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1      The DNA break-induced missegregation of acentric and centric chromosome fragments provides a nov
2 er replication arrest, and are resolved into acentric and dicentric chromosomes in G2.
3 blation studies demonstrate that segregating acentrics are mechanically associated with microtubules.
4 resulting in an increase in the frequency of acentric-bearing, lamin-coated micronuclei.
5                                 Unlike other acentric carbonate fluorides, in this example, the inclu
6 uct of assembly is a holo-apoptosome with an acentric CARD-CARD disk and tethered pc-9 catalytic doma
7                        Fragmentation with an acentric CFV directed in a centromere-proximal orientati
8                                          The acentric chromatid poleward movement is mediated through
9  Polo facilitate the accurate segregation of acentric chromatids by maintaining the integrity of the
10                 Our live studies reveal that acentric chromatids segregate efficiently to opposite po
11  function results in abnormal segregation of acentric chromatids, a decrease in acentric chromosome t
12  in cancer cells is often mediated by paired acentric chromatin bodies called double minute chromosom
13 the roles of mitotic proteins in segregating acentric chromatin.
14 ning bodies were formed through both loss of acentric chromosome fragments and by chromosome missegre
15 romosome condensation, an increased yield of acentric chromosome fragments at the first postirradiati
16 ules play a key role in poleward movement of acentric chromosome fragments generated in Drosophila me
17               Lin et al.(1) demonstrate that acentric chromosome fragments generated within micronucl
18                             This behavior of acentric chromosome fragments on anastral plant spindles
19          Here, we find that late-segregating acentric chromosome fragments that rejoin daughter nucle
20 clei were CREST-negative, reflective of lost acentric chromosome fragments.
21 gation of acentric chromatids, a decrease in acentric chromosome tethering, and a great reduction in
22  determine the behavior of kinetochore-free "acentric" chromosome fragments and "monocentric" chromos
23  polyploid, they naturally accumulate broken acentric chromosomes but do not apoptose/arrest the cell
24 lear envelope through which late-segregating acentric chromosomes enter the telophase daughter nucleu
25  We used the endonuclease I-CreI to generate acentric chromosomes in Drosophila larvae.
26 e dynamics of NEF in the presence of lagging acentric chromosomes in Drosophila neuroblasts.
27             While I-CreI expression produces acentric chromosomes in the majority of neuronal stem ce
28          Through live analysis, we show that acentric chromosomes induce highly localized delays in t
29             Although poleward segregation of acentric chromosomes is well documented, the underlying
30                                              Acentric chromosomes often exhibit delayed but ultimatel
31 ng the integrity of the tethers that connect acentric chromosomes to their centric partners.
32 ents that lack centromeric DNA (structurally acentric chromosomes) are usually not inherited in mitos
33                      To survive mitosis with acentric chromosomes, papillar cells require Fanconi ane
34 f isochromosomes as well as isodicentric and acentric chromosomes.
35 equently fuse to form unstable dicentric and acentric chromosomes.
36 ormation of extrachromosomal DNAs (ecDNAs) - acentric, circular DNA molecules ranging from 50 kb to 5
37 cle morphology characterized by a spherical, acentric core and a crescent-shaped, electron-dense shel
38 e benzothiazolium crystals consisting of new acentric core HMB (2-(4-hydroxy-3-methoxystyryl)-3-methy
39                         During activation an acentric disk is formed on the central hub of the apopto
40 ogenic centromere-containing fragment and an acentric distal fragment, with both mis-segregated into
41 attempted to characterize MN with centric or acentric DNA fragments for the presence or absence of fr
42 ases to promote alignment and segregation of acentric DNA produced by double-strand breaks, thus avoi
43  nuclear envelope that extend and retract as acentrics enter nuclei.
44           Double minute (DM) chromosomes are acentric extrachromosomal DNA artifacts that are frequen
45 h as temperature (T(c)) and pressure (P(c)), acentric factor (omega), boiling temperature (T(b)), and
46 ture, critical pressure and temperature, and acentric factor.
