ライフサイエンスコーパス: minichromosome

1 of DDX5 enhanced transcription from the HBV minichromosome.

2 irectly to that of the bulk, non-transcribed minichromosome.

3 protein required for replication of the SV40 minichromosome.

4 a y+ rescue element on a freely segregating minichromosome.

5 ion, but not from the additional copy of the minichromosome.

6 centromere present in the Drosophila Dp1187 minichromosome.

7 e destabilizing drugs and instability of the minichromosome.

8 ole in replication or expression of the rDNA minichromosome.

9 cription of the Tetrahymena thermophila rDNA minichromosome.

10 ciate with cellular histone proteins to form minichromosomes.

11 endogenous origins and at origins located on minichromosomes.

12 stones associated with the transcribing SV40 minichromosomes.

13 aplotypes of the two polymorphic loci on the minichromosomes.

14 DNA ends to generate functional macronuclear minichromosomes.

15 epresentation of IS elements, similar to the minichromosomes.

16 undant telomeres due to the presence of many minichromosomes.

17 iction fragments and at the ends of isolated minichromosomes.

18 cells exhibit reduced microtubule binding to minichromosomes.

19 anized into a large chromosome and 2 related minichromosomes.

20 the mitotic stability of centromere-bearing minichromosomes.

21 s, translocations, and formation of acentric minichromosomes.

22 rase delta (POLD1), DNA primase (PRIM1), and minichromosome 6 (MCM6).

23 an be suppressed by the presence of a second minichromosome, a phenomenon termed "trans-suppression."

24 In this study, by using minichromosome affinity purification (MAP) and mass spec

25 omes are tethered to host histones to form a minichromosome also known as an "episome." Histones, whi

26 cription of the Tetrahymena thermophila rDNA minichromosome and are required for cell cycle-controlle

27 ired for viability, and mutations cause both minichromosome and endogenous chromosome inheritance def

28 ments, rearranged into a 'palindromic' 21 kb minichromosome and extensively amplified.

29 matin structure of this promoter both in the minichromosome and in the genomic STE6 locus.

30 ption in the inactive VSG Basic Copy arrays, minichromosomes and procyclin loci.

31 in required for the efficient replication of minichromosomes and the transcriptional regulation of ea

32 oresis reveal that sisters of 26 kb circular minichromosomes are held together by catenation as well

33 s easily produced in bacteria, and it formed minichromosomes as HBV cccDNA episome DNA does when it w

34 used to a beta-galactosidase gene in a yeast minichromosome, as well as factors that control the chro

35 HPV origin-containing plasmids partition as minichromosomes, attributable to an association of the v

36 HBV covalently closed circular DNA (cccDNA) minichromosome, both in cultured cells in which HBV is r

37 Engineered minichromosomes can be easily constructed by a telomere-

38 For example, minichromosomes can be used as a platform for efficient

39 We employ a biotin-streptavidin minichromosome capture assay to show that yRad51 or hRad

40 red de novo methylation by using replicating minichromosomes carrying various ICs as targets.

41 owever, endogenous centromeres and X-derived minichromosome centromeres in vivo were replicated async

42 , and its suppression, using a non-essential minichromosome, Ch(16), in fission yeast.

43 ue DSB could be generated in a non-essential minichromosome, Ch(16), using the Saccharomyces cerevisi

44 The results show that the two types of minichromosome contain the same number of nucleosomes as

45 In contrast, minichromosomes containing 7 kb of chromosomal DNA inclu

46 iotic centromeric cohesion is compromised in minichromosomes depending on their size and cannot be ma

47 n requirements at the centromere on a set of minichromosome derivatives [4], we tested the role of he

48 two de novo centromeres on Zea mays (maize) minichromosomes derived from euchromatic sites with high

49 A collection of minichromosomes derived from the chromosome type breakag

50 The other eight minichromosomes did not pair with themselves, and the si

51 cohesin rings concatenate individual sister minichromosome DNA molecules.

52 Terminal deletions of a Drosophila minichromosome (Dp(1;f)1187) dramatically increase the p

53 Fourteen minichromosomes from this set could pair with each other

54 s at both telomeres and several cross-linked minichromosomes had t-loops at both ends.

55 fragment taken from the VP1 gene in the SV40 minichromosome has been measured in polyacrylamide gels

56 We conclude that in transcribing SV40 minichromosomes histone hyperacetylation and deacetylati

57 traps sister DNAs of circular but not linear minichromosomes implies that cohesin functions using a t

58 ed with multiple human tumors, persists as a minichromosome in the nucleus of B lymphocytes and induc

59 lity as seen by the high-frequency loss of a minichromosome in yeast.

