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Activity of the RhoU/ Wrch1 GTPase is critical for cranial neural crest cell migration. , Fort P., Dev Biol. February 15, 2011; 350 (2): 451-63.
A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds. , Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
Heading in a new direction: implications of the revised fate map for understanding Xenopus laevis development. , Lane MC ., Dev Biol. August 1, 2006; 296 (1): 12-28.
Transgenic frogs expressing the highly fluorescent protein venus under the control of a strong mammalian promoter suitable for monitoring living cells. , Sakamaki K., Dev Dyn. June 1, 2005; 233 (2): 562-9.
Xenopus nodal related-1 is indispensable only for left- right axis determination. , Toyoizumi R., Int J Dev Biol. January 1, 2005; 49 (8): 923-38.
Teleost Fh14-3-3a protein protects Xenopus oocytes from hyperosmolality. , Kohn A., J Exp Zool A Comp Exp Biol. October 1, 2003; 299 (2): 103-9.
Primitive and definitive blood share a common origin in Xenopus: a comparison of lineage techniques used to construct fate maps. , Lane MC ., Dev Biol. August 1, 2002; 248 (1): 52-67.
Ectopic Hoxa2 induction after neural crest migration results in homeosis of jaw elements in Xenopus. , Pasqualetti M., Development. December 1, 2000; 127 (24): 5367-78.
Gli1 is a target of Sonic hedgehog that induces ventral neural tube development. , Lee J ., Development. July 1, 1997; 124 (13): 2537-52.
Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. , Turner DL., Genes Dev. June 15, 1994; 8 (12): 1434-47.
Developmental and regional expression of thyroid hormone receptor genes during Xenopus metamorphosis. , Kawahara A., Development. August 1, 1991; 112 (4): 933-43.
Localization of c- myc expression during oogenesis and embryonic development in Xenopus laevis. , Hourdry J., Development. December 1, 1988; 104 (4): 631-41.
The restrictive effect of early exposure to lithium upon body pattern in Xenopus development, studied by quantitative anatomy and immunofluorescence. , Cooke J., Development. January 1, 1988; 102 (1): 85-99.