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1 ressed PTF1A protein C-terminal to the basic-helix-loop-helix domain.
2  regions, either side of the conserved basic Helix-Loop-Helix domain.
3 erated I-repeats, each containing a putative helix-loop-helix domain.
4 eins that contain the highly conserved basic helix-loop-helix domain.
5 ies three nuclear localization signals and a helix-loop-helix domain.
6 id region in E47-(477-530) distinct from the helix-loop-helix domain.
7 tive transcription factor possessing a basic helix-loop-helix domain.
8  chromosome condensation domain and myc-type helix-loop-helix domains.
9 ted from a library of randomly mutated basic helix-loop-helix domains.
10                            Here we show that helix-loop-helix domain 4 is necessary and sufficient fo
11 protein of 1072 amino acids and contains six helix-loop-helix domains, a hydrophobic leucine zipper-l
12 a DNA-binding domain at the C terminus and a helix-loop-helix domain (also called a pointed domain) a
13  mapped the interaction interface to the MYC helix-loop-helix domain and a novel 15-residue MYC-bindi
14  both homology in structure across the basic helix-loop-helix domain and in expression during mesoder
15 re characterized by the presence of multiple helix-loop-helix domains and a leucine zipper motif.
16                       GTF3 contains multiple helix-loop-helix domains and an amino-terminal leucine z
17 e GCGTG recognition site, whereas both their helix-loop-helix domains and periodicity-ARNT-single-min
18 ons, tetratricopeptide repeats (TPRs), and a helix-loop-helix domain, and mutagenesis studies have im
19                            The basic region, helix-loop-helix domain, and WRPW motif have been charac
20 that differences in the IKKalpha and IKKbeta helix-loop-helix domains are primarily responsible for d
21 or novel direct interactions between the E47 helix-loop-helix domain (Arg 357 or Asp 358) and the Pip
22  kinase domain, a leucine zipper motif and a helix-loop-helix domain at their carboxyl terminus.
23             The TAL-1 gene specifies a basic helix-loop-helix domain (bHLH) transcription factor, whi
24  showed that NUCB2 (nucleobindin 2), via its helix-loop-helix domains, binds the ARTS-1 extracellular
25 n and a region with similarity to a Myc-type helix-loop-helix domain but does not include the zinc fi
26                                    The basic helix-loop-helix domain-containing transcription factors
27 and CiMDFb contained the cysteine-rich/basic-helix loop helix domain (Cys-rich/bHLH) present in all M
28       ref-1 encodes a protein with two basic helix-loop-helix domains distantly related to those of t
29  DNA binding basic region and helix 1 of the Helix-Loop-Helix domain; dMax interacts with c-Myc in vi
30  Drosophila ortholog of the vertebrate basic helix-loop-helix domain-encoding genes capsulin and musc
31 interact on the MIC-1 promoter via the basic helix-loop-helix domain in DEC1 and the tetramerization
32                                              Helix-loop-helix domains in other proteins demonstrate h
33                           The N-terminal TEL helix-loop-helix domain is essential for TEL/AML-1B-medi
34  proteins of the TFII-I family with multiple helix-loop-helix domains known as I repeats.
35 ontains three LIM domains, which bind to the helix-loop-helix domain of Id proteins in vitro and in v
36                     A motif within the basic helix-loop-helix domain of Myf5 (R93 to Q101) resembles
37              We found that Serine 147 in the helix-loop-helix domain of OLIG2 was phosphorylated duri
38  Tel-AML-1 fusion protein, indicate that the helix-loop-helix domain of Tel only partially inhibits t
39                                    The basic helix-loop-helix domain of the Drosophila transcription
40  occurred when the template bulge neared the helix-loop-helix domain of the polymerase thumb.
41  deletion constructs indicate that the basic helix-loop-helix domain of USF interacts directly with t
42 inding by the Zn2+ fingers of Sp1, the basic helix-loop-helix domain of USF, and the rel domain of NF
43 riments showed that amino acids flanking the helix-loop-helix domain plus three residues in the first
44                     XopD contains a putative helix-loop-helix domain required for DNA binding and two
45 nct regions of homology, indicating that the helix-loop-helix domain structure of the GTF2IRD2 gene h
46 he first 533 amino acids and contain a basic helix-loop-helix domain that is 100% identical to human
47 re that includes kinase, leucine zipper, and helix-loop-helix domains, they exhibit marked difference
48 Two serines N terminal to the deltaE47 basic helix-loop-helix domain were found to be phosphorylated
49 or (the cyclin Pho80) and a C-terminal basic helix-loop-helix domain, which mediates DNA binding and
50 riptional repressor related within its basic helix-loop-helix domain with the Drosophila Hairy, Enhan

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