ライフサイエンスコーパス: -binding protein

1 e major EF-hand-containing, calcium (Ca(2+))-binding proteins with crucial roles in plant development

2 100A4, a member of the S100 family of Ca(2+)-binding proteins, is a key regulator of cell migration a

3 eukaryotic translation initiation factor 4E-binding protein 1 during postexercise recovery (all P <

4 (eukaryotic translation initiation factor 4E-binding protein).

5 tion initiation factor 4E, phosphorylated 4E-binding protein 1, and p-S6 ribosomal protein.

6 led by the 3' poly(A) tail (PAT) and poly(A)-binding protein (PABP).

7 at regulated expression of cytosolic poly(A)-binding protein 1 (PABPC1) modulates protein synthetic c

8 y induction through interaction with poly(A)-binding proteins.

9 se maternal mRNAs is facilitated by an m(6)A-binding protein, Ythdf2.

10 -loop receptor subunits and an acetylcholine-binding protein (AChBP).

11 a beta-barrel protein, rat liver fatty acid-binding protein (rLFABP), to reveal the effect of differ

12 sion of C/EBPalpha, PPARgamma and fatty acid-binding protein 4 (FABP4).

13 k decreased hepatic expression of fatty acid-binding protein 4 and increased subcutaneous inguinal ad

14 ing icosapent ethyl and adipocyte fatty-acid-binding protein.

15 lso affected the degradation of nucleic acid-binding protein substrates of Lon, intracellular localiz

16 We identify the endothelial actin-binding protein CD2-associated protein (CD2AP) as a nove

17 We recently found that the F-actin-binding protein afadin is required for lumen continuity

18 Twinfilin 2a (Twf2a) is a small actin-binding protein that inhibits actin filament assembly by

19 ge of the closing VBW that express the actin-binding protein transgelin (TAGLN) and TGFbeta receptor

20 5)P2], regulate the activities of many actin-binding proteins (ABPs), including profilin, cofilin, Di

21 in these processes is mediated by many actin-binding proteins, among which the cofilin family plays u

22 member of the NETWORKED superfamily of actin-binding proteins.

23 a vast array of intricately regulated actin-binding proteins.

24 beta-III-spectrin, and likely similar actin-binding proteins, interact with actin, and how this mech

25 mini of SK2 channels interact with the actin-binding proteins alpha-actinin2 and filamin A, respectiv

26 ytoskeleton in IECs via changes in the actin-binding proteins VIL1 and GSN.

27 -binding proteins, which, along with annexin-binding protein S100A4, regulated fusogenic activity of

28 on of adenylate-uridylate-rich element (ARE)-binding protein BRF1, a target of PI3K-Akt.

29 se seeded by the aggregation of specific ASO-binding proteins such as FUS/TLS (FUS) and PSF/SFPQ (PSF

30 SlRd2 was an ATP-binding protein that formed homodimers in planta.

31 lly targets light-harvesting chlorophyll a/b-binding proteins (LHCP) to the thylakoid membrane.

32 f a B12-based chemical probe to identify B12-binding proteins in a nonphototrophic B12-producing bact

33 yme 1 (IRE1) and its downstream target X-box-binding protein 1 (XBP1) drive B-cell differentiation to

34 P particles were identified, including Y box-binding protein 1 (YB-1) and fragile X mental retardatio

35 co-evolution hypothesis of MBF1 and TATA-box-binding proteins.

36 patterns conserved for recruiting human C4b-binding protein (C4BP).

37 de-3-phosphate dehydrogenase (GPDH), calcium-binding protein, and phosphoglycerate mutase were also i

38 se, myosin light chain, sarcoplasmic calcium-binding protein, and hemocyanin are the most relevant.

39 3p must be in complex with the small calcium-binding protein Cdc31p to be active.

40 ted with the expression of the small calcium-binding protein S100A4.

