ライフサイエンスコーパス: associated protein

1 t chain 3 (LC3), the autophagosomal membrane-associated protein.

2 he prosurvival transcriptional regulator Yes-associated protein.

3 p box 1 gene (HMGB1), a nonhistone chromatin-associated protein.

4 mall nuclear ribonucleoprotein particles and associated proteins.

5 lation of cell-cycle progression and mitosis-associated proteins.

6 prototype to model large, dynamic, membrane-associated proteins.

7 ion of lateral interactions between membrane-associated proteins.

8 del did not alter the expression of integrin-associated proteins.

9 lasma membrane and astrocyte-derived, matrix-associated proteins.

10 browse, search and download phase separation associated proteins.

11 ntaining and assembling plasma membranes and associated proteins.

12 variants determining the blood levels of AD-associated proteins.

13 del did not alter the expression of integrin-associated proteins.

14 iven by smoking and elevated levels of 6 age-associated proteins.

15 yeast and Adh2 in hyphae among the cell wall-associated proteins.

16 a large number of transmembrane and membrane-associated proteins.

17 sis of proteins targeted for secretion as EV-associated proteins.

18 t of abundant nuclear-encoded photosynthesis-associated proteins.

19 ce and sequence features of phase separation associated proteins.

20 Multidrug resistance-associated protein 1 (adenosine triphosphate-binding cas

21 Inactivating mutations in BRCA1-associated protein 1 (BAP1) are associated with metastas

22 Cyclase-associated protein 1 (CAP1) is a conserved actin-regulat

23 Death-associated protein 1 (DAP1) was implicated as a candidat

24 tions in ganglioside-induced differentiation-associated protein 1 (GDAP1) alter mitochondrial morphol

25 Here, we identified PDGFA-associated protein 1 (Pdap1) as an essential regulator o

26 RAD51-associated protein 1 (RAD51AP1) plays an integral role i

27 (UAF1) is an integral component of the RAD51-associated protein 1 (RAD51AP1)-UAF1-ubiquitin-specific

28 l-xL and the tumor suppressor retinoblastoma-associated protein 1 (RB1).

29 They bind to S-phase kinase-associated protein 1 (SKP1) through the F-box motif and

30 alyze prolyl-hydroxylation of S-phase kinase-associated protein 1 (Skp1), a reaction enabling adaptat

31 Yes-associated protein 1 (YAP) is a transcriptional regulato

32 Both TEAD4 and its cofactor, yes-associated protein 1 (YAP1), are specifically expressed

33 clusters that all expressed the oncogene Yes-associated protein 1 (YAP1).

34 amine and HIV proteins increased microtubule-associated protein 1 light chain 3 beta-II (LC3B-II) lip

35 ts negative regulator, KEAP1 (Kelch-like ECH-associated protein 1).

36 l phosphoprotein integrin cytoplasmic domain-associated protein-1 (ICAP1) results in recruitment of i

37 Yet, microfibril-associated protein-1 (MAGP1)-rich ciliary zonules that o

38 ne H2A lysine 119 deubiquitinase BAP1 (BRCA1 Associated Protein-1) associates with a history of chron

39 synaptic density-95 (PSD-95) and microtubule-associated protein 1A (MAP1A) in PV(+) neurons.

40 Here, we identify cytoplasmic linker-associated protein 2 (CLASP2), a +TIP that captures cort

41 Here, we reveal that cytoplasmic linker-associated protein 2 (CLASP2), a key regulator of cortic

42 itochondrial damage, and reduced microtubule-associated protein 2 (MAP2) dendrites in human neurons.

43 appaB signaling pathway modulates metastasis-associated protein 2 (MTA2), a component of the nucleoso

44 binding protein 1 (DDB1), and S-phase kinase-associated protein 2 (SKP2) as components of E3 ubiquiti

45 cided with increased expression of caspase-8-associated protein 2, a known microRNA-210 target and ap

46 Among these RBPs, the ubiquitin-associated protein 2-like (UBAP2L) protein interacts wit

47 ronides are effluxed by multidrug resistance-associated proteins 2 and 3.

