ライフサイエンスコーパス: nuclear protein

1 the absence of TDP-43 aggregation or loss of nuclear protein.

2 -3 or AIB1), a large and mostly unstructured nuclear protein.

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

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

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

6 ntrolling the subnuclear localization of the nuclear proteins.

7 ill no reliable and quantitative resource of nuclear proteins.

8 ell immunoblots to detect both cytosolic and nuclear proteins.

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

10 correlates with increased ubiquitination of nuclear proteins.

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

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

13 atrophy restricted the transport of smaller nuclear proteins.

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

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

16 ohydrate modification found on cytosolic and nuclear proteins.

17 to investigate cofractionation of groups of nuclear proteins.

18 important role for export in the turnover of nuclear proteins.

19 r (EGFR) that phosphorylates cytoplasmic and nuclear proteins.

20 neutrophil extracellular traps that contain nuclear proteins.

21 disorganization of lamin A/C and leakage of nuclear proteins.

22 otein lamin A distorts nuclei and sequesters nuclear proteins.

23 HBoV1 encodes a small nonstructural protein, nuclear protein 1 (NP1), that plays an essential role in

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

25 poptotic markers and increased expression of nuclear protein 1 and tribbles related protein-3 compare

26 re, a process governed in part by Transition Nuclear Proteins 1 and 2 (TNP1 and TNP2).

27 ity of the nuclear lamina and leakage of the nuclear protein 53BP1 to the cytosol.

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

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

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

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

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

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

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

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

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

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

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

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

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

41 AFFL-2 is a broadly expressed nuclear protein, and nuclear localization of AFFL-2 is n

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

43 -redundant: USP28 stabilizes c-MYC and other nuclear proteins, and USP25 regulates inflammatory TRAF

44 d B cells; NO generation; S-nitrosylation of nuclear proteins; and DNA accessibility as reflected by

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

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

47 Biological functions of nuclear proteins are regulated by post-translational mod

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

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

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

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

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

53 ShMYB78 was shown to be a nuclear protein based on its presence in sugarcane inter

54 Nuclear proteins bind chromatin to execute and regulate

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

56 ficant SNP, rs4730222, exhibits differential nuclear protein binding in electrophoretic mobility shif

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 ormation are found not only in cytosolic and nuclear proteins, but also in membrane-associated protei

61 cause nuclear rupture and mislocalization of nuclear proteins, but damage to DNA remains uncertain, a

62 syltransferase that modifies cytoplasmic and nuclear protein by transfer of N-acetylglucosamine (O-Gl

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

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

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 Nuclear protein co-immunoprecipitation demonstrated an i

69 Other loci recovered were the nuclear protein-coding genes for antithrombin or SerpinC

70 ,389 mutants in the library, covering 83% of nuclear protein-coding genes, are available to the commu

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

72 odelling, replacing the separate cytoplasmic/nuclear protein compartments that were characteristic of

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

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

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

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

77 We demonstrate that TaHRC encodes a nuclear protein conferring FHB susceptibility and that a

78 inct substructures and distinguishes between nuclear proteins confined to the nucleus and those that

79 The nuclear protein constitutive active/androstane receptor

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

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

82 Although nuclear proteins could be degraded by importing proteaso

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

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

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

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

87 How nuclear proteins diffuse and find their targets remains

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

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

90 Regulated transport of nuclear proteins (e.g., transcription factors) between m

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

92 ivity is critically dependent on C11orf46, a nuclear protein encoded in the chromosome 11p13 WAGR ris

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

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

95 ticularly dependent on the EBV SM protein, a nuclear protein expressed early during lytic reactivatio

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

97 To test the relevance to nuclear proteins expressed in skeletal muscle, we studie

98 AF upregulated nuclear protein expression of IP(3)R1 (IP(3)R-type 1) an

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

100 responses, we performed mass spectrometry on nuclear proteins extracted from Cre-negative controls an

101 Nuclear protein extracts from megakaryocytes, endothelia

102 based on its presence in sugarcane internode nuclear protein extracts, and protoplast transactivation

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

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

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

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

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

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

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

110 role of the nucleosome in regulating diverse nuclear protein functions.

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

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

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

114 erizing a Phaeodactylum tricornutum bHLH-PAS nuclear protein, hereby named RITMO1, we shed light on t

115 CpG-binding-Protein 2 (MeCP2) is an abundant nuclear protein highly enriched in neurons.

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

117 aneous modification and translocation of the nuclear protein HP1alpha in live cells.

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

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

120 where colloid osmotic pressure generated by nuclear protein import inflates the nucleus.

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

122 We propose that CidB targets nuclear-protein import and protamine-histone exchange an

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

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

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

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

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

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

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

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

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

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

133 e demonstration of O-GalNAc glycosylation of nuclear proteins in mammalian cells reported here has im

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

135 e long-standing knowledge gap is the role of nuclear proteins in mRNA translation.

136 that the transport properties of these model nuclear proteins in myotubes depended on molecular weigh

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

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

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

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

141 -linked glycosylation (O-GalNAc) as a PTM of nuclear proteins in the human cell has not been previous

142 an biosynthesis, representing a novel PTM of nuclear proteins in the nucleus of human cells, with an

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

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

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

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

147 ty is mediated in part by S-nitrosylation of nuclear proteins, including MTA3 (Metastasis Associated

148 eles showed differential binding to multiple nuclear proteins, including stronger IRF2 binding to the

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

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

151 5fC uniquely interacts and reacts with key nuclear proteins, indicating functions in genome regulat

152 Yet not all nuclear proteins interact with importins, necessitating

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

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

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

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

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

158 , and Runt-related transcription factor 2, a nuclear protein involved in osteoblastic differentiation

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

160 eome analysis highlighted acetylation on key nuclear proteins involved in the DNA damage response and

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

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

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

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

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

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

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

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

169 in kinase (HIPK) family is comprised of four nuclear protein kinases, HIPK1-4.

