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1 first enters a mitotic-like state (premature chromatin condensation).
2 ry step in cell replication and is linked to chromatin condensation.
3 ould then be disassembled to allow metaphase chromatin condensation.
4 ted with DNA replication, transcription, and chromatin condensation.
5 y, nucleus position, nucleolus position, and chromatin condensation.
6 es; DNA methylation likely occurred prior to chromatin condensation.
7 tion of these chromosomes without detectable chromatin condensation.
8 pological state, chromosome segregation, and chromatin condensation.
9  accelerates its proteolytic degradation and chromatin condensation.
10 ng of transcription factors and the level of chromatin condensation.
11 cleus and the inhibition of acinus-dependent chromatin condensation.
12 ists against apoptotic cleavage and prevents chromatin condensation.
13        Cytochrome c was also found to induce chromatin condensation.
14 echanical properties of the nucleus and also chromatin condensation.
15 ment of a sub-G(0)/G(1) region, and distinct chromatin condensation.
16 ncident with the first detectable changes in chromatin condensation.
17 oisson's ratio, apparent elastic modulus and chromatin condensation.
18 f the gene to DNA demethylation but not with chromatin condensation.
19 electively killing cancer cells by premature chromatin condensation.
20 anscriptional silencing, in part by inducing chromatin condensation.
21 g of P2 and, consequently, the completion of chromatin condensation.
22  domain results in histone deacetylation and chromatin condensation.
23 removal, tau is hyperphosphorylated prior to chromatin condensation.
24 me filament, with a role similar to that for chromatin condensation.
25 transcription complexes and locally blocking chromatin condensation.
26 ing somatic cells during S phase to maintain chromatin condensation.
27 ntiation, meiotic cell divisions and extreme chromatin condensation.
28  and caspases completely abolishes apoptotic chromatin condensation.
29 is not essential for histone displacement or chromatin condensation.
30 hondrial transmembrane potential and nuclear chromatin condensation.
31 ssive effects of histone hypoacetylation and chromatin condensation.
32 ase in response to DL, blocking load-induced chromatin condensation.
33 d by deacetylation of histone H4 lysines and chromatin condensation.
34 biotin nick end labeling, DNA laddering, and chromatin condensation.
35 ation, extensive surface bleb formation, and chromatin condensation.
36 nocytes and thymocytes are also resistant to chromatin condensation.
37 of short, active transcription units hinders chromatin condensation.
38  it was surprising that transfection induced chromatin condensation.
39 ot the result of the temperature shift or of chromatin condensation.
40 disrupt nucleosomal dynamics due to aberrant chromatin condensation.
41  phosphatidylserine exposure, DNA damage and chromatin condensation.
42 e associations within an array, facilitating chromatin condensation.
43 sine residues in histone tails, resulting in chromatin condensation.
44  histone acetylation and inducing peripheral chromatin condensation.
45 NA Polymerase II, perhaps by promoting local chromatin condensation.
46 miR-191 or knockdown of Riok3 or Mxi1 blocks chromatin condensation.
47 esistant form of cyclin A2 partially rescued chromatin condensation.
48 re and block the binding of the regulator of chromatin condensation 1 (RCC1) acidic patch-binding pro
49                  SAB1 encodes a Regulator of Chromatin Condensation 1 (RCC1) family protein and is ex
50 ulators, and phosphorylation of regulator of chromatin condensation 1 (RCC1), a key protein for spind
51                   Moreover, the regulator of chromatin condensation 1-like domain of PAM (amino acids
52                Furthermore, the regulator of chromatin condensation 1-like domain of PAM is sufficien
53 nine nucleotide exchange factor regulator of chromatin condensation 1.
54 t HP1(Hsalpha)-nucleosome interactions cause chromatin condensation, a process that regulates many ch
55 ol cells in that they show reduced degree of chromatin condensation, absent nuclear fragmentation, in
56 ine methylation, histone hypoacetylation and chromatin condensation act together in a discrete region
57 is capable of inducing DNA fragmentation and chromatin condensation after cleavage by caspase-3.
58 tic phosphoproteins and inhibiting premature chromatin condensation after DNA damage or hydroxyurea.
