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1 hosphorylate and inactivate the proapoptotic forkhead transcription factor.
2 gatively regulates the activity of DAF-16, a Forkhead transcription factor.
3                             Daf-16 encodes a forkhead transcription factor.
4 at are efficiently and specifically bound by Forkhead transcription factors.
5 ypertrophic signaling through its effects on Forkhead transcription factors.
6 that involves regulation of the proapoptotic forkhead transcription factors.
7  activated by IGF/insulin, can phosphorylate forkhead transcription factors.
8 y gonadotrope cells is the FOXO subfamily of forkhead transcription factors.
9 e binding competition between POU5F1 and the forkhead transcription factors.
10 udies show FGF15 signaling decreases hepatic forkhead transcription factor 1 (FoxO1) activity through
11                                              Forkhead transcription factor 3 (FOXO3) was identified a
12                                              Forkhead transcription factor 3 (FoxP3) expression and T
13 ls induced by CpG ODN-activated PDCs express forkhead transcription factor 3 and produce IL-10, TGF-b
14  We suggest that insulin signaling and FOXO (forkhead transcription factor), a downstream molecule in
15 t KM-Brk, blocked the phosphorylation of the forkhead transcription factor, a downstream Akt target.
16 e to stress by regulating the FOXO family of Forkhead transcription factors, a family of proteins tha
17                                         Foxo forkhead transcription factors act as downstream targets
18           These two YF mutants fail to block Forkhead transcription factor activity in 293 cells and
19 ctors glycogen synthase kinase-3beta and the Forkhead transcription factors AFX and FKHR.
20 eduction-of-function mutations in the daf-16/forkhead transcription factor, an effector of the DAF-2/
21 al changes in lipid absorption by regulating forkhead transcription factors and MTP and that inhibiti
22 ce of conserved Akt phosphorylation sites in Forkhead transcription factors and PI3K activity.
23          Akt/protein kinase B phosphorylates forkhead transcription factors and prevents their nuclea
24 tion and inhibition of FKHR and related FOXO forkhead transcription factors and that androgens provid
25  FOX:ETS motif, a composite binding site for Forkhead transcription factors and the Ets transcription
26 rates glycogen synthase kinase (GSK)-3 beta, forkhead transcription factor, and BAD.
27 of Sir2 (SirT1) regulates p53, NF-kappaB and Forkhead transcription factors, and is implicated in str
28 g the pro-apoptotic Bc1-2 family member Bad, Forkhead transcription factors, and the cyclic AMP respo
29                      These data suggest that Forkhead transcription factors are critical effectors of
30                                              Forkhead transcription factors are critical regulators o
31                                              Forkhead transcription factors are essential for diverse
32                               Thus mammalian forkhead transcription factors are involved in Epo and S
33                       From yeasts to humans, forkhead transcription factors are involved in mitotic g
34                                              Forkhead transcription factors are key participants in d
35                                         FoxO Forkhead transcription factors are shown here to act as
36                                              Forkhead transcription factors belonging to the FoxO sub
37 ave identified three consensus sequences for forkhead transcription factor binding in transforming gr
38 e Isl1 SHF enhancer contains three consensus Forkhead transcription factor binding sites that are eff
39                                              Forkhead transcription factor box A2 (FOXA2) is uniquely
40 3 partner molecule, Foxo3a, a subtype of the forkhead transcription factors, by inhibiting its associ
41 ations in Whn (Hfh11, Foxn1), a winged-helix/forkhead transcription factor, cause the nude phenotype,
42           Haploinsufficiency of FOXL2, a new forkhead transcription factor, causes blepharophimosis/p
43 e an evolutionary conserved subfamily of the forkhead transcription factors, characterized by the for
44                        The expression of the forkhead transcription factor checkpoint suppressor 1 (C
45 A), independent of p53, but dependent on the forkhead transcription factor class-O family member, FOX
46  fibroblast growth factor signaling and four Forkhead transcription factors consist the central part
47   The NAD-dependent deacetylase SIR2 and the forkhead transcription factor DAF-16 regulate lifespan i
48 in/IGF-1 signaling pathway, dependent on the forkhead transcription factor DAF-16, but independent of
49 ian homologues of the Caenorhabditis elegans forkhead transcription factor DAF-16, function in the in
50 lization and transcriptional activity of the forkhead transcription factor DAF-16.
51 he sir-2.1 gene in a manner dependent on the forkhead transcription factor DAF-16.
