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1 ls necessary for homologous pairing with the sister chromatid.
2 abling SYCP3 to link distant sites along the sister chromatid.
3 on repair), which is based on the homologous sister chromatid.
4 lete replication and faithful segregation of sister chromatids.
5 d transcription take place in the context of sister chromatids.
6 mitotic recombination occurs solely between sister chromatids.
7 es generate mechanical forces that segregate sister chromatids.
8 s that a single cohesin complex entraps both sister chromatids.
9 or centromeres) to mediate cohesion between sister chromatids.
10 elongating spindle physically segregates the sister chromatids.
11 spindle is crucial to achieve segregation of sister chromatids.
12 mal complex proteins, occurs instead between sister chromatids.
13 central core, which may physically separate sister chromatids.
14 and is required to promote bi-orientation of sister chromatids.
15 by proteolytic cleavage to release pairs of sister chromatids.
16 ich directs Cdt1 accumulation on segregating sister chromatids.
17 ndle during mitosis to capture and segregate sister chromatids.
18 on during mitosis depend on cohesion between sister chromatids.
19 lity for global recombination repair between sister chromatids.
20 hromosomes rather than the equally available sister chromatid, a bias that in Saccharomyces cerevisia
21 tablishment of proteinaceous bridges between sister chromatids, a function provided by a ring-shaped
22 ggered DSBs, at least in barley, involve the sister chromatid and occur during S or G2 phase of the c
25 oci, the cohesion of replicated MUC4 loci on sister chromatids, and their dynamic behaviors during mi
28 rom Separase-mediated cleavage ensuring that sister chromatids are kept together until their separati
29 leads to anaphase bridge formation (in which sister chromatids are linked by catenated strands of DNA
33 to repair rereplication-associated DSBs, and sister chromatids are used as templates for such HR-medi
36 factors in undamaged cells causes diminished sister chromatid association at centromeric sequences.
37 attern in which both homologs separate their sister chromatids at meiosis I; detect selection for hig
40 complex, which ensures proper segregation of sister chromatids at mitosis by mediating the interactio
45 mitosis requires the physical separation of sister chromatids before nuclear envelope reassembly (NE
46 's ability to ensure accurate segregation of sister chromatids, but, as in centromere localization, t
47 3 acetylation locks cohesin rings around the sister chromatids by counteracting an activity associate
48 has been implicated in the alignment of four sister chromatids by forming parallel guanine quadruplex
49 to template switches between homologs versus sister chromatids by using microhomology to prime DNA re
50 ucleate or multinucleate, and the replicated sister chromatids can remain attached and aligned, produ
52 3) heterodimeric ATPase, the kleisin subunit sister chromatid cohesion 1 (Scc1) that links the two AT
54 es, cohesin and condensin, are important for sister chromatid cohesion and condensation, respectively
57 ns to the axis, plays an independent role in sister chromatid cohesion and double-strand break format
58 ing with DNA-entrapping ability that ensures sister chromatid cohesion and enables correct synapsis a
59 hroughout the mitotic cell cycle, modulating sister chromatid cohesion and higher-order chromatin str
60 EJ, in addition to its canonical function in sister chromatid cohesion and its recently suggested fun
61 se that spliceosome components contribute to sister chromatid cohesion and mitotic chromosome segrega
62 rates long-range DNA interactions to mediate sister chromatid cohesion and other aspects of chromosom
63 to the initial steps of the establishment of sister chromatid cohesion and other chromosomal processe
64 tein complex was discovered for its roles in sister chromatid cohesion and segregation, and the Polyc
65 xhibited defects in chromosomal congression, sister chromatid cohesion and spindle positioning, there
66 rt of many chromosomal activities, including sister chromatid cohesion and transcriptional regulation
69 ate early S phase DNA replication and robust sister chromatid cohesion at microtubule attachment site
70 ation and live-cell imaging, that persistent sister chromatid cohesion at telomeres triggers a prolon
71 t role for an lncRNA in the establishment of sister chromatid cohesion by modulating DDX11 enzymatic
73 essential multiprotein complex that mediates sister chromatid cohesion critical for proper segregatio
77 h modify cohesin's Smc3 subunit to establish sister chromatid cohesion during S phase, but differ in
79 usly that HTP-1/2 prevents premature loss of sister chromatid cohesion during the meiotic divisions b
85 depletion of H2A.Z causes precocious loss of sister chromatid cohesion in yeast without loss of Mcd1
92 pl-Pds5 binding to the cohesin subcomplex of sister chromatid cohesion protein 1 (Scc1) and stromal a
94 te the establishment and two-step release of sister chromatid cohesion that underlies the production
95 g S phase is accompanied by establishment of sister chromatid cohesion to ensure faithful chromosome
97 hanistic) importance in linking the sites of sister chromatid cohesion to the chromosomal regions tha
99 mediates DNA-DNA interactions both between (sister chromatid cohesion) and within chromosomes (DNA l
100 ing XPD (nucleotide excision repair), DDX11 (sister chromatid cohesion), and RTEL (telomere metabolis
101 Failure to repair DNA damage or defective sister chromatid cohesion, a process essential for corre
104 n chromosome architecture, such as promoting sister chromatid cohesion, chromosome condensation, DNA
105 rder chromosome structure, thereby promoting sister chromatid cohesion, chromosome condensation, DNA
106 is a conserved protein complex required for sister chromatid cohesion, chromosome condensation, DNA
107 chromatin organization that is critical for sister chromatid cohesion, DNA repair and transcriptiona
109 multi-subunit protein complex essential for sister chromatid cohesion, gene expression and DNA damag
111 iotic prophase chromosome axis that mediates sister chromatid cohesion, homologous recombination and
112 lls depleted of CONCR show severe defects in sister chromatid cohesion, suggesting an essential role
113 without premeiotic chromosomal replication, sister chromatid cohesion, synapsis or recombination.
