ライフサイエンスコーパス: RNA-binding protein

1 ces the AtRAP gene, which encodes a putative RNA binding protein.

2 ith nuclear inclusions or foci containing an RNA binding protein.

3 in, a ubiquitously expressed multifunctional RNA-binding protein.

4 igen B [SSB]) is an abundant multifunctional RNA-binding protein.

5 the LC domain of the fused in sarcoma (FUS) RNA-binding protein.

6 of FMR1, a conserved, ubiquitously expressed RNA-binding protein.

7 Enterococcus faecalis is a sequence-specific RNA-binding protein.

8 rized, abundantly and ubiquitously expressed RNA-binding protein.

9 conserved RNA structure to commandeer a host RNA-binding protein.

10 end 1 (Dnd1), a vertebrate-specific germline RNA-binding protein.

11 A-modified RNAs to low-complexity regions in RNA binding proteins.

12 ced genes, PES4 and MIP6, encoding predicted RNA binding proteins.

13 ble overlap in protein composition including RNA binding proteins.

14 all members of the hnRNP A and D families of RNA binding proteins.

15 yotic, membrane, toxic, and multisubunit DNA/RNA-binding proteins.

16 to cardiac disease, such as those involving RNA-binding proteins.

17 dramatically alters its affinity for cognate RNA-binding proteins.

18 those affecting binding of the PUF family of RNA-binding proteins.

19 m around the long non-coding RNA, Neat1, and RNA-binding proteins.

20 sets of RNA regulators such as microRNAs and RNA-binding proteins.

21 which resulted in reduction of intranuclear RNA-binding proteins.

22 of RNAs with functionally important cognate RNA-binding proteins.

23 a series of interconnected steps mediated by RNA-binding proteins.

24 t also more accurately predicts the DNA- and RNA-binding proteins.

25 onucleoprotein (hnRNP) I and AU-rich element RNA-binding protein 1 (AUF1), respectively, with an oppo

26 Musashi RNA-binding protein 2 (MSI2) has important roles in huma

27 In this syntenic group, the RNA-binding protein 28 (RBM28) was in closest proximity

28 d an in vitro system based on expressing the RNA binding protein 6 to obtain infectious metacyclics a

29 te amount of a binding motif for the quaking RNA binding protein, a sequence we show can significantl

30 The Musashi family of RNA binding proteins act to promote stem cell self-renew

31 he authors demonstrate that TDP-43 and other RNA-binding proteins act as chaperones to regulate the f

32 We find that the Apicomplexan-specific ALBA4 RNA-binding protein acts to regulate development of the

33 IRAV is an RNA binding protein and localizes to cytoplasmic process

34 served and highly dosage-sensitive family of RNA binding proteins and reveal unanticipated roles for

35 La/SS-B (or La) is a 48 kDa RNA-binding protein and an autoantigen in autoimmune dis

36 global Ub screen, we identified hnRNPA1, an RNA-binding protein and auxiliary splicing factor, as a

37 onal regulators, including expression of 110 RNA-binding proteins and 137 long non-coding RNAs, most

38 simonious regulatory model consisting of two RNA-binding proteins and four microRNAs that modulate th

39 ts have shown key interactions between these RNA-binding proteins and other regulatory elements, such

40 ge class of condensates that are enriched in RNA-binding proteins and RNA molecules.

41 Herein, we discuss various RNA-binding proteins and their unique contributions to f

42 ptional mechanisms including noncoding RNAs, RNA binding proteins, and mRNA decay-mediated control of

43 and micro RNA target sites, binding sites of RNA binding proteins, and N6-methyladenosine.

44 e the interactions between HuR, a ubiquitous RNA-binding protein, and Ago2, a core effector of the mi

45 ndent combinations of transcription factors, RNA-binding proteins, and long noncoding RNAs (lncRNAs).