48 markers; neuronal nuclei (NeuN), microtubule-associated protein-2 (MAP-2) and betaIII-tubulin.

49 The role of proliferation-associated protein 2G4 (PA2G4), alternatively known as E

50 family member 3A/3B (KIF3A/3B), and kinesin-associated protein 3 (KAP3), is highly conserved across

51 Of the age-associated proteins, 33.5% and 45.3%, were associated wi

52 e, we discover Enterobacter cloacae CD-NTase-associated protein 4 (Cap4) as a founding member of a di

53 ligand 1 (PD-L1), and cytotoxic T lymphocyte-associated protein 4 (CTLA-4) for cancer immunotherapy,

54 protein 1 (PD-1) and cytotoxic T lymphocyte-associated protein 4 (CTLA-4), which limit T cell activa

55 nd 1 (PD-1:PD-L1) and cytotoxic T lymphocyte-associated protein 4 (CTLA-4):B7-1 are among the most im

56 gand PD-L1 as well as cytotoxic T-lymphocyte-associated protein 4 (CTLA4) have shown impressive clini

57 Microtubule-associated protein 4 (MAP4) interacts with and controls

58 orylation status of stathmin and microtubule-associated protein 4 (MAP4), the latter of which was reg

59 a combination of anticytotoxic T-lymphocyte-associated protein 4 and anti-PD-1 antibodies.

60 of CD45, CD28, CTLA4 (cytotoxic T-lymphocyte-associated protein 4), tumor necrosis factor-R-II, and C

61 tors (ICIs) targeting cytotoxic T lymphocyte-associated protein-4 (CTLA-4) and programmed cell death

62 Growth-associated protein 43 (GAP-43) plays a central role in t

63 MAP-2, betaIII-tubulin in addition to growth-associated protein-43 (GAP-43), Synapsin-I and thermo-se

64 describe a deficiency of cilia and flagella associated protein 45 (CFAP45) in humans and mice that p

65 actor 4GI (eIF4GI) and of its homolog, death-associated protein 5 (DAP5), are elevated.

66 gene I (RIG-I), and melanoma differentiation-associated protein 5 (MDA5) mediate antiviral responses.

67 that are sensed by melanoma differentiation-associated protein 5 (MDA5) to trigger constitutive upre

68 cible I (Rig-I) and melanoma differentiation-associated protein 5 (MDA5), to further amplify IFN prod

69 s Bcl-2-associated X protein (Bax) and death-associated protein 6 (Daxx) and attenuated an Mn-induced

70 deler that forms a complex with Death domain-associated protein 6 (DAXX) to deposit the histone varia

71 ed short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9) functional analyses in Parhy

72 ced short palindromic repeat (CRISPR)-CRISPR associated protein 9 (Cas9) homology directed repair (HD

73 terspaced, short palindromic repeats)/CRISPR-associated protein 9 (Cas9) system has emerged as a powe

74 ced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9) technology has provided a si

75 ularly interspaced short palindromic repeats-associated protein 9 gene editing.

76 CRISPR-associated protein 9 variants with expanded targeting ra

77 In this study, CRISPR/CRISPR-associated protein 9 was used to generate HeLa cell line

78 ry elements used to express the Cas9 (CRISPR Associated protein 9) DNA nuclease and single guide RNA

79 interspaced short palindromic repeats/CRISPR-associated protein 9) to correct the GBE1(102C>A) mutati

80 tically impaired Campylobacter jejuni CRISPR-associated protein 9-fused adenine base editor (CjABE).

81 otein encoded by ALDH2) and Glu4Gly of BRCA1-associated protein (a protein encoded by BRAP).

82 Accumulation-associated protein (Aap) from S. epidermidis has been sh

83 The accumulation-associated protein (Aap) from Staphylococcus epidermidis

84 ar function via Cdc42 and its downstream Yes-associated protein activities.