60 The 17alpha HAC vectors generated artificial minichromosomes in 32-79% of the HT1080 clones screened,

61 The final construct generates minichromosomes in HT1080 cells and the HPRT gene is exp

62 itro it efficiently initiates replication of minichromosomes in membrane-free DNA synthesis reactions

63 Minichromosomes in the nuclear genome of Trypanosoma bru

64 Segregation of T. brucei minichromosomes in these stalled cells is impaired, impl

65 histone H3, a correlate of cohesion, in the minichromosomes in which sister chromatids separated dur

66 s by using patch-methylated stable episomes (minichromosomes) in human cells.

67 Of these, 69 decreased minichromosome inheritance while 9 increased minichromos

68 minichromosome inheritance while 9 increased minichromosome inheritance.

69 Despite this, replication of the rDNA minichromosome initiates precociously.

70 We demonstrate directly that a linear minichromosome introduced into one of the fusion mutant

71 ive to a normal B chromosome, the progenitor minichromosome is estimated to be at least several megab

72 some-free, while that of the non-transcribed minichromosome is nucleosome covered.

73 t minichromosomes or on host chromosomes and minichromosomes, is confirmed using chromosome conformat

74 e acetylation and methylation throughout the minichromosome LCR/hGH-N domain.

75 rapamycin complex 1 (TORC1) by the increased minichromosome loss 1/ GTPase-activating proteins toward

76 nase domain and rad53 null mutants display a minichromosome loss phenotype, Rad53 is important in the

77 lting in an F391I change) showed a classical minichromosome loss phenotype.

78 trains showed little difference in growth or minichromosome loss rate when compared to single deletio

79 Surprisingly, DSB-induced minichromosome loss was significantly reduced in ku70Del

80 F3 complex, results in a higher frequency of minichromosome loss, nocodazole sensitivity, and mitotic

81 elta strains exhibited a modest elevation in minichromosome loss, similar to cbh1Delta or abp1Delta s

82 The minichromosome maintenance (MCM) 2-7 helicase complex fu

83 In the presence of the T. kodakaraensis minichromosome maintenance (MCM) 3' --> 5' DNA helicase,

84 emporally discrete steps: a double hexameric minichromosome maintenance (MCM) complex is first loaded

85 The heterohexameric minichromosome maintenance (MCM) complex is the core com

86 The minichromosome maintenance (MCM) complex is the replicat

87 The minichromosome maintenance (MCM) complex is thought to f

88 one mutation corresponds to a subunit of the minichromosome maintenance (MCM) complex of proteins, MC

89 eukaryotic DNA replication by recruiting the minichromosome maintenance (MCM) complex onto DNA.

90 The origin recognition complex, Cdc6 and the minichromosome maintenance (MCM) complex play essential

91 The minichromosome maintenance (MCM) complex plays essential

92 port the identification of the heterohexamic minichromosome maintenance (MCM) complex that interacts

93 requires the recruitment of the six-subunit minichromosome maintenance (Mcm) complex to chromatin th

94 he remaining factor that is necessary as the minichromosome maintenance (MCM) complex, a cellular hel

95 The minichromosome maintenance (MCM) complex, a replicative

96 hase, inhibition of chromatin loading of the minichromosome maintenance (Mcm) complex, and a reduced

97 In archaea, the replicative helicase is the minichromosome maintenance (MCM) complex.

98 be a functional homologue of the eukaryotic minichromosome maintenance (MCM) complex.

99 sphorylation of target proteins, such as the minichromosome maintenance (Mcm) complex.

100 for the eukaryotic replicative helicase, the minichromosome maintenance (MCM) complex.

101 n complex containing the ATPase Cdc6 and the minichromosome maintenance (Mcm) complex.

102 rated for recombinant archaeal homohexameric minichromosome maintenance (MCM) complexes and their yea

103 Members of the minichromosome maintenance (MCM) family have pivotal rol

104 The eukaryotic minichromosome maintenance (MCM) family of proteins (MCM

105 The minichromosome maintenance (MCM) family of proteins is c

106 The minichromosome maintenance (MCM) gene family is essentia

107 cyclin, E2F1, cell division cycle (CDC), and minichromosome maintenance (MCM) genes.