46 RNA-binding proteins are key regulatory molecules involv

47 Many RNA-binding proteins are methylated, and we previously d

48 They also suggest that globally acting RNA-binding proteins are more common in bacteria than cu

49 Nanos RNA-binding proteins are required for germline developme

50 mental retardation autosomal homolog 1), an RNA-binding protein, are critical to maintain proper car

51 We identify the CsrA RNA binding protein as being responsible for this, and s

52 Our results highlight RNA-binding proteins as regulators of pathogenicity and

53 lts suggest potential involvement of HuR/TTP RNA binding protein axis in regulation of inflammation i

54 ter 2 h of hypoxic exposure might deactivate RNA-binding protein BRF1, hence resulting in the selecti

55 An RNA-binding protein called PABPC1 has an important role

56 in genes that encode ubiquitously expressed RNA-binding proteins cause tissue specific disease.

57 he gene encoding this ubiquitously expressed RNA binding protein causes a specific form of muscular d

58 The RNA binding protein Celf1 regulates alternative splicing

59 Reinduction of a nuclear RNA-binding protein CELF1 (CUGBP Elav-like family member

60 e Qbeta replication), a bacterial Lsm family RNA-binding protein, chaperones RNA-RNA interactions bet

61 oughout the organism, and the cold-inducible RNA-binding protein (CIRBP) is one of the mediators of t

62 ometry (IP-MS) and identified cold inducible RNA-binding protein (CIRP or hnRNP A18) as a telomerase-

63 Cold-inducible RNA-binding protein (CIRP), released into the circulatio

64 In this study, we show that the cytosolic RNA-binding protein clustered mitochondria homologue (CL

65 ding of how the altered splicing function of RNA-binding proteins contributes to myelodysplastic synd

66 use of age-dependent aggregation of Whi3, an RNA-binding protein controlling S-phase entry.

67 b1, but not Ccnb2, mRNAs is dependent on the RNA binding protein CPEB1.

68 nal control of GLUT1 mRNA is dependent of an RNA binding protein, CPEB1, and its binding elements in

69 Here we show that the RNA-binding protein CSDE1 (cold shock domain containing

70 ization of tumor suppressor activities of an RNA binding protein, CUGBP1.

71 We show that the germ cell-specific RNA-binding protein deleted in azoospermia-like (Dazl) i

72 Other RNA-binding proteins depend upon low-complexity regions

73 l opposing temporal gradients of Imp and Syp RNA-binding proteins (descending and ascending, respecti

74 We propose a mechanism whereby diverse RNA-binding proteins directly recruit PABP, in a non-pol

75 The vertebrate-conserved RNA-binding protein DND1 is required for the survival of

76 lative binding affinities of dozens of human RNA binding protein domains as reported in the CISBP-RNA

77 are particularly vulnerable to disruption of RNA-binding protein dosage and dynamics.

78 The double-stranded RNA-binding protein DRB4 of Arabidopsis was shown previo

79 ng for Dicer, Argonaute, and double-stranded RNA-binding proteins (dsRBP) as well as for proteins inv

80 mologs FASTKD1-5 are architecturally related RNA-binding proteins, each having a different function i

81 Biallelic loss-of-function mutations in the RNA-binding protein EIF4A3 cause Richieri-Costa-Pereira

82 We identified TDP-43, a DNA-RNA binding protein encoded by the Tardbp gene, as a str

83 nto ribonucleoprotein particles (RNPs) where RNA binding proteins ensure mRNA silencing and provide a

84 translation machinery and interacts with an RNA-binding protein, FMRP, to promote synapse formation;

85 Analysis of RNA-binding protein footprints revealed that G quadruple

86 tional and post-transcriptional processes by RNA-binding proteins for maintaining cellular identity a

87 isease-causing genes including SF3B1 and the RNA binding protein FUS.

