ライフサイエンスコーパス: cytoskeleton-associated

1 c-Abl phosphorylates the cytoskeleton-associated adaptor protein, Crk, at tyrosin

2 with antibodies recognizing plectin, a large cytoskeleton-associated anchorage protein.

3 ma brucei AIR9-like protein, TbAIR9, is also cytoskeleton-associated and colocalizes with the subpell

4 microscopy, we comprehensively screened 378 cytoskeleton-associated and related proteins for their f

5 The activity regulated cytoskeleton associated (Arc) gene has received wide att

6 igonucleotide against the activity-regulated cytoskeleton-associated (Arc) gene.

7 coding the capsid-forming activity-regulated cytoskeleton-associated (Arc) protein as well as capsid-

8 ess higher levels of the activity-regulated, cytoskeleton-associated (Arc) protein, consistent with n

9 ssociated protein of 43 kDa (GAP43) is a key cytoskeleton-associated component of the presynaptic ter

10 Galpha13 physically interacts with Hax-1, a cytoskeleton-associated, cortactin-interacting intracell

11 show that HDAC6, a cytoplasmic-localized and cytoskeleton-associated deacetylase, is required for eff

12 response, polyamine metabolism, chaperonins, cytoskeleton associated, etc.

13 A significant increase in cytoskeleton-associated ezrin occurred following phospho

14 at integrin-mediated adhesion may regulate a cytoskeleton-associated factor(s) responsible for Raf ac

15 ion of hERG channel from the membrane to the cytoskeleton-associated fractions upon sotalol applicati

16 Bim primarily localized to mitochondrial and cytoskeleton-associated fractions.

17 how that MKL1 is a nonredundant regulator of cytoskeleton-associated functions in immune cells and fi

18 xpression signature, consisting of increased cytoskeleton-associated gene expression along with depre

19 Mutations in the cytoskeleton-associated gene filamin A (FlnA) cause the

20 onfirmed the differential expression of four cytoskeleton-associated genes with known functional asso

21 f Rreb1 also resulted in the upregulation of cytoskeleton-associated genes, a change in the organizat

22 We also identify the cytoskeleton-associated growth-associated protein 43 (GA

23 mmediate-early gene Arc (activity-regulated, cytoskeleton-associated) in the dorsomedial (DM) striatu

24 Here, we report the discovery of a cytoskeleton-associated kinase, pseudopodium-enriched at

25 ZNF185 is an actin-cytoskeleton-associated Lin-l 1, Isl-1 and Mec-3 (LIM) d

26 We show that ZNF185 is a novel actin-cytoskeleton-associated Lin-l 1, Isl-1 and Mec-3 (LIM) d

27 results indicate that lipid rafts, including cytoskeleton-associated lipid rafts, are sites of NDV as

28 Given the expression of these cytoskeleton-associated molecules, we hypothesized that

29 small GTP-binding proteins in membrane- and cytoskeleton-associated morphogenetic transformations an

30 We have found that loss of the membrane:cytoskeleton-associated NF2 tumor suppressor, merlin, yi

31 r observations suggest that RBC membrane and cytoskeleton associated NO-inert proteins provide a barr

32 CD66b+ granules, and increased levels of the cytoskeleton-associated phospho-Syk kinase.

33 n src- and ras-transformed cells, is a major cytoskeleton-associated PKC substrate with tumor suppres

34 A431 cells revealed a modest decrease in the cytoskeleton-associated pool of plakoglobin (Pg) and a c

35 trophic factor (Bdnf) and activity-regulated cytoskeleton associated protein (Arc) genes.

36 ural plasticity regulator activity-regulated cytoskeleton associated protein (ARC) were up-regulated

37 Here, we compared activity regulated cytoskeleton associated protein (Arc)/Arg3.1 protein lev

38 cidic acid coiled-coil protein 3 (TACC3) and cytoskeleton associated protein 5 (cKAP5; or colonic hep

39 inal region of kinesin-73 protein contains a cytoskeleton associated protein Gly-rich domain, which i

40 x 10(-)(6)) and neuronal activity-regulated cytoskeleton-associated protein (ARC) (P=3.78 x 10(-)(8)

41 wn to negatively regulate activity-regulated cytoskeleton-associated protein (Arc) and it has been su

42 aptic proteins comprising activity-regulated cytoskeleton-associated protein (ARC) and N-methyl-d-asp

43 xpressed genes, including activity-regulated cytoskeleton-associated protein (ARC) and N-methyl-D-asp

44 Activity-regulated cytoskeleton-associated protein (Arc) expression was kno

45 ein (CREB) activation and activity-regulated cytoskeleton-associated protein (Arc) expression.