108 element (DUE)-binding protein DUE-B and the minichromosome maintenance (MCM) helicase activator Cdc4

109 replication stress presented by a defective minichromosome maintenance (MCM) helicase allele in yeas

110 to replication origins coordinately with the minichromosome maintenance (MCM) helicase and the helica

111 The minichromosome maintenance (MCM) helicase complex is ess

112 st human genome duplication requires loading minichromosome maintenance (MCM) helicase complexes at m

113 aromyces pombe Mcm4,6,7 complex and archaeal minichromosome maintenance (MCM) helicase from Methanoth

114 auses subunit-specific changes of sumoylated minichromosome maintenance (MCM) helicase in addition to

115 The minichromosome maintenance (MCM) helicase is the replica

116 Using minichromosome maintenance (MCM) helicase mutant protein

117 Specifically, minichromosome maintenance (MCM) helicase proteins are l

118 y of a replication origin and recruitment of minichromosome maintenance (MCM) helicase to that origin

119 re-replication complex (pre-RC), such as the minichromosome maintenance (MCM) helicase.

120 Minichromosome maintenance (MCM) helicases are the presu

121 gins requires the loading of two ring-shaped minichromosome maintenance (MCM) helicases around DNA in

122 The solved atomic structure of an archaeal minichromosome maintenance (MCM) homolog provides insigh

123 In many archaea, there is a single minichromosome maintenance (MCM) homologue, presumed to

124 rrent models indicate that direct binding to minichromosome maintenance (MCM) plays a role, but the d

125 The hexameric Minichromosome Maintenance (MCM) protein complex forms a

126 Minichromosome maintenance (MCM) protein complexes have

127 Minichromosome maintenance (Mcm) proteins 2-7 are highly

128 The minichromosome maintenance (Mcm) proteins 2-7 are requir

129 The minichromosome maintenance (MCM) proteins are essential

130 Minichromosome maintenance (MCM) proteins are essential

131 The minichromosome maintenance (MCM) proteins are essential

132 Minichromosome maintenance (MCM) proteins are key elemen

133 Minichromosome maintenance (MCM) proteins are loaded ont

134 The minichromosome maintenance (MCM) proteins are thought to

135 Loading of the six related Minichromosome Maintenance (MCM) proteins as head-to-hea

136 Origin Recognition Complex (ORC) and minichromosome maintenance (MCM) proteins form prereplic

137 Eukaryotes have six minichromosome maintenance (MCM) proteins that are essen

138 This group included all of the minichromosome maintenance (MCM) proteins that are requi

139 and Glossina, but we identified a complex of minichromosome maintenance (MCM) proteins that functiona

140 ication are licensed in G1 by recruiting the minichromosome maintenance (MCM) proteins to form a prer

141 sion yeast) as a mediator for association of minichromosome maintenance (MCM) proteins with chromatin

142 The minichromosome maintenance (MCM) proteins, a family of s

143 th the PBD of Plk1, we identified two of the minichromosome maintenance (MCM) proteins, Mcm2 and Mcm7

144 y involves the Cdc6-dependent loading of six minichromosome maintenance (Mcm) proteins, Mcm2-7, onto

145 The minichromosome maintenance (MCM) proteins, together with

146 s have suggested a two-step binding mode for minichromosome maintenance (MCM) proteins, with transien

147 conserved factors, including Cdc18/CDC6 and minichromosome maintenance (MCM) proteins.

148 Excess dormant origins bound by the minichromosome maintenance (MCM) replicative helicase co

149 The Minichromosome Maintenance (MCM) replicative helicase is

150 Tissue was fixed, immunostained for minichromosome maintenance (MCM)-2, a marker of replicat

151 P(4) reciprocally regulate the expression of minichromosome maintenance (MCM)-2, a protein that is an

152 the origin recognition complex (ORC) and the minichromosome maintenance (MCM)2-7 complex, the replica

153 gin recognition complex (ORC), Cdc6, and the minichromosome maintenance (MCM/P1) proteins produces a

154 leads to the assembly of double hexamers of minichromosome maintenance (Mcm2-7) at origin sites.

155 The heterohexameric minichromosome maintenance (MCM2-7) complex is an ATPase

156 well as decreased levels of chromatin-bound minichromosome maintenance (MCM2-7) complex.