88 RBPs TAR-DNA binding protein 43 (TDP-43) and RNA-binding protein FUS cause amyotrophic lateral sclero

89 The RNA-binding protein FUS participates in several RNA bios

90 Neuronal inclusions of aggregated RNA-binding protein fused in sarcoma (FUS) are hallmarks

91 Cytoplasmic inclusions of the RNA-binding protein fused in sarcoma (FUS) represent one

92 identified multiple long non-coding RNAs and RNA binding protein genes (DA376252, BX089737, LOC101927

93 ed interactions within a set of 14 conserved RNA binding protein genes, generating all possible singl

94 istribution of cytoplasmic PLK-1 couples two RNA-binding protein gradients, thereby partitioning the

95 Many RNA-binding proteins have been reported to play a functi

96 Lin28 RNA-binding proteins have evolutionarily conserved roles

97 RATIONALE: RBPs (RNA-binding proteins) have been described to be expresse

98 We identify the RNA-binding protein hnRNPK as the principal XR-PID bindi

99 ribonucleoprotein complex that involves the RNA-binding proteins HnrnpK and PCBP1 and regulates loca

100 Here we report that HRPU-2, an RNA-binding protein homologous to mammalian heterogeneou

101 ports overwhelmingly support the role of the RNA-binding protein Hu antigen R (HuR) as a positive reg

102 A well-studied RNA-binding protein Hu Antigen-R (HuR), controls post-tr

103 Here we show that a single RNA-binding protein, Hu antigen R (HuR), dictates transl

104 oneurons in vivo that SMN interacts with the RNA binding protein, HuD.

105 ECRG2, via RNA-binding protein human antigen R (HuR), regulated XIA

106 on RNAi or CRISPR approaches implicated the RNA binding protein HuR in preserving survival under nut

107 Here, using RNA-binding protein HuR conditional knock-out (KO) and w

108 The RNA-binding protein HuR functions to promote the stabili

109 The RNA-binding protein HuR regulates the stability and tran

110 rometry, we further uncovered binding of the RNA-binding protein HuR to the -44 region, where it acts

111 Ctn RNA shows enhanced interaction with the RNA-binding proteins HuR and PARN [Poly(A) specific ribo

112 neonatal-specific expression of an oncofetal RNA-binding protein, IGF2BP3, which prevented the destab

113 Using RiboTag immunoprecipitation, RNA binding protein immunoprecipitation, and luciferase

114 HuR is an RNA-binding protein implicated in immune homeostasis and

115 Here, we demonstrate that ASFV-DP is a novel RNA-binding protein implicated in the regulation of mRNA

116 itro icSHAPE measurements can reveal in vivo RNA-binding protein imprints or facilitate the dissectio

117 athways and is in part controlled by the HuR RNA binding protein in Jurkat T cells following activati

118 a rich genetic interaction landscape between RNA binding proteins in maintaining organismal health, a

119 Our findings define roles for the QKI RNA binding proteins in myelin development and maintenan

120 mes, exerting a non-canonical function as an RNA-binding protein in the translation of ER-destined mR

121 The ubiquitous expression of RNA-binding proteins in a wide variety of cell types and

122 scaffold molecules through interactions with RNA-binding proteins in chromatin remodeling complexes,

123 ompare the expression of splicing-regulatory RNA-binding proteins in human islets, brain, and other h

124 genetic mouse model to delete Quaking (QKI) RNA-binding proteins in oligodendrocytes, we identify QK

125 ost-transcriptional control by microRNAs and RNA-binding proteins in the cytoplasm.

126 tructures that comprise ribosomes, mRNA, and RNA binding proteins including Fragile X mental retardat

127 Many RNA-binding proteins including a master regulator of spl

128 ow that Zfp106 interacts with multiple other RNA binding proteins, including the ALS-associated facto

129 Mutations in RNA-binding proteins, including fused in sarcoma (FUS) a

130 Different sets of RNA-binding proteins interact with primary miRs (pri-miR

131 ggesting 4E-T nucleates a complex network of RNA-binding protein interactions.

132 lls, diverse stresses trigger coalescence of RNA-binding proteins into stress granules.