85 , we report that an active form of the ESCRT-associated protein ALIX efficiently recruits ESCRT-III p

86 olocalizes with the Parkinson's disease (PD)-associated protein alpha-synuclein in cells and interact

87 lution insights into the structure of the PD-associated protein alpha-synuclein in complex with the m

88 Moreover, the channel-associated protein alpha2delta localizes independently,

89 se-1 and reduces nuclear accumulation of yes-associated protein and its target gene c-Myc.

90 We suggest that the presence of autophagy-associated proteins and degenerated organelles within ty

91 n of Clec9A facilitates interactions with ER-associated proteins and degradation machinery to control

92 een devoted to identify the phase separation associated proteins and elucidate their functions.

93 ves as a nucleation center for multiple Xist-associated proteins and m(6)A modification.

94 Apart from microtubule-associated proteins and motors, two factors have been sh

95 e then immunostained for different chromatin-associated proteins and mounted for visualization using

96 These areas differ in composition of actin-associated proteins and of phosphoinositides in the memb

97 chitectural and regulatory roles of nucleoid-associated proteins and the implications for bacterial c

98 g protein 4 (BRD4), a regulator of chromatin-associated proteins and transcription factors, which was

99 el matrix components (Odontogenic ameloblast-associated protein) and dentin dysplasia targets (Dentin

100 l of the transcriptional regulators YAP (yes-associated protein) and TAZ.

101 een stomatal regulation and nuclear envelope-associated proteins, and adds two new players to the inc

102 follicular cells by the presence of LDs, LD-associated proteins, and increased TGs.

103 is regulated by a large cohort of chromatin-associated proteins, and inferring their differential bi

104 regulated through a dynamic interplay of DNA-associated proteins, and the composition of gene-regulat

105 relationship between transcription factors, associated proteins, and their target genes.

106 (zif268) and activity regulated cytoskeletal-associated protein (Arc) immediate-early gene (IEG) expr

107 a effects on activity-regulated cytoskeletal-associated protein (ARC) in downstream brain regions.

108 Activity-regulated cytoskeleton-associated protein (Arc) was identified as one of the ca

109 r (Bdnf) and activity-regulated cytoskeleton-associated protein (Arc).

110 compartment, interactions with actin or its associated proteins are also critical for the localizati

111 The mitochondrion and its associated proteins are crucial regulators of these resp

112 ctions between actin filaments (F-actin) and associated proteins are mechanically regulated.

113 dingly, several receptors and other membrane-associated proteins are organized and functional in memb

114 urrent viewpoint that microtubules and their associated proteins are the only significant load-bearin

115 Here, we used the recently identified JBTS-associated protein armadillo repeat motif-containing 9 (

116 lysis suggest a large variability in mineral-associated proteins as a nitrogen source in soils and th

117 he dynamic interaction between lipids and PD-associated proteins assemble yet another piece of the PD

118 We conclude that CMP-associated proteins at 12 weeks' gestation predict the o

119 e mitotic kinase AtAurora 1, the microtubule-associated proteins AtEDE1 and AtMAP65-4, and the vesicl

120 agues provide compelling evidence that BRCA1-associated protein (BAP1) functions as a tumor suppresso

121 altered transcription by targeting chromatin-associated proteins been explored.

122 reported to block the accumulation of the AD-associated proteins beta-amyloid (Abeta) and hyper-phosp

123 ibosome exit tunnel, where multiple ribosome-associated protein biogenesis factors (RPBs) direct nasc

124 the human HepG2 cell line for 208 chromatin-associated proteins (CAPs).

