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1 idence for a genetic effect on mammalian non-disjunction.
2 omosomes may be at an increased risk for non-disjunction.
3 ination and to determine their impact on non-disjunction.
4 kely reflect mechanisms to ensure chromosome disjunction.
5 nteractions which can lead to chromosome non-disjunction.
6 d chromosomes 21 involved in paternal MI non-disjunction.
7  exchanges makes a tetrad susceptible to non-disjunction.
8 junction; and (iii) those leading to MII non-disjunction.
9 ids and a reduced efficiency of distributive disjunction.
10 osomes lacking homology do not pair prior to disjunction.
11  nonexchange chromosomes are paired prior to disjunction.
12 is not consistently linked to mitral annular disjunction.
13 ral valve prolapse (MVP) with mitral annular disjunction.
14 , and destroyed to complete sister chromatid disjunction.
15 ntly ensures genetic exchange and chromosome disjunction.
16 ased risk for UPD in the case of meiotic non-disjunction.
17 om chromosomes and triggers sister-chromatid disjunction.
18  with separase, both failed to induce sister disjunction.
19  are an important contributor to meiotic non-disjunction.
20 re, overexpression of Mad2 inhibited homolog disjunction.
21 e product is essential for proper chromosome disjunction.
22 mitosis was not sufficient to trigger sister disjunction.
23 tor genes, which mediate faithful chromosome disjunction.
24  is an important factor for X chromosome non-disjunction.
25 e know little of the causes of mammalian non-disjunction.
26 ch the Wt Y chromosome is susceptible to non-disjunction.
27 cally, including three STs with transoceanic disjunctions.
28 stakes" dispersal accounts for many of these disjunctions.
29 olutionary arena spanning large geographical disjunctions across the tropics.
30 densation but nonetheless allowed chromosome disjunction, anaphase B, and formation of a cytokinetic
31 t anaphase entry that is associated with non-disjunction and catenation of sister chromatids.
32  POLES, ESP) plays a major role in chromatid disjunction and cell expansion in Arabidopsis thaliana.
33 correlation was found between mitral annulus disjunction and curling (R=0.85).
34 mple and direct connection between defective disjunction and defective sperm development.
35 otic recombination, decreased chromosome non-disjunction and improved spore viability.
36 berates separase triggering sister chromatid disjunction and inactivates cyclin-dependent kinase 1 (C
37 mary counts, and functional summaries of the disjunction and intersection of clusters shared between
38 lar dominant effect on achiasmate chromosome disjunction and mapped the haplo-insufficient meiotic ge
39 driving mitotic events, including centrosome disjunction and separation, and is frequently over-expre
40 , I present an analysis of extensive data on disjunction and sperm survival in rDNA-deficient males c
41 ng meiosis II, resulting in sister chromatid disjunction and the production of haploid gametes.
42  functional annotations and summaries of the disjunctions and intersections of clusters between the c
43 nts (anaphase A, anaphase B, and chromosomal disjunction) and nuclei reentered interphase quickly eve
44 h fibrosis, greater prolapse, mitral annular disjunction, and double-peak strain.
45 ssment of leaflet morphology, mitral annular disjunction, and mitral regurgitation quantification.
46 muscles and inferobasal wall, mitral annulus disjunction, and systolic curling have been recently des
47 pecializing in homolog pairing, the other in disjunction-and each producing both noncrossovers and cr
48 vents; (ii) meiotic events leading to MI non-disjunction; and (iii) those leading to MII non-disjunct
49  factors associated with both MI and MII non-disjunction appear to be different for virtually every c
50 aphy resulting in a distant intercontinental disjunction are poorly understood.
51 mata, that are required to ensure chromosome disjunction, arise via the class I interference-dependen
52 sence of logical abilities is the concept of disjunction as a way into the conception of alternative
53 spect of meiotic prophase I that aids proper disjunction at anaphase I.
54 c chromosomal functions necessary for proper disjunction at meiosis I.
55  available, the extra Y was generated by non-disjunction at meiosis II after a normal chiasmate meios
56 o either a post-zygotic mitotic error or non-disjunction at meiosis II after a nullichiasmate meiosis
57  required during DNA replication, chromosome disjunction at mitosis, and other DNA-related activities
58 ibition is necessary for complete chromosome disjunction, because ribosomal RNA (rRNA) transcripts bl
59 on intermediates to promote sister chromatid disjunction before cell division.
