ライフサイエンスコーパス: binding protein

1 ription factor CREB (cAMP-responsive element binding protein).

2 proteins (staphylococcal nuclease and ribose binding protein).

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

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

5 ing the need to separate the marker from its binding protein.

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

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

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

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

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

11 D anchor for receptor activation and SMAD2/3 binding protein.

12 function was originally identified as a Rab5 binding protein.

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

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

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

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

17 eukaryotes, and recognized as small-molecule binding proteins.

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

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

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

21 cupied by tandem arrays of high-affinity DNA binding proteins.

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

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

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

25 p new therapeutic interventions using glycan-binding proteins.

26 harpens the Ca2+ frequency-dependence of CaM binding proteins.

27 dified RNAs to low-complexity regions in RNA binding proteins.

28 nal repressors via recruitment of C-terminal Binding Proteins.

29 overlap in protein composition including RNA binding proteins.

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

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

32 End binding protein 1 (EB1) is a key element in the complex

33 hylation of 1444 genes, including fatty acid binding protein 1 (FABP1), fatty acid binding protein 2

34 and concentrate the fibroblast growth factor binding protein 1 (FGFBP1) at NMJs.

35 AD1/5 and the expression of inhibitor of DNA binding protein 1 (ID1) were upregulated in HCV-infected

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

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

38 The polyadenylate binding protein 1 (PABPN1) is a ubiquitously expressed R

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

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

41 se-inactive IRE1alpha or the activated X-box binding protein 1 (XBP1), the canonical IRE1alpha target

42 f the transcription factor Xylanase promoter binding protein 1 (Xpp1) in the regulation of both prima

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

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

45 We hypothesized that this requires zipcode binding protein 1 (ZBP1), an mRNA-binding protein that t

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

47 Critically, the sterol regulatory binding protein 1 and its targets are key integrators of

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

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

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

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

52 /2 [LIM domain only 1 or 2]:LDB1 [LIM domain-binding protein 1]) and dynamic recruitment of conserved

53 the transcriptional coregulators C-terminal binding proteins 1 and 2 (CtBP1 and 2) occurs in many hu

54 ncy, B cell-specific CD79a-Cre x XBP1 (X-box binding protein-1) floxed mice (XBP1-conditional knockou

55 The molecular adapter growth factor receptor binding protein 14 (Grb14) is an inhibitor of insulin re

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

57 us sequence in the sterol regulatory-element binding protein-1c (Srebp-1c) promoter.

58 all probes and the compact but disordered 4E binding protein 2 (4E-BP2) protein in [Formula: see text

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

60 y acid binding protein 1 (FABP1), fatty acid binding protein 2 (FABP2), melanocortin 2 receptor (MC2R

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

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

63 Here, we focus on methyl-CpG binding protein 2 (MECP2) restoration for RTT and combin

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

65 by mutations in the gene encoding methyl CpG binding protein 2 (MeCP2) that occur sporadically in 1:1

66 encoding the transcription factor Methyl CpG Binding Protein 2 (MECP2).

67 the activation of sterol regulatory-element binding protein 2 and downregulating low-density lipopro

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

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

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

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

72 transcription of insulin-like growth factor binding protein 3 (IGFBP3), and that this regulates SCC

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

74 Fatty acid binding protein 4 (FABP4) is a fatty acid chaperone, whi

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

76 2 coactivated the transcription factors GATA-binding protein 4 (GATA-4) and hypoxia-inducible factor

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

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

79 TAR DNA binding protein 43 (TDP-43) is another protein linked to

80 Tar DNA binding protein 43 (TDP-43) is the principal component o

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

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

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

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

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

86 of TEC-expressed insulin growth factor (IGF) binding protein-7 (IGFBP7/angiomodulin).

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

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

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

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

91 ies with ligand binding to the acetylcholine binding protein (AChBP), we previously identified a seri

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

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

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

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

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

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

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

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

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

101 n patients with increased lipopolysaccharide binding protein and systemic vascular resistance below t

102 ble the rapid characterization of engineered binding proteins and interaction networks.

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

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

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

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

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

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

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

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

111 SR), or calsequestrin 2 (CASQ2), a SR Ca(2+) binding protein, are linked to CPVT.

112 ty issues, supporting the use of alternative binding proteins as complementary reagents for many appl

113 (BRPF) family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF1L.

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

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

116 nding landscape of C/EBPbeta (CCAAT enhancer binding protein beta) without affecting its expression o

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

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

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

120 2 h of hypoxic exposure might deactivate RNA-binding protein BRF1, hence resulting in the selective d

121 is regulated by histone acetylation and the binding protein bromodomain containing 4 (BRD4) on the t

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

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

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

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

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

127 CCAAT/enhancer binding proteins (C/EBPs) are expressed in various tissu

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

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

130 tial target site, which may be how other DNA binding proteins can steer selection of advantageous tar

131 s kinase activity and the calcineurin B-like binding protein CBL1.

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

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

134 3p must be in complex with the small calcium-binding protein Cdc31p to be active.

