ライフサイエンスコーパス: nuclear protein

1 aggregates are associated with depletion of nuclear protein.

2 ADAR2 is also a constitutively expressed nuclear protein.

3 nucleus and facilitate the degradation of a nuclear protein.

4 -3 or AIB1), a large and mostly unstructured nuclear protein.

5 otein lamin A distorts nuclei and sequesters nuclear proteins.

6 g the linker histone in the context of other nuclear proteins.

7 n RNR and the Fe-S clusters in cytosolic and nuclear proteins.

8 sm distinct from the Srp1-mediated import of nuclear proteins.

9 e and/or threonine residues of cytosolic and nuclear proteins.

10 ohydrate modification found on cytosolic and nuclear proteins.

11 to investigate cofractionation of groups of nuclear proteins.

12 ich have been identified as transmembrane or nuclear proteins.

13 ration of [4Fe-4S] clusters in cytosolic and nuclear proteins.

14 to assemble Fe-S clusters into cytosolic and nuclear proteins.

15 f serine/threonine residues of cytosolic and nuclear proteins.

16 imerize and bind only to cytoplasmic but not nuclear proteins.

17 r San1-mediated PQC degradation of misfolded nuclear proteins.

18 ntrolling the subnuclear localization of the nuclear proteins.

19 reonine residues of membrane, cytosolic, and nuclear proteins.

20 ill no reliable and quantitative resource of nuclear proteins.

21 the export of nuclear RNA and the import of nuclear proteins.

22 Nuclear protein 1 (Nupr1), which mediates stress respons

23 n of liver-integrated stress response-driven nuclear protein 1 (NUPR1).

24 Tumor protein p53-induced nuclear protein 1 (TP53INP1) is involved in cell stress

25 with epidermal growth factor-like domains 2, nuclear protein 1, and growth differentiation factor 15)

26 Ran (Ras-related nuclear) protein, a member of the Ras superfamily of GTP

27 ase of the high-mobility group box 1 (Hmgb1) nuclear protein, activating the sterile inflammatory res

28 SIRT1, a nuclear protein and deacetylase of the AR, is neuroprote

29 group box 1 (HMGB1), a chromatin-associated nuclear protein and extracellular damage-associated mole

30 n increased levels of constitutively cleaved nuclear protein and increased transcription and secretio

31 FTO is a nuclear protein and its physiological function remains l

32 Full-length IL-33 is a nuclear protein and may function as an "alarmin" during

33 ertain nucleoporins and concomitantly affect nuclear protein and poly(A)(+) RNA export.

34 (HMGB1) is an abundant chromatin-associated nuclear protein and released into the extracellular mili

35 mine that SAMHD1 is a strictly non-shuttling nuclear protein and that as expected WT Vpx localizes wi

36 reactivity to the conserved influenza virus nuclear protein and to heterovariant and heterosubtypic

37 e neoplasia, type 1 (MEN1) locus encodes the nuclear protein and tumor suppressor menin.

38 n of OGT affects O-GlcNAcylation of numerous nuclear proteins and acetylation of Lys-9 on histone 3 i

39 buted to PAR modification of p65-interacting nuclear proteins and assembly of the NF-kappaB transcrip

40 Interactions between nuclear proteins and chromatin frequently occur on the t

41 tandem mass spectrometry, we quantified 3987 nuclear proteins and identified significant changes in t

42 d it can be applied to the analysis of other nuclear proteins and pathways.

43 nonstructural proteins, the presence of cell nuclear proteins and the viral nucleocapsid protein incr

44 histones, which are the major components of nuclear proteins and their consequences in COPD, has not

45 SUMO system appears to predominantly target nuclear proteins and, to a lesser extent, cytosolic prot

46 Focusing on the nuclear proteins and/or transcription factors that are e

47 This set is enriched in cytosolic and nuclear proteins, and protein kinases.

48 s lack of understanding of the site(s) where nuclear proteins are degraded because the subcellular di

49 to the nucleus, it is also evident that some nuclear proteins are degraded only after export to cytos

50 Understanding how these nuclear proteins are transported through the nuclear env

51 less dense than normal and accumulated most nuclear proteins as measured by mass spectrometry.

