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1 ar spindle assembly around exogenously added sperm nuclei.
2 in cell-free egg extracts supplemented with sperm nuclei.
3 not the rate of fork progression, in Xenopus sperm nuclei.
4 n of ORC inhibits DNA replication of Xenopus sperm nuclei.
5 uclear theca at the posterior part of mature sperm nuclei.
6 sed to package DNA at very high densities in sperm nuclei.
7 , YY, XY, and total sex-chromosome disomy in sperm nuclei.
8 ructures around unreplicated chromosomes; 2) sperm nuclei added to extracts that cycle through interp
9 e following pathways of spindle assembly: 1) Sperm nuclei added to meiotic extracts, supporting the f
10 amylation increased the deposition of H1M on sperm nuclei and chromatin-coated beads, indicating that
11 e reprogramming of terminally differentiated sperm nuclei and suggest that different epigenetic pathw
12 adient-free spindle assembly occurred around sperm nuclei but not around chromatin-coated beads and r
14 ound chromosomes, reducing the percentage of sperm nuclei capable of forming spindles, and causing dr
16 ation; MyoV was strongly associated with the sperm nuclei during the maturation of the actin-rich inv
18 e-mediated integration (REMI) on decondensed sperm nuclei followed by nuclear transplantation into un
19 ea urchin eggs form nuclear envelopes around sperm nuclei following GTP hydrolysis in the presence of
21 nd centromeres were observed to aggregate in sperm nuclei, forming an average of 20 and 7 clusters, r
24 xtracts requires preincubating the substrate sperm nuclei in an extract under low ATP conditions.
27 ters and spindle assembly, in the absence of sperm nuclei, in a gammaTuRC (gamma-tubulin ring complex
28 ificantly inhibit DNA replication in Xenopus sperm nuclei, little or no inhibition is seen in the cas
29 f 64 cones of actin that assemble around the sperm nuclei, move to the basal end of the tails, formin
31 to centrosomes and its activation by either sperm nuclei or anti-AurA antibody (alphaAurA)-induced d
34 the transgene is incorporated randomly into sperm nuclei that have had their membranes disrupted wit
35 y of licensed replication origins on Xenopus sperm nuclei (the physiological DNA substrate in this sy
38 e transgenic embryos without manipulation of sperm nuclei using microinjection methods that are stand
39 failure of fertilization, since incorporated sperm nuclei were evident in eggs used to measure the Ca
40 ould be allocated for the preparation of the sperm nuclei, which are stored as aliquots for future us
41 scence shows punctate localization of H2B in sperm nuclei, which in part coincides with telomeric DNA
43 tion but did not require added demembranated sperm nuclei with their accompanying centrosomes or acti