ライフサイエンスコーパス: associated protein

1 dhesion molecule 1, and plasmalemmal vesicle-associated protein).

2 ncomitant with an increase in nuclear matrix-associated protein.

3 ed by stable tubulin-only polypeptide, an MT-associated protein.

4 alter the localization and solubility of the associated protein.

5 structural and regulatory interactions with associated proteins.

6 riptional regulators, particularly chromatin-associated proteins.

7 ate localization and activities of chromatin-associated proteins.

8 EGRs target cytoskeleton and plasma membrane-associated proteins.

9 n in vivo requires interaction with telomere-associated proteins.

10 the silicalemma, named SAPs for Silicalemma Associated Proteins.

11 sion, and disrupted localization of adhesion-associated proteins.

12 in turn modulate interactions with membrane-associated proteins.

13 everal phosphatase subunits as potential DSB-associated proteins.

14 BRCA1-associated protein 1 (BAP1) is a potent tumour suppresso

15 redicted relevant proteins, adenylyl cyclase-associated protein 1 (CAP1), SHC-transforming protein 1

16 We identified KRAB-associated protein 1 (KAP1) as the stoichiometric bindin

17 y proteasomal degradation via Kelch-like ECH-associated protein 1 (Keap1), but how Nrf2 is regulated

18 ase substrate adaptor protein Kelch-like ECH-associated protein 1 (KEAP1), the primary negative regul

19 binds to the ubiquitin ligase Kelch-like ECH-associated protein 1 (KEAP1), which targets transcriptio

20 taining have shown that multidrug resistance-associated protein 1 (MRP1) is prevalent in many cancer

21 ns in the KEAP1 gene encoding Kelch-like ECH-associated protein 1 (refs.

22 The transcriptional regulator Yes-associated protein 1 (YAP) is a key regulator of liver s

23 coregulated by the transcription factors Yes-associated protein 1 (YAP1) and transcriptional coactiva

24 mouse models of intestinal HIF-2alpha or Yes-associated protein 1 (YAP1) overexpression indicates a s

25 tion pathways including beta-catenin and Yes-associated protein 1 (YAP1) were repressed.

26 ylation of the transcriptional activator yes-associated protein 1 (YAP1, YAP), which regulates prolif

27 YY1AP1 encodes yin yang 1 (YY1)-associated protein 1 and is an activator of the YY1 tran

28 Yes-associated protein 1 and TAZ activation have been associ

29 utophagy markers, including LC3 (microtubule-associated protein 1 light chain 3) (3,4) .

30 f autophagy markers such as LC3 (microtubule-associated protein 1 light chain 3), Beclin-1, and p62.

31 ophores is crucial for producing microtubule-associated protein 1 light chain 3-II (LC3-II), which is

32 ption of the autophagy component microtubule-associated protein 1 light chain 3beta (Lc3b).

33 YAP1, which encodes the Yes-associated protein 1, is part of the Hippo pathway invol

34 ased levels of its inhibitor, Kelch-like ECH-associated protein 1, were evident in the KO heart, but

35 To examine the BRCA1-associated protein-1 (BAP1) expression of primary uveal

36 Germline mutation of the BRCA1 associated protein-1 (BAP1) gene has been linked to uvea

37 Nucleus accumbens-associated protein-1 (NAC1), a nuclear factor of the BTB

38 taining for the autophagy marker microtubule-associated protein 1A/1B-light chain 3 (LC3).

39 agic structure LC3-I and LC3-II (microtubule-associated protein 1A/1B-light chain 3) fractions, as we

40 activity/anxiety behaviours, and microtubule-associated protein 2 (Map2, rs13475902) was associated w

41 teraction between the AhR and the metastasis-associated protein 2 (MTA2).

42 ch glioma-inactivated 1 (LGI1) and contactin-associated protein-2 (CASPR2), are found in patients wit

43 protein kinase to phosphorylate synaptosome-associated protein 23 (SNAP-23), which in turn enables t

44 e endogenous protein substrate, synaptosomal-associated protein 25 (SNAP-25).