41 We have discovered that the calcium-binding protein nuclebindin-1 (NUCB1) is a novel CLABP.

42 The calcium-binding protein S100A4 is expressed at elevated levels i

43 Calcium-binding proteins such as parvalbumin and calbindin are m

44 S100A8 and S100A9 are calcium-binding proteins predominantly expressed by neutrophils

45 perglycemia, neutrophil-derived S100 calcium-binding proteins A8/A9 (S100A8/A9) interact with the rec

46 ls were found to be negative for the calcium-binding proteins calbindin, parvalbumin, or calretinin.

47 und that CPK28 is a high affinity Ca(2+)/CaM-binding protein.

48 three domains of life as a tight 3',5'-cAMP-binding protein.

49 a single phosphorylation site on the 5' cap-binding protein eIF4E is a critical mechanism for change

50 t between genes for two different carotenoid-binding proteins ancestral to the NTD and CTD.

51 so includes the light-harvesting chlorophyll-binding proteins of photosystems I and II, the early-lig

52 n combination with (15)N-labeled cholesterol-binding proteins (PFO* and ALO-D4, a modified anthrolysi

53 ane to alter the localization of cholesterol-binding proteins, and prevented the association of prese

54 unclear whether PFO* and related cholesterol-binding proteins bind uniformly to the plasma membrane o

55 ring a cavity resembling that of the choline-binding protein ChoX, as revealed by crystal and density

56 (BAF), a small and highly dynamic chromatin-binding protein, which has roles including NE reassembly

57 BACE1 has been described as a copper-binding protein and its oligomeric state as being monome

58 ntal disorder in which the MECP2 (methyl CpG-binding protein 2) gene is mutated.

59 ons in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2) cause Rett syndrome (RTT), a n

60 sed primarily by mutations in the methyl-CpG-binding protein 2 (MECP2) gene, which encodes a multifun

61 The methyl-CpG-binding protein 2 (MeCP2) protein is an epigenetic reade

62 The Rett-syndrome-associated methyl-CpG-binding protein 2 (MeCP2) selectively binds methylated D

63 n 1 (MBD1) belongs to a family of methyl-CpG-binding proteins that are epigenetic "readers" linking D

64 also noted that the acetyltransferases CREB-binding protein and p300 both can acetylate ERK1/2.

65 e acetyltransferase paralogues p300 and CREB-binding protein (CBP) are key transcriptional co-activat

66 nts its interaction with a coactivator, CREB-binding protein, and subsequently reduces the BDNF level

67 of p65 at Thr-305 and Ser-319 increased CREB-binding protein (CBP)/p300-dependent activating acetylat

68 The histone acetyl transferases CREB-binding protein (CBP) and its paralog p300 play a critic

69 we present the solution NMR structure of CUG-binding protein 2 RRM3 in complex with 5'-UUUAA-3' origi

70 report that miRNA 195 (miR-195) and RBP CUG-binding protein 1 (CUGBP1) jointly regulate IGF2R expres

71 lity and translation is regulated by the CUG-binding protein 2 interacting with AU-rich sequences in

72 ared concentrations of 25(OH)D and vitamin D-binding protein (VDBP) in AA and EA women and investigat

73 Despite the hundreds of DISC1-binding proteins reported, almost nothing is known about

74 igh-mobility group protein B1 (HMGB1), a DNA-binding protein capable of inducing secretion of TNF-alp

75 In this paper, we present iDNAProt-ES, a DNA-binding protein prediction method that utilizes both seq

76 ATEMENT CCCTC-binding factor (CTCF) is a DNA-binding protein that organizes nuclear chromatin topolog

77 This system provides a model for any DNA-binding protein that can be posttranslationally modified

78 ted in the genomic context by UV-damaged DNA-binding protein 2 (DDB2), which is part of a multiprotei

79 ared to transactivation response element DNA-binding protein 43 (TDP-43) proteinopathy patients while

80 to any type of yeast surface expressible DNA-binding protein.

