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Summary Literature (5)
Literature for OMIM 113650: BRANCHIOOTORENAL SYNDROME 1; BOR1


Xenbase Articles:
( Denotes literature images)
EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis., Li Y,Manaligod JM,Weeks DL, Biol Cell. February 17, 2010; 102(5):1768-322X.
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.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM,Abbruzzesse G,Bartolo V,Krohn P,Alfandari D,Alfandari D,Moody SA,Kenyon K, Dev Biol. January 15, 2017; 421(2):1095-564X.
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.