45 ding motif (zDABM) sequences of synaptosomal-associated protein 25 (SNAP25) and cysteine string prote

46 pyrimidinase-related protein 1, synaptosomal-associated protein 29, glutamate decarboxylase 1, metabo

47 Microtubule-associated protein 2c (MAP2c) is involved in neuronal de

48 AP3 (brain-specific angiogenesis inhibitor I-associated protein 3), acts in retrograde trafficking by

49 omponents SNX-3 and vacuolar protein sorting-associated protein 35 (VPS-35) did not affect HGRS-1 mic

50 ry antibodies against cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and programmed death recep

51 nd 1 (PD-1/PD-L1) and cytotoxic T lymphocyte-associated protein 4 (CTLA-4) restored antitumor immunit

52 ng antibodies against cytotoxic-T-lymphocyte-associated protein 4 (CTLA4) or programmed cell death 1/

53 he impact of programmed death -1 (PD-1), CTL-associated protein 4 (CTLA4), and T cell Ig and mucin do

54 ll death 1 (PD-1) and cytotoxic T-lymphocyte associated protein 4 (CTLA4), down-regulates the T-cell-

55 Cytotoxic T-lymphocyte-associated protein 4 (CTLA4), which interacts with the m

56 igand 1/2 pathway and cytotoxic T lymphocyte-associated protein 4 are currently the most studied immu

57 machinery in DCs in a cytotoxic T-lymphocyte-associated protein 4-dependent (CTLA4-dependent) manner.

58 ith administration of cytotoxic T-lymphocyte-associated protein 4-Ig reducing disease symptoms and im

59 ese data suggest that cytotoxic T-lymphocyte-associated protein 4-Ig should be evaluated as a potenti

60 tive immunity through cytotoxic-T-lymphocyte-associated protein-4 (CTLA-4).

61 We previously showed increased growth associated protein 43 (GAP-43) expression in brain sampl

62 uences, and heptavalent protein cytoskeleton-associated protein 5 (CKAP5, an alternative name for TOG

63 Disc large homologue-associated protein 5 (HURP/DLGAP5), required for AURKA-d

64 Melanoma differentiation-associated protein 5 (MDA5) mediates the innate immune r

65 We identified keratin-associated protein 5-5 (Krtap5-5) as a candidate.

66 s, we have identified a role for microtubule-associated protein 7 (MAP7) during collateral branch dev

67 opment, we identified a role for microtubule-associated protein 7 (MAP7) in dorsal root ganglion sens

68 Receptor-associated protein 80 (RAP80) helps recruit BRCA1 to dou

69 nucleases (ZFNs), genetically encoded CRISPR/associated protein 9 (Cas9) from Staphylococcus aureus a

70 hort palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) genome-wide loss-of-function

71 ed short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology is a powerful too

72 The RNA-guided endonuclease CRISPR-associated protein 9 (Cas9), in particular, has attracte

73 ed short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9)-mediated editing in 22 steps

74 ed short palindromic repeats (CRISPR) CRISPR-associated protein 9 (CRISPR-Cas9) has garnered a great

75 interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) system is emerging as

76 system consisting of the deactivated CRISPR-associated protein 9 (dCas9) fused with four tandem repe

77 ivator-like effector proteins (TALE), CRISPR associated protein 9 (SpCas9) and the catalytically inac

78 ced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 nuclease (Cas9) system depends on a

79 ularly interspaced short palindromic repeats-associated protein 9) genome editing and confirmed funct

80 larly interspaced palindromic repeats/CRISPR-associated protein 9)-based DNA editing has rapidly evol

81 ed short palindromic repeats (CRISPR)/CRISPR-associated protein-9 (Cas9) technology, simultaneously w

82 terspaced short palindromic repeats (CRISPR)-associated protein-9 nuclease (Cas9), a method called ac

83 II), and vesicle-associated membrane protein-associated protein A (VAP-A).

84 nt of R. equi is the surface bound virulence associated protein A (VapA).