52 Here, we unambiguously identify over 60 nuclear proteins as O-GlcNAcylated, several of which are

53 ochemistry using neuronal (neuronal-specific nuclear protein), astrocytic (glial fibrillary acidic pr

54 Nuclear protein, ataxia-telangiectasia locus (NPAT) and

55 with the C-terminal SANT/Myb-like domain of nuclear protein, ataxia-telangiectasia locus (NPAT), a t

56 s (rat 832/13 and mouse MIN6), and increased nuclear protein binding compared with the rs11708067-G a

57 obility shift assays indicated that specific nuclear protein bindings occur at the three SNPs in HepG

58 RAI1 encodes a nuclear protein but little is known about its molecular

59 smic, also forms nuclear bodies and inhibits nuclear protein but not poly(A)(+) RNA export.

60 ortant regulatory step in the degradation of nuclear proteins by cytosolic proteasomes.

61 slational modification of many cytosolic and nuclear proteins by O-linked beta-N-acetylglucosamine (O

62 gulates mitochondrial respiration, but how a nuclear protein can orchestrate the function of an organ

63 occurs predominantly in the nucleus, but non-nuclear proteins can also be SUMOylated.

64 The evidence that nuclear proteins can be degraded by cytosolic proteasome

65 As many cytoplasmic and nuclear proteins can be glycosylated by O-GlcNAc, we stu

66 merase-1 (PARP-1), a ubiquitous and abundant nuclear protein, catalyzes the synthesis of a negatively

67 endocytosed ligands, and on a motley crew of nuclear proteins, chromatin modifiers, ubiquitin ligases

68 Interplays among lineage-specific nuclear proteins, chromatin modifying enzymes, and the b

69 Nuclear protein co-immunoprecipitation demonstrated an i

70 logeny using the rRNA genes 18S and 28S, the nuclear protein-coding gene EF-1gamma, and a morphologic

71 dy, we characterize the diversity of several nuclear protein-coding genes plus both nSSU-rDNA and mit

72 inth interrelationships based on hundreds of nuclear protein-coding genes, exploring phylogenetic sig

73 x10(-)(3)(5), and stronger EMSA binding of a nuclear protein compared to the T-allele.

74 nservation and regulatory potential, bound a nuclear protein complex composed of NF-kappaB subunits w

75 hat VICTR associates with EDS1 and PAD4 in a nuclear protein complex.

76 criptional repressor and is part of a larger nuclear protein complex.

77 Lamins bind to a growing number of nuclear protein complexes and are implicated in both nuc

78 This study mined a database of nuclear protein complexes to identify a cellular protein

79 ed the presence of Nurr1 and FGFR1 in common nuclear protein complexes.

80 ions of each var gene, are bound by distinct nuclear protein complexes.

81 The nuclear protein constitutive active/androstane receptor

82 JMJ27 is a nuclear protein containing a zinc-finger motif and a cat

83 We also measured mRNA and nuclear protein content of HIF-1alpha, -2alpha, -3alpha

84 hat loss of cellular compartmentalization of nuclear proteins contributes to muscle disease pathogene

85 Although nuclear proteins could be degraded by importing proteaso

86 In this paper, we identified a novel nuclear protein, Csi1, that localized to the site of cen

87 us on the contribution of the 11 zinc finger nuclear protein, CTCF, in mediating loop formation and c

88 tal Cell, Cooper et al. (2014) report that a nuclear protein, cyclin C, is recruited from nuclei to m

89 As a multifunctional nuclear protein, death domain-associated protein 6 (Daxx

90 F4 recognizes poly-SUMO chains to facilitate nuclear protein degradation.

91 trophoretic mobility shift assays with MCF-7 nuclear protein demonstrate differential binding of the

92 A pull-down assay using nuclear proteins demonstrated that the IFN-lambda1 induc

93 elated with downregulation of the neuroblast nuclear protein, Distal antenna (Dan).