52 way negatively regulates the activity of the forkhead transcription factor DAF-16.
53                                          The Forkhead transcription factor DAF-16/FOXO is the major d
54 diated by intrinsic neuronal activity of the forkhead transcription factor DAF-16/FOXO.
55 dylinositol 3-OH kinase (age-1) regulating a forkhead transcription factor (daf-16) [6, 7], as well a
56   Downregulation of this pathway activates a forkhead transcription factor (daf-16), which may regula
57                                          The forkhead transcription factor, DAF-16, a downstream targ
58  overexpressing the phosphatase dPTEN or the forkhead transcription factor dFOXO, prevents the declin
59                                   FoxJ1 is a forkhead transcription factor expressed in multiple tiss
60               Foxp3, an X chromosome-encoded forkhead transcription factor family member, is indispen
61              FOXA1 and FOXA2, members of the forkhead transcription factor family, are critical for e
62                       Mei4p, a member of the forkhead transcription factor family, in turn regulates
63                           FOXO1, a member of forkhead transcription factor family, was phosphorylated
64                         Foxc1 belongs to the forkhead transcription factors family, which plays a cri
65  contains Smad2 or Smad3, Smad4, and a novel forkhead transcription factor, FAST-1, and binds to an e
66                             We find that the forkhead transcription factor FKH-6 promotes male gonada
67                          The activity of the forkhead transcription factor FKH-9 in neurons is requir
68 t early origins through its interaction with forkhead transcription factors Fkh1 and Fkh2.
69                  Here we show that the yeast Forkhead transcription factors, Fkh1 and Fkh2, are globa
70 d Hi-C experiments on cells depleted for the Forkhead transcription factors, Fkh1 and Fkh2, previousl
71  cycle regulation in a mutant that lacks two forkhead transcription factors, Fkh1 and Fkh2.
72                  Here we show that the yeast forkhead transcription factors, Fkh1p and Fkh2p, associa
73 aromyces cerevisiae, Mcm1 interacts with the forkhead transcription factor Fkh2.
74 Akt activation, is a potent inhibitor of the forkhead transcription factor FKHR (FOXO1), identifying
75                    Here we demonstrated that forkhead transcription factor FKHR (FOXO1)-induced death
76  cascade resulting in phosphorylation of the forkhead transcription factor FKHR in a breast cancer ce
77 gen synthase kinase 3beta (GSK3beta) and the Forkhead transcription factor FKHR were phosphorylated a
78 d PDGF-BB-induced phosphorylation of BAD and forkhead transcription factor FKHR-L1, and these events
79 action between ER alpha and the proapoptotic forkhead transcription factor FKHR.
80  apoptosis by phosphorylating the substrates forkhead transcription factor (FKHR) and glycogen syntha
81 ylation of glycogen synthase kinase (GSK)-3, forkhead transcription factor (FKHR), p70(S6K), and ERK,
82  activity, and prevents the translocation of forkhead transcription factors (FKHR).
83 DAF-16, the closely-related FOXO subclass of forkhead transcription factors (FKHR/FOXO1, FKHRL1/FOXO3
84 K), -mammalian target of rapamycin (-mTOR), -forkhead transcription factor (-FKHR), -caspase-9, and -
85  synthase kinase--3 beta (GSK-3 beta), and a forkhead transcription factor, FKHR, in a human T-cell l
86 Akt exhibits a more inhibitory effect on the forkhead transcription factor, FKHR.
87 eins such as the BCL2 family member Bad, the forkhead transcription factor FKHRL-1, and caspase 9.
88 essed the phosphorylation and degradation of forkhead transcription factor FKHRL1 (FOXO3a), resulting
89 Galpha12QL stimulates the phosphorylation of forkhead transcription factor FKHRL1 via AKT in a PDGFRa
90 arly, induction of FasL by the Akt-regulated forkhead transcription factor FKHRL1 was dependent upon
91                                          The Forkhead transcription factor FKHRL1 was observed to pro
92 hat Akt-mediated signals, acting through the forkhead transcription factor FKHRL1, can regulate colla
93 rylate and negatively regulate pro-apoptotic forkhead transcription factor FKHRL1.
94       Recently, two mammalian highly related forkhead transcription factors FKHRL1 and AFX and their
95                            Here we show that Forkhead transcription factors FKHRL1 and FKHR, substrat
96 ltant loss of activity of the FOXO family of forkhead transcription factors FKHRL1 and FKHR.
