ライフサイエンスコーパス: RNA-binding protein

1 ified as binding sites for NC, a Gag-derived RNA-binding protein.

2 omere protein F) and the regulatory Staufen1 RNA-binding protein.

3 omal homologue-1 (FXR1) is a muscle-enriched RNA-binding protein.

4 show that ZC3H5 is an essential cytoplasmic RNA-binding protein.

5 ieving multivalency and can accommodate many RNA binding proteins.

6 ed decay-determinant exons in genes encoding RNA binding proteins.

7 ransferases, ribosomal components, and polyA RNA binding proteins.

8 nscripts, making them responsive to the same RNA binding proteins.

9 kets and binding RNAs for previously unknown RNA binding proteins.

10 icles (RNPs), complexes containing mRNAs and RNA binding proteins.

11 39 cassette exons enriched in genes encoding RNA binding proteins.

12 rough the targeting of selectively essential RNA binding proteins.

13 e method's wide applicability in identifying RNA-binding proteins.

14 tion of similar mechanisms governed by other RNA-binding proteins.

15 d caps, as well as through sequence-specific RNA-binding proteins.

16 HUA-PEP activity, composed of genes encoding RNA-binding proteins.

17 ce of mRNA leaders that use riboswitches and RNA-binding proteins.

18 S directly alters intron retention levels in RNA-binding proteins.

19 ociated proteins, transcription factors, and RNA-binding proteins.

20 low-complexity regions from self-associating RNA-binding proteins.

21 , and occupancy by transcription factors and RNA-binding proteins.

22 have been dedicated to the identification of RNA-binding proteins.

23 action of nuclear encoded ribonucleases and RNA-binding proteins.

24 ed by the conserved trypanosomatid ZC3H39/40 RNA-binding proteins.

25 on the crosstalk between cell signaling and RNA-binding proteins.

26 identify and characterize a conserved SMALL RNA-BINDING PROTEIN 1 (SRBP1) family that mediates non-c

27 he m6A reader protein YTH N6-methyladenosine RNA binding protein 2 (YTHDF2) promotes mRNA decay durin

28 repetitive RNA, which negatively sequesters RNA-binding proteins(5) before its non-canonical transla

29 le X mental retardation protein (FMRP) is an RNA-binding protein abundant in the nervous system.

30 activity for the Drosophila Argonaute family RNA-binding protein AGO1, a component of the miRNA-depen

31 DEAH-box RNA helicase Mtr4 together with an RNA-binding protein (Air1 or Air2) and a poly(A) polymer

32 s containing the fragile X related family of RNA binding proteins along with ribosomes and specific m

33 s and low-complexity protein domains such as RNA-binding proteins also accumulate around sites of tra

34 Arabidopsis, AtSRBP1 is a glycine-rich (GR) RNA-binding protein, also known as AtGRP7, which we show

35 Tristetraprolin (TTP) is an RNA-binding protein and an essential factor of posttrans

36 Although an established RNA-binding protein and histone methyltransferase, EZH2

37 MAARS interacts with HuR/ELAVL1, an RNA-binding protein and important regulator of apoptosis

38 Here we demonstrate that the APUM9 RNA-binding protein and its co-factors play a role in mR

39 targets of La-related protein 1 (LARP1), an RNA-binding protein and mTORC1 effector that has been sh

40 les (MLOs), which majorly consist of RNA and RNA-binding proteins and are formed via liquid-liquid ph

41 mpetition for binding sites among protective RNA-binding proteins and decay factors, PTBP1 promotes d

42 virus-derived sfRNAs interact with cellular RNA-binding proteins and highlight the potential for wid

43 ay, which measures interactions between host RNA-binding proteins and incoming viral RNA, we show tha

44 Consequently, RNA-binding proteins and mRNA-encoded sequence elements

45 ented by low-complexity regions from certain RNA-binding proteins and proteins that form condensates

46 in-29/Zn finger transcription factor, lin-28/RNA binding protein, and the let-7miRNA gene all disrupt

47 FUS is a nuclear RNA-binding protein, and its cytoplasmic aggregation is

48 ite excitement around ProQ as a novel global RNA-binding protein, and its potential to serve as a mat

49 on the p53-inducible gene Zmat3, encoding an RNA-binding protein, and we demonstrate that ZMAT3 is an

50 ptionally stabilized by interacting with the RNA-binding protein ApELAV.