85 s study, we report that the ER-resident VAMP-associated proteins A and B (VAPA and VAPB) interact wit

86 VAPA/B (vesicle-associated membrane protein-associated proteins A/B) and ACBD5 (acyl Co-A binding pr

87 egates contain the neurodegenerative disease-associated proteins alpha-Synuclein, Parkin, and Hunting

88 creased the expression of urothelial barrier-associated protein, altered HA production, and induced a

89 De novo digenic mutations of telomere-associated proteins and inflammasomes initiate many chro

90 VPS4 in HEK293 cells decreases release of EV-associated proteins and miRNA as well as the overall num

91 In contrast, other membrane-associated proteins and non-CME endocytic protein caveol

92 pectrometry identified low-abundance exosome-associated proteins and protein complexes, some with kno

93 via several mechanisms that act on chromatin-associated proteins and provide a rich spectrum of epige

94 screen discovers previously unknown telomere-associated proteins and reveals how homologous proteins

95 minus that mediates its specificity for rDNA-associated proteins and show that this region binds dire

96 f Hippo signaling and its effectors Yap (Yes-associated protein) and Taz (transcriptional coactivator

97 cruits the Hippo pathway effectors, Yap (yes-associated protein) and Taz (transcriptional coactivator

98 of architectural proteins, typical enhancer-associated proteins, and histone modifications, we deter

99 extensive genetic interactions with U2 snRNP-associated proteins, and RNA sequencing (RNA-seq) reveal

100 ization of the filament network, microtubule-associated proteins, and tubulin posttranslational modif

101 Activity-regulated cytoskeleton-associated protein (Arc) is an immediate early gene that

102 ubsequent localization of G3BP1 and other SG-associated proteins around the peripheries of virus-enco

103 nal U2 snRNP (small nuclear RNA [snRNA] plus associated proteins), as H2A.Z shows extensive genetic i

104 on cooperative binding of abundant nucleoid-associated proteins at numerous genomic DNA sites and st

105 protein vesicle-associated membrane protein-associated protein B (VAPB).

106 -replacing antibody antagonizes the membrane-associated protein Basp1, thereby de-repressing nuclear

107 Increased levels of autophagy-associated proteins Beclin-1 and P62, and increased LC3b

108 ated that selective inactivation of the GPCR-associated protein beta-arrestin 2 in hepatocytes of adu

109 lence factors of B. anthracis is the S-layer-associated protein BslA, which endows bacilli with invas

110 Removal of membrane-associated proteins by proteases decreases the area comp

111 Two groups of LD-associated proteins, caleosin/dioxygenase/steroleosin an

112 Although many neurodegenerative-disease-associated proteins can be found in mitochondria, it rem

113 demonstrated how collective action of actin-associated proteins can organize actin filaments into dy

114 cluding neurofascin, contactin and contactin-associated protein, can be linked to phenotypically dist

115 terspaced short palindromic repeats (CRISPR)-associated proteins (Cas) that utilize RNA to find and c

116 ons in over a dozen genes encoding sarcomere-associated proteins cause HCM.

117 in mice lacking the critical slit diaphragm-associated protein CD2AP, highlighting the great potenti

118 fy the endothelial actin-binding protein CD2-associated protein (CD2AP) as a novel interaction partne

119 nerative disorders by investigating glaucoma-associated protein changes in the retina and vitreous hu

120 Cross-reference with previous studies of MPA-associated protein changes widely corroborated these res

121 ls (IECs) fail to express the tight junction-associated protein claudin-7.

122 MyoA is part of a membrane-associated protein complex called the glideosome, which

123 structures of spliceosome intermediates and associated protein complexes shed light on the molecular

124 that this region binds directly to the rDNA-associated protein Csm1.

125 The CRISPR-associated protein Csm6 additionally contributes to inte

126 g with one of two previously uncharacterized associated proteins, Csx27 and Csx28.

127 Here we report that defects in spliceosome-associated protein CWC27 are associated with a spectrum

128 ase (a.k.a. Cdc48) is a key member of the ER-associated protein degradation (ERAD) pathway.

