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1 n part, for modulation of VNTR function as a transcriptional regulatory domain.
2 -C and fuse its DNA-binding domains to novel transcriptional regulatory domains.
3 WS/ets chimera and depends on the functional transcriptional regulatory domains.
4        A347S affects a previously identified transcriptional regulatory domain 3 (TRD3) for which co-
5 peats) that contains a DNA binding domain, a transcriptional regulatory domain, and DAPIN/PAAD, a pro
6 iously demonstrated that the 5-HTT VNTR is a transcriptional regulatory domain, and the allelic varia
7                        The rat GR N-terminal transcriptional regulatory domain contains four major ph
8 entifies the ET domain as a second important transcriptional regulatory domain for Brd4 in addition t
9 nt viruses and identify hundreds of putative transcriptional regulatory domains found in structural p
10 Sequence analysis indicates that many of the transcriptional regulatory domains identified here are c
11                                          The transcriptional regulatory domain of c-Myc was required
12  that is highly homologous to the N-terminal transcriptional regulatory domain of c-Myc.
13 ocated in a proline-rich sequence within the transcriptional regulatory domain of human HSF-1.
14  sites, binds directly to the amino-terminal transcriptional regulatory domain of MYCN.
15                      Prx1 interacts with the transcriptional regulatory domain of the c-Myc oncoprote
16                         Here, we dissect the transcriptional regulatory domains of WT1.
17 ms' tumour suppressor protein WT1 contains a transcriptional regulatory domain that can either activa
18  (ROS), interacts with a region of the c-Myc transcriptional regulatory domain that is essential for
19  complex cellular factor containing multiple transcriptional regulatory domains that play an importan
20      The 63-aa region contains the following transcriptional regulatory domains: the acidic region, t
21 te that Otd requires at least three distinct transcriptional regulatory domains to control photorecep
22 nthetic zinc finger proteins can be fused to transcriptional regulatory domains to create artificial
23 ity in vitro, but it is sufficient to direct transcriptional regulatory domains to specific target ge
24 izer function was examined by fusing defined transcriptional regulatory domains to the Gsc homeodomai
25 evelopment was examined by fusion of defined transcriptional regulatory domains to the siamois homeod
26 P64-p65-Rta (TRIM28(VPR)) or by excising the transcriptional regulatory domain (TRIM28(NFD)).
27 sion of HMGI DNA-binding domains to putative transcriptional regulatory domains was not necessary for
28 nerated polydactyl zinc finger proteins with transcriptional regulatory domains, we developed large c
29 e EWS portion is an intrinsically disordered transcriptional regulatory domain, while the FLI portion
30                  Surprisingly, deletion of a transcriptional regulatory domain within the GR N termin