157 ation is the assembly of the heterohexameric minichromosome maintenance (MCM2-7) helicase complex at

158 We focus on the minichromosome maintenance (MCM2-7) proteins, which form

159 xample, the archaeal Sulfolobus solfataricus minichromosome maintenance (SsoMCM) helicase has been sh

160 soDnaG) with the replicative S. solfataricus minichromosome maintenance (SsoMCM) helicase on DNA.

161 Dbf4-dependent kinase (DDK) phosphorylates minichromosome maintenance 2 (Mcm2) during S phase in ye

162 The MiniChromosome Maintenance 2-7 (MCM2-7) complex provides

163 The MINICHROMOSOME MAINTENANCE 2-7 (MCM2-7) complex, a ring-

164 3 recruits cell division cycle 45 (Cdc45) to minichromosome maintenance 2-7 (Mcm2-7).

165 ontaining the cell division cycle 45 (Cdc45)/minichromosome maintenance 2-7 (Mcm2-7)/Go, Ichi, Nii, a

166 egulation of RBR3-type genes, as well as the MINICHROMOSOME MAINTENANCE 2-7 gene family and PROLIFERA

167 roliferating cell nuclear antigen (PCNA) and minichromosome maintenance 4 (MCM4) proteins without cha

168 ion of PGC-1beta decreased the expression of minichromosome maintenance 4 (MCM4), which leads to a de

169 oblasts (MEFs), we show here that NCOA4 is a minichromosome maintenance 7 (MCM7)-interacting protein

170 the presence of a pathogenic variant of the minichromosome maintenance 8 gene (MCM8, c.446C>G; p.P14

171 onents (origin recognition complex [ORC] and minichromosome maintenance [MCM] complex).

172 ies a subunit of the replicative CMG (Cdc45, minichromosome maintenance [MCM] subunits 2-7, and the G

173 A1, origin recognition complex 2 (ORC2), and minichromosome maintenance complex (MCM) association wit

174 nsing mechanisms that prevent loading of the minichromosome maintenance complex (MCM2-7) onto replica

175 ion complex (ORC), Cdc6/Cdc18, Cdt1, and the minichromosome maintenance complex (Mcm2-Mcm7, or Mcm2-7

176 association of the key replication proteins minichromosome maintenance complex component (MCM7) and

177 S-phase kinase-associated protein 2 (SKP2), minichromosome maintenance complex component 4 (MCM4), a

178 iency as mutation in the MCM4 gene, encoding minichromosome maintenance complex component 4.

179 between a lactase persistence (LP) SNP, the minichromosome maintenance complex component 6 (MCM6)-rs

180 of HPNE and PDAC cells, and correlated with minichromosome maintenance complex components (MCMs) and

181 bited, there is an unexpected loading of the minichromosome maintenance complex onto chromatin.

182 Dpb11 stimulates DDK phosphorylation of the minichromosome maintenance complex protein Mcm4 alone an

183 Cell cycle analysis indicated that the minichromosome maintenance complex protein, MCM3, bound

184 Because minichromosome maintenance complex proteins are thought

185 eregulated cells, consistent with a role for minichromosome maintenance complex proteins in initiatio

186 Y600 to increase its association with other minichromosome maintenance complex proteins, thereby pro

187 nd Cdc6 prereplication proteins, but not the minichromosome maintenance complex, are necessary and bi

188 , Ki-67, proliferating cell nuclear antigen, minichromosome maintenance deficient 3, and phosphorylat

189 of 734 residues of this protein also called minichromosome maintenance deficient 5 (MCM5) or cell di

190 ed with G1/S cell-cycle transition including minichromosome maintenance deficient proteins, as well a

191 quence analysis of beta-tubulin, calmodulin, minichromosome maintenance factor, DNA-dependent RNA pol

192 The minichromosome maintenance genes (MCM2-7) are transcribe

193 The proliferation marker Ki67, minichromosome maintenance genes 2-5, antiapoptotic gene

194 hese reports suggest a critical role for the minichromosome maintenance helicase complex in NK cells

195 The minichromosome maintenance helicase from the archaeon Me

196 f the Methanothermobacter thermautotrophicus minichromosome maintenance helicase is described.

197 ulator of DNA replication through effects on minichromosome maintenance helicase loading and activati

198 In contrast, the minichromosome maintenance helicase was unable to unwind

199 complex and Cdc45 to activate the eukaryotic minichromosome maintenance helicase.

200 Minichromosome maintenance helicases are ring-shaped com

201 iginally identified as proteins required for minichromosome maintenance in Saccharomyces cerevisiae.