125 nterspaced short palindromic repeat (CRISPR)-associated protein (Cas) (CRISPR/Cas), which is by far t

126 tent and sustained upregulation of apoptosis-associated proteins CASP8, TNFSF14, HGF, and TGFB1, with

127 humans, mutations affecting nuclear envelope-associated proteins cause laminopathies, including proge

128 In addition to the known JBTS-associated proteins CEP104 and CSPP1, we identified coil

129 Primarily controlled by nucleoid-associated proteins, chromosome folding is hierarchical,

130 ew in vitro study finds that the microtubule-associated protein CLASP repairs lattice damage by regul

131 in is an evolutionarily conserved chromosome-associated protein complex essential for chromosome segr

132 A conserved MT-associated protein complex, Augmin, recruits gamma-TuRC

133 n, the role of CHCHD10 variants in mitofilin-associated protein complexes in brain has not been exami

134 changes in 12 different mitotic proteins and associated protein complexes in multiple states using 15

135 y regulating the small-GTPase RhoA and actin-associated protein Cortactin.

136 interspaced short palindromic repeats-CRISPR-associated protein (CRISPR-Cas), and mRNA vaccines, and

137 short palindromic repeat (CRISPR) and CRISPR-associated protein (CRISPR/Cas) system, used to target D

138 We also highlight a subset of schizophrenia-associated proteins critically modified by glycosylation

139 e, we demonstrate that the widespread CRISPR associated protein Csx3, previously described as an RNA

140 In endoplasmic reticulum-associated protein degradation (ERAD), membrane proteins

141 lacking the Sel1L-Hrd1 protein complex of ER-associated protein degradation (ERAD).

142 aled downregulation of endoplasmic reticulum-associated protein degradation pathway components upon f

143 quences and co-localized with 23% of all DNA-associated protein degradation sites.

144 s an inhibitor of endoplasmic reticulum (ER) associated protein degradation, Sec61-dependent Ca(2+) h

145 1 and regulate ovarian tumor growth by a yes-associated protein-dependent mechanism.

146 hila melanogaster involving the mitochondria-associated protein Dosmit.

147 modate the import of abundant photosynthesis-associated proteins during photomorphogenesis.

148 suggesting for the first time that integrin-associated proteins dysfunction may contribute to reduce

149 suggesting for the first time that integrin-associated proteins dysfunction may contribute to reduce

150 n the RPE by targeting Ezrin, a cytoskeleton-associated protein essential for the regulation of calci

151 identified 38 envelope membrane intrinsic or associated proteins exhibiting altered abundance after c

152 elative importance of lymphocyte subsets and associated protein expression is incompletely understood

153 C is part of a new complex containing the ER-associated protein FNDC3A, which regulates trafficking a

154 xis structures form in rec8 that recruit DSB-associated protein foci and undergo synapsis, which is f

155 rium glutamicum SepF, the only cell division-associated protein from Actinobacteria known to interact

156 Isolating Zta and associated proteins from Burkitt's lymphoma cells underg

157 Analysis of TRIM32-associated proteins from public databases identified pro

158 Fat mass and obesity-associated protein (FTO), an RNA N(6)-methyladenosine (m

159 equires the RNA-binding protein UPF1 and its associated protein G3BP1.

160 interacts directly with the GABA(A) receptor-associated protein (GABARAP) to stabilize cell surface G

161 RD4 interacting chromatin remodeling complex-associated protein) gene, also known as GLTSCR1, which e

162 uanosine triphosphatase (GTPase) of immunity-associated proteins (GIMAPs).

163 re we determined the expression of ER stress-associated proteins (GRP78, ATF6 and PERK) and correlate

164 Accordingly, many cilia-associated proteins have been described, while those dis

165 Mutations in a number of stress granule-associated proteins have been linked to various neurodeg

166 cumulations of specific nuclear-pore-complex-associated proteins have been reported in multiple neuro

167 e identified and characterized HOS15 and its associated protein HDA9 as negative regulators of immuni

168 cilia disassembly, ciliary entry of membrane-associated protein, Hedgehog signaling, and embryogenesi

169 aining flavoprotein, as a lipid droplet (LD)-associated protein highly enriched in BAT.

