戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              CT-1 action on motoneurons was inhibited by phosphatidyl
2                                              CT-1 also induced the degradation of the NF-kappa B cyto
3                                              CT-1 and gp130/LIF receptor were widely present in the c
4                                              CT-1 and IGF-I may be considered promising candidate tro
5                                              CT-1 induces a distinct pattern of immediate early genes
6                                              CT-1 induces a hypertrophic response in cardiomyocytes t
7                                              CT-1 is a new member of the interleukin 6 (IL-6)/leukemi
8                                              CT-1 is highly expressed in embryonic skeletal muscle, s
9                                              CT-1 is released from the heart in response to hypoxic s
10                                              CT-1 is the first bona fide muscle-derived neurotrophic
11                                              CT-1 may be important in normal motoneuron development a
12                                              CT-1 was injected through the penile vein 30 min before
13                                              CT-1, however, follows a strict degradation pathway afte
14                             Cardiotrophin 1 (CT-1), a potent cardiac survival factor, is capable of i
15 otrophic factor (BDNF), and cardiotrophin-1 (CT-1) are the most potent neurotrophic factors for moton
16                             Cardiotrophin-1 (CT-1) is a potent hypertrophic factor discovered by coup
17  systemic administration of cardiotrophin-1 (CT-1) is able to improve renal function and to decrease
18                             Cardiotrophin-1 (CT-1) was recently isolated by expression cloning based
19                             Cardiotrophin-1 (CT-1), a cytokine related to ciliary neurotrophic factor
20 the metabolic properties of cardiotrophin-1 (CT-1), a member of the interleukin-6 family of cytokines
21                             Cardiotrophin-1 (CT-1), a member of the interleukin-6 superfamily, and en
22                             Cardiotrophin-1 (CT-1), a stress-induced cytokine, belongs to the interle
23  isolated a novel cytokine, cardiotrophin-1 (CT-1), from an in vitro embryonic stem cell system of ca
24 rotrophic factor (CNTF), or cardiotrophin-1 (CT-1).
25 otrophic factor (CNTF), and cardiotrophin-1 (CT-1).
26  the CNTF-LIF family member cardiotrophin-1 (CT-1).
27                                 After E12.5, CT-1 expression is found in other tissues, including ske
28 have developed antibodies directed against a CT-1 fusion protein.
29                                   At PD20, a CT-1-treated eye (2 micro g/2 micro L every 3 days, star
30                               However, acute CT-1 treatment caused an increase in SOCS-3 mRNA in adip
31 un to the SPRR1A promoter was observed after CT-1 stimulation.
32 sphorylated STAT1 and -3 in the retina after CT-1 injection.
33                                     Although CT-1 and ET-1 gene expression in the heart is upregulate
34  RAP-alpha1 variant, which contains NT-1 and CT-1 domains, and T-cell responses were characterized.
35  mice demonstrated increased alpha-actin and CT-1 mRNA expression, and airway myocytes isolated from
36 from the tongue radiolabeled GDNF, BDNF, and CT-1 as well as tetanus toxin.
37                               LIF, CNTF, and CT-1 act through the known receptors LIF receptor beta (
38 eral of these cytokines (LIF, OSM, CNTF, and CT-1) also utilize the LIF receptor (LIFR) as a componen
39 directed against endogenous IGF-I, GDNF, and CT-1, significantly decreased mean single-twitch force.
40 d at synapses more slowly (within 15 h), and CT-1 never associated with synapses.
41 in expression induced by LiCl, SB216763, and CT-1 but not TGF-beta.
42 ial study was carried out with wild-type and CT-1 null mice in fed (ad libitum) and food-restricted c
43 in adipose tissue of both wild-type (WT) and CT-1(-/-) mice.
44 F receptor inhibited basal growth as well as CT-1- or ET-1-stimulated cardiac fibroblast growth.
45                            The median CVS at CT 1 was 5; at CT 2, 4; and at US, 4.
46 derwent all three studies, the median CVS at CT 1 was 5; at CT 2, 4; and at US, 4.
47                    Factors related to CVS at CT 1 were homogeneous versus heterogeneous appearance (s
48 ion, we investigated the interaction between CT-1/gp130/LIF receptor and ET-1/endothelin type A (ET(A
49              eIF2Bepsilon siRNA also blocked CT-1- but not TGF-beta-induced protein synthesis.
50  Together, the inhibitors completely blocked CT-1-dependent NF-kappa B activation and cytoprotection.
51                                         Both CT-1 and LIF, which share the same receptors, dramatical
52 by nuclear run-on transcription assays, both CT-1 and alpha-adrenergic stimulation lead to an increas
53              A partial remission was seen by CT 1 mo after the first radioimmunotherapy, and a furthe
54 e essential for cardiac fibroblast growth by CT-1 and that there is synergism with ET-1/ET(A) recepto
55  kinases, whereas the hypertrophy induced by CT-1 may be mediated by alternative pathways, e.g. Janus
56 ibody completely inhibits c-fos induction by CT-1.