202 Here, we show that Tax associates with the minichromosome maintenance MCM2-7 helicase complex and l

203 In Saccharomyces cerevisiae, minichromosome maintenance protein (Mcm) 10 interacts wi

204 Minichromosome maintenance protein (Mcm) 10 regulates th

205 The minichromosome maintenance protein (MCM) complex is an e

206 Minichromosome maintenance protein 1 (Mcm1) is required

207 ar polyadenylated RNA-binding protein 3, and minichromosome maintenance protein 1.

208 Minichromosome maintenance protein 10 (Mcm10) is an esse

209 The minichromosome maintenance protein 10 (Mcm10) is an evol

210 The Minichromosome maintenance protein 10 (Mcm10), an import

211 n identify colorectal cancer by detection of minichromosome maintenance protein 2 (MCM2) expression i

212 Minichromosome maintenance protein 2 (MCM2) is a compone

213 on of hypoxia-inducible factor-1 (HIF-1) and minichromosome maintenance protein 2 (mcm2).

214 lation sites in the carboxyl terminus of the minichromosome maintenance protein 3 (MCM3), a component

215 e retinoblastoma protein phosphorylation and minichromosome maintenance protein 6 expression.

216 the retinoblastoma protein, and induction of minichromosome maintenance protein 6.

217 hibited the expression of S phase-regulatory minichromosome maintenance protein 6.

218 From this study, we identify minichromosome maintenance protein 7 (MCM7) and p16 as p

219 damage marker gammaH2AX is upregulated under minichromosome maintenance protein 7 (MCM7) knockdown in

220 We then used our mouse model to identify minichromosome maintenance protein 7 (MCM7), an E2F-indu

221 asmid DNA template by DNA polymerases (pol), minichromosome maintenance protein complex (Mcm), topois

222 The heterohexameric minichromosome maintenance protein complex (Mcm2-7) func

223 etylation and RNR levels, maintains helicase minichromosome maintenance protein complexes (Mcm2-7) on

224 The minichromosome maintenance protein homologs MCM8 and MCM

225 The archaeal minichromosome maintenance protein MCM forms a homohexam

226 nd largest subunit of RNA polymerase II, and minichromosome maintenance protein).

227 genome requires the evolutionarily conserved minichromosome maintenance protein, Mcm10.

228 Minichromosome maintenance proteins (Mcm's) are componen

229 Minichromosome maintenance proteins (Mcm) are essential

230 ession of E2F-5, centromere protein A and E, minichromosome maintenance proteins (MCM)-2, -3, -5, -6

231 ognition complex, and the elongation factors minichromosome maintenance proteins (MCM)2-7 and prolife

232 ication, involves the loading of six related minichromosome maintenance proteins (Mcm2-7) into prerep

233 Minichromosome maintenance proteins (MCMs) form a family

234 egulated loading of the replicative helicase minichromosome maintenance proteins 2-7 (MCM2-7) onto re

235 r subsequent use by loading complexes of the minichromosome maintenance proteins 2-7 (Mcm2-7).

236 ereplication complex that contains a Mcm2-7 (minichromosome maintenance proteins 2-7) double hexamer.

237 bers, whereas Double-parked protein/Cdt1 and minichromosome maintenance proteins are apparently essen

238 monstrate that uncontrolled DNA unwinding by minichromosome maintenance proteins upon Cdt1 overexpres

239 (origin recognition complex [ORC], Cdc6, and minichromosome maintenance proteins) causes a cell cycle

240 virions did not reveal the presence of ORCs, minichromosome maintenance proteins, or LANA.

241 ber of other replication proteins, including minichromosome maintenance proteins, the origin recognit

242 group of nuclear proteins, among them MCM5 (minichromosome maintenance) and MCM3, for transcription

243 clear antigen, ribonucleotide reductase, and minichromosome maintenance) and of the retinoblastoma-re

244 The Mcm2-7 (minichromosome maintenance) complex is a toroidal AAA(+)

245 ryotic DNA replicative helicase, the Mcm2-7 (minichromosome maintenance) complex, is loaded at each o

246 litator of chromatin transcription) and MCM (minichromosome maintenance) complexes.

247 INS (go ichi ni san) complex allows the MCM (minichromosome maintenance) helicase to interact with ke

248 the atomic structure of an archaeal MCM (for minichromosome maintenance) homologue.

