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1 mplex is a key determinant of higher-ordered chromosome structure.
2 ole in the control of higher-order bacterial chromosome structure.
3 or clonal subpopulation with a highly stable chromosome structure.
4 xpression and maintain genomic integrity and chromosome structure.
5 complex that links RBF1 to the regulation of chromosome structure.
6 th its proposed function in promoting normal chromosome structure.
7 c elements and for the study of higher-order chromosome structure.
8 lated to fiber-fiber interactions and global chromosome structure.
9 out severely deforming or damaging the local chromosome structure.
10 he genome, perhaps reflecting some aspect of chromosome structure.
11 role for Nse4 in maintenance of higher order chromosome structure.
12 has been difficult to relate linkage maps to chromosome structure.
13 xpression patterns with base composition and chromosome structure.
14 est in the molecular mechanisms that control chromosome structure.
15 hysical contig maps with mitotic and meiotic chromosome structure.
16 y forms, including aneuploidy and changes in chromosome structure.
17 ts constrain models for higher order mitotic chromosome structure.
18 e existence of a novel mechanism controlling chromosome structure.
19 disentanglement, and maintenance of mitotic chromosome structure.
20 een designed to identify genes important for chromosome structure.
21 and elasticity, and provide new insight into chromosome structure.
22 thways that participate in preserving intact chromosome structure.
23 the postreplicative repair pathway influence chromosome structure.
24 limited by the conservation of the existing chromosome structure.
25 r as replicon clusters, form stable units of chromosome structure.
26 fewer cytogenetically evident alterations of chromosome structure.
27 d in genetic screens for genes important for chromosome structure.
28 been proposed as the backbone of interphase chromosome structure.
29 wn to be required for maintenance of correct chromosome structure.
30 can be used as a tool for probing bacterial chromosome structure.
31 hisms in genes affecting recombination or in chromosome structure.
32 are established by higher order features of chromosome structure.
33 y and the establishment of a normal polytene chromosome structure.
34 y and mechanisms that determine higher-order chromosome structure.
35 om forests can generate useful insights into chromosome structure.
36 has important functions in relation to basic chromosome structure.
37 riability in nuclear genome organization and chromosome structure.
38 he interaction between TRF2 and lamin A/C on chromosome structure.
39 evisiae to changes in gene order and overall chromosome structure.
40 ild-type cells and in mutants with disrupted chromosome structure.
41 of cell identity genes and control of local chromosome structure.
42 y reduced cell division and altered polytene chromosome structure.
43 where retrotransposons have a vital role in chromosome structure.
44 chia coli, indicating that the alteration of chromosome structure after DNA damage may be a widesprea
46 ybridization under conditions that preserved chromosome structure, allowing identification of stage-d
48 Identification of components essential to chromosome structure and behaviour remains a vibrant are
50 cate Orc2 protein in chromosome duplication, chromosome structure and centrosome copy number control,
56 parallel roles for titin in both muscle and chromosome structure and elasticity, and provide new ins
58 that are useful for comparative analysis of chromosome structure and evolution and facilitates compa
59 ow-sorted chromosomes enables an overview of chromosome structure and evolution at a resolution never
62 d related the findings to various aspects of chromosome structure and function (DNA sequence organiza
63 ms will provide avenues for studies on plant chromosome structure and function and for future develop
64 ercoiling may modulate epigenetic effects on chromosome structure and function and on prophage behavi
65 ificance of replication-timing boundaries to chromosome structure and function and support the replic
67 that Su(var2-10 controls multiple aspects of chromosome structure and function by establishing/mainta
69 al interactions play an important role in 3D chromosome structure and function, but our understanding
80 egions are organized is a critical aspect of chromosome structure and function; however, the sequence
81 e interrogation of the relationships between chromosome structure and gene control in development and
84 precipitation is providing new insights into chromosome structure and gene regulation and control thr
86 st silencing protein Sir3p functions in both chromosome structure and in transcriptional regulation.