51 We find that mRNAs for pumilio RNA-binding proteins are abundant in synaptic regions, w

52 Yet, the roles of many RNA-binding proteins are not understood.

53 Neuronal splicing programs controlled by RNA-binding proteins, are influenced by chromatin modifi

54 ptionally and how they usurp and modify host RNA binding proteins as well as microRNAs to potentiate

55 tudy in Arabidopsis that employed a designer RNA-binding protein as a psbA RNA affinity tag.

56 are degraded by the proteasome, we uncovered RNA-binding proteins as high-confidence substrates that

57 we identify the Trypanosoma brucei ZC3H39/40 RNA-binding proteins as regulators of the respiratome; t

58 nger 1, encoding a processing body localized RNA-binding protein, as a direct target repressed by PRR

59 We could validate RBMS1, a barely described RNA-binding protein, as a new target gene for oncogenic

60 mphocytes expressed Lin28b, which encodes an RNA-binding protein associated with fetal hematopoietic

61 recruited in phase-separated forms of human RNA-binding proteins associated with SG formation.

62 captures global structural features, such as RNA-binding-protein binding sites and reactivity differe

63 Release factor homolog C12orf65 (mtRF-R) and RNA binding protein C6orf203 (MTRES1) eject the nascent

64 LS) and frontotemporal dementia (FTD)-linked RNA-binding protein called FUS (fused in sarcoma) has be

65 establish that non-amyloid self-assembly of RNA-binding proteins can drive a form of epigenetics bey

66 s that RsmA associates with and that the two RNA-binding proteins can exert regulatory effects on com

67 nonclassical NLSs within the cold-inducible RNA-binding protein (CIRBP).

68 Extracellular cold-inducible RNA-binding protein (CIRP) exaggerates inflammation and

69 A growing body of evidence indicates that RNA binding proteins control an array of processes in be

70 Deleted in azoospermia-like (DAZL) is an RNA-binding protein critical for gamete development.

71 ibonuclear protein K (hnRNPK) is an abundant RNA-binding protein crucial for a wide variety of biolog

72 ore, our results showed increased binding of RNA-binding protein CUGBP1 with occludin and E-cadherin

73 Aggregates of a prion-like RNA-binding protein, cytoplasmic polyadenylation element

74 recruiting aggregates, stress granules, and RNA-binding proteins, directing their elimination and as

75 mice homozygous for the Ter mutation in the RNA-binding protein Dnd1 (Dnd1(Ter/Ter) ), many male ger

76 ins, suggesting a feedback between effective RNA-binding protein dosage and protein quality control i

77 Specific interactions of MYC-sensitive RNA-binding proteins (e.g., SRSF1/RBM42) with 5'UTR sequ

78 Extracellular cold-inducible RNA-binding protein (eCIRP) is a damage-associated molec

79 Here, we show that three ELAV/Hu RNA binding proteins (Elav, Rbp9, and Fne) have similar

80 on of a newly synthesized mRNA by a class of RNA binding proteins (ELAVs).

81 s of human and mouse NMD targets, especially RNA-binding proteins, encode potential Split-ORFs, some

82 Tristetraprolin (TTP), an RNA-binding protein encoded by the ZFP36 gene, is vital

83 CRISPR knockout of LIN28B-an oncofetal RNA-binding protein exerting diverse effects via negativ

84 We find that two PUF family RNA-binding proteins FBF-1 and FBF-2 have opposite effec

85 This motif binds the RNA binding protein FMR1 and directs miRNA loading into

86 Loss of the RNA binding protein FMRP causes Fragile X Syndrome (FXS)

87 La-related protein 6 (Larp6) is a conserved RNA-binding protein found across eukaryotes that has bee

88 We demonstrate how RNA binding protein FOX-1 functions as a dose-dependent

89 e 1 (TAK1) variable exon 12 requires another RNA-binding protein, Fox-1 homolog 2 (Rbfox2), which bin