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

171 formability by twofold overexpression of the nuclear protein lamin A or we introduce into the cells s

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

173 Mutations in LMNA, which encodes the nuclear proteins Lamin A/C, can cause cardiomyopathy and

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

175 the formation of NETs through proteolysis of nuclear proteins leading to chromatin decondensation.

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

177 dementia (IBM-PFD)-together with its adaptor nuclear protein localization (NPL)4, specifically intera

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

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

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

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

182 emporal expression window of BTB-zinc finger nuclear protein, Mamo.

183 ple motile cilia (RGMC), have implicated the nuclear protein MCIDAS (MCI), in the transcriptional reg

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

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

186 signaling molecules (FTL3-ITD, RAS) and the nuclear protein NPM1).

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

188 Nuclear protein of the testis (NUT) midline carcinoma (N

189 teins identified HAI1-Interactor 1 (HIN1), a nuclear protein of unknown function which could be depho

190 a gene encoding a beta cell/stomach-enriched nuclear protein of unknown function.

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

192 ve cellular injury results in the release of nuclear proteins, of which histones are the most abundan

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

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

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

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

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

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

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

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

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

202 r, unlike NMNAT1, NAMPT is not known to be a nuclear protein, prompting the question of how the nucle

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

204 m chloroplasts and mitochondria merge at the nuclear protein RADICAL-INDUCED CELL DEATH1 (RCD1).

205 9 (HEAT9) loop, which regulates GTP-binding nuclear protein Ran binding and cargo release, contains

206 fects on the nucleus by trapping Ras-related nuclear protein (RAN) and preventing it from transportin

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

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

209 to those found in the eukaryotic Ras-related nuclear protein (Ran) guanine nucleotide exchange factor

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

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

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

213 rate that endogenous cGAS is predominantly a nuclear protein, regardless of cell cycle phase or cGAS

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

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

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

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

218 Interestingly, the nuclear protein SIRT6 presents the greatest inhibitory e

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

220 Reversible lysine acetylation of nuclear proteins such as histones is a long-established

221 RAN) and preventing it from transporting key nuclear proteins such as, DNMT3A, for maintaining normal

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

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

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

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

226 Ramazzottius varieornatus contains a unique nuclear protein termed Dsup, for damage suppressor, whic

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

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

229 NKAP is a multifunctional nuclear protein that associates with the histone deacety

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

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

232 es pombe histone chaperone Sim3 is a soluble nuclear protein that binds the histone variant CenH3 and

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

234 MeCP2 is a nuclear protein that binds to sites of cytosine methylat

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

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

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

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

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

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

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

242 5 and the active kinase domain of JAK2, is a nuclear protein that has the ability to bind to wild-typ

243 Rad23 can bind Ho-endonuclease (Ho-endo), a nuclear protein that initiates mating-type switching in

244 The product of Pten-NOLC1 is a nuclear protein that interacts and activates promoters o

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

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

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

248 TEX15 is predominantly a nuclear protein that is not required for piRNA biogenesi

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

250 JNK links to 53BP1, a nuclear protein that negatively regulates DNA double-str

251 WDR5 is a highly-conserved nuclear protein that performs multiple scaffolding funct

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

253 hatase 1 (NIPP1) is a ubiquitously expressed nuclear protein that regulates functions of protein seri

254 Here we show that AKAP95, a nuclear protein that regulates transcription and RNA spl

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

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

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

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

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

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

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

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

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

264 Furthermore, nuclear proteins that participate in mRNA export, such a

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

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

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

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

269 es the trafficking of histone protein H2B, a nuclear protein, to the mitochondria in cancer cells.

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

271 These results reveal nuclear protein trafficking as a function affected by AI

272 highlight a disruption of multiple essential nuclear protein trafficking pathways by polyQ-ataxin-1,

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

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

275 We have developed a mathematical model of nuclear protein transport within a myotube that recapitu

276 By interacting with another nuclear protein TYROSYL-DNA PHOSPHODIESTERASE1 (TDP1), A

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

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

279 EBV nuclear proteins usurp normal transcriptional programs t

280 A rapid digestion of nuclear protein was performed to minimize enzymatic DNA

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

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

283 eased the transport of high molecular weight nuclear proteins, while atrophy restricted the transport

284 little or no (15)N-protein contents in most nuclear proteins, while there were a broad range of (14)

285 SPOCD1 is a nuclear protein whose expression is restricted to the pe

286 Nuclear proteins whose localization varies during the ce

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

288 zymes in the prenylation pathway and SAFB, a nuclear protein with both DNA and RNA binding domains.

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

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

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

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

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

294 PARP1 is an abundant nuclear protein with many pleiotropic functions involved

295 SAF-A/hnRNPU is an abundant nuclear protein with RNA-to-DNA tethering activity, coor

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

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

298 used to predict the spatial distributions of nuclear proteins within a myotube.

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

300 , the principles underlying the transport of nuclear proteins within multinucleated cells remain poor