97 or proteins, glycogen synthase kinase-3, and forkhead transcription factors, FKHRL1/FOXO3 and FKHR/FO
98                 We used this assay to screen Forkhead transcription factors for control of periodic g
99  revealed an inverse correlation between the Forkhead transcription factor Forkhead box class O (FOXO
100 ia complementation group D2 (FANCD2) and the forkhead transcription factor forkhead box O 3a (FOXO3a)
101 ance was mediated directly by inhibiting the Forkhead transcription factor Forkhead box O3a (FOXO3a).
102 oinsufficiency of the Foxo1 gene, encoding a forkhead transcription factor (forkhead box transcriptio
103 regeneration phenotypes and that RNAi of the forkhead transcription factor FoxA, which is expressed i
104              We have previously shown that a forkhead transcription factor Foxa1 interacts with andro
105                             We find that the forkhead transcription factor, FoxA1, is required to gen
106  in normal mice, plasma insulin inhibits the forkhead transcription factor Foxa2 by nuclear exclusion
107 or Tbx1 failed to activate expression of the forkhead transcription factor Foxa2 in the pharyngeal me
108                            We found that the forkhead transcription factor Foxa2, acting in progenito
109 sis and defined a CSVD locus adjacent to the forkhead transcription factor FOXC1.
110 ng, nonsense and frameshift mutations in the forkhead transcription factor FOXC2 in affected members
111                                              Forkhead transcription factor Foxc2 is an essential regu
112                                              Forkhead transcription factor FOXC2 is an important regu
113 ctional and positional candidate gene, helix/forkhead transcription factor (FOXC2), by sequencing and
114 en reported to be caused by mutations in the forkhead transcription factor, FOXC2.
115 ere dominated by less-known factors, such as forkhead transcription factor FOXD1.
116 ies described in this report reveal that the forkhead transcription factor, Foxd1, is not expressed i
117                      Genetic deletion of the forkhead transcription factor, Foxd1, results in strikin
118 nic stem to epiblast cells and uncovered the forkhead transcription factor FOXD3 as a major regulator
119 sing a neural crest-specific deletion of the Forkhead transcription factor Foxd3, we ablated neural c
120 ment of RCs is additionally dependent on the forkhead transcription factor Foxd3, which is more broad
121           Here, we describe mutations in the forkhead transcription factor FOXE3 that predispose muta
122 t fibroblast growth factor signaling and the forkhead transcription factor FoxF directly upregulate t
123  mesodermal precursors expressing or not the Forkhead transcription factor FOXF1.
124  we show that the closely linked mesenchymal forkhead transcription factors Foxf1 and Foxl1 are part
125 vestigated how in intestinal fibroblasts the forkhead transcription factor Foxf2 controls Wnt signali
126 ory that is defined by the expression of the forkhead transcription factor, foxg.
127            We observe that expression of the forkhead transcription factor FoxG1 is dynamically regul
128               Here, the authors identify the forkhead transcription factor Foxh1 as regulating FLK1+
129                              We identify the forkhead transcription factor Foxh1, in part through Eom
130 membrane transport proteins regulated by the forkhead transcription factor FOXI1.
131         Here, we show that expression of the forkhead transcription factor FoxJ1 in mice is required
132  which is dependent on the expression of the forkhead transcription factor Foxj1 in mice.
133                                          The forkhead transcription factor Foxj1 inhibits spontaneous
134            Previous studies suggest that the forkhead transcription factor Foxj1 inhibits spontaneous
135 lling-regulated transcriptome identified the forkhead transcription factor Foxj1.
136 tify a novel interaction between SRF and the Forkhead transcription factor FOXK1 in human cells.
137 ns as well as novel E1A targets, such as the forkhead transcription factors, FOXK1/K2.
138                       While mutations of the forkhead transcription factor FOXL2 are associated with
139     We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophas
140 c analysis identified a central role for the forkhead transcription factor FOXM1 and its targets, and
141                            Expression of the forkhead transcription factor FoxM1 correlates with prol
142                                          The forkhead transcription factor FOXM1 has a key role in DN
143                                          The forkhead transcription factor FoxM1 has been reported to
144       Here we define a critical role for the Forkhead transcription factor FoxM1 in modulating the de
145 (PA) in mice increased the expression of the forkhead transcription factor FoxM1 in type II cells coi
146                                          The forkhead transcription factor FoxM1 is essential for end
147 nstrate that the expression of the oncogenic forkhead transcription factor FOXM1 is upregulated by GO
148 rongly correlated with the expression of the forkhead transcription factor FoxM1, which binds to the
149 ide chromatin binding mechanisms used by the forkhead transcription factor FOXM1.