94 K51 by Sirt1 allows LC3 to interact with the nuclear protein DOR and return to the cytoplasm with DOR

95 rential mobility shifting to chromaffin cell nuclear proteins during EMSA, binding of endogenous c-FO

96 The recruitment is absolutely dependent on nuclear proteins EBNA3A and EBNA3C; what is more, epitop

97 e provide definitive evidence that the viral nuclear protein EBNA3C is essential in EBV-infected prim

98 on of most nuclear proteins, suggesting that nuclear protein export had occurred.

99 nucleophagy pathways but is compromised when nuclear protein export is blocked.

100 Here we assessed the role for Geminin, a nuclear protein expressed in embryonic cells, during neu

101 Antigen Ki-67 is a nuclear protein expressed in proliferating mammalian cel

102 orylation of PLCgamma2 and ERK and decreased nuclear protein expression of NF-kappaB p50.

103 ant in vitro cleavage assay system, in which nuclear protein extracts from Arabidopsis (Arabidopsis t

104 Nuclear protein extracts from megakaryocytes, endothelia

105 DNA was much lower in mitochondrial than in nuclear protein extracts, and resulted in persistent DNA

106 As a nuclear protein, FBP1 may translocate to the cytoplasm i

107 e formation of microscopically visible RAD51 nuclear protein foci occurring in the absence of any DNA

108 Thus, PARG release of PAR attached to nuclear proteins, followed by ARH3 cleavage of PAR, is e

109 Of 130 nuclear proteins found associated with the lamin A tail,

110 DNA sequence forms multiunit complexes with nuclear proteins from adult and embryonic striata of mic

111 of rs2978974 showed strong interaction with nuclear proteins from five cell lines tested, implying a

112 t, including both endogenous cytoplasmic and nuclear proteins from individual mammalian cells.

113 th cytosolic, microsomal, mitochondrial, and nuclear proteins from rat liver homogenate and resolved

114 EMSAs) were performed to investigate whether nuclear proteins from these cell lines bind SNP alleles

115 lase (MCM3AP) and germinal-centre associated nuclear protein (GANP) are transcribed from the same loc

116 X-2 is based on a germinal-centre associated nuclear protein (GANP) scaffold to which ENY2, PCID2 and

117 Here, we demonstrate that the nuclear protein Geminin is required to restrain commitme

118 idate mitochondrial regulators including the nuclear protein GLTSCR2, also known as PICT1.

119 Disturbing the RAN (Ras-related nuclear protein)-GTP gradient decoupled nuclear size fro

120 SUMO-modification of nuclear proteins has profound effects on gene expression

121 The extracellular nuclear proteins, histone H4 (H4) and high mobility grou

122 Here we show that the nuclear protein HP1BP3 is widely expressed in most verte

123 sically and functionally interacts with some nuclear proteins, i.e. the lymphoid enhancer-binding fac

124 ch DNA end from rotating by interacting with nuclear proteins; i.e., DNA-binding proteins.

125 110; p110(nrb)/SART3/p110) is an RNA-binding nuclear protein implicated in the regulation of HIV-1 ge

126 Interestingly, several nuclear proteins implicated in posttranscriptional RNA p

127 ortin-beta is the main vector for interphase nuclear protein import and plays roles after nuclear env

128 ent of IMPbeta1- or IMPalpha/beta1-dependent nuclear protein import specifically, whereas specific al

129 most nucleoporins into nuclear pores and for nuclear protein import.

130 ling, and forms the foundation to define the nuclear proteins important for puberty and estrous cycli

131 Shifts in the gene expression of nuclear protein in chronic obstructive pulmonary disease

132 approximately 5 x 10(5) molecules per cell) nuclear protein in HeLa cells.

