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Summary Literature (4)
Literature for DOID 0060232: branchiootic syndrome


Xenbase Articles :
( Denotes literature images)
Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors., Neilson KM,Pignoni F,Yan B,Moody SA, Dev Dyn. December 1, 2010; 239(12):1058-8388.
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM,Krohn P,Baxi AB,Tavares ALP,Sullivan CH,Chillakuru YR,Majumdar HD,Neilson KM,Moody SA, Dis Model Mech. March 3, 2020; 13(3):1754-8411.
Mcrs1 interacts with Six1 to influence early craniofacial and otic development., Neilson KM,Keer S,Bousquet N,Macrorie O,Majumdar HD,Kenyon KL,Alfandari D,Alfandari D,Moody SA, Dev Biol. November 1, 2020; 467(1-2):1095-564X.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.