60                                          The disjunction between arrestin recruitment and internaliza
61 ee alternative hypotheses to account for the disjunction between modern and archaeological herring po
62                                         This disjunction between phenology at low and high altitudes
63 ognitive reserve was born to account for the disjunction between the objective extent of brain damage
64 oal-directed action propose that experienced disjunctions between an action and its specific conseque
65 ivo target coverage was not practical due to disjunctions between enzyme and cell data, complex and a
66 rs, or long-distance dispersal in explaining disjunctions between the two regions, dismissing the con
67 es that mediate the influence of experienced disjunctions between these events are unknown.
68 o estimate the frequency of transcontinental disjunctions, biome shifts and evolutionary transitions
69 een offered is that pairing not only ensures disjunction, but also changes the physical state of chro
70 uish between the different mechanisms of non-disjunction by analysing DNA polymorphisms at the distal
71 NA topologic entanglements during chromosome disjunction by introducing transient DNA double-stranded
72                                     Synaptic disjunction by retraction of rod spherules, quantified b
73              We showed that transcontinental disjunctions confined within the Succulent Biome are fre
74 d more bileaflet involvement, mitral annular disjunction, curling, and abnormal valvular-myocardial m
75                   We assessed mitral annular disjunction, curling, global longitudinal strain, segmen
76  cyclin A degradation facilitates chromosome disjunction, cyclin B destruction is required for anapha
77               The presence of mitral annular disjunction, defined as separation between the left atri
78  proteolysis at the time of sister chromatid disjunction destabilizes kinetochore-microtubule attachm
79 dean, Amazonian and Atlantic Forests and one disjunction distribution in southern Chile.
80 a Ca(2+)-dependent manner whereas non-claret disjunction, Drosophila kinesin, and KCBP that lack a CB
81 ls of the chromokinesin NOD (no distributive disjunction; Drosophila melanogaster kinesin-10).
82 ms: p53 inactivation and abnormal chromosome disjunction due to telomere fusions (TFs).
83 cks in preparation for homologous chromosome disjunction during anaphase I.
84  at the metaphase plate and their subsequent disjunction during anaphase I.
85 role for Aurora B in telomere dispersion and disjunction during fission yeast mitosis.
86 romosomes is necessary for proper chromosome disjunction during meiosis I.
87 her, creating chiasmata that ensure accurate disjunction during reductional division.
88 king (such as the conjunction fallacy or the disjunction effect), question order effects, conceptual
89                                              Disjunction efficiency decreases linearly as heterochrom
90  germ cell proliferation, meiotic chromosome disjunction, egg shell formation, and the normal rate of
91  classifying cases according to stage of non-disjunction error.
92 s well as a high frequency of chromosome non-disjunction errors leading to aneuploidy (50%) in the oo
93 or (I or II) and the individual in which non-disjunction event occurred, as well as the crossover loc
94 ivative 22 syndrome owing to 3:1 meiotic non-disjunction event.
95                        Surprisingly, the non-disjunction events are largely restricted to the earlies
96 s occurring at MI, and suggests that all non-disjunction events may be initiated during MI and simply
97 rnal meiosis I (MI) and meiosis II (MII) non-disjunction events.
98 we show that a novel chromatin factor, X non-disjunction factor 1 (xnd-1), is responsible for the glo
99 le, at least four were due to meiosis II non-disjunction following a normal chiasmate meiosis I.
100  the first analysis of recombination and non-disjunction for a large paternally derived population of
101 al loss of APC/Apc: mutation in APC/Apc, non-disjunction, homologous somatic recombination and epigen
102 d genera (eastern Asia-eastern North America disjunction) implies significant periods of separation s
103 itral annulus showed a longer mitral annulus disjunction in 50 sudden death patients with MVP and LV
104 large proteins that mediate sister chromatid disjunction in all eukaryotes.
105 PICH(-/-) cells undergo sister chromatid non-disjunction in anaphase, and frequently abort cytokinesi
106 rements for achiasmate (nonexchange) homolog disjunction in Drosophila female meiosis I have been ide
107     During fieldwork, we found a substantial disjunction in flowering time that is correlated with so
108 first molecular correlate identified for non-disjunction in humans.
