coppenrath K,Khan D,Lin Z,Horb M,Saint-Jeannet JP,
Dis Model Mech. March 1, 2025; 18(3):1754-8411.
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