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Matches in Nanopublications for { ?s ?p "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." ?g. }

• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _7 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.
• _5 value "We found that ANCO-1 and likely its related protein ANCO-2 may represent a novel class of nuclear receptor corepressors that may inhibit transcriptional activity of NRs through interfering with the coactivator function of p160 by recruiting HDACs. We found that both ANCO-1C and the ANCO-1Ct fragment (amino acids 2597-2663) bound strongly to the full-length RAC3, TIF2, and SRC-1 (Fig. 1C)." provenance.