133 Here we document that BTBD18 is a pachytene nuclear protein in mouse testes that occupies a subset o

134 roscopy that Ago2 is distributed mainly as a nuclear protein in primary human foreskin keratinocytes

135 es reveals that Ago2 exhibits primarily as a nuclear protein in skin, normal cervix, and cervical can

136 valuation in a phase I/II clinical trial for nuclear protein in testis (NUT) midline carcinoma and ot

137 me translocation-mediated fusion of the NUT (nuclear protein in testis) gene on chromosome 15 to a fe

138 ain helicase DNA-binding protein 5) and NUT (nuclear protein in testis) were also demonstrated to be

139 indicated that rs8023462 and rs6495309 bind nuclear proteins in an allele-specific way.

140 lyP-mediated proinflammatory effects of both nuclear proteins in cellular and in vivo systems.

141 Because many cytoplasmic and nuclear proteins in diverse pathways are O-GlcNAc target

142 proteasome-dependent degradation of specific nuclear proteins in mammalian cells and zebrafish embryo

143 that NAD(+)-dependent SIRT1, RELB, and SIRT6 nuclear proteins in monocytes regulate a switch from the

144 ERbeta interacting mitochondrial as well as nuclear proteins in mouse brain using pull-down assay an

145 etter, we mapped sites of O-GlcNAcylation of nuclear proteins in mouse embryonic stem cells (ESCs).

146 ich showed strong allele-specific binding of nuclear proteins in several cell lines.

147 oteins, including membrane, cytoplasmic, and nuclear proteins in T cells and embryonic stem cells.

148 s the gold-standard technique for localizing nuclear proteins in the genome.

149 control molecules, generally presumed to be nuclear proteins in the human beta-cell, are in fact con

150 nrichment of cytoplasmic, cell membrane, and nuclear proteins in the three respective buffer system f

151 hiff-base conjugates with Lys side chains of nuclear proteins in vitro and in vivo.

152 xploring San1, which ubiquitinates misfolded nuclear proteins in yeast for proteasomal degradation.

153 ting with a small G-protein Ran (RAs-related nuclear protein), in the nucleus.

154 sly shown to interact with a growing list of nuclear proteins including chromatin remodeling complexe

155 BRMS1 interacts with several nuclear proteins including SIN3:HDAC chromatin remodelin

156 n enables OGT to catalyze O-GlcNAcylation of nuclear proteins, including Pdx-1.

157 intained by the concerted action of numerous nuclear proteins, including that of the linker histone H

158 ccinylation is also present on cytosolic and nuclear proteins; indeed, we show that a substantial fra

159 Yet not all nuclear proteins interact with importins, necessitating

160 -dependent differences for rs13082711 in DNA-nuclear protein interactions, where the risk allele is a

161 AF-A), originally identified as a structural nuclear protein, interacts with chromatin-associated RNA

162 UHRF2 encodes a nuclear protein involved in cell-cycle regulation.

163 merase IIbeta (Top2b), a broadly distributed nuclear protein involved in chromatin modifications duri

164 nji domain-containing protein 6 (JMJD6) is a nuclear protein involved in histone modification, transc

165 ed here demonstrate that CPS1 is a bona fide nuclear protein involved in homocitrullination (hcit), i

166 talloproteinases-2 and -9), and nucleolin (a nuclear protein involved with synthesis and maturation o

167 Using an interferon-inducible nuclear protein Ipr1 as a biomarker of macrophage activa

168 ne (GlcNAc) to Ser or Thr in cytoplasmic and nuclear proteins is a well known post-translational modi

169 An unexpected attribute of these nuclear proteins is their antimicrobial activity.

170 in beta-catenin turnover, but its effect on nuclear proteins is unknown.

171 SP110b, an IFN-induced nuclear protein, is the nearest human homologue to the m

172 hown that p63, a member of the p53 family of nuclear proteins, is expressed in proliferative cytotrop

173 One hour postinhalation, sputum was induced, nuclear proteins isolated from purified macrophages, and

174 result of SIRT6-mediated deacetylation, PKM2 nuclear protein kinase and transcriptional coactivator f

175 evation of nuclear calcium and activation of nuclear protein kinase D (PKD).