89 epithelial cancers, triggers instability in chromosome structure and number, which are thought to ar
92 ant nonlinear DNA structures that may define chromosome structure and organization, as well as interm
93 tic interactions between mutations affecting chromosome structure and partitioning in Bacillus subtil
94 tative DNA translocase) and smc (involved in chromosome structure and partitioning) caused a syntheti
97 mmon mechanism for establishing higher order chromosome structure and proper X chromosome gene expres
98 g the influence of two major forces, spatial chromosome structure and purifying (or negative) selecti
101 nce of Ki-67 and the chromosome periphery in chromosome structure and segregation, but little is know
102 etion of SMC-4/MIX-1 causes aberrant mitotic chromosome structure and segregation, but not dramatic d
106 monstrate the importance of transcription in chromosome structure and the plasticity of supercoil dom
107 ed in polyacrylamide to maintain both native chromosome structure and the three dimensionality of the
108 microscopy approaches that directly examine chromosome structure and then on population-averaged bio
110 e1's pivotal role in regulating higher-order chromosome structure and X-chromosome-wide gene expressi
111 ve chromatin mesh that organizes large-scale chromosome structures and protects the genome from insta
112 enter M phase without repair of the aberrant chromosome structures and undergo cell death during mito
113 ing, chromatin modification, organization of chromosome structure, and ATP-dependent nucleosome slidi
114 gene expression, connect gene expression to chromosome structure, and contribute to human disease.
117 g how modular organization underlies dynamic chromosome structure, and how this structure is probabil
119 lays several key roles in DNA metabolism and chromosome structure, and it is the primary cytotoxic ta
120 chore positions shift in response to altered chromosome structure, and kinetochore complex numbers ch
122 by searching in three dimensions, modifying chromosome structure, and spreading to newly accessible
123 d for gene silencing, as cellular probes for chromosome structure, and therapeutic applications.
126 maintain genome integrity and sense altered chromosome structure are invariably subverted in cancer
128 chromosome number, and the same stability of chromosome structure, as the RER colon cancers with wild
129 ong DNA sequence, meiotic recombination, and chromosome structure at a genome-wide scale has been dif
131 tion-averaged biochemical methods that infer chromosome structure based on the interaction frequencie
133 her order folding transitions that stabilize chromosome structure beyond the 30-nm diameter fiber.
134 comparative genomics framework for studying chromosome structure, broadly applicable to other organi
135 dence that the establishment of higher-order chromosome structure by a condensin complex regulates cr
136 major NAP, HU, acting together organize the chromosome structure by establishing multiple DNA-DNA co
137 protein complexes that mediates higher-order chromosome structure by tethering different regions of c
138 nce that the control of key genes depends on chromosome structures called insulated neighborhoods, we
142 evolution of mutation rate, genome size, and chromosome structure can therefore be extremely rapid an
143 SB distribution is influenced by large-scale chromosome structures, chromatin, transcription factors,
144 Long considered an intriguing component of chromosome structure, common fragile sites have taken on
145 Long considered an interesting component of chromosome structure, common fragile sites have taken on
146 ic) genes, RED1 and MEK1/MRE4, that encode a chromosome structure component and a protein kinase, res
149 Nucleosomes, the basic unit of eukaryotic chromosome structure, cover most of the DNA in eukaryote
150 meiotic cells, and that features of meiotic chromosome structure determine whether one or the other
151 d to developmental problems or underdominant chromosome structure differences between the parents.
155 tion requires highly orchestrated changes of chromosome structure during the mitotic cell cycle.
156 eristic size pertinent to the description of chromosome structure, e.g. there does not exist any sing
157 s as a self-limiting system in which meiotic chromosome structures establish an environment that prom
158 current arsenal of techniques used to query chromosome structure, focusing first on single-cell fluo
159 lement recognition allow decoupling of local chromosome structure from transcription initiation.
160 DNA segments called transposable elements to chromosome structure, function, and evolution in virtual
161 to ask otherwise intractable questions about chromosome structure, function, and evolution with a bot
163 ur understanding of the relationship between chromosome structure, gene activity, and recombination.
