ライフサイエンスコーパス: nuclear matrix

1 ied subnuclear fractions (e.g., nucleoli and nuclear matrix).

2 XL9 was also found to be associated with the nuclear matrix.

3 Ralpha immobilization and degradation to the nuclear matrix.

4 all amount of both proteins localized to the nuclear matrix.

5 in or LexA relocalized these proteins to the nuclear matrix.

6 RNA splicing and attachment of dsRNA to the nuclear matrix.

7 tained by interaction with the RNA-dependent nuclear matrix.

8 soluble nuclear substructures, including the nuclear matrix.

9 on the CD4 silencer via association with the nuclear matrix.

10 hat the PROP1 protein is associated with the nuclear matrix.

11 at least one of the HS appears bound to the nuclear matrix.

12 attachment of the inserted sequences to the nuclear matrix.

13 ng within the nucleus and for binding to the nuclear matrix.

14 ible roles in the organization of DNA on the nuclear matrix.

15 ts of the gypsy insulator are present in the nuclear matrix.

16 in the interaction of the telomeres with the nuclear matrix.

17 soluble nuclear fraction, referred to as the nuclear matrix.

18 creased association of the receptor with the nuclear matrix.

19 ar network of nonhistone proteins called the nuclear matrix.

20 obility of Ku70-GFP and its association with nuclear matrix.

21 e have shown that p53 can associate with the nuclear matrix.

22 ion experiments suggest that this represents nuclear matrix.

23 s on either side predicted to associate with nuclear matrix.

24 enhancer regions into close proximity at the nuclear matrix.

25 e nucleus and association of the GR with the nuclear matrix.

26 to 98) appeared important for binding to the nuclear matrix.

27 that is known to occur predominantly at the nuclear matrix.

28 t of cohesin was found to associate with the nuclear matrix.

29 occurs on a nuclear sub-structure termed the nuclear matrix.

30 gest a role for FA proteins in chromatin and nuclear matrix.

31 proposed to be a component of an underlying nuclear matrix.

32 lls and found to localize exclusively to the nuclear matrix.

33 the lack of FA proteins in chromatin or the nuclear matrix.

34 ructurally and functionally organized by the nuclear matrix.

35 untingtin fragments, which tightly bound the nuclear matrix.

36 ARs), domains that organize DNA loops on the nuclear matrix.

37 ) was originally isolated from avian oviduct nuclear matrix.

38 ecyl sulfate-soluble and associated with the nuclear matrix.

39 at Lhx3 is found in both the nucleoplasm and nuclear matrix.

40 Hic-5 in Cos-1 cells was associated with the nuclear matrix.

41 TA binding protein from association with the nuclear matrix.

42 C domain, independently associated with the nuclear matrix.

43 phorylated and specifically localized to the nuclear matrix.

44 spermatids and associated with chromatin and nuclear matrix.

45 n redistribution between the nucleoplasm and nuclear matrix.

46 dition to being an integral component of the nuclear matrix.

47 n, both being localized primarily within the nuclear matrix.

48 as important for PDLIM2 to interact with the nuclear matrix.

49 mmobile FGFR1 population associated with the nuclear matrix.

50 s but not proteins bound to chromatin or the nuclear matrix.

51 n isoform associated with PML bodies and the nuclear matrix.

52 r components such as the nuclear envelope or nuclear matrix.

53 of estrogen receptor-alpha (ERalpha) in the nuclear matrix accompanied by rapid degradation by the u

54 tem cells and is dependent on the C-terminal nuclear matrix anchor domain of CIZ1 and the E repeats o

55 Telomeres are associated with the nuclear matrix and are thought to be heterochromatic.

56 ch likely pulls the HIV DNA segment into the nuclear matrix and away from transcriptional machinery,

57 on reveals that the FA proteins are found in nuclear matrix and chromatin and that treatment with mit

58 pithelial cells, NuMA is present in both the nuclear matrix and chromatin compartments.

59 C results in increase of the FA proteins in nuclear matrix and chromatin fractions.

60 ear organization by tethering the DNA to the nuclear matrix and creating chromatin loops.

61 lay neurons marked during development by the nuclear matrix and DNA binding factor Satb2 (ISR(Satb2))

62 ar substrates that includes both DNA and the nuclear matrix and may represent a mechanism for repair

63 to fulvestrant-induced immobilization to the nuclear matrix and protein degradation.