81 For the chromodomain helicase DNA-binding protein 1 (Chd1) remodeler, nucleosome sliding h

82 ction mutations in chromodomain helicase DNA-binding protein 7 (CHD7(LOF)) and lysine (K) methyltrans

83 found that ATPases chromodomain helicase DNA-binding protein 9 (CHD9) and Brahma homologue (BRM, a pr

84 ce deposited, mCA is bound by the methyl-DNA-binding protein MECP2 and functions in a rheostat-like m

85 s with the specificity of a programmable DNA-binding protein by using protein trans-splicing to ligat

86 eration (FTLD) with transactive response DNA-binding protein (TDP) inclusions in 40.5%, FTLD-tau in 4

87 es a direct role of transactive-response DNA-binding protein 43 (TDP-43) in the pathology of ALS and

88 dementia (FTD) with transactive response DNA-binding protein of 43 kD (TDP-43)-positive inclusions an

89 rated that Hop1 is a structure-selective DNA-binding protein exhibiting high affinity for the Hollida

90 lex, incorporating the sequence-specific DNA-binding protein Cep3 together with regulatory subunits C

91 EBNA1 is a sequence-specific DNA-binding protein that is consistently expressed in EBV tu

92 cation requires only the single-stranded DNA-binding protein gp32 from bacteriophage T4 and a strand-

93 ing the telomeric repeat single-stranded DNA-binding protein Teb1 and its heterotrimer partners Teb2

94 oms, mutations in the DCTN1 gene and TAR DNA-binding protein 43 (TDP-43) pathology.

95 nature with numerous round, hyaline, TAR DNA-binding protein 43 (TDP-43)-positive inclusions.

96 ize the cell-to-cell transmission of TAR DNA-binding protein and alpha-synuclein, involved in amyotro

97 Transactivation response element (TAR) DNA-binding protein 43 (TDP-43) misfolding is implicated in

98 ving nonstructural proteins, such as the DNA-binding protein P1 and the genome terminal protein (P4),

99 rvation protein A (SspA) complex and the DNA-binding protein pathogenicity island gene regulator (Pig

100 n yeast cells carrying a mutation in the DNA-binding protein Sap1 show defects in DNA replication pro

101 We have recently identified Z-DNA-binding protein 1 (ZBP1) as an innate sensor of influenz

102 er-inducing interferon-beta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of IFN-

103 lix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

104 DNA-binding proteins play a very important role in the struc

105 ifically measuring target site search by DNA-binding proteins via intersegmental translocation.

106 Single-stranded DNA-binding proteins (SSBs) play a key role in genome mainte

107 Open chromatin provides access to DNA-binding proteins for the correct spatiotemporal regulati

108 ium Deinococcus radiodurans contains two DNA-binding proteins from starved cells (Dps): Dps1 (DR2263)

109 NKX2.2), paired box 6 (PAX6), and LIM domain-binding protein 1 (LDB1) serve to maintain mature adult

110 /2 [LIM domain only 1 or 2]:LDB1 [LIM domain-binding protein 1]) and dynamic recruitment of conserved

111 be blocked by the expression of viral dsRNA-binding proteins.

112 multidomain components, E1, E3, E2 and an E3-binding protein (E3BP), the latter two forming the core

113 by translation initiation factor 4E (eIF4E)-binding proteins (4E-BPs).

114 parallel to Atf4 in the regulation of eIF4E-binding protein 1 (4ebp1), a mammalian target of rapamyc

115 ic inactivation of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCA

116 ted receptor gamma/sterol regulatory element-binding protein 1/CD36 in hepatocytes from high fat-fed

117 WT mice, including sterol regulatory element-binding protein 1c target gene fatty-acid synthase (3.0-

118 show that the carbohydrate response element-binding protein (ChREBP) coordinates an adaptive respons

119 is a direct target of cAMP response element-binding protein (CREB) that is activated by beta-adrener

120 e --> cAMP --> PKA --> cAMP response element-binding protein pathway mediating cell survival and the

121 nvolving Akt1/Akt2 and cAMP response element-binding protein.

