???pagination.result.count???
Bone morphogenetic protein function is required for terminal differentiation of the heart but not for early expression of cardiac marker genes. , Walters MJ, Wayman GA, Christian JL ., Mech Dev. February 1, 2001; 100 (2): 263-73.
Dissection of inhibitory Smad proteins: both N- and C-terminal domains are necessary for full activities of Xenopus Smad6 and Smad7. , Nakayama T , Berg LK, Christian JL ., Mech Dev. February 1, 2001; 100 (2): 251-62.
The Xvex-1 antimorph reveals the temporal competence for organizer formation and an early role for ventral homeobox genes. , Shapira E, Marom1 K, Levy V, Yelin R , Fainsod A ., Mech Dev. January 1, 2000; 90 (1): 77-87.
Evidence for a role of Smad6 in chick cardiac development. , Yamada M, Szendro PI, Prokscha A, Schwartz RJ, Eichele G., Dev Biol. November 1, 1999; 215 (1): 48-61.
Can't get no SMADisfaction: Smad proteins as positive and negative regulators of TGF-beta family signals. , Christian JL , Nakayama T ., Bioessays. May 1, 1999; 21 (5): 382-90.
A molecular basis for Smad specificity. , Lagna G, Hemmati-Brivanlou A ., Dev Dyn. March 1, 1999; 214 (3): 269-77.
Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis. , Nakayama T , Gardner H, Berg LK, Christian JL ., Genes Cells. June 1, 1998; 3 (6): 387-94.
Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer. , Casellas R, Brivanlou AH ., Dev Biol. June 1, 1998; 198 (1): 1-12.
Smad6 inhibits BMP/ Smad1 signaling by specifically competing with the Smad4 tumor suppressor. , Hata A, Lagna G, Massagué J, Hemmati-Brivanlou A ., Genes Dev. January 15, 1998; 12 (2): 186-97.