57                               Cardiotrophin (CT-1) is a naturally occurring protein member of the int
58 ), Interleukin-11 (IL-11) and Cardiotrophin (CT-1).
59 lation, have residual abnormalities at chest CT 1 year after presentation.
60                            Moreover, chronic CT-1 treatment resulted in the development of insulin re
61 ice and characterization of 24-h circulating CT-1 profiles in normal-weight and overweight/obese subj
62 therapy, all patients underwent planning CT (CT 1) at 3-mm section intervals.
63 9), followed by DeALPS-CT-2 (588) and DeALPS-CT-1 (330).
64 levels of IgG anti-LPS (DeALPS-CT-2 > DeALPS-CT-1 > cellular vaccine).
65  was disrupted in aged obese CT-1-deficient (CT-1(-/-)) mice (12 mo).
66 binding of CT-1 to CNTFR alpha was detected, CT-1 may use a novel cytokine receptor alpha subunit.
67 ere absorbed (>75%) by LPS but not by either CT-1 or CT-2.
68 d by an Ab directed at a C-terminal epitope (CT-1) but not with an Ab recognizing a protected intralu
69                                    Exogenous CT-1 markedly stimulated [(3)H]thymidine and [(3)H]proli
70 cells stimulated by endogenous and exogenous CT-1 requires gp130/LIF receptor as well as ET(A) recept
71  but not bovine insulin-primed CTL expressed CT-1, a carbohydrate epitope of CD45, and bovine insulin
72 either to increase levels of trophic factors CT-1, IGF-I, glial cell line-derived neurotrophic factor
73 t study documents that gp130 is required for CT-1 signaling in cardiomyocytes, by demonstrating that
74 -kappa B and that NF-kappa B is required for CT-1 to mediate its full cytoprotective effects in cardi
75 se observations suggest a potential role for CT-1 in the regulation of metabolic circadian rhythms.
76                                In the heart, CT-1 is primarily expressed in myocardial cells, and not
77                                   In humans, CT-1 plasma profile exhibited a 24-h circadian rhythm in
78           As assessed by immunolocalization, CT-1 is predominantly expressed in the early mouse embry
79          However, the pattern was altered in CT-1(-/-) mice toward a lower percentage of the rhythm o
80 induced adipose tissue lipid mobilization in CT-1 null mice.
81 r antagonist, BQ123, significantly inhibited CT-1-stimulated DNA synthesis.
82  rhythms of Vo2 were conserved in young lean CT-1(-/-) mice (2 mo), CT-1 deficiency caused a phase sh
83 ssays assessed IL-6, IL-11, IL-27, OSM, LIF, CT-1, CLC, and CNTF signaling.
84 nserved in young lean CT-1(-/-) mice (2 mo), CT-1 deficiency caused a phase shift of the acrophase.
85                                    Moreover, CT-1 mRNA levels in adipose tissue showed significant ci
86            Our studies revealed that neither CT-1 nor ciliary neurotrophic factor treatment affected
87 ption rate (Vo2) was disrupted in aged obese CT-1-deficient (CT-1(-/-)) mice (12 mo).
88             We also confirmed the ability of CT-1 to induce signaling in fat cells in vivo.
89 nal cell survival, we studied the ability of CT-1 to promote cardiac myocyte survival and proliferati
90 igned to identify the presence and action of CT-1 and its receptor complex, glycoprotein130 (gp130) a
91                   Repeated administration of CT-1 resulted in significant survival of photoreceptors.
92                    Chronic administration of CT-1 to 3T3-L1 adipocytes resulted in a decrease of both
93                          Since no binding of CT-1 to CNTFR alpha was detected, CT-1 may use a novel c
94 AP kinase pathway for the survival effect of CT-1.
95 AP kinase, as well as the survival effect of CT-1.
96 on, as well as the cytoprotective effects of CT-1 against hypoxic stress.
97 family cytokines, we examined the effects of CT-1 on 3T3-L1 adipocytes.
98                               The effects of CT-1 on SOCS-3 and PPARgamma mRNA were independent of MA
99                             These effects of CT-1 seem to be mediated by reduction in oxygen-radical
100 l cells blocked the antiapoptotic effects of CT-1, indicating a requirement of the MAP kinase pathway
101 tely inhibited the cytoprotective effects of CT-1.
102 e the developmental pattern of expression of CT-1 during murine embryogenesis, we have developed anti
103                 Confocal laser microscopy of CT-1 stimulated cells reveals the assembly of sarcomeric
104                          The 24-h pattern of CT-1 was characterized by a pronounced increase during t
105           Finally, the physiological role of CT-1 in fasting is confirmed by the impaired food restri
106 reviously unrecognized physiological role of CT-1 in metabolic adaptations, through the regulation of
107      Here, we aimed at analyzing the role of CT-1 in response to these metabolic changes.
108 c response elicited following stimulation of CT-1.