166 exhibit phenotypic similarities in terms of chromosome structure in both diploid and polyploid cells
169 ween chromatin modification and higher-order chromosome structure in long-range regulation of gene ex
170 atment and the role of programmed changes in chromosome structure in replication control are discusse
172 ely separated target genes, and organize the chromosome structure in space, thereby likely contributi
177 ns not only of chromosome number but also of chromosome structure including chromosomal deletions, in
178 ost extreme differences relate to changes in chromosome structure, including the emergence of African
179 s studies of effects of nucleases on mitotic chromosome structure, indicate that mild proteolysis gra
181 tiate recombination in meiosis, we show that chromosome structure influences the choice of proteins t
185 ng late S phase and that nurse cell polytene chromosome structure is controlled by regulating whether
190 opoisomerase II mutant, defective in mitotic chromosome structure, is also due to the retention of co
191 le element shown to have a bona fide role in chromosome structure, maintenance of telomeres in Drosop
192 limited amount of structural data on mitotic chromosome structure makes it impossible to distinguish
193 ity, proximity to centromeric sequences, and chromosome structure may all play a role in low recombin
194 regulating chromosome segregation as well as chromosome structure may be governed by the conserved BR
195 specific genes, establishment of the meiotic chromosome structure, meiosis-specific telomere behavior
197 ided early insight into the consequences for chromosome structure of an ancient large-scale duplicati
202 the suggestion that features of higher-order chromosome structure or chromosome dynamics act in a tar
203 ese results suggest that the requirements of chromosome structure place significant constraints on eu
205 otspots, including HIS2, suggest that global chromosome structure plays a significant role in recombi
207 has been recognized for several decades that chromosome structure regulates the capacity of replicati
208 the cytoplasmic filaments may be involved in chromosome structure, segregation, or the cell division
209 exually reproducing single-cell organisms to chromosome-structured sexually reproducing species.
210 mbles a holocentric chromosome, which is the chromosome structure shared by the closest relatives of
211 ing method for measuring gene expression and chromosome structure simultaneously on single chromosome
213 n Drosophila exhibit disrupted sarcomere and chromosome structure, suggesting that giant proteins may
214 ually fast rate of evolution with respect to chromosome structure, suggesting that this classic case
215 facilitates the formation of a higher-order chromosome structure that could also influence gene expr
217 rposes and for investigations of features of chromosome structure that influence gene expression.
218 ion fork, thereby leading to a disruption in chromosome structure that interferes with the meiotic di
219 identifies an activity critical for mitotic chromosome structure that is inactivated by Repo-Man-PP1
220 ntial tissue or developmental differences in chromosome structure that might be informative for compa
221 enhancer-driven genes generally occur within chromosome structures that are formed by the looping of
222 landscape is locally funneled toward "ideal" chromosome structures that represent hierarchical fibril
223 stribution of meiotic recombination, such as chromosome structure, that influences meiotic recombinat
225 methylation and chromatin remodeling affect chromosome structure, their impact on meiotic recombinat
227 lue of microfluidics as a tool for examining chromosome structure, these results lend support to cert
228 ates Ca2+, Mg2+, Na+, and K+ in higher order chromosome structure through electrostatic neutralizatio
229 erstanding of gene function, gene order, and chromosome structure through the de novo synthesis of ge
231 oxygen and nutrient availability with global chromosome structure, thus providing a mechanistic insig
232 mechanism involving changes in higher-order chromosome structure to achieve chromosome-wide effects.
233 es crossover formation, which in turn alters chromosome structure to inhibit other crossovers at addi
234 t the natural stochastic fluctuations of the chromosome structure to map both the spatial and tempora
236 that EFO1 and EFO2 are targeted to different chromosome structures to help establish or maintain sist
237 ocesses, including DNA repair, regulation of chromosome structure, transcriptional regulation, mitosi
238 f Su(Hw) causes global defects in nurse cell chromosome structure, we demonstrate that these architec
239 regulators of viral oncogene expression and chromosome structure were identified and validated, reve
241 objective function was designed for modeling chromosome structures, which was optimized by a gradient
242 involved in the organization of higher-order chromosome structure-which is essential for accurate chr
243 tive COH-3/4 complexes modulate higher-order chromosome structure, while WAPL-1-refractory REC-8 comp
245 of condensin I in the maintenance of mitotic chromosome structure with unprecedented temporal resolut
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