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1 to the establishment of exclusive homologous chromosome pairing.
2 ential for proper SC assembly and homologous chromosome pairing.
3 ion by the genetic system regulating meiotic chromosome pairing.
4 ic relationships of diploid species based on chromosome pairing.
5 ation, meiotic recombination, and homologous chromosome pairing.
6 ded duration of nuclear division, or homolog chromosome pairing.
7 ide by side in a process known as homologous chromosome pairing.
8 aused by relaxed natural selection on proper chromosome pairing.
9 vation center, thereby inducing homologous X chromosome pairing.
10 it may function during the earlier stages of chromosome pairing.
11 g RNA implicated in allelic choice through X-chromosome pairing.
12 l terminus may be important in hom(e)ologous chromosome pairing.
13 omosome motion but an intermediate defect in chromosome pairing.
14 t interhomolog interactions promote accurate chromosome pairing.
15  interactions are dispensable for homologous chromosome pairing.
16  chromosomal domain, which leads to abnormal chromosome pairing.
17 s, including Ph1, the principal regulator of chromosome pairing.
18 c prophase, is thought to promote homologous chromosome pairing.
19 ase I in C. elegans males, is due to lack of chromosome pairing.
20 at a level other than non-coding RNA species-chromosome pairing.
21 chromosomes in maize mutants with defects in chromosome pairing.
22 ecombination machinery in promoting accurate chromosome pairing.
23 earch by spontaneous base pairing to mediate chromosome pairing.
24 ion is hypothesized to facilitate homologous chromosome pairing.
25 ntaining their chromosome numbers and proper chromosome pairings.
26 e sexual population showed proper homologous chromosome pairings.
27  hybrid, which exhibited strong preferential chromosome pairing (94% of the examined cells had 24 biv
28     Somatic XCI is regulated by homologous X-chromosome pairing and counting, and by the random choic
29 hierarchy, and regulates XCI by triggering X-chromosome pairing and counting.
30 rganization that ultimately restore bivalent chromosome pairing and disomic inheritance, and resolve
31 nd Mnd1 work as a complex to promote meiotic chromosome pairing and DSB repair.
32 YNAPSIS1 (PHS1) gene acts in coordination of chromosome pairing and early recombination steps in plan
33 dicates that RAD51 is required for efficient chromosome pairing and its absence results in nonhomolog
34 log Meu13 are required for proper homologous chromosome pairing and recombination during meiosis.
35        Depletion of Oct4 blocks homologous X-chromosome pairing and results in the inactivation of bo
36 ate factors influencing meiotic homoeologous chromosome pairing and reveal the type and extent of kar
37 us recombination that is crucial for meiotic chromosome pairing and segregation.
38 ly long telomeres, exhibit severely impaired chromosome pairing and synapsis and reduced meiotic reco
39                                   Homologous chromosome pairing and synapsis are prerequisite for acc
40 suggest that RAD51 function is essential for chromosome pairing and synapsis at early stages in meios
41 n yeast and plants, especially the fact that chromosome pairing and synapsis depend on the function o
42  studies have shown that these sites mediate chromosome pairing and synapsis during meiosis, and that
43 51 mutant that exhibits completely disrupted chromosome pairing and synapsis during meiosis.
44  of these double mutants revealed incomplete chromosome pairing and synapsis in meiotic prophase, and
45 ation intermediates or defects in homologous chromosome pairing and synapsis independent of DNA damag
46 the noncoding genomic sequence important for chromosome pairing and synapsis may be the culprit.
47 tological analyses of mum2 mutants show that chromosome pairing and synapsis occur, although at reduc
48 al studies in an Atmlh3 mutant indicate that chromosome pairing and synapsis proceed with normal dist
49 al chromosome dynamics, affecting homologous chromosome pairing and synapsis.
50 catalyzed solely by HOP2 supports homologous chromosome pairing and synapsis.
51 1 locus, a locus ensuring correct homologous chromosome pairing, and discover that bouquet formation
52  spatiotemporal initiation of recombination, chromosome pairing, and synapsis.
53 o-like kinase PLK-2 to induce NE remodeling, chromosome pairing, and synapsis.