90 ragile X syndrome results from a loss of the RNA-binding protein fragile X mental retardation protein

91 The RNA-binding protein fragile-X mental retardation autosom

92 RNA-binding motif protein 10 (RBM10) is an RNA-binding protein frequently deleted or mutated in lun

93 SERBP1 is the first example of an RNA-binding protein functioning as a central regulator o

94 Mutations in the RNA-binding protein FUS cause amyotrophic lateral sclero

95 Dysregulation of the DNA/RNA-binding protein FUS causes certain subtypes of ALS/F

96 es, such as the 214-residue LC domain of the RNA-binding protein FUS, is particularly intriguing from

97 The RNA-binding protein fused in sarcoma (FUS) can form path

98 Mutations in the RNA-binding protein Fused in Sarcoma (FUS) cause early-o

99 The RNA-binding protein fused in sarcoma (FUS) forms physiol

100 gile X mental retardation protein (FMRP), an RNA-binding protein, has previously been shown to affect

101 targets, and signaling circuitry surrounding RNA-binding proteins have become better understood, in p

102 Many proteins, such as RNA-binding proteins, have complex folding landscapes.

103 by small RNAs in Escherichia coli depends on RNA binding proteins Hfq and ProQ, which bind mostly dis

104 We discovered a role for the RNA binding protein hnRNP H in methamphetamine reward an

105 or pathologically associated with tau (e.g. RNA binding protein HNRNPA1).

106 Among these, LC/MS analysis identified the RNA binding protein, HNRNPD.

107 We additionally show that the related RNA-binding proteins hnRNPF and hnRNPH bind directly to

108 P1 family proteins have long been considered RNA-binding proteins, however, our results identified 40

109 Lastly, we demonstrate that the neuronal RNA-binding protein HuD binds to circHomer1a and can inf

110 Here, we report that the RNA-binding protein HuR (ELAVL1) forms complexes with NA

111 Here, we investigated the role of RNA-binding protein HuR (human antigen R) in the posttra

112 iting p53 protein synthesis by degrading the RNA-binding protein HuR in response to UV radiation.

113 igated the cell-intrinsic processes by which RNA-binding protein HuR orchestrates Th17 cell fate deci

114 umanized livers through its interaction with RNA-binding protein HuR.

115 Here, we report the identification of the RNA-binding protein HuR/ELAVL1 as a central oncogenic dr

116 In this study, we used TRIBE (targets of RNA-binding proteins identified by editing) as an approa

117 n the cytoplasm, where it interacts with the RNA binding protein IGF2BP2/IMP2, facilitating its bindi

118 tion using a combination of transcriptomics, RNA-binding protein immunoprecipitation, CRISPR-mediated

119 asts) are controlled by the highly conserved RNA binding protein Imp (IGF2BP), via one of its top bin

120 e, we report that follicle cells lacking the RNA-binding protein IMP go through one extra division ow

121 Opposing gradients of two RNA-binding proteins Imp and Syp comprise the intrinsic

122 in sarcoma (FUS) is a ubiquitously expressed RNA-binding protein implicated in familial ALS and front

123 AD-box family of proteins are ATP-dependent, RNA-binding proteins implicated in many aspects of RNA m

124 es in RNA expression and the central role of RNA binding proteins in preserving neuronal integrity.

