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1 to reinstate the apoptotic response to the X univalent.
2 seven bivalents and 21 chromosomes remain as univalents.
3 proposed to explain the lack of response to univalents: (1) reduced stringency of the oocyte SAC to
6 We used a laser microbeam to either sever a univalent along the plane of sister chromatid cohesion o
7 ationic to anionic charge ratio, TE data for univalent and multivalent cationic lipids merged into a
11 rmation of mIgM cross-links: (1) more stable univalent binding and (2) a tendency for monogamous bind
12 tion exhibited wild-type tetramer binding in univalent binding assays, but reduced binding affinity i
13 with reduced chiasma formation and frequent univalents, but is normal in allotetraploid hybrids, ind
17 oalumino-phosphate with the RHO topology and univalent cation forms of the zeolite ZK-5 were measured
19 experiments confirm that the selectivity of univalent cations for the strong sites on the G-quadrupl
22 , the currents were predominantly carried by univalent cations with a slightly greater selectivity fo
24 cytokinesis and for directional stability of univalent chromosome movements, and cyclin B3 degradatio
25 ple meiotic defects which are represented by univalent chromosomes and chromosome fragmentation at me
27 premature separation of homologs results in univalent chromosomes at MI, and univalents constrained
29 prophase spermatocytes, and, if not, whether univalent chromosomes could align normally on the meioti
32 mature chromatid separation (predivision) of univalent chromosomes producing either a balanced (2 + 2
33 poptotic elimination of cells with unpaired (univalent) chromosomes at the first meiotic metaphase (M
34 n N-terminal peptides can form tetramer-like univalent complexes, but they cannot evaluate effects of
36 her uniquely mapped onto separate effectors (univalent conditions) or else mapped onto shared effecto
38 results in univalent chromosomes at MI, and univalents constrained to form monopolar attachments sho
39 neutral hosts with dicationic guests having univalent counterions includes two possible modes: (1) d
44 n addition, YY1-deficient spermatocytes show univalent formation, increased aneuploidy, and pachytene
46 ion of bivalent chromosomes resulting in two univalents going to the same pole and, second, nondisjun
47 mutations that exhibit wild-type binding in univalent head-to-head assays are located in the interst
48 The presence of many multivalents and few univalents in meiotic chromosome preparations of spore m
49 ion of rod bivalents over ring bivalents and univalents, indicating that there is a mechanism present
50 nesis and that 11 cosegregating markers with univalent inheritance are completely associated with dip
51 ection against the parthenogenetic locus and univalent inheritance of the region bearing diplospory.
56 e long-term evolutionary consequence for the univalents is likely to be genetic degradation through a
59 tic effects are negligible for monolayers of univalent lipids, emphasizing the unique importance of e
60 00) (1.1 nM) had tumor uptake similar to the univalent LLP2A-DOTA but higher liver, marrow, and kidne
62 upon deoxygenation and was permeable to both univalent (Na+, K+, Rb+) and also divalent (Ca2+, Mg2+)
66 ny dehydratases are susceptible to damage by univalent oxidants that convert the clusters to an inact
67 sters of dehydratases are rapidly damaged by univalent oxidants, including hydrogen peroxide, superox
70 xidized intermediate diiron species, and (3) univalent oxidation of Y177 by one of these intermediate
71 hydratases that are notoriously sensitive to univalent oxidation, and experiments confirmed that othe
73 nd B genes were labeled at saturation with a univalent probe consisting of Fab coupled to R-phycoeryt
74 imizing the redox cycling attendant upon the univalent reduction of nitro compounds, quinones, and dy
75 tracellular superoxide was generated through univalent reduction of oxygen by reduced demethylmenaqui
77 an then mediate O2.- production by cycles of univalent reduction, to the corresponding monocation rad
79 ter chromatid cohesion or knock out one of a univalent's two kinetochores to release one or both from
80 ately 9x10(-4) (ng/mul)(-1) s(-1) for 100 mM univalent salt buffer, with a very small off-rate at zer
81 magnesium binding; the strong dependence on univalent salt concentration, and its substantial antico
83 , we find that the model also reproduces the univalent salt-dependence and the anticooperativity of M
84 tely modeled using either a one-dimensional, univalent, site-specific Ising lattice approximation, or
85 nt responses, depending on the rule, whereas univalent target stimuli were associated with fixed resp
86 tramers through mechanisms not probed by the univalent tetramer binding assay or represent polymorphi
87 e 21 unpaired chromosomes probably remain as univalents through multiple generations and do not recom
88 r than solely reflecting the ability of some univalents to adopt a meiosis II-like orientation on the
89 chromosome behavior, and (2) the ability of univalents to satisfy the SAC by forming bipolar attachm
94 pairs formed bivalents at metaphase and many univalents were observed, leading to chromosome nondisju
96 studies demonstrate that segregation of the univalent X chromosome at the first meiotic division is
97 MI spermatocytes is seen in response to the univalent X chromosome of XSxr(a)O male mice [2], in whi
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