133 TDP-43 is a well known RNA binding protein involved in the pathogenesis of Amyo

134 ll restricted intracellular antigen-1) is an RNA-binding protein involved in splicing and translation

135 repeat (PPR) proteins are a large family of RNA-binding proteins involved in RNA metabolism in plant

136 maturely placed polyA tails by a specialized RNA-binding protein is a novel nucleic-acid-based survei

137 utcome of individual RNA contacts made by an RNA-binding protein is subject to extensive context-spec

138 ssential pentatricopeptide repeat-containing RNA binding protein, kinetoplast polyadenylation factor

139 CCUG repeats bind and sequester a family of RNA-binding proteins known as Muscleblind-like 1, 2, and

140 The cancer-associated RNA-binding protein La is posttranslationally modified b

141 The RNA binding protein, LARP1, has been proposed to functio

142 ntaining RNA forms aggregates that sequester RNA binding proteins, leading to altered RNA metabolism

143 rmed by elongated DMPK transcripts sequester RNA-binding proteins, leading to mis-splicing of numerou

144 The aggregation and mislocalization of RNA-binding proteins leads to the aberrant regulation of

145 enhancer region of these genes by binding to RNA-binding protein Matrin 3 that, in turn, associates w

146 We show that the RNA-binding protein, ME31B, binds to and represses the e

147 hat governs breast cancer metastasis through RNA-binding protein-mediated transcript stabilization.

148 etric division of the C. elegans zygote, the RNA-binding protein MEX-5 forms an anterior-rich cytopla

149 We found that expression of the RNA-binding protein Mex3a labels a slowly cycling subpop

150 tro data but indicated that a so far unknown RNA binding protein might exist in B. subtilis that can

151 e of transcription, by the YTH domain of the RNA-binding protein Mmi1 and degraded by the nuclear exo

152 wth by the combined action of the YTH-family RNA-binding protein Mmi1 and the nuclear exosome.

153 A "trigger" sequence, creating a regulatable RNA-binding protein motif that retains its functional ac

154 In summary, the RNA-binding protein Msi1 competes with miR130a and -206

155 1 and revealed the clinical relevance of the RNA-binding protein MSI2 in breast cancer.

156 The RNA-binding protein Musashi-1 (MSI1) exerts essential ro

157 Here we report that the neural RNA-binding protein Musashi-1 (MSI1) interacts with the

158 Here we show that overexpression of the RNA-binding protein Musashi-2 (MSI2) induces multiple pr

159 The conserved RNA-binding protein Musashi1 (MSI1) has been characteriz

160 The repeat transcripts sequester the RNA binding protein Muscleblind-like protein 1 (MBNL1) a

161 it to gain insight into the function of the RNA-binding protein Nab3.

162 Knockdown of translation of the RNA-binding protein Nanos2 by morpholino antisense oligo

163 roglia, regulated in part by neuron-specific RNA-binding proteins NOVA2 and PTBP2.

164 RNA-binding proteins of the Musashi (Msi) have been impl

165 RNA-binding proteins of the ZFP36 family are best known

166 e 3'UTRome as binding sites for microRNAs or RNA binding proteins, or during alternative polyadenylat

167 rast, the amyloid-like state of the neuronal RNA binding protein Orb2 in Drosophila was recently impl

168 Downregulation of oo18 RNA-binding proteins (ORBs) in any of these MBONs impair

169 Polyadenosine RNA-binding proteins (Pabs) regulate multiple steps in g

170 RNA-binding proteins play a key role in post-transcripti

171 RNA-binding proteins play a key role in shaping gene exp

172 rmed by specific recognition between RNA and RNA-binding proteins play an important role in biologica

173 RNA-binding proteins play central roles in RNA regulatio

174 Rbfox RNA-binding proteins play important roles in the regulat

175 Liquid-liquid phase separation (LLPS) of RNA-binding proteins plays an important role in the form

176 or-rich cytoplasmic gradient that causes the RNA-binding protein POS-1 to form an opposing, posterior

177 FMRP is a RNA-binding protein predominantly resident in cytoplasm.

178 We find that RBM38, an erythroid-specific RNA-binding protein previously implicated in splicing, i

179 Here we have shown that the RNA-binding protein PSPC1, a component of the paraspeckl

180 igration, which requires the Pumilio-related RNA-binding protein Puf118.