249 The MCM2-7 (minichromosome maintenance) proteins are a family of evo

250 The six MCM (minichromosome maintenance) proteins are essential DNA r

251 fi1, Dnt1 is required for rDNA silencing and minichromosome maintenance, and both Dnt1 and Net1/Cfi1

252 e-3-phosphate dehydrogenase, proteoglycan 4, minichromosome maintenance, complex component 9, high mo

253 The antibody against minichromosome maintenance-2 (MCM2) protein was tested f

254 atients identified a variant (c.71-1insG) in minichromosome maintenance-deficient 4 (MCM4) that was p

255 Mcm4 (minichromosome maintenance-deficient 4 homolog) encodes

256 oth Set1 and Bre1 are required for efficient minichromosome maintenance.

257 In the present study, we employ a novel minichromosome model of the hGH-N regulatory domain and

258 he transgenes would reside on an independent minichromosome, not linked to any endogenous genes; thus

259 telomeres that cap the linear chromosome and minichromosomes of Borrelia burgdorferi.

260 n approach is feasible for the generation of minichromosomes of normal A chromosomes by selection of

261 Twenty-two minichromosomes of related origin but varying in size ar

262 we follow the catenation status of circular minichromosomes of three sizes during the Saccharomyeces

263 Minichromosomes of wild-type polyomavirus were previousl

264 ranscription units, whether on two different minichromosomes or on host chromosomes and minichromosom

265 lar chromosome and two large megaplasmids or minichromosomes, pNRC100 and pNRC200.

266 g emulsion PCR (LE-PCR) enables formation of minichromosomes preserving phase information of two poly

267 In anaphase II, the minichromosomes progressed to one pole or the other.

268 bstitutes for outer repeats on plasmid-based minichromosomes, promoting de novo CENP-A(Cnp1) and kine

269 d whether incorporation of Sir proteins into minichromosomes regulates early steps of recombinational

270 h the initiation and the elongation steps of minichromosome replication in vitro.

271 iz- cells shows that SUMO E3 is required for minichromosome segregation and thus has a positive role

272 SIZ1 and SIZ2 genes we demonstrate that the minichromosome segregation defect and dicentric minichro

273 In addition, our analysis of the plasmid minichromosome shows that T(3)-bound TR disrupts the nor

274 ichromosome segregation defect and dicentric minichromosome stabilization, both characteristic for Sm

275 We used a "sensitized" minichromosome substrate (J21A) to screen approximately

276 l centromeres in vivo, using a budding yeast minichromosome system and temperature-sensitive mutation

277 The engineered minichromosome technology can also be used in combinatio

278 With the advent of engineered minichromosome technology in plants, an understanding of

279 Minichromosome technology provides one solution to the s

280 Tetrahymena thermophila ribosomal DNA (rDNA) minichromosome that are required for origin activation.

281 nal regulatory region of the simian virus 40 minichromosome that is being transcribed in the cell is

282 the nucleus of the infected hepatocyte as a minichromosome that serves as the transcription template

283 n-Barr virus (EBV) persists as chromatinized minichromosomes that are replicated by the host replicat

284 meiosis I, is still present at anaphase I on minichromosomes that divide equationally.

285 ell lines and in larval tissues that contain minichromosomes that have structurally defined centromer

286 ts into cells, where they are assembled into minichromosomes that the cellular machinery replicates a

287 ence of the HBV genome, which forms a stable minichromosome, the covalently closed circular DNA (cccD

288 vely with origin sequences in the 21 kb rDNA minichromosome, the interaction between ORC and the non-

289 In plants containing one minichromosome, the sister chromatids also separated at

290 In cells containing thousands of minichromosomes, we found (using fluorescence in situ hy

291 Engineered minichromosomes were constructed in maize by modifying n

292 nd H3 in transcribing simian virus 40 (SV40) minichromosomes were determined.

293 st to the hypoacetylated state of NG59, NG59 minichromosomes were hypermethylated at specific lysines

294 romatin in vivo in Saccharomyces cerevisiae, minichromosomes were isolated using an immobilized lac r

295 Many minichromosomes were lost after long-term culture in the

296 Maize meiotic mutants and minichromosomes were used to study the role of H2AThr133

297 can be recapitulated on intracellular human minichromosomes where immunoglobulin 12- and 23-signals

298 Coating of non-cross-linked minichromosomes with Escherichia coli single-strand bind

299 nto extrachromosomal arrays resembling extra minichromosomes with repetitive structures.

300 Minichromosomes with structurally intact centromeres wer