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 (1語後でソート)

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 (q) protein, suggesting cooperation with Lbc/alpha-catulin.
2 ting protein of relatively unknown function, alpha-catulin.
3 ans genetic study, we demonstrate that CTN-1/alpha-catulin, a cytoskeletal protein, physically intera
4     Mechanistic investigations revealed that alpha-catulin activated Akt-NF-kappaB signaling downstre
5                         Here, we report that alpha-catulin also drives malignant invasion and metasta
6 dy demonstrates that the interaction between alpha-catulin and alpha-dystrobrevin is evolutionarily c
7     Clinically, high levels of expression of alpha-catulin and ILK were associated with poor overall
8   These results suggest a novel function for alpha-catulin and imply that alpha-catenin and alpha-cat
9 d endogenous alpha-catulin product, document alpha-catulin and Lbc co-expression in multiple human ce
10 ssion in multiple human cell lines, and show alpha-catulin and Lbc subcellular co-fractionation and i
11 exin, alpha-Liprin, SYDE, ELKS/CAST, RIM-BP, alpha-Catulin, and MAGI1.
12                                              Alpha-catulin appears to inhibit Ras-mediated signals to
13         Taken together, our study implicates alpha-catulin as a unique regulator of GPCR signaling an
14                                Thus, the Lbc/alpha-catulin axis participates in 5-HT-induced PASMC mi
15 hment for LT-HSCs and sixfold enrichment for alpha-catulin+c-kit+ HSCs, and yielded HSCs with superio
16                                 Furthermore, alpha-catulin co-expression enhances Lbc-induced GTP-Rho
17                                Functionally, alpha-catulin co-expression leads to increased Lbc-induc
18                               Interestingly, alpha-catulin expression attenuates the activation of th
19 itutively upregulated Wnt signaling, whereas alpha-catulin expression had no effect.
20                                    The human alpha-catulin gene (CTNNAL1) maps to 9q31-32.
21 ted as alpha-catulin(GFP)), we discover that alpha-catulin(GFP) is expressed by only 0.02% of bone ma
22 e gene Ctnnal1 in mice (hereafter denoted as alpha-catulin(GFP)), we discover that alpha-catulin(GFP)
23 l imaging, allowing us to image thousands of alpha-catulin-GFP(+)c-kit(+) cells and to digitally reco
24 titution of irradiated mice, indicating that alpha-catulin-GFP(+)c-kit(+) cells are comparable in HSC
25            We find that approximately 30% of alpha-catulin-GFP(+)c-kit(+) cells give long-term multil
26                          The distribution of alpha-catulin-GFP(+)c-kit(+) cells indicated that HSCs w
27 ifferences in femurs and sterna, their adult alpha-catulin-GFP+ HSCs had similar distributions.
28 both had indistinguishable localization from alpha-catulin-GFP+ HSCs.
29                       We found adult femoral alpha-catulin-GFP+ or Mds1GFP/+Flt3Cre HSCs proximal to
30 pha-catulin and imply that alpha-catenin and alpha-catulin have distinct activities that downregulate
31 increased, suggesting a compensatory role of alpha-catulin in dystrophic muscle.
32 apped, and complex formation between Lbc and alpha-catulin in mammalian cells was detected.
33 paB or alphavbeta3 was sufficient to inhibit alpha-catulin-induced cell migration and invasion.
34                                              alpha-Catulin interacted with integrin-linked kinase (IL
35             The required regions for Lbc and alpha-catulin interaction were mapped, and complex forma
36                                              alpha-Catulin is an oncoprotein that helps sustain proli
37 tation and blot overlay assays indicate that alpha-catulin is directly recruited to the alpha(1D)-AR
38 strophin, we discover that the expression of alpha-catulin is increased, suggesting a compensatory ro
39                We further show that in mouse alpha-catulin is localized at the sarcolemma and neuromu
40 ith alpha-dystrobrevin and that the level of alpha-catulin is reduced in alpha-dystrobrevin-deficient
41 we show that CTN-1, a homologue of mammalian alpha-catulin, is required for subcellular localization
42                                 Furthermore, alpha-catulin knockdown attenuated 5-HT-induced PASMC th
43      Here, based on evidence suggesting that alpha-catulin may associate with a beta-catenin fraction
44         Taken together, our study shows that alpha-catulin plays a critical role in cancer metastasis
45    Here we identify the predicted endogenous alpha-catulin product, document alpha-catulin and Lbc co
46 ort the concept that the recently identified alpha-catulin protein may modulate Rho pathway signaling
47 t and is identical to the alpha-catenin-like alpha-catulin protein of unknown function.
48                        Attenuation of ILK or alpha-catulin reciprocally blocked cell migration and in
49 eased association between Lbc, RhoA, and the alpha-catulin scaffold.
50 eomic and biochemical analysis revealed that alpha-catulin supersensitizes alpha(1D)-AR functional re
51                                              alpha-Catulin was upregulated in highly invasive non-sma
52 identified an alpha-catenin-related protein, alpha-catulin, whose function is poorly understood, as p