122 by its human homolog Ras-responsive element-binding protein 1 (RREB-1).

123 ed by hepatic cholesterol responsive element-binding protein and featured portal/lobular inflammation

124 nhibition of carbohydrate-responsive element-binding protein-beta, pyruvate kinase L, SCD-1, and DGAT

125 Sterol regulatory element-binding proteins (SREBPs) in the fission yeast Schizosac

126 tion of tristetraprolin, two AU-rich element-binding proteins.

127 in the spatiotemporal expression of EB1 (end-binding protein 1), a +TIP (MT plus-end tracking protein

128 tubule network and the microtubule minus end-binding protein, Patronin.

129 n vivo Furthermore, live-cell imaging of end-binding protein 3 tagged with EGFP (EB3-GFP) in primary

130 Ablation of CCAAT-enhancer-binding protein homologous protein (CHOP), the major ER

131 pogenic transcription factors CCAAT/enhancer-binding protein alpha (C/EBPalpha), C/EBPbeta, C/EBPdelt

132 th Tbeta4 and is recruited by CCAAT/enhancer-binding protein beta (C/EBPbeta) to discrete regulatory

133 ursors up-regulates c-Fos and CCAAT/enhancer-binding protein-alpha (C/EBPalpha), two critical OC tran

134 A, TcrA, FsrR, RpoN and its cognate enhancer-binding protein EbpA, which is required for the inductio

135 ells with computationally predicated ethanol-binding proteins and experimentally identified ethanol t

136 cle arrest (urine insulin-like growth factor-binding protein 7) and, finally, by functional markers o

137 nto a hexameric coiled-coil bundle and an Fc-binding Protein A fragment, we generated the Hex nanocar

138 l wall-anchored proteins such as fibronectin-binding protein A (FnBPA) that bind to host ligands (e.g

139 The SaeRS-modulated factor fibronectin-binding protein A (FnBPA) also contributed to the fermen

140 s deficient in expression of the fibronectin-binding protein SfbA.

141 high homology to genes encoding fibronectin-binding proteins of Gram-positive pathogens.

142 Cryptochromes are flavin-binding proteins that act as blue light receptors in bac

143 inhibition of HAdV-5-FX interaction with FX-binding protein (X-bp) inhibited transduction in the pre

144 2 coactivated the transcription factors GATA-binding protein 4 (GATA-4) and hypoxia-inducible factor

145 Glycan-binding proteins, which include galectins, are involved

146 rs investigations into the biology of glycan-binding proteins, which in turn complicates the biomedic

147 Probing the array with several glycan-binding proteins uncovered that not only terminal glycoe

148 The PUL also includes two glycan-binding proteins, confirmed by beta-mannan affinity elec

149 p new therapeutic interventions using glycan-binding proteins.

150 nucleotide exchange factor (GEF) for its GTP-binding protein partner eIF2 via interaction with eIF2.G

151 1) is sex biased whereby coupling to its GTP-binding protein, Gs, is greater in females, whereas beta

152 The ARL15 gene encodes a small GTP-binding protein whose function is currently unknown.

153 ), a negative regulator of the Ras small GTP-binding protein.

154 Septins are filament-forming GTP-binding proteins involved in many essential cellular eve

155 post-translational prenylation of small GTP-binding proteins such as Rho and Rac, and their downstre

156 Human guanylate-binding protein 1 (hGBP1), the founding member of GBPs,

157 ciated genes, such as IFN-beta and guanylate-binding proteins (GBPs), are downregulated in STING knoc

158 IFN-inducible family of DLPs, the guanylate-binding proteins (GBPs), is involved in antimicrobial an

159 nitrite reductase gene (aniA), the factor H-binding protein gene (fHbp), and the capsule biosyntheti

160 atica that belongs to a broad family of heme-binding proteins (MF6p/helminth defense molecules (HDMs)

