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Summary Literature (7)
Literature for DOID 9258: Waardenburg syndrome


Xenbase Articles :
( Denotes literature images)
Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction., Monsoro-Burq AH,Wang E,Harland R, Dev Cell. February 1, 2005; 8(2):1878-1551.
The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS,Saint-Jeannet JP, Mol Biol Cell. June 1, 2007; 18(6):1939-4586.
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C,Maczkowiak F,Roche DD,Monsoro-Burq AH, Proc Natl Acad Sci U S A. April 2, 2013; 110(14):1091-6490.
Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL,Park TJ,Woods JO,Cha HJ,Wallingford JB,Marcotte EM, Proc Natl Acad Sci U S A. April 6, 2010; 107(14):1091-6490.
Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells., Okuno H,Okano H, Regen Ther. August 24, 2021; 18:2352-3204.
Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB,Nemes P,Moody SA, iScience. September 15, 2023; 26(9):2589-0042.
Xenopus as a model system for studying pigmentation and pigmentary disorders., El Mir J,Nasrallah A,Thézé N,Cario M,Fayyad-Kazan H,Thiébaud P,Rezvani HR, Pigment Cell Melanoma Res. January 7, 2024; 38(1):1755-148X.