109 ces the B subunit (but not the A subunit) of CT-1.
110 t a subset of gp130 cytokines, in particular CT-1, LIF, and OSM, has the ability to impair subsequent
111 ined with positron emission tomography (PET)/CT 1 and 15 hours after an oral Copper-64 ( 64 Cu) dose.
112 18 MBq of (61)Cu-PSMA and then underwent PET/CT 1, 2, and 4 hours after administration and blood samp
113                                          PET/CT-1 was compared with routine staging, and response on
114        PET/CT was performed at baseline (PET/CT-1) and after 3 cycles of neoadjuvant chemotherapy (PE
115 o have uptake in cervical lymph nodes on PET/CT-1, and 2 of 3 IRSS stage IIIB patients with pathologi
116 7 patients without optic nerve uptake on PET/CT-1.
117                All 25 patients underwent PET/CT-1, and 21 of 25 patients underwent PET/CT-2.
118    Moreover, the circadian pattern of plasma CT-1 levels was evaluated in normal-weight and overweigh
119                                  Recombinant CT-1 was injected intravitreally into eyes of heterozygo
120  ERK, or Akt pathways each partially reduced CT-1-mediated NF-kappa B activation, as well as the cyto
121                       Cytokine arrays showed CT-1 (cardiotrophin-1) to be a mediator of Aldo-induced
122                     PI was followed by SPECT/CT 1-3 h after injection of (99m)Tc-colloid particles.
123                        In the present study, CT-1 activated p38 and ERK MAPKs as well as Akt in cultu
124                                  In summary, CT-1 is a potent regulator of signaling in adipocytes in
125 ell epitopes may vary antigenically and that CT-1 may be differentially expressed with respect to the
126     Northern blot analysis demonstrated that CT-1 gene expression was present in normal atrium and ve
127                 This study demonstrates that CT-1 and its receptors are present in cardiac fibroblast
128 ponsible for this effect, we documented that CT-1 activated both signal transducer and activator of t
129    A cell proliferation assay documents that CT-1 provokes an approximate 2-fold increase in embryoni
130 sphorylated, providing further evidence that CT-1 signals through the gp130/LIFRbeta heterodimer in c
131                  These studies indicate that CT-1 can activate a distinct form of myocardial cell hyp
132                  These results indicate that CT-1 promotes photoreceptor survival and that Muller cel
133                  These results indicate that CT-1 signals through p38, ERK, and Akt in a parallel man
134                  Our studies have shown that CT-1 administration results in a dose- and time-dependen
135        Therefore, these results suggest that CT-1 administration prevents IRI and it might be used as
136      Sequence similarity data suggested that CT-1 is a novel member of a family of structurally relat
137 fic phospholipase C (PIPLC), suggesting that CT-1 may act through a GPI-linked component.
138  cavity volume decreased somewhat during the CT 1-to-CT 2 interval.
139 (LIFRbeta) antagonist effectively blocks the CT-1 induction of c-fos, indicating a requirement for LI
140                    The T-cell epitope in the CT-1 domain was mapped to aa 436 to 465 (VNSEKVDADDAGNAE
141                              Survival in the CT-1-treated group was higher than in the untreated grou
142 ontrast to alpha-adrenergic stimulation, the CT-1 responsive cis-regulatory elements are located outs
143 cids [aa] 144 to 187), and one mapped to the CT-1 variable domain (aa 386 to 480).
144                                   Therefore, CT-1 promotes cardiac myocyte survival via the activatio
145                                        Thus, CT-1 may play an autocrine role during cardiac chamber g
146 ter; none of these were changed at follow-up CT 1 year later.
147 hymic masses, 25 were evaluated at follow-up CT 1 year later: Five had increased in diameter, two had
148 rotype Inaba, to cholera toxin (CT) variants CT-1 and CT-2.
149 tential activation of atrial and ventricular CT-1 expression in pacing-induced experimental congestiv
150 s a positive correlation between ventricular CT-1 mRNA and left ventricular mass index.
151                                    In vitro, CT-1 kept 43% of purified E14 rat motoneurons alive for
152                                     In vivo, CT-1 protected neonatal sciatic motoneurons against the
153    In the present study, we analyzed whether CT-1 also acts to peripherally regulate metabolic rhythm
154                             Stimulation with CT-1 results in an increase in cardiac cell size that is
155                        Upon stimulation with CT-1, both gpl30 and the LIFRbeta are tyrosine-phosphory
156                               Treatment with CT-1 or IGF-I significantly increased the mean single-tw

 
Page Top