47                            In klp3a mutants, acentrics fail to localize and segregate along the perip
48 ormation: following a double-strand break an acentric fragment forms, during either meiosis or mitosi
49                                          The acentric fragment is lost when cells divide and the dice
50                      The open DNA end of the acentric fragment is stabilized by the formation of an i
51 a- or metaphase were cut with the laser, the acentric fragments (lacking kinetochores) that were gene
52 chromosome fragmentation at metaphase I, and acentric fragments and chromatin bridges in meiosis I an
53                     Etoposide induced mostly acentric fragments and deletions, types of aberrations e
54                                              Acentric fragments and monocentric chromosomes generated
55 mosomes with live-cell imaging and show that acentric fragments cluster in close spatial proximity th
56        When this occurred, we found that the acentric fragments cosegregated into either the mother o
57  a single centromere, it remains unclear how acentric fragments derived from shattered chromosomes ar
58 it is unknown whether these late-segregating acentric fragments influence NEF to ensure their inclusi
59 tic clustering facilitates the reassembly of acentric fragments into rearranged chromosomes lacking t
60          Inactivation of CIP2A-TOPBP1 caused acentric fragments to disperse throughout the mitotic cy
61                         At anaphase, control acentric fragments typically remained unoriented between
62                                         When acentric fragments were generated in taxol-treated sperm
63                        Significant levels of acentric fragments were induced by all chemicals, which
64                              Sub-chromosomal acentric fragments were prone to replication and collect
65 broken chromosome (rejoining the centric and acentric fragments) occurred in either the mother or dau
66 or during prometaphase/metaphase II, whereas acentric fragments, also generated by afd1, fail to alig
67 ere given and chromosome damage (dicentrics, acentric fragments, micronuclei, chromatid gaps/breaks)
68 aphase cells with lagging chromosomes and/or acentric fragments.
69 al fragments, albeit to a lesser extent than acentric fragments.
70                    Membrane encompassing the acentrics fuses with the nuclear membrane, facilitating
71 zed from the vapour phase into intrinsically acentric, high-quality, micrometre-scale films.
72 re squamous epithelial cells that contain an acentric, hyperchromatic nucleus that is displaced by a
73 ar membrane, facilitating integration of the acentrics into newly formed nuclei.
74 P4B and CHMP2B, facilitates reintegration of acentrics into nuclei.
75 pe that facilitates the inclusion of lagging acentrics into telophase daughter nuclei.
76  a new general mechanism is proposed for the acentric inv dup marker formation: following a double-st
77  the previously suggested model by which the acentric inv dup markers form through inter-chromosomal
78                                              Acentric inverted duplication (inv dup) markers, the lar
79      Chromosome arm level CNAs also generate acentric lagging chromatin and micronuclei containing th
80                         The achiral nonpolar acentric material is second harmonic generation (SHG) ac
81                          The chiral nonpolar acentric material shows second-harmonic generation (SHG)
82 irst-order hyperpolarizabilities (beta) into acentric microstructures for electro-optic (EO) applicat
83                    Here we report that these acentric mini-chromosomes bind the centromere-specific p
84 rmally non-centromeric DNAs present in these acentric mini-chromosomes have acquired centromere funct
85 elanogaster mini-chromosome, of structurally acentric mini-chromosomes that display efficient mitotic
86                       The sequences in these acentric mini-chromosomes were derived from the tip of t
87 inversions, translocations, and formation of acentric minichromosomes.
88 to functional neocentromeres of structurally acentric minichromosomes; and (c) the localization of bo
89                              Such inherently acentric networks exhibit intensive nonlinear optical pr
90 normal virion maturation; virions containing acentric nucleoid structures comprised 90 to 99% of all
91 matter material system, leading to increased acentric order and EO activity.
92 ivate new experimental approaches to achieve acentric order in both bulk-phase and thin film structur
93 l role of the small potassium cations in the acentric packing of the [NbOF5]2- anion.
94                                 We show that acentrics pass through membrane-, lamin-, and nuclear po
95                                    Normally, acentric poleward segregation occurs at the periphery of
96 that from the X-ray crystal structure of the acentric racemic (+/-)-(1pR,1' 'R)(1pS,1' 'S)-[Cr(CO)(3)
97                        The local symmetry of acentric regions present in BaTiO(3) nanocrystals, parti
98                                              Acentrics segregate with either telomeres leading or lag
99             Finally, we show that successful acentric segregation requires the chromokinesin Klp3a.
100  role for interpolar microtubules in driving acentric segregation.
101  both, consistent with a model in which both acentric sister chromatid fragments are passaged into th
102                                          The acentric structure is described by a superposition of 16
103        The LGYSB:Nd-type crystals exhibit an acentric structure similar to that of the natural minera
104  at the nanoscale can be utilized to produce acentric structures markedly different than their consti
105 e formation of a dicentric chromosome and an acentric, telomere-bearing, chromosome fragment in somat
106 se via directed hydrogen-bond networks, into acentric thin films.
107                                          Two acentric vector arms were utilized; these carry autonomo

 
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