54 tiation, including DNA double-strand breaks, chromosome pairing, and synaptonemal complex formation.
55 led a role for Zfy2 in promoting meiotic sex chromosome pairing, and uncovered unexpected effects of
56 ing mutant male meiosis, although homologous chromosome pairing appeared normal at metaphase I, chrom
57  our results reveal significant preferential chromosome pairing at meiosis in an F1 hybrid population
58      This process may initiate or facilitate chromosome pairing before recombination and meiosis.
59 IM-1 and an SMC subunit decreased homologous chromosome pairing before synapsis, revealing a new role
60 s the nature of polyploidy and its impact on chromosome pairing behavior.
61                                      Meiotic chromosome pairing between homoeologous chromosomes was
62 f the numbers of orthologues observed in the chromosome pairings between the two species and by deter
63 heir gametes usually experienced problems in chromosome pairing, but females also produced a certain
64  QPh.ucd-5S expression increased homeologous chromosome pairing by 1.6 chiasmata/cell in T. aestivum
65 observations show that Phl does not regulate chromosome pairing by premeiotic chromosome alignment an
66 o crossing-over also facilitate the intimate chromosome pairing called "synapsis." Many organisms--in
67 a simultaneous estimation of the linkage and chromosome pairing configuration-a cytological parameter
68                                              Chromosome pairing constitutes an important level of gen
69  X chromosome fate by controlling homologous chromosome pairing, counting, and mutually exclusive cho
70  of L2-CRM function including evidence for a chromosome pairing-dependent process that promotes trans
71 ese iab-2 PHO sites are required in vivo for chromosome pairing-dependent repression of a mini-white
72 g first centriole duplication and homologous chromosome pairing/DNA cross-over events, forming multip
73 se, a small amount of cohesin remains at the chromosome-pairing domain, mainly at the centromeres, wh
74 ly described mutation (Mcm5A7) that disrupts chromosome pairing, DSB repair is initiated by homologou
75  suggest a potential mechanism of homologous chromosome pairing during meiosis in allopolyploid parth
76 13+, which has been implicated in homologous chromosome pairing during meiosis in Schizosaccharomyces
77 anchorage, nuclear migration, and homologous chromosome pairing during meiosis.
78 ntified a checkpoint mechanism that monitors chromosome pairing during meiosis.
79 romosome movement is critical for homologous chromosome pairing during meiosis.
80 t-like structure that facilitates homologous chromosome pairing during meiosis.
81 gh homologous recombination is essential for chromosome pairing during prophase I, the resulting cros
82 ic analysis of this hybrid revealed multiple chromosome pairing errors, indicating hybrid sterility.
83  were observed in abnormal cells that showed chromosome-pairing errors affecting these chromosomes.
84 er meiosis, but they show defects in meiotic chromosome pairing, establishment of the XY body and pro
85               In meiosis in male fruitflies, chromosome pairing events do not facilitate genetic exch
86 propose that innate preference of homologous chromosome pairing exists in nascent allopolyploids and
87  one describing the preference of homologous chromosome pairing (expressed as the preferential pairin
88 gh small in size, has retained essential sex chromosome pairing functions despite its rapid rate of e
89     Analysis of mutants defective in meiotic chromosome pairing has uncovered a role for Caenorhabdit
90 licated until after karyogamy and subsequent chromosome pairing have taken place.
91 d by the Ph1 gene via preventing homeologous chromosome pairing (HECP).
92 ogical applications for the understanding of chromosome pairing, homoeologous recombination, and geno
93 le for Rad51 in the homology search phase of chromosome pairing in addition to its known role in meio
94 that would eventually block all homoeologous chromosome pairing in allopolyploids.
95 oint protein is somehow required for meiotic chromosome pairing in C. elegans, thus providing a direc
96     In the 1920s, Jozsef Gelei proposed that chromosome pairing in flatworms resulted from the format
97 l techniques, the early stages of homologous chromosome pairing in male Drosophila have not been obse
98 s display sterility associated with abnormal chromosome pairing in meiosis.
99 se mice is affected due to the disruption of chromosome pairing in prophase I.