176 Here we identify a family of nuclear protein kinases, designated Photoregulatory Prot

177 ell-conserved family of essential eukaryotic nuclear proteins known to be stress activated and involv

178 ure aging disease caused by mutations in the nuclear protein lamin A.

179 l disorder caused by increased levels of the nuclear protein, Lamin B1.

180 cription predominantly through increased Sp1 nuclear protein levels and increased Sp1 binding to its

181 Excluded are mostly nuclear proteins, like proteins involved in nucleotide b

182 Target of Egr1 (TOE1) is a nuclear protein localized primarily in nucleoli and Caja

183 In this study, we found that a nuclear protein, LYAR (human homologue of mouse Ly-1 ant

184 ist that upregulates CD1d expression via the nuclear protein, lymphoid enhancer-binding factor 1 (LEF

185 pathway regulated by retinoic acid-regulated nuclear protein made the largest contribution to this ge

186 The novel nuclear protein nBMP2 is synthesized from the BMP2 gene

187 the presence of immunoreactivity to neuronal nuclear protein (NeuN-IR) using a mouse monoclonal antib

188 Previously we identified the multifunctional nuclear protein NONO as a partner of circadian PERIOD (P

189 We report that the structural nuclear protein NuMA accumulates at sites of DNA damage

190 of Ty 6 (Spt6) and a homologue of mammalian nuclear protein of the ataxia telangiectasia-mutated loc

191 GRD encodes a small nuclear protein of the RWP-RK family and is broadly tran

192 ion of Ser and Thr residues on cytosolic and nuclear proteins of higher eukaryotes catalyzed by O-Glc

193 Regarding nuclear proteins of NF-kB subunits, Liv-Ikk2ca mice had

194 Whereas menin is largely regarded as a nuclear protein, our data demonstrate a novel cytoplasmi

195 The nuclear protein p54(nrb)/NONO belongs to the Drosophila

196 Here, we show that the nuclear protein p54(nrb)/Nono is highly expressed in bre

197 by the single-chain antibody HF1 and by the nuclear protein PARP-1, both of which are known to recog

198 Damaged DNA-binding protein 2 (DDB2), a nuclear protein, participates in both nucleotide excisio

199 Here, we report that the recently described nuclear protein, Pax2 transactivation domain interaction

200 Nuclear protein peptidyl-prolyl isomerase Pin1-mediated

201 The nuclear protein poly(ADP-ribose) polymerase-1 (PARP-1) h

202 DUF2128 family is related to the eukaryotic nuclear protein positive cofactor 4 (PC4) family and to

203 ormaldehyde (FA) that binds to cytosolic and nuclear proteins producing proteotoxic stress and genoto

204 GANP (germinal- centre associated nuclear protein) promotes the transfer of mRNAs bound to

205 and bulbar muscular atrophy (SBMA), and the nuclear protein PTIP (Pax Transactivation-domain Interac

206 mmarize the known and implicated pathways of nuclear protein quality control, and identify the unreso

207 to selectively detect misfolded proteins for nuclear protein quality control.

208 9 (HEAT9) loop, which regulates GTP-binding nuclear protein Ran binding and cargo release, contains

209 Upon Ras-related nuclear protein (RAN) depletion, cytoplasmic PS-body-lik

210 Accurate control of the Ras-related nuclear protein (Ran) GTPase cycle depends on the regula

211 further show that the flagellar Ras-related nuclear protein (Ran) guanosine 5'-triphosphate (GTP) gr

212 ctroscopy technique to study the ras-related nuclear protein (Ran) pathway, which forms soluble gradi

213 tional insight into the details of misfolded nuclear protein recognition and demonstrate that there i

214 Here, we show that the nuclear protein RED, also called IK, a down-regulator of

215 e (O-GlcNAc) modification of cytoplasmic and nuclear proteins regulates fundamental cellular processe

216 HMGB1 (high mobility group box 1), a nuclear protein released by necrotic and severely stress

217 phila syncytial embryos, we demonstrate that nuclear proteins reorganize during mitosis to form a hig

218 nal interactions between CtBP and Pygopus, a nuclear protein required for Wingless signalling, suppor

219 hemical approach, we establish that Id1 is a nuclear protein restricted to proliferating intestinal c

220 Immunofluorescence microscopy studies of nuclear proteins revealed costaining between PABP1 and m

221 assays revealed that XLG2 interacts with the nuclear protein RTV1 (related to vernalization 1).