129 asome-a pathway termed endoplasmic reticulum-associated protein degradation (ERAD).

130 e provide detailed measurements of human-Yes-associated protein diffusion dynamics in a human gastric

131 us polyposis coli (APC), which is a known MT-associated protein, directly nucleates actin assembly to

132 ors relevant to CNS disorders typically have associated proteins discretely expressed in specific neu

133 Here, we found that the parkinsonism-associated protein DJ-1 and its bacterial homologs Hsp31

134 Recently, the Parkinsonism-associated protein DJ-1 was described in vitro to have g

135 underline the dynamic nature of even tightly associated protein-DNA complexes such as nucleosomes.

136 in DNA-binding activity and induction of Yes-associated protein expression.

137 cell as part of the soluble and/or membrane-associated protein fraction.

138 tically, R-2HG inhibits fat mass and obesity-associated protein (FTO) activity, thereby increasing gl

139 e molecular mechanisms by which many spindle-associated proteins function remains unknown.

140 of RhoB in Gamma-aminobutyric acid receptor-associated protein (GABARAP)+ autophagosomes and endosom

141 LGMD 2C is caused by loss of the dystrophin-associated protein, gamma-sarcoglycan.

142 acting protein (MTIP) and several glideosome-associated proteins (GAPs).

143 ence genes that are silenced by the nucleoid-associated protein H-NS and regulated positively or nega

144 The nucleoid-associated protein H-NS is a key global regulator in Gra

145 cholerae, LeuO cooperates with the nucleoid-associated protein H-NS to repress vieSAB transcription.

146 orted as an interferon (IFN)-inducible tumor-associated protein, harbors nucleic acid-binding domains

147 If any of the EV-associated proteins identified were to be correlated to

148 is suppressed by the binding of two nucleoid associated proteins, IHF and Fis.

149 c spindle and to phosphorylate a microtubule-associated protein important for mitotic spindle formati

150 milarity between sigma1.1 and delta, an RNAP-associated protein in B. subtilis, bearing implications

151 pate in pore formation are e, f, g, diabetes-associated protein in insulin-sensitive tissues (DAPIT),

152 e tolerance processes, is a critical spindle-associated protein in mouse ES(mES) cells.

153 chitecture, suggesting important roles of NM-associated proteins in genome organization.

154 aim of this study was to identify novel T2D-associated proteins in Mexican patients.

155 l linker between kAE1 and actin cytoskeleton-associated proteins in polarized cells.

156 l injury only (EC) (n = 10), 92 inflammation-associated proteins in serum obtained: <1 hr (within 1-h

157 can reduce aggregation of neurodegeneration-associated proteins in vitro and in vivo; however, the r

158 e downstream Hippo pathway effector YAP (Yes-associated protein) in Drosophila and MCF10A cells.

159 leoprotein U (HNRNPU), a nuclear matrix (NM)-associated protein, in 3D genome organization.

160 L ACYLTRANSFERASE1 and the OLEOSIN1 oil body-associated protein, in the adg1suc2 mutant doubled leaf

161 nducible changes in expression of cell cycle-associated proteins including MCM2 and cyclins A, E, D1/

162 s are significantly enriched in cytoskeletal-associated proteins including proteins activating the Rh

163 After SPB insertion, membrane-associated proteins including the conserved Ndc1 encircl

164 onucleosomes and identified multiple H3K4me1-associated proteins, including many involved in chromati

165 e to up-regulate the expression of autophagy-associated proteins, including p62/SQSTM1.

166 the interaction of PorB with outer membrane-associated proteins, including PorA and RmpM.