100  genes acting together increased homeologous chromosome pairing in T. aestivum x Ae. speltoides hybri
101 of Su1-Ph1 and Su2-Ph1 increased homeologous chromosome pairing in T. aestivum x Ae. speltoides hybri
102                           However, examining chromosome pairing in the allotetraploid Brassica napus
103 al and inverted X chromosomes; (2) meiotic X chromosome pairing in these individuals is likely initia
104  the Ph1 locus, which prevents heterogenetic chromosome pairing in wheat, is also investigated.
105 at are implicated in controlling homeologous chromosome pairing in wheat.
106          Disruption of microtubules inhibits chromosome pairing, indicating that these connections pr
107                                   Homologous chromosome pairing is a prerequisite to establish physic
108                                              Chromosome pairing is an essential meiotic event that en
109  for successful interhomologue events before chromosome pairing is complete.
110     How heterochromatin could act to promote chromosome pairing is discussed here.
111 f spermatocytes is acquired after homologous chromosome pairing is established and is coincident with
112                             Thus, homologous chromosome pairing is favored to partners with the most
113                       In C. elegans, meiotic chromosome pairing is initiated by association of chromo
114         In polyploid wheat, the diploid-like chromosome pairing is principally controlled by the Ph1
115            In meiotic prophase I, homologous chromosome pairing is promoted through chromosome moveme
116 ution of the bouquet structure to homologous chromosome pairing is uncertain.
117                                              Chromosome pairing, isozyme, and restriction fragment le
118                     InDrosophila, homologous chromosome pairing leads to "transvection," in which the
119          Recent reports suggest homologous X chromosome pairing may be a prerequisite for silencing,
120 olyploids, different degrees of preferential chromosome pairings may occur during meiosis.
121 epigenetic silencing; underlying controls of chromosome pairing; mechanisms and functional significan
122 ysis for autopolyploids, based on the random chromosome pairing model.
123 monstrated a role in centromere function and chromosome pairing, necessary to ensure proper chromosom
124 s segregate as in a diploid, indicating that chromosome pairing occurs exclusively (or almost so) amo
125  most allopolyploid plants, only homogenetic chromosome pairing occurs in meiosis, as a result of the
126 have characterized meiotic and early somatic chromosome pairing of homologous chromosomes in flies th
127                             These changes in chromosome pairing parallel changes in large-scale chrom
128 sence of the wheat suppressor of homeologous chromosome pairing, Ph1.
129                             We conclude that chromosome pairing plays an important role in trans-supp
130 ssociations play active roles in the meiotic chromosome pairing process, analogous to those of the te
131                Here, we find that homologous chromosome pairing protein 2 (Hop2) functions as an inhi
132                                       Sister chromosome pairing provides a mechanism for the maintena
133 ariety of external factors, which can impact chromosome pairing, recombination, and fertility.
134 ound to detect mutations that impair meiotic chromosome pairing, recombination, or segregation.
135  inactive centromere are present, homologous chromosome pairing reduces the frequency of intrachromos
136 mes in the tetraploid progeny was similar to chromosome pairing reported for A. hypogaea, with recomb
137 viously been shown to function as cis-acting chromosome pairing/segregation sites.
138 esis and nucleolar formation and also as sex chromosome pairing sites in male meiosis.
139                       Strikingly, this early chromosome pairing still requires SPO11 but is not depen
140 re there are no intrinsic barriers to normal chromosome pairing, synapsis, double-strand break format
141 a cytological parameter determining bivalent chromosome pairings (the preferential pairing factor).
142  (SC) and its role in maintaining homologous chromosome pairings, the critical roles of the meiosis-s
143  initiation of inactivation is preceded by X chromosome pairing; their results implicate this pairing
144 pairing homoeologous) system which restricts chromosome pairing to strictly homologous.
145 ved in Cdk2 KO mice including non-homologous chromosome pairing, unrepaired double-strand breaks, und
146                                       During chromosome pairing, we consistently found two contiguous
147 y the relationship between recombination and chromosome pairing, we examined the distribution of RAD5
148 t pachytene, the stage of maximum homologous chromosome pairing, we found a mean of 70.3 foci (i.e.,

 
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