64 lex but is also suggested to localize to the nuclear matrix and regulate chromatin structure.

65 raction of cyclin D3 was associated with the nuclear matrix and repression of >200 genes including th

66 oAF cells were associated with the HeLa cell nuclear matrix and silenced.

67 that Sp2 preferentially associates with the nuclear matrix and speculate that this subcellular local

68 determinants that target this protein to the nuclear matrix and to discrete subnuclear sites.

69 key nuclear structures (e.g., chromatin and nuclear matrix), and enables its recombinational repair

70 y within subnuclear foci associated with the nuclear matrix, and 2) these foci are distinct from prom

71 CGBP associates with the nuclear matrix, and fragments of CGBP that fail to assoc

72 ith 81 proteins from chromatin modification, nuclear matrix, and RNA remodeling pathways.

73 hermore, menin is localized to chromatin and nuclear matrix, and the association with nuclear matrix

74 stem to study how transcription factors, the nuclear matrix, and the cytoskeleton interact to control

75 subnuclear domains, including chromatin, the nuclear matrix, and the nuclear envelope, where sphingol

76 n co-localized with endogenous AKAP95 in the nuclear matrix, and the physical interaction between fid

77 nx complexes are associated in situ with the nuclear matrix, and this association requires the intran

78 ecent work that bears on the mystique of the nuclear matrix are addressed in this essay.

79 romere protein F (CENPF), a component of the nuclear matrix, are severely reduced at kinetochores in

80 for repair of double-strand breaks using the nuclear matrix as a scaffold.

81 othelial cells, cyclin E is recruited to the nuclear matrix as cells differentiate and this can be ma

82 at this predominant binding state is not the nuclear matrix, as some studies have suggested.

83 nteracting zinc finger protein 1 (CIZ1) is a nuclear matrix associated protein that facilitates a num

84 h differential association of E mu MARs with nuclear matrix- associated PML NBs and LANDs.

85 poptosis) demonstrated dynamic modulation of nuclear matrix-associated B23 without a significant chan

86 in CEM cells preferentially localize to the nuclear matrix-associated DNA indicating their in vivo M

87 Here we show that a variant form of the nuclear matrix-associated DNA replication factor Ciz1 is

88 hereas the U(L)31 gene product of HSV-1 is a nuclear matrix-associated phosphoprotein previously show

89 drawing the receptor into close proximity to nuclear matrix-associated proteasomes that facilitate ER

90 leophosmin/numatrin (B23) is a key nucleolar/nuclear matrix-associated protein required for cell grow

91 olocalized and coimmunoprecipitated with the nuclear matrix-associated protein Runx2 in osteoblasts.

92 s decreased, concomitant with an increase in nuclear matrix-associated protein.

93 ese proteins are usually referred to as the 'nuclear matrix-associated proteins'.

94 mponents of the spliceosome as well as other nuclear matrix-associated proteins.

95 Nuclear matrix-associated regions (MARs) organize chroma

96 s directed by the ETO component to alternate nuclear matrix-associated sites.

97 Two were identified as SRm160, a nuclear matrix-associated splicing coactivator, and hPrp

98 Our studies indicate that both nuclear matrix association and DNA binding are required

99 hese results provide the first evidence that nuclear matrix association dynamically mediates the loop

100 ts are likely to be mediated by the enhanced nuclear matrix association of the ubiquitylation-resista

101 For IgH transactivation, Bright binds to nuclear matrix association regions upstream of certain v

102 t zinc-"finger" that is sufficient to direct nuclear matrix association, and this region also encodes

103 uired for efficient nuclear localization and nuclear matrix association.

104 ount of initial template associated with the nuclear matrix at 15 unique regions spanning the beta-gl

105 Moreover, ETO is nuclear matrix attached at sites coincident with histone

106 Interestingly, nuclear matrix attachment and thus silencing of specific

107 pUC18 and pUC18 plasmids containing various nuclear matrix attachment region (MAR) sequences suggest

108 ond, structural boundary is represented by a nuclear matrix attachment region (MAR), situated about 3

109 ductase origin of replication is a prominent nuclear matrix attachment region (MAR).