125 We highlight the role of RNA binding proteins in shaping selective translational

126 eserved expression patterns of the targeting RNA binding proteins in subsets of germ cells-suggest th

127 ntly, ProQ has been shown to act as a global RNA-binding protein in Salmonella and Escherichia coli,

128 ding to a toxic protein or RNA binding to an RNA-binding protein in the case of liquid-liquid phase s

129 les in pathological hypertrophy, the role of RNA-binding protein in this process has received little

130 RNAs, and that they bound a diverse array of RNA binding proteins, including p300 but not CBP.

131 On a diverse set of challenging RNA-binding proteins, including Fem-3-binding-factor 2,

132 7 biogenesis is tightly regulated by several RNA-binding proteins, including Lin28A/B, which represse

133 factor receptor A (PDGFRA), as well as novel RNA-binding protein interactors ZC3H14 (zinc finger CCCH

134 e fragile X protein family consists of three RNA-binding proteins involved in translational regulatio

135 genome-wide detection of in vivo binding of RNA-binding proteins is greatly facilitated by the enhan

136 The Musashi family of RNA-binding proteins is known for its role in stem-cell

137 8 (also known as Lin28A), a highly conserved RNA-binding protein, is associated with PVT1-214.

138 RNA-binding proteins like human antigen R (HuR) are key

139 ght the exquisite specificity that conserved RNA-binding proteins like RBM24 mediate in the post-tran

140 lel to let-7-family microRNAs, the conserved RNA-binding protein LIN-28 and its downstream gene lin-4

141 n-29a, and of HBL-1 for lin-29b, whereas the RNA-binding protein LIN-28 coordinates LIN-29 isoform ac

142 The RNA-binding protein LIN28 controls progenitor and neuron

143 Here, we demonstrate that the RNA binding protein LIN28B plays an important role in th

144 proteomic analyses, we demonstrate that the RNA-binding protein LIN28B, which is developmentally exp

145 lls (HSPCs) caused by high expression of the RNA-binding protein Lin28b.

146 y describes an unexpected mechanism by which RNA-binding protein, MBNL1, activity is inhibited in hyp

147 d that three maternally deposited Drosophila RNA-binding proteins (ME31B, Trailer Hitch [TRAL], and C

148 cing, RNA editing, nuclear pore composition, RNA-binding protein motif enrichment, and RNA secondary

149 Ssd1 and another RNA-binding protein, Mpt5 (Puf5), have parallel roles in

150 Recently, the RNA-binding protein Musashi-1 (Msi1), which mediates the

151 From this screen, we identified an RNA binding protein, Musashi (msi), as one of the possib

152 Evolutionarily conserved RNA-binding protein Musashi1 (Msi1) can regulate develop

153 e assembly requires NEAT1 recruitment of the RNA-binding protein NONO, however the NEAT1 elements res

154 Blocking PKR using PKR-K296R, the TAR RNA binding protein or PKR-KO cells, reduces RAN protein

155 evidence that it specifically interacts with RNA-binding proteins or mRNA.

156 tion specificity factor, as well as by other RNA-binding proteins, particularly splicing factors.

157 This is of interest considering RNA binding proteins play key roles in post-transcriptio

158 Consequently, RNA-binding proteins play a critical role in the regulat

159 y expressed gene 3 (Meg3) interacts with the RNA binding protein polypyrimidine tract binding protein

160 to the canonical CBP20-CBP80 CBC, and/or an RNA-binding protein - possibly in association with the e

161 To identify RNA binding proteins potentially driving these patterns,

162 Hfq is an RNA-binding protein present in diverse bacterial lineage

163 cytes to functional neurons by depleting the RNA-binding protein PTB (also known as PTBP1).

164 eracting this mechanism, the multifunctional RNA-binding protein PTBP1 regulates the balance of short

165 The sequence-specific RNA-binding proteins PTBP1 (polypyrimidine tract-binding

166 Here we show that the Xist RNA-binding proteins PTBP1(9), MATR3(10), TDP-43(11) and

167 cepts through experimental examples with the RNA-binding protein Puf4.

168 5AS interfered with interactions between the RNA-binding protein Raly and the CCR5 3' untranslated re

169 We focused on two RNA-binding proteins, RALY and hnRNP-C, which we confirm

170 regulation of a non-muscle splice isoform of RNA-binding protein RBFOX2 in DM1 heart tissue-due to al

171 sible to detect the binding peaks of a given RNA binding protein (RBP) at transcriptome scale.

