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Summary Literature (5)
Literature for DOID 14702: branchiootorenal syndrome


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. May 1, 2010; 102(5):1768-322X.
Using Xenopus to study genetic kidney diseases., Lienkamp SS, Semin Cell Dev Biol. March 1, 2016; 51:1096-3634.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM,Abbruzzesse G,Kenyon K,Bartolo V,Krohn P,Alfandari D,Alfandari D,Moody SA, Dev Biol. January 15, 2017; 421(2):1095-564X.
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. January 1, 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. January 1, 2020; 467(1-2):1095-564X.