129 We suggest that, in the absence of SeqA, the sister-chromatid cohesion 'safety spacer' is destabilize
130 ires coordination between the dissolution of sister-chromatid cohesion and the establishment of prope
131 on at the centromere region until release of sister-chromatid cohesion at the metaphase II/anaphase I
132 physically interacts with Naa50, rescues the sister-chromatid cohesion defects and the resulting mito
136 ilitating the recruitment of kinetochore and sister-chromatid cohesion proteins, both required for co
138 proteins SOLO, SUNN, and ORD is required for sister-chromatid cohesion, localizes to the centromeres
139 Kleisin-like protein and ORD is required for sister-chromatid cohesion, we tested the hypothesis that
143 ional meiosis I division in which replicated sister chromatids comigrate, rather than separate as in
144 r kinetochores during meiosis I may underlie sister chromatid comigration in diverse organisms, but d
146 icated DNA, fully replicated and intertwined sister chromatids--commonly referred to as DNA catenatio
147 ge of centromeric cohesin by separase allows sister chromatids connected to microtubules from opposin
148 cumstantial evidence has linked condensin to sister chromatid decatenation but, because of the diffic
151 ls, where they are the consequence of failed sister chromatid disentanglement during chromosome compa
152 lexes ensure timely chromosome condensation, sister chromatid disentanglement, and maintenance of mit
154 venting cyclin B1 proteolysis at the time of sister chromatid disjunction destabilizes kinetochore-mi
156 indle assembly checkpoint (SAC) ensures that sister chromatids do not separate until all chromosomes
158 n addition, condensin promotes resolution of sister chromatids during anaphase, a function that is co
165 he symmetric tethering of plasmid sisters to sister chromatids embodies the replication-dependent com
166 studies demonstrate that H3T3P distinguishes sister chromatids enriched with distinct pools of H3 in
167 , called Strand-seq, that can be used to map sister chromatid exchange (SCE) events genome-wide in si
168 the simultaneous high-resolution mapping of sister chromatid exchange (SCE), facilitating the study
172 centromeric CO-FISH patterns consistent with sister chromatid exchange at the frequency of 5% in prim
175 BLM, telomeric circle formation and telomere sister chromatid exchange, both arising out of nucleolyt
176 on can be induced display elevated levels of sister chromatid exchange, gross chromosomal aberrations
177 s can occur by replication slippage, unequal sister chromatid exchange, homologous recombination, and
178 ary Pml(C62A/C65A) cells exhibited increased sister-chromatid exchange and chromosome abnormalities.
180 c mitotic recombination, a high frequency of sister chromatid exchanges and double strand DNA breaks,
184 cause in its absence cells display increased sister chromatid exchanges, replication origin firing an
185 d telomere shortening, elevation of telomere sister-chromatid exchanges and increased aphidicolin-ind
192 owing the reproducibility of banding between sister chromatids, homologue pairs and from one metaphas
193 ys, including homologous recombination (HR), sister chromatid HR, resolution of branched HR intermedi
197 sess the resection needed for repair between sister chromatids in G-2 arrested cells of random, radia
198 otubule attachment/centromere, and co-orient sister chromatids in meiosis I in Saccharomyces cerevisi
199 hich condensin complexes compact and resolve sister chromatids in mitosis and by which cohesin genera
201 oint system prevents premature separation of sister chromatids in mitosis and thus ensures the fideli
202 oint system prevents premature separation of sister chromatids in mitosis and thus ensures the fideli
203 that, despite a loss in centromere cohesion, sister chromatids in STAG2 mutant tumor cells maintain c
204 al genome fails to condense and resolve into sister chromatids in synchrony with the maternal genome.