59  hypoacetylation of associated histones, and chromatin condensation, all characteristics of a transcr
60 nd microtubule depolymerization and changing chromatin condensation altered volume, shape, and dry ma
61 ctivated state showing a decrease in nuclear chromatin condensation, altered histone deacetylase expr
62 ifferentiate, they are capable of undergoing chromatin condensation, although many abnormal cells are
63 he N-termini perform essential roles in both chromatin condensation and also bind specific chromatin-
64 ations, centriole separation, and prophase I chromatin condensation and also cause anaphase I bridges
65 nstrated that overexpression of Plk3 induces chromatin condensation and apoptosis.
66 is in a cell-free system revealed a block in chromatin condensation and apoptotic body formation when
67 slocates into the nucleus, where it promotes chromatin condensation and apoptotic cell death.
68 rough the determination of apoptosis-related chromatin condensation and biochemically through the mea
69 istics of PCD of mammalian cells: NO induced chromatin condensation and caspase-like activity in Arab
70 s sensor with reporter dyes for detection of chromatin condensation and cell death, enabling studies
71 totic entry, presumably as a prerequisite to chromatin condensation and cell division.
72 tin F confers protection against TPT-induced chromatin condensation and cleavage of PARP, cell detach
73 suggests that chondrocytes likely experience chromatin condensation and decondensation during a daily
74        UBF trimethylation leads to nucleolar chromatin condensation and decreased rDNA transcriptiona
75 are advantageous, allowing tunable levels of chromatin condensation and DNA accessibility/interaction
76 plicity of infection (MOI) of 25:1 developed chromatin condensation and DNA fragmentation at 4 h and
77 r77 induction, which is involved in inducing chromatin condensation and DNA fragmentation.
78 adative events of apoptosis, such as nuclear chromatin condensation and DNA fragmentation.
79  the induction of apoptotic cell morphology, chromatin condensation and DNA fragmentation.
80 of MST1, which functions to induce apoptotic chromatin condensation and DNA fragmentation.
81  modifications could affect gene regulation, chromatin condensation and DNA packaging.
82 nd extend the argument that the processes of chromatin condensation and DNA replication are linked.
83 ll death (PCD) at late stages typically show chromatin condensation and endonucleolytic cleavage prio
84 ythroblasts resulted in severe inhibition of chromatin condensation and enucleation but otherwise had
85 lation of miR-191 is essential for erythroid chromatin condensation and enucleation by allowing up-re
86     Hypermethylation in Th2 cells results in chromatin condensation and exclusion of CREB proteins fr
87   This result was confirmed using assays for chromatin condensation and for DNA fragmentation.
88           However, the normal progression of chromatin condensation and fragmentation accompanying pr
89 s from synaptosomes exposed to Abeta induced chromatin condensation and fragmentation in isolated nuc
90 ADP-ribose) polymerase was cleaved, and (iv) chromatin condensation and fragmentation of cellular DNA
91 LZ increased Caspase -3, -8 and -9 activity, chromatin condensation and fragmentation, data indicativ
92 age, membrane blebbing, vesicle release, and chromatin condensation and fragmentation.
93           Histone H1 phosphorylation affects chromatin condensation and function, but little is known
94 thin the gene body of SLFN11, inducing local chromatin condensation and gene silencing.
95 tant epigenetic mark that is known to induce chromatin condensation and gene silencing.
96 f the condensin complex that plays a role in chromatin condensation and has also been associated with
97 pase proteolysis of RAD21 precedes apoptotic chromatin condensation and has important functional cons
98  a substantial ( approximately 7 h) delay in chromatin condensation and histone H3 phosphorylation, a
99 eplacement results in an abnormal pattern of chromatin condensation and in reduced fertility.
100 tone-modifying enzymes that together promote chromatin condensation and inactivation.
101 vealed widening of intercellular spaces with chromatin condensation and margination in the upper stra
102 cytoplasmic membrane blebbing (zeiosis), and chromatin condensation and margination, and decrease in
103  the mechanism by which DFF40/CAD influences chromatin condensation and nuclear collapse during apopt
104                     The distinct features of chromatin condensation and nuclear DNA fragmentation ind
105 sphorylation of nuclear targets critical for chromatin condensation and nuclear envelope breakdown.
106  activation of caspases and characterized by chromatin condensation and nuclear fragmentation (type I
107 aspase-3-like proteases preceded TAM-induced chromatin condensation and nuclear fragmentation, the ty
108 d to the cytoplasm early in apoptosis before chromatin condensation and nuclear fragmentation.