172 a from our lab implicate autoimmunity to the RNA binding protein (RBP) heterogeneous nuclear ribonucl

173 translation of distinct mRNA isoforms of the RNA binding protein (RBP), Elavl4, in radial glia progen

174 Computational prediction of RNA binding proteins (RBP) motifs and UV-cross-linking a

175 ulated during development through changes in RNA-binding protein (RBP) activities.

176 imidine tract-binding protein 1 (PTBP1) is a RNA-binding protein (RBP) expressed throughout B cell de

177 etween the oncogenic microRNA miR-21 and the RNA-binding protein (RBP) human antigen R (HuR) in respo

178 constrained, and enriched for cis-eQTLs and RNA-binding protein (RBP) interactions.

179 tified that La-related protein 4 (LARP4), an RNA-binding protein (RBP) known to enhance mRNA stabilit

180 Here we report that the RNA-binding protein (RBP) nucleolin, which interacts wit

181 Predicting RNA-binding protein (RBP) specificity is important for u

182 with MEF2C mRNA and the presence of HuR, an RNA-binding protein (RBP) with affinity for both transcr

183 Recent studies suggest that the RNA-binding protein (RBP) ZMAT3 is important in mediatin

184 RNA-binding protein (RBP)/helicase DDX3 (DEAD-box helica

185 as9 (dCas9)-based CARRY (CRISPR-assisted RNA-RNA-binding protein [RBP] yeast) two-hybrid assay to ass

186 resent evidence that the rice (Oryza sativa) RNA-binding protein, RBP-L, like its interacting RBP-P p

187 RNA binding proteins (RBPs) are a large protein family t

188 The crosslinked RNA binding proteins (RBPs) are purified by solid-phase

189 RNA binding proteins (RBPs) are the primary gene regulat

190 RNA binding proteins (RBPs) frequently regulate the expr

191 egulatory RNA motifs in human transcripts by RNA binding proteins (RBPs) is essential for gene regula

192 The cell-context dependency for RNA binding proteins (RBPs) mediated control of stem cel

193 to study the in vivo regulatory networks of RNA binding proteins (RBPs).

194 a highly interconnected network enriched in RNA-binding proteins (RBPs) and EV cargoes.

195 RNA-binding proteins (RBPs) and long non-coding RNAs (ln

196 ybrid screen for interactions between murine RNA-binding proteins (RBPs) and motor proteins, here we

197 Interactions between RNA-binding proteins (RBPs) and RNAs are critical to cel

198 ce of a standard TRIzol extraction to enrich RNA-binding proteins (RBPs) and their cognate bound RNA.

199 RNA-binding proteins (RBPs) are essential modulators of

200 RNA-binding proteins (RBPs) are key mediators of RNA met

201 Identifying binding targets of RNA-binding proteins (RBPs) can greatly facilitate our u

202 RNA-binding proteins (RBPs) comprise a large class of ov

203 Engineering of functionalized RNA-binding proteins (RBPs) could therefore have many ap

204 RNA-binding proteins (RBPs) function as master regulator

205 Advances in high-throughput profiling of RNA-binding proteins (RBPs) have resulted inCLIP-seq dat

206 using mouse models, we explored the role of RNA-binding proteins (RBPs) in regulation of the biologi

207 a role for neurodegenerative disease-linked RNA-binding proteins (RBPs) in the cellular stress respo

208 Oligomeric assemblies of tau and the RNA-binding proteins (RBPs) Musashi (MSI) are reported i

209 ng the interaction mechanism and location of RNA-binding proteins (RBPs) on RNA is critical for under

210 RNA-binding proteins (RBPs) play crucial roles in almost

211 RNA-binding proteins (RBPs) play key roles in post-trans

212 RNA-binding proteins (RBPs) regulate RNA metabolism at m

213 The molecular functions of the majority of RNA-binding proteins (RBPs) remain unclear, highlighting

214 mediated mRNA decay and associate with major RNA-binding proteins (RBPs) such as Hfq and ProQ.