222 o nuclei, thus favoring local NO production, nuclear protein S-nitrosylation, and induction of mitoch

223 ese promoters and specifically bound amoebic nuclear protein(s).

224 tibody response and a reduction in influenza nuclear protein-specific CD8(+) T cells compared with mi

225 In order to determine whether activated nuclear protein STAT3 binds to the MMP3 promoter and reg

226 AHLs also share interactions with other nuclear proteins, such as transcription factors, suggest

227 Lov is a nuclear protein, suggesting a role as a transcriptional

228 liver revealed a striking depletion of most nuclear proteins, suggesting that nuclear protein export

229 he SUMO pathway and caused a global shift in nuclear protein SUMOylation patterns.

230 A nuclear protein, SYDN-1, which regulates neuronal develo

231 smablast response to the conserved influenza nuclear protein, than IIV.

232 p15(PAF) is a 12 kDa nuclear protein that acts as a regulator of DNA repair d

233 me to our knowledge that TRAF3 is a resident nuclear protein that associates with the transcriptional

234 RTT is caused by mutations in MECP2, a nuclear protein that becomes phosphorylated at S421 in r

235 ribose) polymerase 1 (PARP-1) is an abundant nuclear protein that binds chromatin and catalyzes the t

236 Here we investigate the role of Ldb1, a nuclear protein that binds directly to all LIM-HD factor

237 Deleted in breast cancer 1 (DBC1) is a nuclear protein that binds to and regulates both Rev-erb

238 RBM14 that is associated with XPO1 (CRM1), a nuclear protein that binds to the HIV-1 Rev protein and

239 up protein B-1 (HMGB1) is a highly conserved nuclear protein that can be actively secreted by innate

240 We show that alpha-cat is a nuclear protein that can interact with beta-catenin (bet

241 We show that Nito is a ubiquitous nuclear protein that controls the alternative splicing o

242 HOP-10) is a novel developmentally regulated nuclear protein that emerges as a critical transcription

243 Promyelocytic Leukemia (PML) is a nuclear protein that forms sub-nuclear structures termed

244 Pre-mRNA processing protein 40 (Prp40) is a nuclear protein that has a role in pre-mRNA splicing.

245 PARP-1 is a nuclear protein that has important roles in maintenance

246 5 and the active kinase domain of JAK2, is a nuclear protein that has the ability to bind to wild-typ

247 e regulatory protein (GKRP), a predominantly nuclear protein that inhibits hepatic glucokinase (GCK)

248 RNF34 is a nuclear protein that interacts with and ubiquitinates PG

249 e show that HDC1 is a ubiquitously expressed nuclear protein that interacts with at least two deacety

250 Here we identify Castor (Cas) as a nuclear protein that is expressed in FSCs and early foll

251 Defective entry into mitosis 1 (Dim1) is a nuclear protein that is implicated in pre-mRNA splicing

252 angiectasia mutated (ATM) is predominantly a nuclear protein that is involved in the early recognitio

253 -binding protein-1 (PQBP-1) is a 265-residue nuclear protein that is involved in transcriptional regu

254 ependent mutations in PRDM6, which encodes a nuclear protein that is specific to vascular smooth musc

255 CCS52A2 messenger RNA encoding a nuclear protein that promotes a shift from mitosis to en

256 NPM1 is a nuclear protein that regulates a variety of cell functio

257 ocm encodes a large nuclear protein that shares a novel cysteine rich motif

258 asis suppressor 1 (BRMS1) is a predominantly nuclear protein that suppresses metastasis in multiple h