109 % versus 8.7%, respectively), as detected by chromatin condensation and nuclear fragmentation.
110 ding cytoplasmic shrinkage and condensation, chromatin condensation and nuclear membrane blebbing.
111       DNA methylation has been implicated in chromatin condensation and nuclear organization, especia
112 ethylation, and show a strong correlation of chromatin condensation and nuclear stiffness with the ex
113 reorganization within the nucleus, including chromatin condensation and nucleoprotein immobilization.
114 2 activity is necessary for death-associated chromatin condensation and other manifestations of apopt
115                                    Following chromatin condensation and perinuclear centrosome aggreg
116 uding apoptotic morphology with mitosis-like chromatin condensation and prelytic genome digestion.
117 es to the nuclei of hepatic cells to control chromatin condensation and proliferation.
118 at has been implicated in inducing apoptotic chromatin condensation and regulating mRNA processing.
119 gical changes suggesting that the process of chromatin condensation and rod cell structural integrity
120  death was apoptotic, as indicated by marked chromatin condensation and the requirement for caspase-3
121 monstrate the presence or absence of nuclear chromatin condensation and thus confirm that ISEL-positi
122 tivator-dependent histone acetylation had on chromatin condensation and to ascertain whether acetylat
123  of core histone N-terminal tails influences chromatin condensation and transcription.
124 of histones by histone deacetylases promotes chromatin condensation and transcriptional repression.
125 A/B and histone deacetylases to induce local chromatin condensation and transcriptional repression.
126 7), which serves as an epigenetic signal for chromatin condensation and transcriptional repression.
127 ranscription factors, resulting in localized chromatin condensation and transcriptional silencing.
128 other chromatin-associated proteins to cause chromatin condensation and transcriptional silencing.
129 ted DNA, resulting in histone deacetylation, chromatin condensation and transcriptional silencing.
130 rget HDAC activity to chromatin resulting in chromatin condensation and transcriptional silencing.
131      Electron microscopic examination showed chromatin condensation and vacuolization in a fraction o
132 d caspase-3 activation and apoptotic nuclear chromatin condensation and was inhibited by the proteaso
133 totic markers such as nuclear fragmentation, chromatin condensation, and accumulation of reactive oxy
134 cking down of acinus substantially decreases chromatin condensation, and depletion of Akt provokes th
135  assessed by plasma membrane bleb formation, chromatin condensation, and DNA fragmentation.
136 fnt, all of which are required for germ cell chromatin condensation, and drastically altered pattern
137          It also lacks caspase-3 activation, chromatin condensation, and endonuclease-mediated DNA de
138 uclear morphology consistent with apoptosis, chromatin condensation, and formation of apoptotic bodie
139 iated with triggering histone deacetylation, chromatin condensation, and gene silencing.
140                             Cell morphology, chromatin condensation, and genomic DNA fragmentation me
141 cleosomal interactions during salt-dependent chromatin condensation, and here we used it to examine i
142 ternalization, increased caspase-3 activity, chromatin condensation, and nuclear fragmentation.
143 rks of PCD such as accumulation of H(2)O(2), chromatin condensation, and oligonucleosomal fragmentati
144  nuclear opening formation, histone release, chromatin condensation, and terminal erythroid different
145 a high frequency as shown by TUNEL staining, chromatin condensation, and the appearance of morphologi
146 e key implications for both the mechanism of chromatin condensation, and the regulation of genomic fu
147 lts in rapid deacetylation of histone H4 K8, chromatin condensation, and transcription silencing.
148  morphology in which nuclear changes such as chromatin condensation are absent or reduced; in additio
149 ylation of histone H4 lysines and coincident chromatin condensation are critically involved in the si
150  TGHQ-induced histone H3 phosphorylation and chromatin condensation are inhibited by PD098059, which
151              Apoptotic DNA fragmentation and chromatin condensation are mediated by the caspase-activ
152 es have implicated histone deacetylation and chromatin condensation as critical mechanisms of transcr
153 duced apoptosis in C6 cells morphologically (chromatin condensation as detected by light microscopy)
154  with drug resistance, showed characteristic chromatin condensation as well as distinct poly(ADP-ribo
155 of histone H3 is accompanied by increases in chromatin condensation, as observed with the use of 4,6-
156 tive EGL cells includes a failure to exhibit chromatin condensation (assessed with TOPRO), phosphatid
157 ytes in cultures that contained 2.4G2 showed chromatin condensation, binding of Annexin-V, and fas in
158 nucleus, histone displacement, initiation of chromatin condensation, binding of protamines to DNA, or
159 vented DNA fragmentation and reduced nuclear chromatin condensation but also preserved mitochondrial
160 ce cells treated with toxic ONs did not show chromatin condensation, but did exhibit high-extracellul
161 with higher levels of actin organization and chromatin condensation, but only after 24 h in culture.
