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In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives. , Griffin C., Dev Biol. February 1, 2024; 506 20-30.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
Transcriptional regulator PRDM12 is essential for human pain perception. , Chen YC , Chen YC ., Nat Genet. July 1, 2015; 47 (7): 803-8.
Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling. , Watanabe T., Genesis. October 1, 2014; .
The evolutionary history of vertebrate cranial placodes--I: cell type evolution. , Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning. , Schlosser G ., Dev Biol. May 1, 2014; 389 (1): 98-119.
Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/ β-catenin-mediated lung specification in Xenopus. , Rankin SA , Rankin SA ., Development. August 1, 2012; 139 (16): 3010-20.
Myogenic waves and myogenic programs during Xenopus embryonic myogenesis. , Della Gaspera B ., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm. , Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
Origin and segregation of cranial placodes in Xenopus laevis. , Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis. , Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus. , Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
Hairy2- Id3 interactions play an essential role in Xenopus neural crest progenitor specification. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Expression of TFAP2beta and TFAP2gamma genes in Xenopus laevis. , Zhang Y ., Gene Expr Patterns. August 1, 2006; 6 (6): 589-95.
Induction and specification of cranial placodes. , Schlosser G ., Dev Biol. June 15, 2006; 294 (2): 303-51.
Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation. , Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation. , Taylor KM., Dev Cell. November 1, 2005; 9 (5): 593-603.
Evi-1 expression in Xenopus. , Mead PE ., Gene Expr Patterns. June 1, 2005; 5 (5): 601-8.
Molecular anatomy of placode development in Xenopus laevis. , Schlosser G ., Dev Biol. July 15, 2004; 271 (2): 439-66.
Specification of the otic placode depends on Sox9 function in Xenopus. , Saint-Germain N ., Development. April 1, 2004; 131 (8): 1755-63.
A role for Xlim-1 in pronephros development in Xenopus laevis. , Chan TC ., Dev Biol. December 15, 2000; 228 (2): 256-69.
Synergism between Pax-8 and lim-1 in embryonic kidney development. , Carroll TJ ., Dev Biol. October 1, 1999; 214 (1): 46-59.