170 py) the effect of pressure on the chromosome-associated protein HU and on the ParB partition protein

171 proximity-labeling proteomic profile of INM-associated proteins in Arabidopsis, we identify critical

172 crease of actin and microtubule cytoskeleton-associated proteins in both control and LIV groups while

173 The increased expression of ER stress-associated proteins in EOC suggests a role for ER stress

174 an increased identification of peptides and associated proteins in global proteome, as compared to t

175 revealed two rice (Oryza sativa) microtubule-associated proteins in the phragmoplast and uncovered a

176 Using proteomics, we identified 377 IVC-associated proteins in yeast cells grown under steady-st

177 reased expression and activation of YAP (yes-associated protein) in renal proximal tubule epithelial

178 Trp226LeufsTer4) in M1AP, encoding meiosis 1 associated protein, in three unrelated men.

179 Several sarcolemma-associated proteins, including dystrophin and sarcoglyca

180 tumor cells produced a diverse array of ECM-associated proteins, including secreted factors and modu

181 matin remodeler (ATRX), a DAXX (death domain-associated protein) interacting protein, is often lost i

182 plicability of TurboID in capturing membrane-associated protein interactomes using Lotus japonicus sy

183 The discrimination of sEV-associated proteins is a minimally invasive method with

184 slation of axonal mRNAs encoding some injury-associated proteins is known to be increased with Ca(2+)

185 YAP1 (YES-associated protein) is highly expressed in rhabdomyosarc

186 MEK-ERK pathway, the first described mitogen-associated protein kinase (MAPK) cascade, mediates multi

187 ion of GABAergic markers were rescued by Rho-associated protein kinase (ROCK)/protein kinase A (PKA)

188 kinase (LYN), zeta chain of T-cell receptor-associated protein kinase 70 (ZAP-70), and three mitogen

189 tion of Zap70 (zeta chain of T cell receptor-associated protein kinase 70).

190 Our work also predicts that nucleoid-associated proteins known to wrap DNA must form higher p

191 ns in LMNA, which encodes the nuclear lamina-associated protein lamin A/C.

192 type1 NI immunopositivity for the autophagy-associated proteins LC3B, ubiquitin, p62/sequestosome1,

193 and increased expression of the microtubule-associated protein light chain 3 (LC3), the autophagosom

194 Contactin-associated protein-like 2 (Caspr2) is a neurexin-like pr

195 that are genetically deficient for contactin-associated protein-like 2 (Cntnap2)(5), fragile X mental

196 Mutants in the gene encoding mitochondrion-associated protein LRPPRC were found to be associated wi

197 Microtubule-associated protein (MAP) 2 has been perceived as a stati

198 the combinatory effects of four microtubule-associated proteins (MAPs), namely EB1, XMAP215, CLASP2,

199 IRE1alpha, an ER membrane-associated protein mediating unfolded protein response (

200 gical contexts, it functions as a melanosome-associated protein, membrane-bound surface receptor, sol

201 cell lines suggest a role for this new JBTS-associated protein module in ciliary stability.

202 anslational specificity switches from injury-associated protein mRNA translation to CK2alpha translat

203 valosin-containing protein (VCP), an ATPase-associated protein newly identified in the heart, acts a

204 reported that adipocyte SNAP23 (synaptosome-associated protein of 23 kDa) deficiency blocks the acti

205 orrect the T-cell immunodeficiency in a zeta-associated protein of 70 kDa (ZAP-70)-deficient murine m

206 Such signals include membrane-associated proteins of the oligodendrocyte plasma membra

207 Here, we show MLL3/MLL4/PTIP-associated protein PAGR1 (also known as PA1) cooperates

208 associated with increased mitophagy and the associated protein Parkin.

209 44 to study the role of the receptor and its associated protein phosphatase 2A (PP2A) in macrophage a

210 Here, we report that SDE2, a PCNA-associated protein, plays a key role in maintaining acti

211 ne module, we identified plasmalemma vesicle-associated protein (PLVAP) as a protein amply expressed

212 ndency of TRF2-null ES cells on the telomere-associated protein POT1B and on the chromatin remodellin

213 The ribosome-associated protein quality control (RQC) system that res

214 We also discuss alterations of ribosome-associated proteins (RAPs), with a particular focus on t

215 raction between S18-2 and the retinoblastoma-associated protein (RB) and hypothesized that the simult

216 ile isomerase-binding to a separate, disease-associated protein region opposes aggregation.