150          Increased hepatic expression of the Forkhead transcription factor FoxM1B in adult mice accel
151  the key nodes in the metabolic network, the forkhead transcription factor FOXO has been shown to int
152                                              Forkhead transcription factor FOXO-1, activated by SIRT-
153 evelopment by regulating the activity of the forkhead transcription factor Foxo.
154 ressed in adult worms, and this requires the forkhead transcription factor (FOXO) encoded by daf-16.
155                       Second, we deduced the forkhead transcription factor (FOXO) family to be a down
156 ans extends lifespan by activating DAF-16, a forkhead transcription factor (FOXO) repressed by insuli
157  to do so by converging on the regulation of forkhead transcription factor (FOXO).
158 factor 1 (HIF-1) through the inactivation of Forkhead transcription factors (FOXO) in PTEN-null cells
159  physiological roles in this process are the forkhead transcription factor FOXO1 (also known as FKHR)
160                                              Forkhead transcription factor FoxO1 also is an important
161                                              Forkhead transcription factor FoxO1 and the NAD(+)-depen
162 ce, but Akt-dependent phosphorylation of the forkhead transcription factor FoxO1 at serine 256, which
163                                          The forkhead transcription factor Foxo1 has previously been
164 ng evidence documents a key function for the forkhead transcription factor FoxO1 in cellular metaboli
165                                          The Forkhead transcription factor FoxO1 inhibits through its
166                                          The forkhead transcription factor FoxO1 is a critical regula
167                                          The forkhead transcription factor Foxo1 is regulated by insu
168    We report that haploinsufficiency for the forkhead transcription factor Foxo1 reverses beta cell f
169                                          The forkhead transcription factor FOXO1, a downstream target
170  determined the molecular mechanisms whereby forkhead transcription factor Foxo1, a key downstream si
171 is associated with reduced expression of the forkhead transcription factor Foxo1, a substrate of the
172                         Disinhibition of the forkhead transcription factor FoxO1, increases expressio
173 se AKT and subsequent phosphorylation of the forkhead transcription factor FOXO1.
174                                              Forkhead transcription factors FOXO1 (FKHR), FOXO3a (FKH
175                                          The forkhead transcription factor (FoxO1) binds the PDK4 gen
176 an target of rapamycin (mTOR), the family of forkhead transcription factors (FOXO1, FOXO3a, and FOXO4
177 glycogen synthase kinase-3alpha/beta and the forkhead transcription factor, FoxO1, in protection of F
178 rmone deficiencies, we are investigating the forkhead transcription factor, FOXO1, which has been imp
179                                              Forkhead transcription factor FOXO3 plays a critical rol
180 D31 signals prevents the localization of the forkhead transcription factor FoxO3 to the nucleus, thus
181  demonstrated that Sirt6 can be recruited by forkhead transcription factor FoxO3 to the proximal prom
182 s primordial follicle activation through the forkhead transcription factor Foxo3.
183                         In this context, the Forkhead transcription factor, Foxo3, amplified GATA-1-m
184 acetylates and represses the activity of the forkhead transcription factor Foxo3a and other mammalian
185                         Here we identify the forkhead transcription factor FOXO3a as a key target of
186                       The phosphorylation of forkhead transcription factor FOXO3a by Akt is critical
187                     Nuclear exclusion of the forkhead transcription factor FOXO3a by protein kinase A
188                              The role of the Forkhead transcription factor FOXO3a in processes that p
189             Here we examined the role of the forkhead transcription factor FOXO3a, a downstream targe
190 e the first linkage by the identification of Forkhead transcription factor FOXO3a, the PI3K/Akt downs
191 n of the SIRT1 deacetylase and activates the Forkhead transcription factor Foxo3a.