181 genetic studies have identified the neuronal RNA binding protein, Rbfox1, as a candidate gene for aut

182 s a model system that SMN interacts with the RNA binding protein (RBP) HuD in motoneurons in vivo dur

183 mes, allowing identification of differential RNA binding protein (RBP) recognition sites.

184 wing Sarcoma protein (EWS) is a multifaceted RNA binding protein (RBP) with established roles in tran

185 We have previously shown that the RNA-binding protein (RBP) CUG-BP1 is overexpressed in es

186 ucleoprotein A1 (hnRNP A1) is a multipurpose RNA-binding protein (RBP) involved in normal and patholo

187 ry elements that are controlled by the viral RNA-binding protein (RBP) NS1.

188 ry-Protein 1 (Esrp1) is a cell-type specific RNA-binding protein (RBP) that is essential for mammalia

189 HCC samples revealed that a large numbers of RNA binding proteins (RBPs) are dysregulated and that RB

190 Recent data has recognized the importance of RNA binding proteins (RBPs) in DNA damage repair (DDR) p

191 consistently with binding sites of the same RNA binding proteins (RBPs) or (2) are transcribed in co

192 RNA binding proteins (RBPs) play important roles in post

193 RNA binding proteins (RBPs) provide one mechanism for mo

194 RNA binding proteins (RBPs) regulate the lives of all RN

195 RNA binding proteins (RBPs), in turn, are important regu

196 rsity in adult neurons is partly mediated by RNA binding proteins (RBPs), including the RBFOX factors

197 a role for tau in regulating the biology of RNA binding proteins (RBPs).

198 RNA-binding proteins (RBPs) acting at various steps in t

199 olves nuclear retention of expansion RNAs by RNA-binding proteins (RBPs) and an acute phase in which

200 ) granules are enriched in specific RNAs and RNA-binding proteins (RBPs) and mediate critical cellula

201 ukaryotic mRNA decay is tightly modulated by RNA-binding proteins (RBPs) and microRNAs (miRNAs).

202 RNA-binding proteins (RBPs) are important regulators of

203 RNA-binding proteins (RBPs) are involved in mRNA splicin

204 RNA-binding proteins (RBPs) are pivotal in orchestrating

205 We extend our technology to yeast RNA-binding proteins (RBPs) by tracking their propensity

206 heir association with microRNAs (miRNAs) and RNA-binding proteins (RBPs) can influence gene expressio

207 RNA-binding proteins (RBPs) control the fate of nearly e

208 MicroRNAs (miRNAs) and RNA-binding proteins (RBPs) critically regulate gene exp

209 g, in a proteome-wide manner, the regions of RNA-binding proteins (RBPs) engaged in native interactio

210 RNA-binding proteins (RBPs) have emerged as important re

211 The mammalian MSI family of RNA-binding proteins (RBPs) have important roles as onco

212 Characterizing the binding behaviors of RNA-binding proteins (RBPs) is important for understandi

213 MZT, post-transcriptional gene regulation by RNA-binding proteins (RBPs) is the dominant force in emb

214 Collaboration among the multitude of RNA-binding proteins (RBPs) is ubiquitous, yet our under

215 RNA-binding proteins (RBPs) play a critical role in the

216 The identity of the RNA-binding proteins (RBPs) that govern cancer stem cell

217 monstrate that regulation of the affinity of RNA-binding proteins (RBPs) to export receptors along wi

218 e show that in developing B lymphocytes, the RNA-binding proteins (RBPs) ZFP36L1 and ZFP36L2 are crit

