PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10075933-5 1999 Our results provide evidence that CBP functions as a co-activator during Dpp signalling, and they suggest that Mad may recruit CBP to effect the transcriptional activation of Dpp-responsive genes during development. dipalmitoylphosphatidylserine 73-76 Mothers against dpp Drosophila melanogaster 111-114 11222150-7 2001 In spite of the uniform expression of Scw, pMad expansion is restricted to the dorsal domain of the embryo where Dpp is expressed. dipalmitoylphosphatidylserine 113-116 Mothers against dpp Drosophila melanogaster 43-47 11222150-9 2001 Indeed, the early pMad pattern is abolished when either the Scw receptor Saxophone (Sax), the Dpp receptor Thickveins (Tkv), or Dpp are removed. dipalmitoylphosphatidylserine 94-97 Mothers against dpp Drosophila melanogaster 18-22 11222150-11 2001 From this stage onward, activation by Scw is no longer required, and Dpp suffices to induce high levels of pMad. dipalmitoylphosphatidylserine 69-72 Mothers against dpp Drosophila melanogaster 107-111 21671915-8 2011 We focused on the inhibitory Smad, daughters against dpp (dad), which is induced by Dpp signaling and negatively regulates Dpp activity. dipalmitoylphosphatidylserine 53-56 Mothers against dpp Drosophila melanogaster 29-33 17092951-0 2006 Threshold response of C15 to the Dpp gradient in Drosophila is established by the cumulative effect of Smad and Zen activators and negative cues. dipalmitoylphosphatidylserine 33-36 Mothers against dpp Drosophila melanogaster 103-107 17092951-8 2006 Thus, the combinatorial action of Smad and Zen activators bound to a number of adjacent sites, and competing negative cues allows for proper gene response to lower than peak levels of the Dpp morphogen. dipalmitoylphosphatidylserine 188-191 Mothers against dpp Drosophila melanogaster 34-38 10075933-5 1999 Our results provide evidence that CBP functions as a co-activator during Dpp signalling, and they suggest that Mad may recruit CBP to effect the transcriptional activation of Dpp-responsive genes during development. dipalmitoylphosphatidylserine 175-178 Mothers against dpp Drosophila melanogaster 111-114 9693372-4 1998 Mothers against dpp (Mad) is a pathway-specific Smad, whereas Daughters against dpp (Dad) is an inhibitory Smad genetically shown to antagonize Dpp signaling. dipalmitoylphosphatidylserine 16-19 Mothers against dpp Drosophila melanogaster 21-24 9693372-4 1998 Mothers against dpp (Mad) is a pathway-specific Smad, whereas Daughters against dpp (Dad) is an inhibitory Smad genetically shown to antagonize Dpp signaling. dipalmitoylphosphatidylserine 16-19 Mothers against dpp Drosophila melanogaster 48-52 9693372-4 1998 Mothers against dpp (Mad) is a pathway-specific Smad, whereas Daughters against dpp (Dad) is an inhibitory Smad genetically shown to antagonize Dpp signaling. dipalmitoylphosphatidylserine 16-19 Mothers against dpp Drosophila melanogaster 107-111 9299558-0 1997 Drosophila MAD, a member of the Smad family, translocates to the nucleus upon stimulation of the dpp pathway. dipalmitoylphosphatidylserine 97-100 Mothers against dpp Drosophila melanogaster 32-36 8681796-0 1996 Mad acts downstream of Dpp receptors, revealing a differential requirement for dpp signaling in initiation and propagation of morphogenesis in the Drosophila eye. dipalmitoylphosphatidylserine 79-82 Mothers against dpp Drosophila melanogaster 0-3 8681796-2 1996 We show that the Mothers against dpp (Mad) gene is required for dpp signaling during eye development. dipalmitoylphosphatidylserine 33-36 Mothers against dpp Drosophila melanogaster 38-41 8681796-4 1996 Mad-mediated dpp signaling is absolutely required for the initiation of the morphogenetic furrow in the eye, but has only a minor role in its subsequent propagation across the eye disc. dipalmitoylphosphatidylserine 13-16 Mothers against dpp Drosophila melanogaster 0-3