259 High-mobility group box 1 (HMGB1) is a nuclear protein that triggers inflammation when released

260 s in methyl-CpG-binding protein 2 (MeCP2), a nuclear protein that, in neurons, regulates transcriptio

261 nd out that MUF1 is a ubiquitously expressed nuclear protein that, upon coexpression with RhoBTB, par

262 High Mobility Group Box 1 (HMGB1) is a nuclear protein that, when released on injury, triggers

263 allowing for the cytoplasmic accumulation of nuclear proteins that are then available to function in

264 MGN) is a family of intrinsically disordered nuclear proteins that bind to nucleosomes, alters the st

265 vation of STAT-3, and increased abundance of nuclear proteins that bind to the STAT-3-responsive elem

266 nate chromosomal regions via modification of nuclear proteins that in turn may regulate genes in the

267 alian mRNA m(6)A methylosome is a complex of nuclear proteins that includes METTL3 (methyltransferase

268 chromatography-mass spectrometry to identify nuclear proteins that interact with the -794 CATT5-8 sit

269 H1 (or linker) histones are basic nuclear proteins that possess an evolutionarily conserve

270 Transcription factors are essential nuclear proteins that trigger the expression of gene pro

271 on of ERbeta with specific mitochondrial and nuclear proteins through consensus CK2, PKC phosphorylat

272 at vertebrate CTCF may also align with other nuclear proteins to accomplish similar functions.

273 n of lncRNAs could serve as "grip holds" for nuclear proteins to pull the genome into new positions.

274 pplied a method for large-scale profiling of nuclear proteins to quantify vasopressin-induced changes

275 xcessive DNA methylation, reduced binding of nuclear proteins to the methylated region and altered ex

276 1 recruits the small GTPase Ran (Ras-related nuclear protein) to chromatin and sets up a Ran-GTP grad

277 each other and themselves, as well as other nuclear proteins, to form complexes which modulate plant

278 Previously, we showed that nuclear protein TOX is also required for murine CD4(+) T

279 the transcription factor ATF4 and identified nuclear protein transcriptional regulator 1 (Nupr1), a s

280 control transcriptional regulation and intra-nuclear protein translocation of FoxM1 in polyploid cell

281 et al. shows that lamin B2, well known as a nuclear protein, undergoes regulated synthesis in axons,

282 reveal an increased association of TFEB with nuclear proteins upon GSK3 and mTOR inhibition suggestin

283 normal isoaspartyl residues predominantly in nuclear proteins upon seed-specific expression in Arabid

284 Given that SF-1 is a nuclear protein, we sought to define the molecular mecha

285 ly interacted with Acinus (Acn), a primarily nuclear protein, which promotes starvation-independent,

286 TDP-43 is a predominantly nuclear protein, which regulates the transcription of th

287 Nuclear proteins whose localization varies during the ce

288 Bypass of Ess1 (Bye1) is a nuclear protein with a domain resembling the central dom

289 we identify the oncoprotein DEK, an abundant nuclear protein with a previously enigmatic in vivo func

290 that HP1BP3 is a ubiquitous histone H1 like nuclear protein with distinct and non-redundant function

291 Although EDM2 encodes a nuclear protein with features commonly observed in epige

292 ve also shown this STR to bind to an unknown nuclear protein with high specificity.

293 SFPQ) is a ubiquitously expressed, essential nuclear protein with important roles in DNA damage repai

294 Methyl-CpG binding protein 2 (MeCP2) is a nuclear protein with important roles in regulating chrom

295 plicate high-mobility group box 1 (HMGB1), a nuclear protein with inflammatory cytokine activities, i

296 ifies HMGN5 as a rapidly evolving vertebrate nuclear protein with species-specific properties.

297 genetic screen in mice to identify ZFP318, a nuclear protein with two U1-type zinc fingers found in R

298 ted modifier (SUMO) to a large collection of nuclear proteins, with studies in Arabidopsis (Arabidops

299 it macroautophagy to capture cytoplasmic and nuclear proteins within autophagosomes.

300 CIP encodes a nuclear protein without recognizable motifs.