219 RNA-binding proteins (RBPs), in addition to their functi

220 by an expanding, yet incomplete, catalog of RNA-binding proteins (RBPs), many of which lack characte

221 ranule marker ROX8 and additional endogenous RNA-binding proteins (RBPs), suggesting that these patho

222 ealed that motor-neuron disease (MND)-linked RNA-binding proteins (RBPs), TDP-43, FUS, and hnRNPA2B1,

223 ed by multiple regulatory factors, including RNA-binding proteins (RBPs), that bind to specific RNA s

224 ounding member of the conserved family of Hu RNA-binding proteins (RBPs), which play crucial and dive

225 Here, we describe four conserved RNA-binding proteins (RBPs)-PUF-8, MEX-3, GLD-1, and CGH

226 tionally regulated by cellular microRNAs and RNA-binding proteins (RBPs).

227 through influencing their interactions with RNA-binding proteins (RBPs).

228 ites on RNAs that are in direct contact with RNA-binding proteins (RBPs).

229 ST-trAnscriptional Regulation coordinated by RNA-binding proteins (RBPs).

230 RNA transcripts are bound and regulated by RNA-binding proteins (RBPs).

231 lation via interactions of G4 with potential RNA-binding proteins (RBPs).

232 ure human circRNA is associated with diverse RNA binding proteins reflecting its endogenous splicing

233 igned using a new dataset with both DNA- and RNA-binding proteins, regression that penalizes cross-pr

234 e demonstrate that the levels of Imp and Syp RNA-binding proteins regulate NB decommissioning.

235 How methylation of specific RNA-binding proteins regulates RNA granule assembly has

236 The functions of many bacterial RNA-binding proteins remain obscure because of a lack of

237 of mRNA-specific translational activation by RNA-binding proteins remain poorly understood.

238 Neuronal protein 3.1 (P311), a conserved RNA-binding protein, represents the first documented pro

239 RNA binding proteins required for the maintenance of mye

240 The protein kinase Ime2 and RNA binding protein Rim4 are general regulators of meiot

241 The aim of this study was to examine RNA binding protein (RNABP) HuR/TTP axis in endometriosi

242 ol, operating post-transcriptionally via the RNA-binding proteins RsmA, RsmE and RsmI, is unraveled.

243 We found that the RNA- binding protein Sam68 (Khdrbs1) is strongly express

244 y retained introns are enriched for specific RNA binding protein sites and are often retained in clus

245 regulatory networks, via conserved miRNA and RNA binding protein sites.

246 Absence of SR-like RNA-binding protein Slr1 slows hyphal formation and decr

247 alize to all RNA-protein interaction as some RNA binding proteins specifically recognize more complex

248 First, we find that two RNA-binding proteins specifically expressed in germ cell

249 7SL1, an endogenous RNA normally shielded by RNA binding proteins SRP9/14.

250 Moreover, UPF1 and its interaction with the RNA binding protein STAU2 are necessary for proper trans

251 s, and are linked neuropathologically by the RNA binding protein TDP-43 (TAR DNA binding protein-43 k

252 all patients with ALS have aggregates of the RNA-binding protein TDP-43 in their brains and spinal co

253 s exhibit aberrant localization of a nuclear RNA binding protein, TDP-43, into cytoplasmic aggregates

254 Defects in the RNA-binding protein, TDP-43, are known to cause a variet

255 Carbon Storage Regulator A (CsrA) is an RNA binding protein that acts as a global regulator of d

256 we identified Musashi2 (MSI2), an oncogenic RNA binding protein that is required for blast crisis CM

257 fied a neural progenitor cell (NPC)-specific RNA binding protein that may underlie the high levels of

258 ntigen R (HuR) and Tristetraprolin (TTP) are RNA binding proteins that competitively bind to cytokine

259 Defining the interplay between RNA binding proteins that couple mRNA biogenesis events

260 We have also identified a range of RNA binding proteins that recognize the loop of miR-132

261 is a highly conserved and essential DNA- and RNA-binding protein that controls gene expression throug