217 an mitochondrial ribosome (mitoribosome) and associated proteins regulate the synthesis of 13 essenti

218 tein Neurobeachin-like (NBEAL) 1 as a Golgi- associated protein required for regulation of cholestero

219 es (against agrin, adipocyte plasma membrane-associated protein, Rho GDP-dissociation inhibitor 2 [AR

220 EM) to investigate the functions of two NPET-associated proteins, ribosomal protein uL4 and assembly

221 Signaling lymphocytic activation molecule-associated protein (SAP), a critical intracellular signa

222 ion, as well as insertion of the silicalemma-associated protein SAP1 into the SDVs.

223 ecovery after photobleaching of tagged Nexus-associated proteins showed that mobility in plaque domai

224 llar ataxia, autosomal recessive 20 (SCAR20)-associated protein Snx14, an endoplasmic reticulum (ER)-

225 Here we show that the RNA-associated protein Srrt/Ars2 sustains embryonic stem cel

226 ntified the serine threonine kinase receptor-associated protein (STRAP) as a putative spliceosome-ass

227 While ZO-1-associated proteins such as vinculin, connexin 43, N-cad

228 tio to PSD-95 of Transmembrane AMPA-Receptor-associated Proteins (TARPs), which mediate binding of AM

229 (C9orf72), progranulin (GRN) or microtubule-associated protein tau (MAPT) and their first-degree bio

230 horylation of target residues in microtubule-associated protein tau (MAPTAU) contributes to MAPTAU hy

231 primarily of hyperphosphorylated microtubule-associated protein tau (p-tau) and extracellular plaques

232 regates of Abeta peptide and the microtubule-associated protein tau are key molecular hallmarks of Al

233 The microtubule-associated protein tau has a central role in the pathoge

234 a) protein precedes and requires microtubule-associated protein tau in a sort of trigger-bullet mecha

235 The microtubule associated protein tau is another neuronal protein criti

236 urodegenerative diseases is tau (microtubule-associated protein tau), which can cause frontotemporal

237 diated by the phosphorylation of microtubule-associated protein tau.

238 hyperphosphorylated forms of the microtubule-associated protein tau.

239 not bind to any of the 5,300 human membrane-associated proteins tested.

240 Tau is a microtubule-associated protein that becomes dysregulated in a group

241 ified protein kinase C (PKC)zeta as a TRIM32-associated protein that contributes to the regulation of

242 finger protein 1 (CIZ1) is a nuclear matrix associated protein that facilitates a number of nuclear

243 d in textbooks so far, is a ribonucleocapsid-associated protein that interacts with P, thereby increa

244 er, our work suggests that PCARE is an actin-associated protein that interacts with WASF3 to regulate

245 Tau, a microtubule-associated protein that modifies the dynamic properties

246 Tau is a microtubule-associated protein that plays a major role in Alzheimer'

247 sferase PCAF (p300/CBP-associated) as a fork-associated protein that promotes fork degradation in BRC

248 n target of SC35 mAb is SRRM2, a spliceosome-associated protein that sharply localizes to NS.

249 abolished TG, suggesting the presence of MV-associated proteins that are essential for contact activ

250 gions, chromosomes are highly decorated with associated proteins that may block sliding.