167 at PfAP2-I associates with several chromatin-associated proteins, including the Plasmodium bromodomai

168 Several cytosolic and membrane-associated proteins, including the Rab family members Ra

169 YAP (Yes-associated protein) is a coactivator protein which, upon

170 loss activated NFkB and upregulated the EGFR-associated protein KIAA1199/CEMIP, which is known to opp

171 Three membrane-associated proteins, Kibra, Merlin, and Expanded, regula

172 RhoA cell invasiveness is increased in a Rho-associated protein kinase (ROCK) activation and cell con

173 Rho-associated protein kinase (ROCK) is required for both hi

174 g RIG-I activity, which is mediated by death associated protein kinase 1 (DAPK1).

175 ants of the conserved tumor suppressor death-associated protein kinase dapk-1 We have previously repo

176 zing the importance of the activated mitogen-associated protein kinase pathway in this disease.

177 rench et al. (2017) show that the centromere-associated protein KNL-2/M18BP1 reads the centromere epi

178 PHB2 binds the autophagosomal membrane-associated protein LC3 through an LC3-interaction region

179 Previously, we showed that the LD-associated proteins (LDAPs) are a family of plant-specif

180 ome 1, and the lipidated form of microtubule-associated protein light chain 3 isoform B.

181 ur data also revealed that RNA-polymerase-II-associated proteins like PAF1 and RTF1 antagonize PIWI-d

182 l-D-aspartate receptor (NMDAR) and contactin-associated protein-like 2 (CASPR2) in maternal sera, and

183 in certain social responses in the contactin-associated protein-like 2 (Cntnap2) mouse model for ASD.

184 ar gamma-aminobutyric acid (GABA)-A-receptor-associated protein-like 2 (Gabarapl2; also known as Gate

185 ere we identified a novel actin stress fiber-associated protein, LIM and calponin-homology domains 1

186 In this work, we found that SG-associated proteins localized to the periphery of virus-

187 cluding a chaperonin (GroEL1) and a nucleoid-associated protein (Lsr2), although how their activities

188 To report the identification of microtubule-associated protein (MAP) 1B as the antigen of the previo

189 increased, and the expression of microtubule-associated protein (MAP)-1A was significantly up-regulat

190 signated AUG) including AUG8, which is an MT-associated protein (MAP).

191 ement inhibitor, mannan-binding lectin (MBL)-associated protein (MAp)44, in regulating the compositio

192 tified an accessory protein, 17 kDa membrane-associated protein (MAP17), that increased SGLT2 activit

193 we uncovered a new role for the microtubule-associated protein MAP1B in modulating access of AMPARs

194 crotubules are bound by numerous microtubule-associated proteins (MAPs) that have the capacity to aff

195 anization of the MT array is regulated by MT-associated proteins (MAPs), which include a subset of hi

196 of starch was restricted by the presence of associated protein matrix and enzyme inhibitors, but acc

197 rexpressing an invasive isoform of the actin-associated protein Mena.

198 We further found that the phagocytosis-associated protein MERTK was significantly reduced in CE

199 cogenes TERT and PIK3CA, and alter chromatin-associated proteins (MLL3, ARID1A, CHD6 and KDM6A) and e

200 -dependent and is guided by several nucleoid-associated proteins (NAPs) and at least one nucleoid-ass

201 Nucleoid-associated proteins (NAPs) facilitate chromosome organiz

202 nd gene expression are modulated by nucleoid-associated proteins (NAPs), but little is known about ho

203 nction of Gin4 is taken over by the bud neck-associated protein Nba1.

204 The nucleolar and spindle-associated protein NUSAP1 is a microtubule-binding prote

205 Eml1, a microtubule (MT)-associated protein of the EMAP family, is impaired in th

206 mycin complex 1/2 protein subunit regulatory associated protein of the MTOR complex 1 (RAPTOR), the s

207 in interactome and function of PhIL1, an IMC-associated protein on the motile and invasive stages of

208 cells as well as to isolate and enrich GAGs-associated proteins on cell membrane.

209 However, the effect of MLR and MLR-associated proteins on neuronal aging is unknown.

210 The ORC-associated protein (ORCA/LRWD1) stabilizes ORC on chroma

211 nd inhibited the expression of the apoptosis-associated proteins PARP, Bax, and caspase-3.