205 TB plasmid sisters are tightly correlated to sister chromatids in the extents of co-segregation as we
207 nable to support stable bipolar alignment of sister chromatids, indicating failure of kinetochore-mic
209 ion, topoisomerase II (topo II) must resolve sister chromatid intertwines (SCI) formed during deoxynu
212 l regions as circular "loop outs" to convert sister chromatid intertwines into catenated circles.
218 ge effect." During meiosis, cohesion between sister chromatids keeps recombinant homologs physically
219 he SAC coordinates the correct attachment of sister chromatid kinetochores to the mitotic spindle wit
220 mmonly referred to as DNA catenation--and as sister chromatid linkages generated by homologous recomb
225 ate chromosome segregation, cohesion between sister chromatids must be released in a controlled manne
226 ICRF-193-treated PICH(-/-) cells undergo sister chromatid non-disjunction in anaphase, and freque
228 ted by a chromothripsis event involving both sister chromatids of the Robertsonian chromosome, a nove
229 During hermaphrodite spermatogenesis, the sister chromatids of the X chromosomes separate during m
230 h single-chromosome resolution and show that sister chromatids of X and Y chromosomes, but not autoso
231 generated the triplication occurred between sister chromatids on the duplication-bearing chromosome
232 paired by homologous recombination using the sister chromatid or the homologous chromosome (homolog)
233 the formation of DNA intermediates, in which sister chromatids or homologous chromosomes are covalent
234 olliday junctions (HJs) that physically link sister chromatids or homologous chromosomes are formed a
236 eiotic-specific cohesin member, required for sister chromatid pairing and for preventing telomere sho
237 t (SAC) delays mitotic progression until all sister chromatid pairs achieve bi-orientation, and while
238 It is important that preceding exit, all sister chromatid pairs are correctly bioriented, and tha
240 ng chromosomes once each cell cycle produces sister chromatid pairs, which separate accurately at ana
242 talled replication forks may be processed by sister chromatid recombination (SCR), generating error-f
245 ation in rate of both interhomolog and intra/sister chromatid recombination in the CUP1 array; recomb
248 und centromeres is protected by shugoshin-2, sister chromatids remain attached through centromeric/pe
251 romoting complex/cyclosome (APC/C) regulates sister chromatid segregation and the exit from mitosis.
252 promoting complex/cyclosome (APC/C) controls sister chromatid segregation, cytokinesis and the establ
255 ts and H2AThr133ph on maize lines containing sister chromatids separate precociously in anaphase I re
256 er-sister kinetochore distance and premature sister chromatid separation (PSCS), suggesting aberrant
257 s induced bone marrow aplasia with premature sister chromatid separation and revealed an absolute req
259 erference-mediated knockdown of SENP1 delays sister chromatid separation at metaphase, whereas SENP2
264 catenation is resolved, permitting complete sister chromatid separation in the ensuing anaphase.
266 SAC) ensures genomic stability by preventing sister chromatid separation until all chromosomes are at
271 gulation through its prevention of premature sister-chromatid separation and the formation of DNA loo
272 ent of attachment monitoring mechanisms when sister chromatids split and tension is lost at anaphase
273 required both for the tethering together of sister chromatids (termed cohesion) and subsequent conde
274 break hotspots form more frequently between sister chromatids than between homologs, but a novel spe
276 ggesting that it controls the segregation of sister chromatids through heterochromatin modification.
278 me segregation requires centromeres on every sister chromatid to correctly form and attach the microt
279 points in the cell cycle when the lack of a sister chromatid to serve as a homologous template preve
282 plexes that mediate the physical coupling of sister chromatids to spindle microtubule bundles (called
283 chores are large protein complexes that link sister chromatids to the spindle and transduce microtubu
286 rnover to one capable of tenaciously holding sister chromatids together for extended periods of time,
287 ell cycle, sister-chromatid cohesion tethers sister chromatids together from S phase to the metaphase
288 The cohesin ring holds newly replicated sister chromatids together until their separation at ana
289 rase-mediated cleavage, in order to maintain sister chromatids together until their separation in mei
290 oval of cohesin, the protein complex holding sister chromatids together, first from arms in meiosis I
293 e assembly checkpoint prevents separation of sister chromatids until each kinetochore is attached to
296 mitosis requires the physical separation of sister chromatids which depends on correct position of m
297 The unpaired X precociously separates into sister chromatids, which co-segregate with the autosome
298 Cohesin complex mediates cohesion between sister chromatids, which promotes high-fidelity chromoso
299 mitotic fidelity as evidenced by unresolved sister chromatids with marked accumulation of H1S/T18ph
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