215 Here, we uncover a network of RNA-binding proteins (RBPs) that enhances the translatio

216 ng individual guide RNAs (gRNA), we identify RNA-binding proteins (RBPs) that influence the formation

217 These pathways include a plethora of RNA-binding proteins (RBPs) that modulate all steps of t

218 zinc finger (TZF) domains are found in many RNA-binding proteins (RBPs) that regulate the essential

219 ional elements in Xist RNA, their associated RNA-binding proteins (RBPs), and the downstream pathways

220 s in the human genome that are recognized by RNA-binding proteins (RBPs), generated as part of the En

221 s are capable of hijacking the expression of RNA-binding proteins (RBPs), leading to dysfunctional ge

222 The human genome encodes for over 1,500 RNA-binding proteins (RBPs), which coordinate regulatory

223 cytoplasmic condensates are rich in RNA and RNA-binding proteins (RBPs), which undergo liquid-liquid

224 ssion of RNA requires the action of multiple RNA-binding proteins (RBPs).

225 d protein components of complexes of RNA and RNA-binding proteins (RBPs).

226 ntial for their function and are mediated by RNA-binding proteins (RBPs).

227 e functions through direct interactions with RNA-binding proteins (RBPs).

228 grams are primarily controlled by regulatory RNA-binding proteins (RBPs).

229 ironmental stress are frequently mediated by RNA-binding proteins (RBPs).

230 f lincNORS requires the presence of RALY, an RNA-binding protein recently found to be implicated in c

231 Integrator is another RNA binding protein recruited to the promoters and enhan

232 Finally, we observed a DNV burden in RNA-binding-protein regulatory sites (OR = 1.13, 95% CI

233 echniques to quantify mRNA interactions with RNA-binding proteins relevant for tumorigenesis and canc

234 TDP-43 is an RNA-binding protein responsible for regulating RNA trans

235 1 is recruited to mRNAs by sequence-specific RNA-binding proteins, resulting in stabilization of the

236 es of TRAMP components with multiple nuclear RNA binding proteins, revealing preferential colocalizat

237 meric condensate that consists of ubiquitous RNA-binding proteins, revealing an unanticipated mechani

238 Our analysis of RNA-binding proteins reveals ILF3 as a potential regulat

239 on mRNA using amyloid-like assemblies of the RNA-binding protein Rim4.

240 Finally, we show that caspase-7 prefers RNA-binding proteins (RNA-BPs) as substrates compared to

241 RNA-binding proteins (RNA-BPs) play critical roles in de

242 QTLs and are enriched with binding sites of RNA-binding proteins, RNA structure-changing variants an

243 HIV Tat is a well-known RNA binding protein secreted by HIV.

244 We identify the RNA-binding protein SERBP1 as a novel regulator of gliob

245 these data identify HIN1 as a plant-specific RNA-binding protein, show a specific effect of drought a

246 s and destabilizing interactions with varied RNA-binding proteins, suggest that RNA pseudouridylation

247 s differed in their dependence on 3'UTRs and RNA binding proteins, suggesting diverse regulatory mech

248 oth RG/RGG and RSY regions in numerous other RNA-binding proteins suggests that the interaction of TN

249 cular junction is regulated by the conserved RNA binding protein Syncrip/hnRNP Q.

250 l level and involves an interaction with the RNA-binding protein TAR DNA-binding protein 43 kDa (TDP-

251 zer, and then, graphically displays enriched RNA-binding protein target sites.

252 The RNA binding protein TDP-43 forms intranuclear or cytopla

253 display pathological mislocalization of the RNA-binding protein TDP-43 and that mutations in its gen

254 Aberrant aggregation of the RNA-binding protein TDP-43 in neurons is a hallmark of f

255 The RNA-binding protein TDP-43 is present in several MLOs, u

256 Mutations in TARDBP, encoding the RNA-binding protein TDP-43, are one cause of ALS, and TD

257 te stress-induced nuclear condensates of the RNA-binding protein TDP-43, uncovering a protective func

258 hyperexcitability and mislocalization of the RNA-binding protein TDP43 are highly conserved features

259 d networks of both transcription factors and RNA-binding proteins (TFs and RBPs).