212 osin/dioxygenase/steroleosin and LD/oil body-associated proteins, participate in cellular stress defe

213 Tau, as a microtubule (MT)-associated protein, participates in key neuronal functio

214 03 cytoplasmic domain and the focal adhesion-associated protein paxillin (Pxn) in downstream signalin

215 dentified the first LD motif (LD1) of the FA-associated protein paxillin as the binding partner of th

216 rmal progenitors deficient in the peroxisome-associated protein Pex11b failed to segregate peroxisome

217 Cytoskeletal-associated proteins play an active role in coordinating

218 nd the membrane-proximal regions of membrane-associated proteins play important roles in regulating m

219 (Ab/SOD, size 10nm) to plasmalemmal vesicle-associated protein (Plvap) that is specifically localize

220 This emerging pharmacology of receptor-associated proteins provides a new approach for improvin

221 he binding properties of LRP1 using receptor-associated protein (RAP) as a model ligand due to its ti

222 By contrast, the LRP1 ligand, receptor-associated protein (RAP), robustly activated microglia,

223 oinflammatory LRP1 ligands, such as receptor-associated protein (RAP), which included sustained Ikapp

224 is modulated by the LRP chaperone, Receptor-Associated Protein (RAP).

225 unexpectedly identifies hundreds of ribosome-associated proteins (RAPs) from categories including met

226 gene Retinal Degeneration 3 (RD3) is a Golgi-associated protein required for efficient trafficking of

227 luding defense-related genes like senescence-associated proteins, resveratrol synthase, 9s-lipoxygena

228 bulin as well as the assembly of microtubule-associated protein rich tubulin.

229 d transcription factor DnaA and the nucleoid-associated protein Rok of Bacillus subtilis.

230 Importantly, mice deficient in the Vps34-associated protein Rubicon, which is critical for a nonc

231 of signalling lymphocyte activation molecule-associated protein (SAP) adaptors.

232 als in both cell types, mediated by the SLAM-associated protein (SAP) family of adaptors.

233 s, signaling lymphocytic activation molecule-associated protein (SAP) was functionally and mechanisti

234 aling lymphocytic activation molecule (SLAM)-associated protein (SAP)-deficient mouse model.

235 The MT-associated protein She1 regulates dynein activity along

236 The synaptosomal-associated protein SNAP25 is a key player in synaptic ve

237 that PC2 binds two isoforms of the retromer-associated protein sorting nexin 3 (SNX3), including a n

238 y exposes unexpected binding of the ribosome-associated protein SRA.

239 The microtubule-associated protein Stu2 (XMAP215) has the remarkable abi

240 ytoskeletal stability and the activity of MT-associated proteins such as kinesins.

241 tations in the gene encoding the microtubule-associated protein TAU (MAPT).

242 The microtubule-associated protein tau (MAPT, tau) forms neurotoxic aggr

243 interaction between CDA and the microtubule-associated protein Tau deficiencies, and report that Tau

244 n between cytidine deaminase and microtubule-associated protein Tau deficiencies.

245 bcellular mislocalization of the microtubule-associated protein Tau is a hallmark of Alzheimer diseas

246 Microtubule-associated protein tau is an axonal phosphoprotein.

247 The microtubule-associated protein tau is implicated in various neurodeg

248 The MT-associated protein tau is known to mediate actin/MT inte

249 The microtubule-associated protein Tau plays a central role in the patho

250 ins to be determined whether the microtubule-associated protein tau regulates the differentiation and

251 thway from the natively unfolded microtubule-associated protein Tau to a highly structured amyloid fi

252 n of aberrantly aggregated MAPT (microtubule-associated protein Tau) defines a spectrum of tauopathie

253 nt regulator of this system, the microtubule-associated protein Tau, has been shown to participate in

254 h the cytoplasmic aggregation of microtubule-associated protein tau.

