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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.
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance. , Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.
On the origin of vertebrate somites. , Onai T., Zoological Lett. June 15, 2015; 1 33.
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development. , Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
Sp8 regulates inner ear development. , Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
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.
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm. , Janesick A ., Development. March 1, 2012; 139 (6): 1213-24.
PAPC and the Wnt5a/ Ror2 pathway control the invagination of the otic placode in Xenopus. , Jung B., BMC Dev Biol. June 10, 2011; 11 36.
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.
XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis. , Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.