251 ediating interactions with numerous membrane-associated proteins, they are key components in the esta

252 ipogenesis; decreased expression of invasion associated proteins through AMPK activation; and potenti

253 ution of ribosome heterogeneity and ribosome-associated proteins to the molecular control of proteome

254 NP) consisting of a dimeric viral genome and associated proteins, together constituting the viral cor

255 regulate gene expression, such as chromatin-associated proteins, transcription factors, and RNA-bind

256 erived cardiac fibroblasts based on YAP (yes-associated protein)-transcriptional enhanced associate d

257 e mechanosensitive transcription factors Yes-associated protein/Transcriptional coactivator with PDZ

258 ocardin-related transcription factor and Yes-associated protein/transcriptional coactivator with PDZ-

259 Studies of lysosome associated protein transmembrane 4B (LAPTM4B) have mainl

260 he relevance of spatial control in chromatin-associated protein ubiquitination and define a novel rol

261 by urokinase plasminogen activator receptor-associated protein (uPARAP or Endo180), which is also a

262 ed degradation of extracellular and membrane-associated proteins using conjugates that bind both a ce

263 e used to assess the expression levels of ER-associated proteins using immunohistochemistry (IHC).

264 egation of the amyotrophic lateral sclerosis-associated protein variant superoxide dismutase 1 (SOD1)

265 We show that integrin beta2 and its associated protein vinculin localize as distinct patches

266 The novel concept of Well-Associated Proteins (WAPs) introduced herein-gene produc

267 MURC, a plasma membrane-associated protein, was found to be more abundant in mus

268 ar vesicles containing endoplasmic reticulum-associated proteins, web-like adhesions between cultured

269 mitochondria nor abundance of mitochondrial associated proteins were affected by NR.

270 Mitophagy-associated proteins were sequentially recruited to depol

271 posed of core receptor proteins and receptor-associated proteins, which have profound effects on the

272 axis regulates the expression of cell cycle-associated proteins, which then inhibit EBV-associated t

273 ecies, and endoplasmic reticulum (ER) stress-associated proteins, which were attenuated by the coincu

274 ism, the innate immune system, and glutamate-associated proteins while simultaneously providing organ

275 uced apoptosis in the terminal ileum via Fas-associated protein with death domain protein repression

276 , block the interaction with coactivator yes-associated protein with nanomolar apparent IC(50) values

277 undamental role of FTO (fat mass and obesity-associated protein) within obesity; however, its functio

278 reconstituted with frataxin, indicated HS-1-associated protein X-1 (HAX-1) as the most significantly

279 vation of actin-dependent mechanosensors Yes-associated protein (YAP) and myocardin-related transcrip

280 lso activates the mechanically sensitive yes-associated protein (YAP) and promotes the excessive prol

281 ppo pathway transcriptional coactivators Yes-associated protein (YAP) and transcriptional coactivator

282 regulation of the downstream effectors, Yes-associated protein (YAP) and transcriptional coactivator

283 The paralogous transcriptional cofactors Yes-associated protein (YAP) and transcriptional coactivator

284 , this signature enriched for targets of Yes-associated protein (Yap) and transcriptional coactivator

285 Yes-associated protein (YAP) and transcriptional coactivator

286 the levels of the Hippo pathway effector Yes-associated protein (Yap) are sharply induced upon the ac

287 his study, we examined the regulation of yes-associated protein (YAP) localization, phosphorylation,

288 Yes-associated protein (YAP) signaling has emerged as a cruc

289 The Hippo-Yes-associated protein (YAP) signaling network plays a centr

290 phosphorylation but was independent from yes-associated protein (YAP) signaling.

291 ncreased transcriptional activity of the Yes-associated protein (YAP), a key downstream component of

292 f hepatocyte nuclear factor (Hnf)4alpha, Yes-associated protein (Yap), and transforming growth factor

293 osuppressive transcriptional coactivator Yes-associated protein (YAP), is critical for mechanotransdu

294 Yes-associated protein (YAP), the main transcriptional coact

295 nduction of transcriptional coactivator, Yes-associated protein (YAP), which is later degraded with a

296 ression of the transcriptional co-factor Yes-associated protein (Yap).

297 ent fibrosis in ADPKD as well as that of yes-associated protein (YAP).

298 tinal Wnt inhibition by Lats deletion is Yes-associated protein (YAP)/transcriptional activator with

299 ion of the Hippo pathway and increase in yes-associated protein (Yap1).

300 reased all-cause mortality, smoking, and age-associated proteins, yet multiple previous studies found