109 address the underlying causes of meiotic non-disjunction in humans.
110 chromosomes exhibit an absence of chromosome disjunction in meiosis I and an infrequent chromosome di
111 help prepare the chromosome pairs for proper disjunction in meiosis I.
112 on in meiosis I and an infrequent chromosome disjunction in meiosis II.
113 l recombination appears to predispose to non-disjunction in MI, the presence of a proximal exchange p
114 ce of a proximal exchange predisposes to non-disjunction in MII.
115                               Mitral annular disjunction in patients with MVP and MR was associated w
116  adjacent to a region of intron I at which a disjunction in sequence similarity between RBCS1B and RB
117 es and the mechanisms that ensure chromosome disjunction in the absence of recombination.
118 romosomal interactions that promote accurate disjunction in the first of two segregation events to ge
119 rt a highly significant association: MII non-disjunction involves increased recombination that is lar
120               Explanations for biogeographic disjunctions involving South America and Africa typicall
121                               Mitral annulus disjunction is a constant feature of arrhythmic MVP with
122 ansposon silencing, while meiotic chromosome disjunction is affected in rsd-6 mutants.
123                               Mitral annular disjunction is increasingly recognized as an important a
124 se results, we propose that sister-chromatid disjunction is often incomplete in human cells even afte
125 rinsic defect; however, the incidence of non-disjunction is significantly influenced by strain backgr
126 tween altered recombination and maternal non-disjunction is well documented: reductions in recombinat
127  the literature pertaining to mitral annular disjunction, its clinical implications, and areas needin
128 ble cyclin A prolonged or blocked chromosome disjunction, leading to metaphase arrest.
129                               Mitral annular disjunction length, referring to true MAD, was measured
130 igate the prognostic value of mitral annulus disjunction (MAD) and myocardial fibrosis at late gadoli
131 ricular arrhythmias (VA), and mitral annular disjunction (MAD) has been reported as a risk factor.
132                               Mitral annular disjunction (MAD) has received particular interest in pa
133                               Mitral annular disjunction (MAD) has recently been recognized as an arr
134 mic functional feature called mitral annular disjunction (MAD) have remained widely disputed.
135 o determine the prevalence of mitral annular disjunction (MAD) in patients undergoing cardiac MRI for
136                               Mitral annular disjunction (MAD) refers to atrial displacement of the h
137 e, marked leaflet redundancy, mitral annulus disjunction (MAD), a larger left atrium and left ventric
138                   The defect in distributive disjunction may be attributable to overloading of the di
139 eneral complete bipartite graphs and logical disjunctions may be of broader use than that the specifi
140                               Mitral annulus disjunction (median: 4.8 versus 1.8 mm; P<0.001), end-sy
141 anced, Cardiac, Mitral Valve, Mitral Annular Disjunction, Mitral Valve Prolapse, Floppy Mitral Valve,
142                                 The error of disjunction must occur either during paternal meiosis II
143     Conclusion In contrast to mitral annulus disjunction, myocardial fibrosis determined according to
144 est to determine when errors of Y chromosome disjunction occur.
145                                   Chromosome disjunction occurred normally, but anaphase-like movemen
146  one crossover per bivalent, below which non-disjunction occurred.
147 combination are associated with maternal non-disjunction occurring at both meiosis I (MI) and meiosis
148 P1 and cohesin Rad21 from telomeres, whereas disjunction occurs at anaphase after the phosphorylation
149  segregation system helps to ensure faithful disjunction of autosomes during spermatogenesis.
150                                 Paternal non-disjunction of chromosome 21 accounts for 5-10% of Down
151                             The cause of non-disjunction of chromosome 21 remains largely unknown.
152 age, distinguishing our results from MII non-disjunction of chromosomes 18 or 21.
153 en homologous chromosomes facilitates proper disjunction of chromosomes during meiosis I.
154 lin A degradation, and functions to time the disjunction of chromosomes in the early embryo.