162 uces apoptotic morphological changes such as chromatin condensation, but the mechanism is not clear.
163 spermatids as they undergo restructuring and chromatin condensation, but unlike SSTK, is not retained
164       Using time course AFM, we observe that chromatin condensation by H1.5 is dynamic, whereas using
165  other hand, knocking down cyclin B1 delayed chromatin condensation by only about one hour.
166                     In vitro, H2A.W enhances chromatin condensation by promoting fiber-to-fiber inter
167  modification at lysine 9 directly regulates chromatin condensation by recruiting MENT to chromatin i
168  Motivated by recent evidence that modifying chromatin condensation can change nuclear morphology, we
169  in addition, Crb1 delays UV and blue cones' chromatin condensation caused by UV light irradiation.
170 equired cell-autonomously for proper meiotic chromatin condensation, cell cycle progression and sperm
171 n both cell lines, and there was evidence of chromatin condensation, cell shrinkage and apoptotic bod
172 as mitochondria degeneration, alterations in chromatin condensation, cell vacuolization and extracell
173  that is characterized by DNA fragmentation, chromatin condensation, cellular swelling with big bubbl
174 ion in bcl-2 protein expression, followed by chromatin condensation, chromosomal DNA fragmentation, a
175 r-chromatid cohesion (Cohesin: Smc1 & Smc3), chromatin condensation (Condensin: Smc2 & Smc4), and DNA
176 n of histone H1 is thought to have a role in chromatin condensation/decondensation, and we asked whet
177 hestrated developmental process during which chromatin condensation decouples transcription from tran
178                 dCap-D3 mutants also exhibit chromatin condensation defects, and mutant alleles of dC
179 t Jhdm2a-deficient mice exhibit post-meiotic chromatin condensation defects, and that JHDM2A directly
180 g presence of intracellular EMCV virions and chromatin condensation; detection of virus-induced chrom
181 aracteristics of apoptosis assessed included chromatin condensation, DNA cleavage, and phosphatidylse
182 in synthesis because cycloheximide inhibited chromatin condensation, DNA fragmentation and activation
183 bility was due to apoptosis characterized by chromatin condensation, DNA fragmentation by agarose gel
184 is, resulting in decreased colony formation, chromatin condensation, DNA fragmentation, and caspase a
185                        These cells exhibited chromatin condensation, DNA fragmentation, and laddering
186                    Further, 11 and 18 caused chromatin condensation, DNA fragmentation, and loss of m
187 or phenotypes following peptide binding were chromatin condensation, DNA fragmentation, annexin V bin
188 ifferent cell lines as evidenced by enhanced chromatin condensation, DNA fragmentation, or an enhance
189 cal features similar to apoptosis, including chromatin condensation, DNA laddering, cell shrinkage, a
190 se to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression.
191                           Thus, Akt inhibits chromatin condensation during apoptosis by phosphorylati
192 icient to trigger both DNA fragmentation and chromatin condensation during apoptosis.
193                            The mechanisms of chromatin condensation during erythropoiesis are unclear
194 e from the opening is a critical step toward chromatin condensation during erythropoiesis in mice.
195 to be important for histone displacement and chromatin condensation during mammalian spermatogenesis.
196 rbf1 mutant larvae have extensive defects in chromatin condensation during mitosis.
197 rly genes upon mitogenic stimulation, and to chromatin condensation during mitotic/meiotic events.
