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The balance of two opposing factors Mad and Myc regulates cell fate during tissue remodeling. , Okada M., Cell Biosci. April 19, 2018; 8 51.
High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis. , Michiue T ., Dev Biol. June 15, 2017; 426 (2): 270-290.
Exposure to the herbicide acetochlor alters thyroid hormone-dependent gene expression and metamorphosis in Xenopus Laevis. , Crump D., Environ Health Perspect. December 1, 2002; 110 (12): 1199-205.
The bHLH class protein pMesogenin1 can specify paraxial mesoderm phenotypes. , Yoon JK., Dev Biol. June 15, 2000; 222 (2): 376-91.
Alternative splicing and embryonic expression of the Xenopus mad4 bHLH gene. , Newman CS., Dev Dyn. June 1, 1999; 215 (2): 170-8.
Thylacine 1 is expressed segmentally within the paraxial mesoderm of the Xenopus embryo and interacts with the Notch pathway. , Sparrow DB ., Development. June 1, 1998; 125 (11): 2041-51.
Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins. , Sparrow DB ., Mech Dev. February 1, 1998; 71 (1-2): 151-63.
Remarkable sequence conservation of transcripts encoding amphibian and mammalian homologues of quaking, a KH domain RNA-binding protein. , Zorn AM ., Gene. April 1, 1997; 188 (2): 199-206.
Analysis of a variant Max sequence expressed in Xenopus laevis. , Tonissen KF ., Oncogene. January 1, 1994; 9 (1): 33-8.
Expression of two distinct homologues of Xenopus Max during early development. , King MW , King MW ., Cell Growth Differ. February 1, 1993; 4 (2): 85-92.