192  we show that such inflammation requires the forkhead transcription factor Foxo3a: Foxo3a-deficient m
193 vation of a ubiquitously expressed mammalian forkhead transcription factor, Foxo3a, induces cerebral
194                             In addition, the forkhead transcription factor, FoxO3a, interacts with ea
195                                The mammalian forkhead transcription factors, FOXO3a (FKHRL1), FOXO1a
196  the in vitro interactions among 14-3-3, the Forkhead transcription factor FOXO4, and its target DNA,
197                                          The forkhead transcription factor FoxO6 is prominently expre
198                                              Forkhead transcription factors (FOXOs) alter a diverse a
199 pproaches were used to evaluate the roles of forkhead transcription factors (FoxOs) in endoplasmic re
200                       Down-regulation of the forkhead transcription factor Foxp1 by integrin engageme
201                            We found that the forkhead transcription factor Foxp1 is crucial for maint
202                            Expression of the forkhead transcription factor FOXP1 is essential for ear
203                                          The forkhead transcription factor FOXP1 is involved in B-cel
204 strate that absence of the gene encoding the forkhead transcription factor Foxp1 resulted in a profou
205              Heterozygous disruptions of the Forkhead transcription factor FoxP2 impair acquisition o
206                                          The forkhead transcription factors Foxp2 and Foxp1 are expre
207                Here, we demonstrate that two Forkhead transcription factors, Foxp2 and Foxp4, are pro
208                                          The forkhead transcription factor Foxp3 (forkhead box P3) is
209       Here, we present data arguing that the forkhead transcription factor Foxp3 acts as the regulato
210                                Expression of forkhead transcription factor Foxp3 defines a distinct l
211                                          The forkhead transcription factor FOXP3 is necessary for ind
212                      Here we report that the forkhead transcription factor Foxp3 is specifically expr
213 alogous cooperative complex of NFAT with the forkhead transcription factor FOXP3, a lineage specifica
214 lls, both mRNA and protein expression of the forkhead transcription factor Foxp3, a specific marker o
215 , they efficiently induced expression of the forkhead transcription factor FoxP3, the master regulato
216 al circumstances, male mice deficient in the forkhead transcription factor FoxP3, which lack regulato
217 and function with particular emphasis on the forkhead transcription factor Foxp3.
218 and function are critically dependent on the forkhead transcription factor Foxp3.
219                                          The forkhead transcription factor, FoxP3, is a key molecule
220                                          The forkhead transcription factor, Foxp3, is thought to act
221 ntified stomach-restricted expression of the forkhead transcription factor FOXQ1.
222 nd -gamma), members of the FoxA subfamily of forkhead transcription factors, function as initial chro
223 esenchymal markers, including members of the forkhead transcription factor gene family, have been det
224                       The recently described forkhead transcription factor gene Foxe3 was shown to be
225                             Mutations in the forkhead transcription-factor gene (FOXC1), have been sh
226                                          The forkhead transcription factor genes Foxc1 (formerly Mf1
227 ed members of the Fox family of winged-helix/forkhead transcription factor genes.
228                                              Forkhead transcription factors have been found to play a
229                                          The forkhead transcription factor hepatocyte nuclear factor
230                                   FOXP2 is a forkhead transcription factor implicated in developmenta
231 onstrating a critical role for at least this forkhead transcription factor in the regulation of B lym
232 he phosphorylation and hence inactivation of forkhead transcription factors in a p66Shc-dependent man
233                           There are numerous forkhead transcription factors in mammalian cells but we
234 he Forkhead box, class O (FOXO) subfamily of Forkhead transcription factors in the regulation of BIM
235 t Isl1 is a direct transcriptional target of Forkhead transcription factors in the SHF and establish
236 f genetic programs induced by a subfamily of forkhead transcription factors including AFX.
237            FOXO3a, a member of the family of Forkhead transcription factors, interacted with the prom
238  as a primary downstream target for Foxn4, a forkhead transcription factor involved in the genesis of
239     We show here that the Foxn4 winged helix/forkhead transcription factor is coexpressed with the bH
240    Here, we show that the Foxn4 winged helix/forkhead transcription factor is expressed in a subset o
241      Finally, a putative binding element for forkhead transcription factors is necessary for promoter
242  Forkhead box gene, group O (FoxO) family of Forkhead transcription factors is phopsphorylated and in
243                                    DAF-16, a forkhead transcription factor, is a key regulator of lon
244                                Sep1, another forkhead transcription factor, is an activator for a sma
245                                     Foxn4, a forkhead transcription factor, is expressed in the commo
246 malian FOXO3, a member of the FOXO family of Forkhead transcription factors known to promote resistan
247 osphorylation of FOXO3a, a tumor suppressive forkhead transcription factor, leading to its cytoplasmi
248 ted a physical interaction of SMA-3 with the forkhead transcription factor LIN-31, which is enhanced
249 nase promoter and that increased activity of forkhead transcription factors may underlie the increase
250 iogenesis, transcriptionally suppresses AFX1 forkhead transcription factor-mediated apoptosis and inc
251 e mutation in a gene encoding a winged helix/forkhead transcription factor ( Mf1 ).