161 get protease kallikrein 7 (KLK7) are heparin-binding proteins, and inhibition of KLK7 by vaspin is ac

162 The ligand requirements of HS-binding proteins have, however, been defined in only a f

163 ously that AIBP (apolipoprotein A-I [apoA-I]-binding protein)-regulated cholesterol efflux in endothe

164 s study, we identified and characterized IgE-binding proteins from the mosquito species Aedes aegypti

165 Some patient sera revealed IgE-binding proteins matching LTP and/or profilin.

166 hermore, we report that calcium and integrin-binding protein 2 binds to the components of the hair ce

167 n with remote homology to bacterial integrin-binding proteins.

168 A soluble lipid-binding protein, MlaC, ferries lipids between MlaD and a

169 The C-Mad2-binding protein p31(comet) and the ATPase TRIP13 promote

170 action of the TRIP13 AAA-ATPase and the Mad2-binding protein p31(comet) Now we have isolated from ext

171 o), glutathione S-transferase (GST), maltose-binding protein (MBP), N-utilisation substance protein A

172 din (SA-CAP-1 or 2) or nonallergenic maltose-binding protein (MBP; MBP-CAP-1 to 4) and binding to a p

173 elta, the concentrations of several membrane-binding proteins were reduced in the CR and/or on the PM

174 e-associated protein NUSAP1 is a microtubule-binding protein implicated in spindle stability and chro

175 es zipcode binding protein 1 (ZBP1), an mRNA-binding protein that transports beta-actin mRNA and rele

176 encoding beta-myosin heavy chain and myosin-binding protein C, respectively, are the 2 most common g

177 Cardiac myosin-binding protein C (cMyC) is a cardiac-restricted protein

178 MYBPC3, encoding cMyBP-C (cardiac myosin-binding protein C), is the most frequently mutated HCM g

179 and in cells expressing low levels of myosin-binding protein C.

180 e identify previously uncharacterized myosin-binding proteins, putative myosin adaptors that belong t

181 Thus, HO-2 is a cellular myristate-binding protein that negatively regulates both virus rep

182 ation and characterization of a novel Notch1-binding protein, N9, obtained by screening of a combinat

183 scaffolding protein Sir4, and the nucleosome-binding protein Sir3.

184 mJHBP is a member of the odorant-binding protein (OBP) family, and orthologs are present

185 on to dentilisin, most notably, oligopeptide-binding proteins (OBPs) and the beta-barrel of BamA.

186 g affinity as tablysin-15, a known palmitate-binding protein.

187 chromatin condensation 1 (RCC1) acidic patch-binding protein.

188 ch in a manner similar to other acidic patch-binding proteins such as herpesvirus latency-associated

189 Penicillin-binding protein PBP 2B is a key cell division protein in

190 An enzyme, called penicillin-binding protein 2a (PBP2a), is brought into this biosynt

191 ss A, C and D beta-lactamases and penicillin-binding proteins, resulting in intrinsic antibacterial a

192 in concert with the PG synthases penicillin-binding proteins PBP3 and PBP1b.

193 The family of bacterial Penicillin-binding-protein And Serine/Threonine kinase-Associated (

194 proteins that have extracellular penicillin-binding-protein and serine/threonine kinase-associated (

195 n extracellular annexins, phosphatidylserine-binding proteins, which, along with annexin-binding prot

196 Here, we report that the phospholipid-binding protein, annexin A2 (ANXA2) functions to maintai

197 sence of autoantibodies against phospholipid-binding proteins (aPLs), such as beta2 glycoprotein I (b

198 PNA-binding proteins may also participate in the patterning

199 d the somites that is normally formed by PNA-binding proteins that block entry to medial pathways.

200 terminal expanded polyalanine tract in polyA-binding protein nuclear 1 (PABPN1).

201 nd cofilin, which we identified as novel PSA-binding proteins.