262 RBM10 is an RNA-binding protein that plays an essential role in deve

263 The Human antigen R protein (HuR) is an RNA-binding protein that recognizes U/AU-rich elements i

264 gile X mental retardation protein (FMRP), an RNA-binding protein that regulates local protein transla

265 Yeast Ssd1 is an RNA-binding protein that shuttles between the nucleus an

266 opoiesis and that enrich for target sites of RNA-binding proteins that are specific to hematopoietic

267 d by effector proteins that are recruited by RNA-binding proteins that bind to 3'-UTR cis-elements.

268 ucleoproteins (hnRNP) form a large family of RNA-binding proteins that exert numerous functions in RN

269 Also, novel putative DNA/RNA-binding proteins that it predicts share similar subc

270 tory protein 1 (IRP1) belongs to a family of RNA-binding proteins that modulate metazoan iron metabol

271 eoprotein U (hnRNP U) belongs to a family of RNA-binding proteins that play important roles in contro

272 This removal is controlled in part by RNA-binding proteins that regulate alternative splicing

273 ectrometry identified numerous non-canonical RNA-binding proteins that stabilize ribozyme folding; th

274 stic insight into RNA networks controlled by RNA-binding proteins that underlie self-renewal and prov

275 )A 'writer'), not only specifically bound by RNA-binding proteins (the m(6)A 'readers'), but also rem

276 ces of altering the levels of this important RNA-binding protein through the analysis of cardiac-spec

277 repeat) domain-containing-2 (nhl-2), encode RNA-binding proteins, thus delineating a previously unkn

278 , including stress granules that contain the RNA binding protein Tia1.

279 inhibit the binding of human antigen R (HuR) RNA-binding protein to tumor necrosis factor-alpha mRNA.

280 otein-modifying enzymes, receptors, ligands, RNA-binding proteins, transcription factors and co-facto

281 endent diffusion of transactivation response RNA binding protein (TRBP) on dsRNA, yet the mechanistic

282 Human Dicer associates with HIV TAR RNA-binding protein (TRBP) or protein activator of PKR (

283 rylation of the RNA-silencing factor HIV TAR-RNA-binding protein (TRBP) promotes binding and stabiliz

284 Transactivation response element RNA-binding protein (TRBP; TARBP2) is known to play impo

285 We have identified the RNA-binding protein Tristetraprolin (TTP) as a negative

286 he reversed balance in the expression of the RNA-binding proteins tristetraprolin (TTP, ZFP36) and Hu

287 otein 1 (PABPN1) is a ubiquitously expressed RNA binding protein vital for multiple steps in RNA meta

288 e discovered a novel function for MYF5 as an RNA-binding protein which associated with a subset of my

289 TRs have enriched binding motifs for several RNA-binding proteins, which implies extensive translatio

290 XR1P) is a member of the fragile X family of RNA-binding proteins, which includes FMRP and FXR2P.

291 Human antigen (Hu) R is an RNA-binding protein whose overexpression in human cancer

292 Thus, these studies identify Zfp106 as an RNA binding protein with important implications for ALS.

293 -induced protein 1 (MCPIP1) is a zinc-finger RNA binding protein with important roles in mediating in

294 We show that ProQ is an abundant RNA-binding protein with a wide range of ligands and a g

295 ultiple neurite-targeted non-coding RNAs and RNA-binding proteins with potential regulatory roles.

296 Our results indicate that the RNA-binding protein YBX1, which is required for the sort

297 and knockdown approaches, we find that Xist RNA-binding proteins, YY1 and hnRNPU, are critical for r

298 codes a ubiquitously expressed polyadenosine RNA-binding protein, ZC3H14 (Zinc finger CysCysCysHis do

299 We identified the RNA-binding protein Zfp36l1 as an FXR target gene and de

300 amic actin cytoskeleton, and the transacting RNA-binding protein, Zipcode-binding protein 1 (ZBP1).