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The function and developmental expression of alternatively spliced isoforms of amphioxus and Xenopus laevis Pax2/5/8 genes: revealing divergence at the invertebrate to vertebrate transition. , Short S, Kozmik Z, Holland LZ ., J Exp Zool B Mol Dev Evol. November 1, 2012; 318 (7): 555-71.
Essential role of Dkk3 for head formation by inhibiting Wnt/ β-catenin and Nodal/ Vg1 signaling pathways in the basal chordate amphioxus. , Onai T, Takai A, Setiamarga DH, Holland LZ ., Evol Dev. July 1, 2012; 14 (4): 338-50.
Opposing Nodal/ Vg1 and BMP signals mediate axial patterning in embryos of the basal chordate amphioxus. , Onai T, Yu JK, Blitz IL , Cho KW , Holland LZ ., Dev Biol. August 1, 2010; 344 (1): 377-89.
Neofunctionalization in vertebrates: the example of retinoic acid receptors. , Escriva H, Bertrand S, Germain P, Robinson-Rechavi M, Umbhauer M , Cartry J, Duffraisse M, Holland L , Gronemeyer H, Laudet V ., PLoS Genet. July 1, 2006; 2 (7): e102.
An amphioxus LIM-homeobox gene, AmphiLim1/5, expressed early in the invaginating organizer region and later in differentiating cells of the kidney and central nervous system. , Langeland JA, Holland LZ , Chastain RA, Holland ND., Int J Biol Sci. January 1, 2006; 2 (3): 110-6.
Heads or tails? Amphioxus and the evolution of anterior- posterior patterning in deuterostomes. , Holland LZ ., Dev Biol. January 15, 2002; 241 (2): 209-28.
Evolutionary conservation of the presumptive neural plate markers AmphiSox1/2/3 and AmphiNeurogenin in the invertebrate chordate amphioxus. , Holland LZ , Schubert M, Holland ND, Neuman T., Dev Biol. October 1, 2000; 226 (1): 18-33.