260 ists of genes regulated by MYC and NELFE, an RNA binding protein that enhances MYC-induced hepatocarc

261 le X Mental Retardation Protein (FMRP) is an RNA binding protein that regulates translation and is re

262 f the FMR1 gene and loss of encoded FMRP, an RNA binding protein that represses translation of some o

263 Gag is an RNA binding protein that selects and packages HIV-1 RNA

264 In this study, we use Staufen, an RNA-binding protein that colocalizes with osk mRNA, as a

265 The FinO-domain-protein ProQ is an RNA-binding protein that has been known to play a role i

266 TDP-43 is a DNA/RNA-binding protein that in ALS and FTD translocates fro

267 mediated by La-related protein 6 (LARP6), an RNA-binding protein that is enriched in protrusions.

268 CSTF2 encodes an RNA-binding protein that is essential for mRNA cleavage

269 indings demonstrate that FUS is an important RNA-binding protein that mediates translational repressi

270 tion of the antisense transcripts by FCA, an RNA-binding protein that physically interacts with RNA 3

271 pathogen Pseudomonas aeruginosa, RsmA is an RNA-binding protein that plays critical roles in the con

272 ZFP36L1 is a tandem zinc-finger RNA-binding protein that recognizes conserved adenylate-

273 Pumilio is an RNA-binding protein that represses a network of mRNAs to

274 of a long 26 hr period phenotype, encodes an RNA-binding protein that stabilizes the ck-1a transcript

275 ika viruses interact with a common set of 21 RNA-binding proteins that contribute to the regulation o

276 otemporal gene regulation is often driven by RNA-binding proteins that harbor long intrinsically diso

277 FUS (fused in sarcoma) are aggregation-prone RNA-binding proteins that in ALS can mislocalize to the

278 tids such as trypanosomes depends heavily on RNA-binding proteins that influence mRNA decay and trans

279 post-transcriptional gene control, often via RNA-binding proteins that use a YT521-B homology (YTH) d

280 -containing complexes reproducibly contained RNA-binding proteins that were previously found associat

281 We show that the RNA-binding protein THRAP3 (thyroid hormone receptor-ass

282 otein kinase 2 (MK2) but is inhibited by the RNA-binding protein tristetraprolin (TTP, encoded by the

283 kely mechanism of splicing repression by the RNA-binding protein UNC-75/CELF via interactions with ci

284 The decay pathway requires the RNA-binding protein UPF1 and its associated protein G3BP

285 we devised a cell-based functional screen of RNA-binding proteins using a let-7 sensor luciferase rep

286 SLIRP (SRA stem-loop interacting RNA binding protein) was identified as a candidate prote

287 eate filamentous fungus Ashbya gossypii, the RNA-binding protein Whi3 regulates the cell cycle and ce

288 TDP-43 is an RNA-binding protein which forms aggregates in neurons of

289 uitously expressed and predominantly nuclear RNA binding proteins, which form pathological cytoplasmi

290 NONO is a DNA/RNA-binding protein, which plays a critical regulatory r

291 SRSF7 is an essential RNA-binding protein whose misexpression promotes cancer.

292 he binding motifs and expression patterns of RNA binding proteins with exon splicing profiles, we unc

293 ing protein 1 (IGF2BP1) is a multifunctional RNA-binding protein with an oncofetal pattern of express

294 ZC3H14 has recently emerged as an important RNA-binding protein with multiple roles in posttranscrip

295 s a spliceosome recycling factor and nuclear RNA-binding protein with no previously reported role in

296 We show here that in medaka, two RNA-binding proteins with antagonizing properties target

297 umulating evidence suggests participation of RNA-binding proteins with intrinsically disordered domai

298 Here, we found that isoforms of the RNA-binding protein ZAP functioned as both a direct anti

299 Our previous research identified the RNA-binding protein ZC3H5 as possibly involved in gene r

300 RNA-binding protein ZFP36L1 functions as a tumor suppres