110 ese results suggest that NPM associates with nuclear matrix attachment region DNA in heat-shocked cel

111 Nuclear matrix attachment regions (MAR) have been implic

112 lating the human CD8 gene complex, we mapped nuclear matrix attachment regions (MARs) and DNase I hyp

113 ce with different configurations of flanking nuclear matrix attachment regions (MARs) encompassing th

114 as identified as a protein that bound to the nuclear matrix attachment regions (MARs) of the immunogl

115 Nuclear matrix attachment regions (MARs), which flank th

116 ls lie near cellular sequences identified as nuclear matrix attachment regions (MARs), while integrat

117 These sequences were shown to function as nuclear matrix attachment regions (MARs).

118 that this domain exhibits characteristics of nuclear matrix attachment regions (MARs): an exceptional

119 ed nuclease sensitivity flanked by 5' and 3' nuclear matrix attachment regions was defined.

120 also conformed to the consensus sequence for nuclear matrix attachment regions.

121 on with nucleosomal DNA and association with nuclear matrix attachment regions.

122 otein, two methods were employed to localize nuclear matrix attachment sites within intron 1 of the h

123 This complex is flanked by nuclear matrix attachment sites.

124 t least in part be achieved through aberrant nuclear matrix attachment.

125 otein belongs to the same family as SATB1, a nuclear matrix-attachment region binding protein implica

126 ndings suggest that BLM is part of a dynamic nuclear matrix-based complex that requires PML and funct

127 ation, HP1, and SATB1, topoisomerase engages nuclear matrix binding as minor marks of histone acetyla

128 etween the highly conserved PIASy N-terminal nuclear matrix binding domain (SAPD) and the C/EBPdelta

129 also found that TCF-4, beta-catenin, and the nuclear matrix binding protein SMAR1 tether at the -143-

130 These data support that the nuclear matrix binding site (acceptor site) for PR in th

131 experiments suggested that BLM resides in a nuclear matrix-bound complex in which association with h

132 y function in the nucleus in the assembly of nuclear matrix-bound protein complexes involved with tra

133 interact with proteins to form a filamentous nuclear matrix, but this idea became less popular as mor

134 high molecular weight DNA fragments from the nuclear matrix by promoting topoisomerase II-catalyzed D

135 volved in the attachment of chromatin to the nuclear matrix, chromatin remodeling and transcription r

136 istant to salt extraction and behaves like a nuclear matrix/chromosome scaffold-associated structure.

137 he ATPase activity, HELLS is retained at the nuclear matrix compartment, defined in part by lamin B1.

138 A potential nuclear matrix component for this association is actin.

139 Cenp-F is a nuclear matrix component that localizes to kinetochores

140 ded here demonstrate that examination of the nuclear matrix composition allows differentiation of col

141 ar protein in carrot (Daucus carota), called Nuclear Matrix Constituent Protein1 (NMCP1), which conta

142 These nuclear matrix constituent proteins (NMCPs) play importa

143 hat attachment of genes to the NaCl-isolated nuclear matrix correlates with their silencing in HeLa c

144 rescence microscopy, MINT adopts a reticular nuclear matrix distribution that overlaps transcriptiona

145 d by the enhanced localization of CKB to the nuclear matrix during colon tumorigenesis.

146 gesting that the observed high CKB levels in nuclear matrix extracts are caused by the enhanced local

147 ents of CGBP that fail to associate with the nuclear matrix fail to localize to nuclear speckles and

148 helix crippled PDLIM2 in shutting Tax to the nuclear matrix for ubiquitination-mediated degradation,

149 nsformed cells, PDLIM2 shuttles Tax into the nuclear matrix for ubiquitination-mediated proteasomal d

150 p91(phox) promoter binds specifically to the nuclear matrix fraction in vitro.

151 essing was measured in RNA isolated from the nuclear matrix fraction of mouse liver.

152 Pol epsilon, but not Pol delta, was found in nuclear matrix fraction throughout the cell cycle.

153 ; however, Y102E is more associated with the nuclear matrix fraction.

154 pliced and spliced RNA, respectively, in the nuclear matrix fraction.

155 leus to actively expressed chromatin and the nuclear matrix fraction.

156 inity of SMARCA3 and its localization to the nuclear matrix fraction.

157 r, was found to be in the 2 m NaCl-insoluble nuclear matrix fraction.

158 oplasmic/nucleoplasmic, chromatin-bound, and nuclear matrix fractions) showed increased hyperphosphor

159 C3G is associated with chromatin and nuclear matrix fractions.

160 lized to the soluble nuclear, chromatin, and nuclear matrix fractions.

