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Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease. , Coppenrath K ., Genesis. December 1, 2021; 59 (12): e23453.
Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells. , Okuno H., Regen Ther. August 24, 2021; 18 275-280.
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. , Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.
Myogenic waves and myogenic programs during Xenopus embryonic myogenesis. , Della Gaspera B ., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns. , Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.
The mych gene is required for neural crest survival during zebrafish development. , Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.
Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis. , Showell C ., Dev Dyn. June 1, 2006; 235 (6): 1623-30.