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1 the salivary placodes by fork head (fkh), a winged helix transcription factor.
2 of the foxd3 gene, which encodes a conserved winged-helix transcription factor.
3 , including fork head (fkh), which encodes a winged-helix transcription factor.
4 fespan extension requires DAF-16, a forkhead/winged-helix transcription factor.
5 loss-of-function mutations in Whn (Hfh11), a winged-helix transcription factor.
6 member of the regulatory factor X family of winged helix transcription factors.
7 al that this gene falls into Class II of the winged helix transcription factors.
8 a protein that belongs to the family of the winged helix transcription factors.
11 ent of this activity revealed it to be a new winged-helix transcription factor and a direct target fo
12 Members in the superfamily of the forkhead/winged-helix transcription factors are known to play a c
13 ell phenotypes, suppressor ability, forkhead winged/helix transcription factor box P3 (FOXP3) gene, a
14 ported that expression of the human forkhead/winged helix transcription factor, CHES1 (checkpoint sup
18 rm/mesenchyme forkhead 2) encodes a forkhead/winged helix transcription factor expressed in numerous
20 ires the organ specification factor PHA-4, a winged-helix transcription factor expressed in all phary
22 study, we describe two novel isoforms of the winged helix transcription factor family, HNF-3/fork hea
25 3/forkhead homologue 4 (HFH-4) is a forkhead/winged-helix transcription factor family member that has
27 from Smad2 in regulating transcription by a winged-helix transcription factor, FAST-2, on an activin
29 a 35,000-fold higher expression of forkhead/winged helix transcription factor forkhead box (FOXF1) n
31 ed genome-wide binding sites of the forkhead/winged helix transcription factor Foxa1, which functions
33 we demonstrate novel roles for the forkhead/winged helix transcription factors Foxa1 and Foxa2 in th
36 l YAC-based Foxa3Cre transgene to delete the winged helix transcription factor Foxa2 (formerly HNF-3b
37 tro analysis has suggested that the forkhead/winged helix transcription factor Foxa2 (formerly HNF-3b
39 nd cell type-specific gene ablation that the winged helix transcription factor Foxa2 is required for
40 onditional deletion of the gene encoding the winged-helix transcription factor Foxa2 (Forkhead box a2
41 over a dramatic and unpredicted role for the winged-helix transcription factor Foxa2 (formerly HNF-3
42 In this study, we elucidate the roles of the winged-helix transcription factor Foxa2 in ventral CNS d
47 We show in both mouse and zebrafish that the winged helix transcription factor Foxg1 is expressed in
48 teracts with and inhibits DNA binding by the winged-helix transcription factor FoxH1 (FAST), a critic
55 ro, as demonstrated by cytokine and forkhead/winged helix transcription factor (FoxP3) gene and prote
56 beta induce naive T cells to become forkhead/winged helix transcription factor (Foxp3) positive regul
57 of the T(reg) cell lineage factor, Forkhead/winged helix transcription factor (Foxp3), and tolerance
60 opulation does acquire the X-linked forkhead/winged helix transcription factor, FoxP3, which is assoc
61 duction in the CD4(+)CD25(+)CD62L(+)forkhead/winged helix transcription factor gene (Foxp3(+)) compar
62 cell-specific transcription factor forkhead/winged helix transcription factor gene (FOXP3) in CD4+CD
63 tabolite NAD induce death in murine forkhead/winged helix transcription factor gene-expressing CD4+CD
64 ed mice possess increased levels of forkhead/winged helix transcription factor gene-expressing CD4+CD
68 eveloping liver coincident with the forkhead/winged helix transcription factor, Hepatocyte Nuclear Fa
71 differ significantly from those of bona fide winged-helix transcription factors (HNF-3gamma and RFX1)
73 Mice homozygous for a null mutation in the winged helix transcription factor HNF3alpha showed sever
75 the current study, we demonstrated that the winged-helix transcription factor IL-2 enhancer binding
76 of XBF-1, an anterior neural plate-specific winged helix transcription factor, in controlling the pa
77 tis elegans indicate that daf-16, a forkhead/winged-helix transcription factor, is a major target of
81 generation of allospecific CD4CD25 forkhead/winged helix transcription factor P3 (FOXP3) T-regulator
82 L, however, significantly increased forkhead/winged helix transcription factor P3 (FOXP3) Tregs, wher
84 D25+ glucocorticoid-inducible TNFR+-Forkhead/winged helix transcription factor+ populations and effic
86 RovA, a member of the MarR/SlyA family of winged-helix transcription factors, regulates expression
87 ances is restrained by CD4(+)CD25(+)forkhead/winged helix transcription factor(+) regulatory T cells.
88 hymic mice depleted of CD4(+)CD25(+)forkhead/winged helix transcription factor(+) regulatory T cells.
90 XBF-1 is an anterior neural plate-specific, winged helix transcription factor that affects neural de
94 ist), a novel member of the Foxi-subclass of winged-helix transcription factors that is involved in t
96 -beta and -gamma) constitute a sub-family of winged helix transcription factors with multiple roles i
97 2/Mfh1 genes encode closely related forkhead/winged helix transcription factors with overlapping expr
98 (previously, Mf1 and Mfh1), encode forkhead/winged helix transcription factors with virtually identi
99 expression in the embryo and encode forkhead/winged helix transcription factors with virtually identi
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