161 showed PELP1 association with chromatin and nuclear matrix fractions.

162 In mammalian cells, the nuclear matrix functions in gene expression and DNA repl

163 ing evidence for this functional role of the nuclear matrix has been elusive and has recently been fu

164 that the dynamic interaction of p53 with the nuclear matrix has to be considered for a full understan

165 Numerous studies of nuclear matrix have failed to provide evidence of the ex

166 sitively with the level of expression of the nuclear matrix high mobility group (HMG) proteins HMGI(Y

167 Pem introns and pre-mRNA accumulated in the nuclear matrix, high salt-soluble, and DNase-sensitive f

168 iated gene activation shifted FGFR1 from the nuclear matrix (immobile) to chromatin (slow) and reduce

169 end of the 20th century, the concept of the nuclear matrix implies the existence of a nuclear skelet

170 nt promoter in vitro and associates with the nuclear matrix in a DNA-independent fashion, 3) zebrafis

171 for the first time, that p53 is bound to the nuclear matrix in primary cultures of normal mammalian c

172 To address the role of the nuclear matrix in SATB1-mediated repression, a series of

173 the insulator tethers the SP-10 gene to the nuclear matrix in somatic tissues, sequestering the core

174 s an essential role in anchoring Xist to the nuclear matrix in specific somatic lineages.

175 hat cyclin E, but not A, is mounted upon the nuclear matrix in sub-nuclear foci in differentiated ver

176 ysis of the results obtained in the study of nuclear matrix in the light of current views on the orga

177 of the polycomb complex and the role of the nuclear matrix in the process of X chromosome inactivati

178 have identified p53 in association with the nuclear matrix in viral- and non-viral transformed cell

179 t bore no relation to their affinity for the nuclear matrix in vitro.

180 obulin (betalg) gene that interacts with the nuclear matrix in vitro.

181 s DNA elements that bind specifically to the nuclear matrix in vitro.

182 hey also mediate binding of chromatin to the nuclear matrix in vivo and alter the topology of the gen

183 distinguish between a network-like 'internal nuclear matrix' (INM) and a 'nuclear shell' that connect

184 The pattern of the nuclear matrix interaction correlated directly with the

185 malignant transformation compromises the DNA-nuclear matrix interface.

186 A preferentially relocalized Dnmt3a from the nuclear matrix into the chromatin fraction.

187 of a well defined locus control region, the nuclear matrix is considered the primary candidate regul

188 and nuclear matrix, and the association with nuclear matrix is enhanced by gamma-irradiation.

189 ts of p53 revealed that association with the nuclear matrix is independent of the tertiary and quater

190 The assembly of E4-ORF3 into a multivalent nuclear matrix is required to target PIAS3.

191 The nuclear matrix is the structural scaffolding of the nucl

192 ed at least three AKAP95-binding proteins in nuclear matrix isolated from rat brain.

193 to a brief heat shock, or destruction of the nuclear matrix lead to disruption of the loop.

194 progesterone-regulated avian c-myc gene, and nuclear matrix-like attachment sites flank the RBF eleme

195 ike the fibrogranular structures termed the "nuclear matrix." Like the residual material seen in nucl

196 We have previously isolated a novel nuclear matrix-localized protein (MFP1) from tomato (Lyc

197 nuclear entry, association of Lhx3 with the nuclear matrix may contribute to LIM homeodomain factor

198 mans, dynamic alterations in the chromosomal nuclear matrix may modulate the -sigma of certain DNA re

199 The nuclear matrix (NM) is a structure resulting from the ag

200 evated in rapidly proliferating tissues, and nuclear matrix (NM) is an important subnuclear locale of

201 eous Nuclear Ribonucleoprotein U (HNRNPU), a nuclear matrix (NM)-associated protein, in 3D genome org

202 teraction of the Ifng gene promoter with the nuclear matrix occurred differentially in a lineage-spec

203 ermatocyte stage with the recruitment to the nuclear matrix of a large approximately 9.6-kb region ju

204 d to localize strongly to the nuclei and the nuclear matrix of cultured urothelial cells.