202 acids stimulate recruitment of the PtdIns3P-binding protein FYCO1 to lysosomes and promote contacts

203 ously shown that the scaffolding protein Ran-binding protein 9 (RanBP9), which is highly elevated in

204 These findings identify an estrogen receptor-binding protein as a critical mediator of HER2-driven br

205 Plasmodium falciparum reticulocyte-binding protein homologue 2b (PfRh2b) is an invasion lig

206 cycle proteins, interphotoreceptor retinoid-binding protein and stimulated by retinoic acid 6 protei

207 rkers of dedifferentiation, cellular retinol-binding protein 1, and matrix metalloproteinase 2, compa

208 or 32 pmol/L), vitamin A deficiency (retinol-binding protein <14.7 mug/mL or 0.70 mumol/L) and inflam

209 Similarly, serum levels of retinol-binding protein 4 and retinoids were significantly lower

210 tation-mass spectrometry identified ribosome-binding protein 1 (RRBP1) as SYNJ2BP's ERM binding partn

211 n synapses by perturbing the function of RIM-binding proteins (RBPs) as central active-zone scaffoldi

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

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

214 ind that the Apicomplexan-specific ALBA4 RNA-binding protein acts to regulate development of the para

215 bal Ub screen, we identified hnRNPA1, an RNA-binding protein and auxiliary splicing factor, as a subs

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

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

218 RBM10 is an RNA-binding protein that plays an essential role in developm

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

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

221 tal retardation autosomal homolog 1), an RNA-binding protein, are critical to maintain proper cardiac

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

223 The cancer-associated RNA-binding protein La is posttranslationally modified by ph

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

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

226 n this study, we show that the cytosolic RNA-binding protein clustered mitochondria homologue (CLUH)

227 2 h of hypoxic exposure might deactivate RNA-binding protein BRF1, hence resulting in the selective d

228 MR1, a conserved, ubiquitously expressed RNA-binding protein.

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

230 1 (Dnd1), a vertebrate-specific germline RNA-binding protein.

231 s a ubiquitously expressed polyadenosine RNA-binding protein, ZC3H14 (Zinc finger CysCysCysHis domain

232 tion, which requires the Pumilio-related RNA-binding protein Puf118.

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

234 tion of the RNA-silencing factor HIV TAR-RNA-binding protein (TRBP) promotes binding and stabilizatio

235 The RNA-binding protein FUS participates in several RNA biosynth

236 s overwhelmingly support the role of the RNA-binding protein Hu antigen R (HuR) as a positive regulat

237 The RNA-binding protein HuR functions to promote the stability o

238 try, we further uncovered binding of the RNA-binding protein HuR to the -44 region, where it acts as

239 We found that expression of the RNA-binding protein Mex3a labels a slowly cycling subpopulat

240 transcription, by the YTH domain of the RNA-binding protein Mmi1 and degraded by the nuclear exosome

241 d revealed the clinical relevance of the RNA-binding protein MSI2 in breast cancer.

242 patients with ALS have aggregates of the RNA-binding protein TDP-43 in their brains and spinal cords,

243 Our results indicate that the RNA-binding protein YBX1, which is required for the sorting

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

245 RNA-binding proteins (RBPs), in addition to their functions

246 RNA-binding proteins of the Musashi (Msi) have been implicat

247 RNA-binding proteins play a key role in shaping gene express

248 MicroRNAs (miRNAs) and RNA-binding proteins (RBPs) critically regulate gene express

249 ple neurite-targeted non-coding RNAs and RNA-binding proteins with potential regulatory roles.

250 so more accurately predicts the DNA- and RNA-binding proteins.

251 of RNA regulators such as microRNAs and RNA-binding proteins.