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

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

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

138 class of chaperones, chaperone-like amyloid binding proteins (CLABPs), has been shown to interfere w

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

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

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

142 ncreased levels of the cAMP response element binding protein (CREB), a transcriptional factor involve

143 ar signaling molecule, cAMP-response element binding protein (CREB), which serves as a pivotal transc

144 lic adenosine monophosphate response element binding protein (CREB)-regulated transcription coactivat

145 transcription factor cAMP-responsive element binding protein (Creb1) and its transcriptional co-activ

146 the histone acetyl-transferases (HATs) CREB binding protein (CREBBP) and EP300 are recurrently mutat

147 The Duffy binding protein (DBP) dimerization with its cognate rece

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

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

150 omal S6 kinase 1, or cAMP responsive element binding protein DNA-binding activity prevented the proli

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

152 SMP (synaptotagmin-like mitochondrial-lipid binding protein) domain.

153 dynamic microtubules in the presence of end binding proteins (EBs).

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

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

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

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

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

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

160 ssess significant chemical diversity; glycan binding proteins (GBPs) recognize specific glycans to tr

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

162 The ssDNA binding protein [gene product 32 (gp32)] of the T4 bacte

163 nteractions within a set of 14 conserved RNA binding protein genes, generating all possible single an

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

165 e and cooperative interactions between actin binding proteins help define their associations with dif

166 Cyclic AMP-responsive element binding protein, hepatocyte specific (CREBH), is a liver

167 ional complexation with human growth hormone binding protein (hGHBp) to the different NOTA-modified s

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

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

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

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

172 We measured plasma intestinal fatty acid binding protein (I-FABP), soluble CD14 (sCD14), interleu

173 own-regulation of insulin-like growth factor binding protein (Igfbp) genes when Ng2/Cspg4 is depleted

174 by its naturally occurring antagonist, IL-18 Binding Protein (IL-18BP).

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

176 it was previously shown that the major AAV2 binding protein in membrane preparations of human cells

177 tion buffer that separates 25(OH)D3 from its binding protein in situ, eliminating the need for sample

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

179 of peptide toxins to two ion channels and a binding protein in which the peptide toxins successfully

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

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

182 tin, serum transferrin receptor, and retinol binding protein) in settings of prevalent inflammation a

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

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

185 TDP-43 is a well known RNA binding protein involved in the pathogenesis of Amyotrop

186 HP1) family proteins are conserved chromatin binding proteins involved in gene silencing, chromosome

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

188 The recognition protein (FK506 binding protein) is inserted into functionally-inactivat

189 The RNA binding protein, LARP1, has been proposed to function do

190 C5A anaphylatoxin (C5A), lipopolysaccharide binding protein (LBP), C-reactive protein (CRP), ILT-4,

191 tion in phosphorylated cAMP-response element binding protein levels in the NAcSh that could account f

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

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

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

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

196 PNA-binding proteins may also participate in the patterning

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

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

199 ly, 5hmC colocalized with the methylated DNA binding protein MeCP2 and with the active chromatin hist

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

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

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

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

204 that the interaction between the lncRNA, its binding protein MYH9, and the coding gene FOXE1 underlie

205 ity and are mediated through the periplasmic binding protein NspS and the transmembrane bis-(3'-5') c

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

207 Mttp-LKO mice, on either the liver FA binding protein null or Apobec-1 null background (i.e.,

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

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

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

211 ubunit 6A (CCT6A) as an inhibitor and direct binding protein of SMAD2 and found that CCT6A suppresses

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

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

214 ex have been identified, including oxysterol binding protein (OSBP) and phosphatidylinositol 4-kinase

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

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

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

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

219 Often, the interactions of IDPRs with their binding protein partner(s) lead to transition from the s

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

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

222 ols activity of the bi-functional penicillin binding protein PBP A1, we discovered that GpsB influenc

223 rial cell wall, is synthesised by penicillin binding proteins (PBPs).

224 arrangement of the C-terminal domain of heme binding protein (PhuS) is required for interaction with

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

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

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

228 uthors show in murine HSCs that the telomere binding protein POT1a inhibited the production of reacti

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

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

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

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

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

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

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

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

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

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

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

240 re we examined the role of zebrafish retinol binding protein receptor 2 (Rbpr2) for RBP4-retinol upta

241 human circRNA is associated with diverse RNA binding proteins reflecting its endogenous splicing and

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

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

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

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

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

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

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

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

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

251 , an endogenous RNA normally shielded by RNA binding proteins SRP9/14.

252 E. coli single strand (ss) DNA binding protein (SSB) is an essential protein that binds

253 ) is notable for its interactions with ssDNA binding proteins (SSBs) during fundamentally important b

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

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

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

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

258 pecificity, outside of extremely modular DNA binding proteins such as TAL effectors, has generally pr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

274 translocation to pair barcodes representing binding proteins, thousands of distinct interactions can

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

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

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

278 sma renin, noradrenaline, lipopolysaccharide binding protein, troponin T, and brain natriuretic pepti

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

280 aminoglycans (GAG), and lectins/carbohydrate binding proteins using matrix-assisted laser desorption/

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

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

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

284 n 1 (PABPN1) is a ubiquitously expressed RNA binding protein vital for multiple steps in RNA metaboli

285 , and seven highly-expressed hippocampal CaM binding proteins, we find that competition for CaM bindi

286 Among several putative binding proteins, we identified tripartite motif-contain

287 vels of troponin T and heart-type fatty acid binding protein were increased (P < 0.05) after pneumoco

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

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

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

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

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

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

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

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

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

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

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

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

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