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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
6 dy demonstrates that the interaction between alpha-catulin and alpha-dystrobrevin is evolutionarily c
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
19 ted as alpha-catulin(GFP)), we discover that alpha-catulin(GFP) is expressed by only 0.02% of bone ma
20 e gene Ctnnal1 in mice (hereafter denoted as alpha-catulin(GFP)), we discover that alpha-catulin(GFP)
21 l imaging, allowing us to image thousands of alpha-catulin-GFP(+)c-kit(+) cells and to digitally reco
22 titution of irradiated mice, indicating that alpha-catulin-GFP(+)c-kit(+) cells are comparable in HSC
25 pha-catulin and imply that alpha-catenin and alpha-catulin have distinct activities that downregulate
32 tation and blot overlay assays indicate that alpha-catulin is directly recruited to the alpha(1D)-AR
33 strophin, we discover that the expression of alpha-catulin is increased, suggesting a compensatory ro
35 ith alpha-dystrobrevin and that the level of alpha-catulin is reduced in alpha-dystrobrevin-deficient
36 we show that CTN-1, a homologue of mammalian alpha-catulin, is required for subcellular localization
40 Here we identify the predicted endogenous alpha-catulin product, document alpha-catulin and Lbc co
41 ort the concept that the recently identified alpha-catulin protein may modulate Rho pathway signaling
45 eomic and biochemical analysis revealed that alpha-catulin supersensitizes alpha(1D)-AR functional re
47 identified an alpha-catenin-related protein, alpha-catulin, whose function is poorly understood, as p
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