46 he enhancer region of the activity-regulated cytoskeleton-associated protein (Arc) immediate-early ge

47 y increased expression of activity-regulated cytoskeleton-associated protein (Arc) in the amygdala in

48 Activity-regulated cytoskeleton-associated protein (Arc) is an immediate ea

49 The activity-regulated cytoskeleton-associated protein (Arc) is an immediate ea

50 A significant increase in activity-regulated cytoskeleton-associated protein (Arc) mRNA and Arc and c

51 ulted in higher levels of activity-regulated cytoskeleton-associated protein (Arc) mRNA induction tha

52 Activity-regulated cytoskeleton-associated protein (Arc) was identified as

53 cogene homolog (CFOS) and activity-regulated cytoskeleton-associated protein (ARC), and the neureguli

54 The immediate early gene, activity-regulated cytoskeleton-associated protein (Arc), has been implicat

55 neages, and expressed the activity-regulated cytoskeleton-associated protein (Arc), suggesting their

56 ription factor Elk-1, and activity-regulated cytoskeleton-associated protein (Arc).

57 trophic factor (Bdnf) and activity-regulated cytoskeleton-associated protein (Arc).

58 his mechanism is based on activity-regulated cytoskeleton-associated protein (Arc)/ARG3.1-dependent p

59 r induce transcription of activity-regulated cytoskeleton-associated protein (Arc/Arg3.1) and transpo

60 Activity-regulated cytoskeleton-associated protein (Arc/Arg3.1) is an immed

61 Activity-regulated cytoskeleton-associated protein (Arc/Arg3.1) is an immed

62 g AS (AS mice) accumulate activity-regulated cytoskeleton-associated protein (ARC/ARG3.1), a neuronal

63 richment was observed for activity-regulated cytoskeleton-associated protein (P=0.23) or N-methyl-D-a

64 ays we show that the mitotic spindle protein Cytoskeleton-Associated Protein 2 (CKAP2) has a strong e

65 stitution experiments have demonstrated that Cytoskeleton-Associated Protein 2 (CKAP2) increases micr

66 Cytoskeleton-associated protein 2, CKAP2, is a microtubu

67 ng adenocarcinoma samples, we identified the cytoskeleton-associated protein 2-like (CKAP2L) as a pot

68 Asnfs( *)6), in CKAP2L, encoding the protein cytoskeleton-associated protein 2-like (CKAP2L).

69 adder carcinoma cells in vitro by binding to cytoskeleton-associated protein 4 (CKAP4) and altering t

70 Here, we identified cytoskeleton-associated protein 4 (CKAP4) as a DKK1 rece

71 Previously, we identified cytoskeleton-associated protein 4 (CKAP4) as a major sub

72 eagues demonstrate that DKK-1 interacts with cytoskeleton-associated protein 4 (CKAP4) to promote act

73 This study demonstrates that cytoskeleton-associated protein 4/p63 (CKAP4/p63), a typ

74 other RNA sequences, and heptavalent protein cytoskeleton-associated protein 5 (CKAP5, an alternative

75 ess the expression of the activity-regulated cytoskeleton-associated protein Arc at various times aft

76 mediate early gene called activity-regulated cytoskeleton-associated protein Arc.

77 nase II, neurogranin, and activity-regulated cytoskeleton-associated protein are coassembled into the

78 helial protein lost in neoplasm (EPLIN) is a cytoskeleton-associated protein characterized by the pre

79 overexpressed gene (TOG) protein, encoded by cytoskeleton-associated protein CKAP5, is a microtubule-

80 helial protein lost in neoplasm (EPLIN) is a cytoskeleton-associated protein encoded by a gene that i

81 transitions in the RPE by targeting Ezrin, a cytoskeleton-associated protein essential for the regula

82 ion of the cdc42-interacting protein CIP4, a cytoskeleton-associated protein for which expression was

83 Here, we report a structure of the cytoskeleton-associated protein glycine-rich (CAP-Gly) d

84 ) contains an N-terminal microtubule-binding cytoskeleton-associated protein glycine-rich (CAP-Gly) d

85 This 191-residue region encompasses the cytoskeleton-associated protein glycine-rich domain, the

86 e observation that CLIP-170 has two CAP-Gly (cytoskeleton-associated protein glycine-rich) motifs and

87 The local translation of the cytoskeleton-associated protein Homer2 in particular mig

88 AIR9 is a cytoskeleton-associated protein in Arabidopsis thaliana

89 uding the PSD-95 complex, activity-regulated cytoskeleton-associated protein interactors, the fragile

90 We found that TRIOBP, a cytoskeleton-associated protein mutated in human heredit

91 etroviral Gag lattice and activity-regulated cytoskeleton-associated protein oligomers.

92 The actin cytoskeleton-associated protein talin binds to integrins

93 GAS2L3 is a recently identified cytoskeleton-associated protein that interacts with acti

94 NF2) tumor suppressor, Merlin, is a membrane/cytoskeleton-associated protein that mediates contact-de

95 ng protein 280 (ABP-280), a widely expressed cytoskeleton-associated protein that plays an important

96 EPLIN is a cytoskeleton-associated protein that was initially ident

97 We analyzed the role of host cell c-Src, a cytoskeleton-associated protein tyrosine kinase, in C. p

98 ecific gene two (GAS2) is a highly conserved cytoskeleton-associated protein whose in vivo function r

99 immediate-early gene Arc (activity-regulated cytoskeleton-associated protein) at the level of mRNA an

100 ce of Copia and the Arc1 (activity-regulated cytoskeleton-associated protein) homolog.