155    In these cells, taxol did not inhibit the disjunction of chromosomes nor prevent their poleward se
156 nalyzing each subset defined by the union or disjunction of groups within the Venn diagram, and inclu
157                                       Proper disjunction of homologous chromosomes requires the misma
158 d appears to promote crossing over to ensure disjunction of homologous chromosomes.
159                                         Both disjunction of mini-X pairs and multivalent formation ar
160 D, provides a tool with which to explore the disjunction of mitosis and cytokinesis in cell cultures,
161  Bub1 and 3, and Mps1, may prevent premature disjunction of sister chromosomes, the other, consisting
162 sed cyclin A proteolysis and delayed mitotic disjunction of sister chromosomes.
163                                            A disjunction of such motifs often can represent the entir
164 tionally implicated in the regulation of the disjunction of the centrosome, the assembly of the mitot
165       The inseparabile mutation also affects disjunction of the chromosome 4 in males.
166                                      Mitotic disjunction of the repetitive ribosomal DNA (rDNA) invol
167 here are at least two mechanisms causing non-disjunction of the Y chromosome.
168 ttern evolved recently and expanded, causing disjunctions of more ancestral patterns.
169  are conjectured to compute conjunctions and disjunctions of oriented features.
170            Examples include intercontinental disjunctions of tropical plants, the spread of plant lin
171 nal detachment (RD) causes damage, including disjunction, of the rod photoreceptor-bipolar synapse, w
172 e N or C terminus of a minus-end (non-claret disjunction) or C terminus of a plus-end (Drosophila kin
173 de precipitation prompted geographical range disjunctions over Earth's history, leading to high rates
174 oup I and group II, repair during pachytene (disjunction pathway) is associated with interference and
175  triggering the abscission checkpoint if non-disjunction persists.
176                                      The non-disjunction phenotype has both cis and trans components:
177 vity or securin can prevent sister chromatid disjunction, principally by overexpression of non-degrad
178 e earliest cell divisions in mammals are non-disjunction-prone, an interpretation which provides an e
179 at in addition to promoting accurate homolog disjunction, recombination can also function to partiall
180                                   Given this disjunction, regulating those advertisements may be an a
181 a computer program that constructs models of disjunctions, represents possible destinations, and veri
182                                    Efficient disjunction requires 1000 kilobases of overlap in the ce
183 bryonic lethality and meiotic chromosome non-disjunction respectively, when separase function is comp
184 they suggest that virtually all maternal non-disjunction results from events occurring in meiosis I.
185  imaging risk factors such as mitral annular disjunction, severe mitral regurgitation, or replacement
186 r abandoned leads, imaging of mitral annular disjunction, specificity of the Lung Imaging Reporting a
187  kinase 2 (Nek2), which regulates centrosome disjunction/splitting, binds to and phosphorylates beta-
188 eywords: MR Imaging, Cardiac, Mitral Annular Disjunction Supplemental material is available for this
189 e dispersion initiates in metaphase, whereas disjunction takes place in anaphase.
190 predicted, children (as per logic of negated disjunction) tended to increase their speed of checking
191 ons are associated with a higher risk of non-disjunction than others.
192 tes, allowing these insects to cross habitat disjunctions that would have represented major or comple
193 uch as bileaflet involvement, mitral annular disjunction, the double-peak strain pattern, mechanical
194 ii) mitotic checkpoints regulate chromosomal disjunction to generate fissioned karyotypes.
195 efore investigated maternal X chromosome non-disjunction, to determine whether the effects of recombi
196      A high frequency of sex chromosomal non-disjunction, unrelated to the BN: mutation, was also ide
197 ase A of meiosis I, thus preventing complete disjunction until mid- to late anaphase A.
198 ents possible destinations, and verifies the disjunctions using the truth values in our experiments.
199                               Mitral annular disjunction was present in 2 generations among 3 familie
200                               Mitral annular disjunction was surgically corrected in all patients.
201    To assess the drivers of these geographic disjunctions, we combined ecological niche modeling, pal
202  simulations, speciation resulted from range disjunctions, whereas extinction occurred when no suitab
203 omenon, which is called preplay, occurred in disjunction with sequences of replay of a familiar exper
204                                  The current disjunctions within B. alternifolia might result from vi
205 g processes that generate and maintain large disjunctions within plant species can provide valuable i

 
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