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Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos. , Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network. , Yan B ., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/ Smad1 pathway. , Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
Function of the two Xenopus smad4s in early frog development. , Chang C ., J Biol Chem. October 13, 2006; 281 (41): 30794-803.
Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos. , Hino J ., Dev Biol. August 1, 2003; 260 (1): 138-57.
Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2. , Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
Paraxial-fated mesoderm is required for neural crest induction in Xenopus embryos. , Bonstein L., Dev Biol. January 15, 1998; 193 (2): 156-68.
Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus. , McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
Mechanisms of dorsal- ventral patterning in noggin-induced neural tissue. , Knecht AK., Development. June 1, 1997; 124 (12): 2477-88.
Distinct expression and shared activities of members of the hedgehog gene family of Xenopus laevis. , Ekker SC ., Development. August 1, 1995; 121 (8): 2337-47.
Anterior neurectoderm is progressively induced during gastrulation: the role of the Xenopus homeobox gene orthodenticle. , Blitz IL ., Development. April 1, 1995; 121 (4): 993-1004.