101 nor the increase in Arc (activity-regulated cytoskeleton-associated protein) levels in response to m

102 e expression level of the activity-regulated cytoskeleton-associated protein, Arc.

103 luster significantly increased and reduced a cytoskeleton-associated protein, Enigma homolog 1 (ENH1)

104 that these proteins (eg, activity-regulated cytoskeleton-associated protein, focal adhesion kinase,

105 This mutation in the conserved cytoskeleton-associated protein, glycine-rich (CAP-Gly)

106 the three-dimensional structure of CAP-Gly (cytoskeleton-associated protein, glycine-rich) domain of

107 sactivated the Galpha(i2) gene promoter; the cytoskeleton-associated protein, Keap1, abrogated this e

108 ing microtubules, requiring the NH2-terminal cytoskeleton-associated protein-glycine rich domain, but

109 Cytoskeleton-associated proteins (CAPs) are involved in

110 ity biotinylation, we identified a subset of cytoskeleton-associated proteins (CAPs) as KLIF-proximal

111 molecules, including transcription factors, cytoskeleton-associated proteins and membrane receptor-l

112 studies reveal that yotiao fractionates with cytoskeleton-associated proteins and with the postsynapt

113 otein of tight junctions (TJs), recruits the cytoskeleton-associated proteins cingulin (CGN) and para

114 ltogether, our results identify a network of cytoskeleton-associated proteins connecting focal adhesi

115 ynergistic decrease of actin and microtubule cytoskeleton-associated proteins in both control and LIV

116 , as a crucial linker between kAE1 and actin cytoskeleton-associated proteins in polarized cells.

117 new evidence for the involvement of cortical cytoskeleton-associated proteins in the regulation of ax

118 haracterized, much less is known about other cytoskeleton-associated proteins in trypanosomes.

119 s, a novel Ser/Thr kinase, and several actin cytoskeleton-associated proteins including actin, profil

120 ila Enabled (Ena) is a member of a family of cytoskeleton-associated proteins including mammalian vas

121 X1 interactome involving plasma membrane and cytoskeleton-associated proteins including the previousl

122 uced the interaction of DPYSL5 with neuronal cytoskeleton-associated proteins MAP2 and BIII-tubulin.

123 The finding that cytoskeleton-associated proteins may be key determinants

124 Cytoskeleton-associated proteins play key roles not only

125 on was associated with the redistribution of cytoskeleton-associated proteins such as actin, alpha-ac

126 We previously discovered a family of cytoskeleton-associated proteins that includes GAS11, a

127 lin, which belongs to the band 4.1 family of cytoskeleton-associated proteins that link cell surface

128 ression or organization of cell adhesion and cytoskeleton-associated proteins were correlated with th

129 Several actin cytoskeleton-associated proteins were identified in the

130 Raft-, non-raft-, and cytoskeleton-associated proteins were simultaneously ima

131 plasmic reticulum and increased synthesis of cytoskeleton-associated proteins, all of which contribut

132 required for tyrosine phosphorylation of the cytoskeleton-associated proteins, focal adhesion kinase

133 analysis identified the genes encoding actin cytoskeleton-associated proteins, including Abra and Arl

134 Ts by arrestin channels Mdm2 activity toward cytoskeleton-associated proteins, increasing their ubiqu

135 t proteins include major signaling proteins, cytoskeleton-associated proteins, membrane transporters,

136 These included membrane proteins, cytoskeleton-associated proteins, nuclear transport fact

137 ored when dealing with reaction-diffusion of cytoskeleton-associated proteins.

138 ound at the C terminus of a variety of actin cytoskeleton-associated proteins.

139 rin, radixin, and moesin) family of membrane:cytoskeleton-associated proteins.

140 The hrs/actinin-4/BERP/myosin V (CART [cytoskeleton-associated recycling or transport]) complex

141 ing complex formed by the activity-regulated cytoskeleton-associated scaffold protein (ARC) of the po

142 may be involved in the formation of membrane cytoskeleton-associated signaling complexes that are imp

143 vealed that ADP-stimulated activation of the cytoskeleton-associated small GTPase Rac1 was independen

144 The NF2 protein, Schwannomin/Merlin, is a cytoskeleton-associated tumor suppressor regulated by ph

145 also known as Pyk2/RAFTK/CAKbeta/FAK2, is a cytoskeleton-associated tyrosine kinase.

146 d in regulating the function of receptor and cytoskeleton-associated tyrosine kinases.

147 and the existence of an enzymatically active cytoskeleton-associated UPase.

148 mall GTPases regulates the dynamics of actin cytoskeleton associated with cell motility.

149 ive F-actin, the dynamic nature of the actin cytoskeleton associated with new AChR clusters was revea

150 Changes in the actin cytoskeleton associated with this switch suggest that th