252 s nuclear retention of expansion RNAs by RNA-binding proteins (RBPs) and an acute phase in which expa

253 al and post-transcriptional processes by RNA-binding proteins for maintaining cellular identity among

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

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

256 We propose a mechanism whereby diverse RNA-binding proteins directly recruit PABP, in a non-poly(A)

257 eat) domain-containing-2 (nhl-2), encode RNA-binding proteins, thus delineating a previously unknown

258 Lin28 RNA-binding proteins have evolutionarily conserved roles in

259 d that motor-neuron disease (MND)-linked RNA-binding proteins (RBPs), TDP-43, FUS, and hnRNPA2B1, bin

260 Many RNA-binding proteins have been reported to play a functional

261 Characterizing the binding behaviors of RNA-binding proteins (RBPs) is important for understanding t

262 Different sets of RNA-binding proteins interact with primary miRs (pri-miRs) a

263 diverse stresses trigger coalescence of RNA-binding proteins into stress granules.

264 G repeats bind and sequester a family of RNA-binding proteins known as Muscleblind-like 1, 2, and 3 (

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

266 otein U (hnRNP U) belongs to a family of RNA-binding proteins that play important roles in controllin

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

268 Downregulation of oo18 RNA-binding proteins (ORBs) in any of these MBONs impaired L

269 on via interactions of G4 with potential RNA-binding proteins (RBPs).

270 re the expression of splicing-regulatory RNA-binding proteins in human islets, brain, and other human

271 have enriched binding motifs for several RNA-binding proteins, which implies extensive translational

272 posing temporal gradients of Imp and Syp RNA-binding proteins (descending and ascending, respectively

273 The identity of the RNA-binding proteins (RBPs) that govern cancer stem cells re

274 onucleoprotein complex that involves the RNA-binding proteins HnrnpK and PCBP1 and regulates local tr

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

276 nious regulatory model consisting of two RNA-binding proteins and four microRNAs that modulate the mR

277 First, we find that two RNA-binding proteins specifically expressed in germ cells, D

278 Herein, we discuss various RNA-binding proteins and their unique contributions to femal

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

280 ine insertion sequence (SECIS) and the SECIS-binding protein Secisbp2.

281 gulation of recombinant recognition sequence-binding protein at the Jkappa site (RBP-J) protein, a po

282 chromatin organizer special AT-rich sequence-binding protein-1 (Satb1) restrains PD-1 expression indu

283 by Ent, neutrophils rely on the siderophore-binding protein lipocalin 2 (Lcn2) in a "tug-of-war" for

284 ll-specific deletion of recombination signal-binding protein for immunoglobulin Jkappa region (RBPJka

285 Mn(II) competition between CP and two solute-binding proteins that Staphylococcus aureus and Streptoc

286 Remarkably, lysenin (a sphingomyelin-binding protein) also bound preferentially to microvilli

287 w that replication protein A (RPA), an ssDNA-binding protein, interacts with RNaseH1 and colocalizes

288 The human mitochondrial ssDNA-binding protein (mtSSB) is a homotetrameric protein, inv

289 PHF11 interacted with the ssDNA-binding protein RPA and was found in a complex with seve

290 ling evidence that AgRP is a heparan sulfate-binding protein and localizes critical regions in the Ag

291 n factor 4E (eIF4E), eIF4G, and poly(A) tail-binding protein (PABP) that circularizes mRNAs, promotin

292 hysical half-life or residence time for TATA-binding protein (TBP) across the yeast genome from compe

293 Recently, TATA-binding protein-related factor 2 (TRF2) rather than the

294 Although the TATA-binding protein (TBP) subunit of TFIID is necessary and

295 related factor 2 (TRF2) rather than the TATA-binding protein (TBP) was found to function in transcrip

296 ce, we show that TERF1 evolved as a telomere-binding protein in the common stem lineage of marsupial

297 al interactions between Blm and two telomere-binding proteins, which may thus recruit or regulate Blm

298 We recently identified TRIOBP-1 (Trio-binding protein 1, also known as Tara) to be another suc

299 -interacting protein (TOLLIP) is a ubiquitin-binding protein that regulates innate immune responses,

300 lated regions (UTRs) of MICA, MICB, and UL16-binding protein 2 were shown to be regulated by RBPs and