205 is present within nuclei and can target the nuclear matrix of CV-1 cells, cultured prostate cancer c

206 high molecular weight DNA fragments from the nuclear matrix of HL-60 leukemia cells, which preceded t

207 The helicase and AKAP95 co-localized in the nuclear matrix of mammalian cells, associated in vitro,

208 Furthermore, aberrations in the nuclear matrix often contribute to genomic instabilities

209 ation may control AHL10 association with the nuclear matrix or with other transcriptional regulators.

210 finity for DNA, transport to the nucleus, or nuclear matrix organization.

211 fically increases mRNA and protein levels of nuclear matrix peptides lamins A and C, suggesting that

212 In osteoblasts, MINT may serve as a nuclear matrix platform that organizes and integrates os

213 ile atrophin-1 and ETO/MTG8 cofractionate in nuclear matrix preparations from brains of DRPLA transge

214 matrix." Like the residual material seen in nuclear matrix preparations, the hnRNP filaments were in

215 Both in intact cells and in nuclear matrix preparations, the majority of Bright and

216 poisomerase II-mediated cleavage in isolated nuclear matrix preparations.

217 eolar phosphoprotein that is concentrated in nuclear matrix preparations.

218 ermediary factor 1 gamma, anti-MDA5 and anti-nuclear matrix protein 2, which are potentially exploita

219 Others, such as nuclear matrix protein 22 (NMP22) and UroVysion, appear

220 rug Administration (FDA) approved the use of Nuclear matrix protein 22 (NMP22) as a monitoring tool f

221 Nmp4/CIZ proteins (nuclear matrix protein 4/cas interacting zinc finger pro

222 (such as ribosomal proteins L3, L5, and L28; nuclear matrix protein 84; matrin cyclophilin; the H3 hi

223 We now report that RGS12TS-S is a nuclear matrix protein and identify structural determina

224 The nuclear matrix protein Cip1-interacting zinc finger prot

225 Matrin3 is an RNA- and DNA-binding nuclear matrix protein found to be associated with neura

226 This work identifies phosphorylation of the nuclear matrix protein matrin 3 as a new conserved targe

227 rupts the 3' UTR of MATR3, which encodes the nuclear matrix protein Matrin 3, and mouse Matr3 is stro

228 member of the BTB/Kelch repeat family, is a nuclear matrix protein normally expressed in neurons but

229 ived 2 (E2)-related factor 2 (NRF2) with the nuclear matrix protein NRP/B was essential for the trans

230 in breast cancer cells, we observed that the nuclear matrix protein NRP/B was expressed and colocaliz

231 Here, we showed that the nuclear matrix protein nuclear restricted protein in bra

232 ting with both the nuclear envelope and DNA, nuclear matrix protein NuMA (Nuclear mitotic apparatus),

233 Here, we show that the nuclear matrix protein SAFA (also known as HnRNPU) funct

234 elopmental Cell, Agrelo et al. show that the nuclear matrix protein SATB1 is a critical determinant o

235 l, Grosschedl and colleagues report that the nuclear matrix protein Satb2 represses Hoxa2 expression

236 Scaffold attachment factor-B1 (SAFB1) is a nuclear matrix protein that has been proposed to couple

237 t in part through the inhibition of SATB2, a nuclear matrix protein that is a critical determinant of

238 he Nrf2 pathway, identifying a novel role of nuclear matrix protein(s) in oxidative stress responses.

239 locytic leukemia zinc finger, nucleophosmin, nuclear matrix protein, and signal transducer and activa

240 Studies of the novel neuronal nuclear matrix protein, NRP/B, reveal that it is an earl

241 Here we report that the nuclear matrix protein, scaffold attachment factor B1 (S

242 Since CDP is a nuclear matrix protein, two methods were employed to loc

243 hypothesis that fulvestrant induces specific nuclear matrix protein-ERalpha interactions that mediate

244 We have characterized previously the nuclear matrix protein/scaffold attachment factor (SAFB)

245 ral scaffolding of the nucleus, and specific nuclear matrix proteins (NMPs) have been identified as a

246 ine novel protein-protein interactions among nuclear matrix proteins and suggest a potential role of

247 Alterations of nuclear matrix proteins are frequently involved in chang

248 was identified as matrin 3, one of the major nuclear matrix proteins.

249 binding to WW domain or SMAD proteins or the nuclear matrix retain this growth regulatory ability.

250 equences that independently target SRm160 to nuclear matrix sites at splicing speckled domains: amino

251 signal sequence that impair its targeting to nuclear matrix sites.