198                         For all tested loci, chromatin condensation during photomorphogenesis does no
199 m female passage of human chromosome 21, the chromatin condensation during spermatogenesis and the ex
200 he p53 gain of function could interfere with chromatin condensation either by blocking mitotic shutdo
201 ty is repressed by overlapping mechanisms of chromatin condensation, epigenetic transcriptional silen
202 r classical features of apoptosis, including chromatin condensation, externalization of phosphatidyls
203  promoter, causing histone deacetylation and chromatin condensation, further reducing ER transcript l
204                                    Apoptotic chromatin condensation has been causally linked to the p
205 cell lines involving CpG island methylation, chromatin condensation, histone deacetylation and MeCP2
206 embrane blebbing, nuclear fragmentation, and chromatin condensation (Hoechst staining), terminal deox
207 perhaps helping to explain how NIMA promotes chromatin condensation in A. nidulans and when expressed
208 d), cytochrome c redistribution, and nuclear chromatin condensation in approximately 12% of the cells
209 aired Chk1 activation, and induced premature chromatin condensation in cells, indicating a defect in
210 , a constitutively nuclear cyclin B1 rescued chromatin condensation in cyclin A2 knockdown cells.
211 oles of various candidate mitotic cyclins in chromatin condensation in HeLa cells.
212                                              Chromatin condensation in interphase cells is characteri
213 uggesting that LMNB1 is required to maintain chromatin condensation in interphase nuclei.
214 PAN/DFF40 [4,7,8] (CAD) can induce apoptotic chromatin condensation in isolated HeLa cell nuclei in t
215  in step 11 to 13 spermatids and progressive chromatin condensation in later spermatids, but condensa
216  fluorescent protein, mMaroon1, to visualize chromatin condensation in mitosis.
217                         Instead, it prevents chromatin condensation in prometaphase, extends the leng
218 hat mediates regulated DNA fragmentation and chromatin condensation in response to apoptotic signals.
219                     These data indicate that chromatin condensation in response to DL is regulated th
220 1), and Prm2, all of which are essential for chromatin condensation in spermatids.
221 are insulated from developmentally regulated chromatin condensation in terminally differentiated cell
222 nsation, endoplasmic reticulum dilation, and chromatin condensation in the COLO 16 cells.
223 ammed cell death (PCD) or apoptosis, such as chromatin condensation in the nucleus and blebbing of th
224 ing by de novo DNA methylation and increased chromatin condensation in the SV40 promoter was the majo
225 ignaling in KRAS-mutant NSCLC cells promotes chromatin condensation in vitro and in vivo, thereby res
226  histones have long been known to facilitate chromatin condensation in vitro.
227 l for the induction of DNA fragmentation and chromatin condensation in vivo, but is not required for
228 cid) induced rapid ATP release, resulting in chromatin condensation independent of loading.
229 )-fluoromethylketone; this failed to inhibit chromatin condensation induced by DNase II.
230 regulation of Claspin augments the premature chromatin condensation induced by hydroxyurea, inhibits
231  h and 8 h, respectively, whereas changes in chromatin condensation induced by MOIs of 10:1 and 1:1 r
232 53 protected granule cells from AraC-induced chromatin condensation, internucleosomal cleavage, and a
233                                              Chromatin condensation is a ubiquitous feature of metazo
234                               Abnormal sperm chromatin condensation is common in sterile men, and our
235                                    Pachytene chromatin condensation is disrupted, and although some m
236 tene when chromosome homologues pair and sex chromatin condensation is initiated.
237 lin A2 knockdowns, arguing that the delay in chromatin condensation is not secondary to a delay in S-
238 nus, a nuclear factor required for apoptotic chromatin condensation, is a direct target of Akt.
239 uires the amino-terminal "RCC1 (regulator of chromatin condensation)-like" GEF domain.
240 ssociated with dramatic nuclear alterations: chromatin condensation, loss of nuclear lamins, and brea
241 el which, along with the rapid nature of the chromatin condensation (<20 s), reveals the basic physic
242 e, hallmark properties of apoptosis, such as chromatin condensation, may be regulated by posttranslat
243 s, short term DL elicits a rapid increase in chromatin condensation, mediated by acto-myosin based ce
244 s was followed by apoptosis, as reflected by chromatin condensation, membrane blebbing, cell detachme
245           During this active phase there was chromatin condensation, mitochondria were swollen but re
246 ence-based cellular assay for MT morphology, chromatin condensation, mitotic arrest, and cellular tox
247 ment of apoptosis was evaluated by examining chromatin condensation, nuclear DNA fragmentation, and c
248 whereas DIDS induced an apoptotic phenotype (chromatin condensation, nuclear fragmentation and cleava
249 ochrome C and apoptosis inducing factor, (4) chromatin condensation, nuclear lamin A and DNA cleavage