255 (H-NS) is an abundant DNA-bridging, nucleoid-associated protein that binds to an AT-rich conserved DN

256 failure-induced gene functioning as an mRNA-associated protein that enhances expression of a subset

257 Tau is a microtubule-associated protein that functions in regulating cytoskel

258 GAS2L3 is a recently identified cytoskeleton-associated protein that interacts with actin filaments a

259 Also, uncommonly, HU, a chromosome-associated protein that is essential in the DNA-RNA inte

260 Tau is a microtubule-associated protein that is highly soluble and natively u

261 We characterize NET2A as a novel actin-associated protein that localizes to punctae at the plas

262 Tau is a microtubule-associated protein that stabilizes microtubules in neuro

263 y conserved modules present in transcription-associated proteins that are termed "reader" proteins.

264 facilitated dissociation of certain nucleoid-associated proteins that exhibit an unbinding rate that

265 ndle is composed of dynamic microtubules and associated proteins that together direct chromosome move

266 ion were dependent on activation of YAP (yes-associated protein)-the downstream effector of Hippo sig

267 We identify a novel Myst2-associated protein, the tumour suppressor protein Niam (

268 olism in almost all eukaryotic cells, and LD-associated proteins tightly regulate their dynamics.

269 -sensitive Sgt1 mutants and for linking Skp1-associated proteins to Hsp90-dependent pathways.

270 Nrf2 reduced PD-associated protein toxicity by a cell-autonomous mechani

271 Prior work demonstrated that a microtubule-associated protein, TPX2, targets kinesin-5 and kinesin-

272 ctive responses in cells, including YAP (Yes-associated protein) transcription factor activity, caspa

273 The translocon-associated protein (TRAP) complex is an integral compone

274 olog the transformation/transcription domain-associated protein TRRAP are members of the phosphatidyl

275 dvanced our understanding of how microtubule-associated proteins tune microtubule dynamics in trans,

276 ese findings identify ACK1 as a novel SLP-76-associated protein-tyrosine kinase that modulates early

277 Framingham Cardiovascular Disease Risk Score-associated proteins using linear mixed-effects models in

278 VAMP/synaptobrevin-associated proteins (VAPs) contain an N-terminal major s

279 Two invasion-associated proteins, vimentin and L-plastin, were strong

280 lei shape and expression of nuclear envelope-associated proteins were accompanied by altered distribu

281 The classical complement pathway associated proteins were activated in the glaucoma sampl

282 By quantitative mass spectrometry, DCV-associated proteins were found to be reduced approximate

283 A total of 151 ECM and ECM-associated proteins were identified by mass spectrometry

284 ic acid (GABA), and acetylcholine, also have associated proteins, which may be druggable.

285 THP1 and NUA were identified as SAC3B-associated proteins whose mutations also caused d35S::LU

286 ition proteins and the adaptor molecules Fas-associated protein with a death domain (FADD) and IMD.

287 Finally, we identify another axis-associated protein with a role in meiotic recombination.

288 aptor protein tumor necrosis factor receptor-associated protein with death domain as an upstream regu

289 ective tissue growth factor (CTGF), a matrix-associated protein with four distinct cytokine binding d

290 ere, we report that UBE3B is a mitochondrion-associated protein with homologous to the E6-AP Cterminu

291 tween infection and expression of cell cycle-associated proteins, with terminally differentiated macr

292 led to rapid HCC formation and activated Yes-associated protein/WW domain containing transcription re

293 The antiapoptotic protein HAX-1 (HS-associated protein X-1) localizes to sarcoplasmic reticu

294 Here we identify Yes-associated protein (Yap) as a critical regulator of the

295 t manner, in part through suppression of yes-associated protein (YAP) function.

296 ranscriptional co-repressor in the Hippo-Yes-associated protein (YAP) pathway.

297 tivator with PDZ binding motif (TAZ) and Yes-associated protein (YAP) proteins via inhibition of the

298 esearch showed that DLG5 is decreased in Yes-associated protein (YAP)-overexpressing cells.

299 via restricting its downstream effector, Yes-associated protein (YAP).

300 Here, it is reported that the Z-ring associated proteins ZapA and ZapB form FtsZ-independent