252 se proteins were coimmunoprecipitated from a nuclear matrix-solubilized fraction, and the purified re

253 ed for interaction with focal adhesions, the nuclear matrix, steroid receptors, and the tau2 domain o

254 nrb), the splicing factor PSF, and the inner nuclear matrix structural protein matrin 3.

255 of RAI1 was found in the chromatin bound and nuclear matrix subcellular fractions while the mutant pr

256 and showed that NCoA62/SKIP was targeted to nuclear matrix subdomains.

257 had a greatly diminished localization to the nuclear matrix, suggesting the presence of a nuclear mat

258 fy determinants for nuclear localization and nuclear matrix targeting of AKAP95.

259 nuclear matrix, suggesting the presence of a nuclear matrix targeting sequence (NMTS).

260 A second nuclear matrix targeting sequence is encoded within the

261 The presence of the nuclear matrix targeting sequence is required for Runx-m

262 The latter region contains the nuclear matrix targeting sequence, which is highly conse

263 ermore, the HTY mutation overlaps the unique nuclear matrix targeting signal of Runx factors and exhi

264 egment that is responsible for localization (nuclear matrix targeting signal).

265 n of physiological signals, and contains the nuclear matrix targeting signal, the protein motif that

266 conservation of the nuclear localization and nuclear matrix targeting signals suggests that the LIM h

267 in, which are also known to be important for nuclear matrix targeting.

268 association or paralogue association and for nuclear matrix targeting.

269 A novel nuclear matrix-targeting sequence was identified that is

270 Furthermore, we show that the nuclear matrix-targeting signal and DNA-binding runt-hom

271 A unique nuclear matrix-targeting signal in the C terminus direct

272 have identified point mutations of the Runx2 nuclear matrix-targeting signal sequence that impair its

273 Runx2 was mapped to a region overlapping the nuclear matrix-targeting signal.

274 The nuclear matrix-targeting site is unique but conserved am

275 ted in situ and found to be dependent on the nuclear matrix-targeting site.

276 fragment is less tightly associated with the nuclear matrix than full-length hbrm.

277 RNA- and DNA-binding protein enriched in the nuclear matrix that also plays a role in the regulation

278 teraction of the Ifng gene promoter with the nuclear matrix that may set off transcription in activat

279 isrupts the association between hbrm and the nuclear matrix; the 160-kDa hbrm cleavage fragment is le

280 ctures are thought to be associated with the nuclear matrix, they appear to be released from this mat

281 n the region interact with components of the nuclear matrix to form a compact stable cluster.

282 Splice variants of the Nmp4 gene include nuclear matrix transcription factors that regulate the t

283 When exposed by epitope retrieval and nuclear matrix unmasking techniques, endogenous SPARC wa

284 reased targeting of androgen receptor to the nuclear matrix upon overexpression of paxillin may be br

285 Attachment of DNA to the nuclear matrix via matrix attachment region (MAR) sequen

286 n monocytes, can tether the TNF locus to the nuclear matrix via matrix attachment region formation, p

287 The interaction of chromatin with the nuclear matrix via matrix attachment regions (MARs) on t

288 Direct binding of AKAP95 to isolated nuclear matrix was demonstrated in situ and found to be

289 s was reduced while its association with the nuclear matrix was increased.

290 Strong association of the promoter with the nuclear matrix was observed only in the Th1 cell subset

291 ell fraction that would today be termed "the nuclear matrix" was first described and patented in 1948

292 n of TPZ is/are thought to be at or near the nuclear matrix, we hypothesized that TPZ may have a majo

293 in was previously shown to reside within the nuclear matrix, we show here that a significant amount o

294 uited Tax from its functional sites into the nuclear matrix where the polyubiquitinated Tax was degra

295 -dependent binding of the XPA protein to the nuclear matrix, which was also observed in UV light-trea

296 ed here is to anchor hyperedited RNAs to the nuclear matrix, while allowing selectively edited mRNAs

297 8 with atrophin-1 recruits atrophin-1 to the nuclear matrix, while atrophin-1 and ETO/MTG8 cofraction

298 d that calspermin does not colocalize to the nuclear matrix with CaMKIV.

299 icited proteasomal degradation of Tax in the nuclear matrix with concomitant inhibition of NF-kappaB

300 terized by heterogeneous condensation of the nuclear matrix without formation of discrete chromatin m