252 e Xenopus and zebrafish homologs of Foxj1, a forkhead transcription factor necessary for ciliogenesis
253                          A homeodomain and a forkhead transcription factor, NKX2.1 and HNF-3, respect
254           Recent studies have indicated that forkhead transcription factor O1 (Foxo1) and silent info
255 atic nuclear receptor 4alpha (HNF4alpha) and forkhead transcription factor O1 (FOXO1), two critical t
256 lycogen synthase kinase-3beta (GSK3beta) and forkhead transcription factor of the O class (FOXO)3A, k
257                                              Forkhead transcription factors of the forkhead box gene,
258                                              Forkhead transcription factors of the FoxO subfamily are
259                                              Forkhead transcription factors of the O class (FOXOs) ar
260                                              Forkhead transcription factors often function in concert
261 es through the inhibitory phosphorylation of forkhead transcription factors, our results describe for
262               Despite elevated expression of forkhead transcription factor P3 (foxP3), they exerted o
263 sure and was mediated through an AKT-1/PDK-1/forkhead transcription factor pathway overlapping with b
264 2 is a let-7 target in seam cells, while the forkhead transcription factor pha-4 is a target in the i
265                                              Forkhead transcription factors play critical roles in th
266                                              Forkhead transcription factors play crucial and diverse
267                                              Forkhead transcription factors play key roles in the reg
268                           The FoxO family of Forkhead transcription factors plays an important role i
269                                   FoxD4/5, a forkhead transcription factor, plays a critical role in
270 escribe a mechanistic model whereby Foxd3, a forkhead transcription factor, prevents neural crest-der
271  mitotic genes in close proximity to Fkh2, a forkhead transcription factor previously implicated in r
272                                              Forkhead transcription factors regulate many aspects of
273                           The FOXO family of Forkhead transcription factors, regulated by the phospho
274 on mutations in Whn (Hfh 11), a winged-helix/forkhead transcription factor, result in the nude mouse
275       Moreover, transcripts dependent on the forkhead transcription factor Sep1, which are expressed
276 e antioxidant defenses and inhibition of the forkhead transcription factor signaling pathways.
277               In addition to inactivation of forkhead transcription factor signaling through enhanced
278 erior domain by activating expression of the forkhead transcription factors sloppy paired 1 and slopp
279                           Akt phosphorylates Forkhead transcription factors such as FKHRL1, leading t
280 f FOXO4 (also known as AFX), a member of the forkhead transcription factor superfamily that is negati
281 ential display PCR, we have cloned an 85-kDa forkhead transcription factor (termed Mac-1-regulated fo
282                                 FoxD4L1 is a forkhead transcription factor that expands the neural ec
283                                    Foxa is a forkhead transcription factor that is expressed in the e
284                 Foxe3 encodes a winged helix-forkhead transcription factor that is initially expresse
285 the nuclear accumulation of DAF-16/FOXO, the forkhead transcription factor that is the major downstre
286 ic protein consisting of MLL fused to AFX, a forkhead transcription factor that normally regulates ge
287                                  FOXO3a is a forkhead transcription factor that regulates a multitude
288            Klotho protein activates the FoxO forkhead transcription factors that are negatively regul
289                AFX belongs to a subfamily of Forkhead transcription factors that are phosphorylated b
290 ar location of FoxO1 and FoxO3a, two Class O Forkhead transcription factors that mediate lymphocyte q
291                          FOXC1 and FOXC2 are forkhead transcription factors that play essential roles
292 cyte nuclear factors-3 (Foxa-1-3) are winged forkhead transcription factors that regulate gene expres
293  homologue (CHES-1-like), two genes encoding forkhead transcription factors that we discovered utiliz
294                                       DAF-16/forkhead transcription factor, the downstream target of
295  on and represses the expression of FOXP2, a forkhead transcription factor tightly associated with sp
296                             Our results link Forkhead transcription factors to a previously unexplore
297  Akt; induces phosphorylation of the FKHRL-1 Forkhead transcription factor; upregulates a series of i
298                        Furthermore, Foxa2, a forkhead transcription factor, was induced by active Wnt
299    FKHR is a member of the FOXO subfamily of Forkhead transcription factors, which are important targ
300 n by up-regulating the expression of Class-O Forkhead transcription factors, which play essential rol

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