250                               Later, nuclear chromatin condensation occurred, a characteristic of apo
251                                           As chromatin condensation occurs even when CAD activity is
252      High expression of CKT2 correlated with chromatin condensation of spermatids in murine testes.
253 ctedly caused hypermethylation and increased chromatin condensation of the transgene in both the G10
254 ytes released by nuclear envelope breakdown, chromatin condensation, or cytokinesis and does not resu
255 , including nuclear crenellation, absence of chromatin condensation, organelle swelling, and accumula
256 olality on nuclear morphology (p < 0.01) and chromatin condensation (p < 0.001) also differed between
257                  Although DEVD inhibited the chromatin condensation, PARP cleavage, release of apopto
258 ssue samples, thereby linking alterations in chromatin condensation patterns to different stages of t
259 they showed altered cytosine methylation and chromatin condensation patterns, and a correlation betwe
260                                    Premature chromatin condensation (PCC) is a hallmark of mammalian
261                                              Chromatin condensation plays an important role in the re
262  and 6 days after ovariectomy showed nuclear chromatin condensation principally in plasma cells.
263 cium signaling as a central mediator of this chromatin condensation process.
264 over an unexpected link between pRB/RBF1 and chromatin condensation, providing a mechanism by which t
265  mechanistic functions of linker histones in chromatin condensation, purified histone H5 has been ass
266 ght while some transcripts for Regulators of Chromatin Condensation (RCC1) declined in the dark.
267  region by lac operator repeats led to local chromatin condensation, recruitment of nuclear receptor
268 ent kinase inhibitor induced cell shrinkage, chromatin condensation, reorganization of actin microfil
269 on inhibits perinatal nucleation of regional chromatin condensation resulting in continued elevated t
270          Evaluation of DNA fragmentation and chromatin condensation revealed that CART 55-102 reduced
271 e chromatin, and the latter revealed various chromatin condensation states in live cells.
272                      The resulting change in chromatin condensation stiffened the MSC nucleus, making
273 to the PIK3CA and PIK3R2 promoters modulates chromatin condensation, suggesting a mechanism by which
274            However, there was a reduction in chromatin condensation, suggesting that changes in the n
275            Mammalian erythropoiesis involves chromatin condensation that is initiated in the early st
276 of loading events led to a greater degree of chromatin condensation that persisted for longer periods
277 by BRG-1 involved nucleosome recruitment and chromatin condensation, thereby abolishing Sp1 binding.
278     Here we show that MST1 induces apoptotic chromatin condensation through its phosphorylation of hi
279 plication of DL elicited a rapid increase in chromatin condensation through purinergic signaling medi
280  modifications of nucleosomal histones alter chromatin condensation to regulate transcriptional activ
281 termini are required to achieve higher order chromatin condensation, two of which apparently involve
282 lear ultrastructure remained normal, without chromatin condensation, until the nuclear envelope fragm
283 il domain performs multiple functions during chromatin condensation via distinct molecular interactio
284 sistent with this possibility, we found that chromatin condensation was tightly associated temporally
285 nce no evidence of tubulin reorganization or chromatin condensation was visible.
286 ex interactions of the H3 tail domain during chromatin condensation, we have developed a new site-dir
287           Endoplasmic reticulum dilation and chromatin condensation were also observed in the rho(0)
288  later when full-blown DNA fragmentation and chromatin condensation were first observed (6 h).
289 anisms underlying the acetylation effects on chromatin condensation were investigated by analyzing th
290 during chromatin assembly and salt-dependent chromatin condensation were investigated using defined c
291 rtain whether acetylation-induced changes in chromatin condensation were related to changes in RNA po
292                         DFF40 also triggered chromatin condensation when incubated with nuclei.
293 2 expression) had little effect on premature chromatin condensation, when combined with ATR-kd expres
294 measured by propidium iodide (PI) uptake and chromatin condensation, whereas they remained relatively
295  propose that lola is necessary for complete chromatin condensation which occurs during programmed ce
296        Our findings suggest that this unique chromatin condensation, which can affect interpretations
297 es in chromatin modifications that result in chromatin condensation, which is a likely contributing f
298 yperosmotic conditions (>400 mOsm/kg) induce chromatin condensation, while hypoosmotic conditions (10
299 ration of 30 kb DNA fragments within 3 h and chromatin condensation within 6 h, when nuclei were incu
300 caspase-3 activation, DNA fragmentation, and chromatin condensation within 72 hours of infection.

 
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