ライフサイエンスコーパス: sperm nuclei

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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 sed to package DNA at very high densities in sperm nuclei.

6 , YY, XY, and total sex-chromosome disomy in sperm nuclei.

7 ructures around unreplicated chromosomes; 2) sperm nuclei added to extracts that cycle through interp

8 e following pathways of spindle assembly: 1) Sperm nuclei added to meiotic extracts, supporting the f

9 amylation increased the deposition of H1M on sperm nuclei and chromatin-coated beads, indicating that

10 e reprogramming of terminally differentiated sperm nuclei and suggest that different epigenetic pathw

11 adient-free spindle assembly occurred around sperm nuclei but not around chromatin-coated beads and r

12 Sperm nuclei can be licensed by a combination of nucleop

13 ound chromosomes, reducing the percentage of sperm nuclei capable of forming spindles, and causing dr

14 By the time pollen tubes reach the ovary, sperm nuclei contain approximately 1.75C DNA.

15 ation; MyoV was strongly associated with the sperm nuclei during the maturation of the actin-rich inv

16 In wild-type plants, generative and sperm nuclei enter S phase soon after inception, implyin

17 e-mediated integration (REMI) on decondensed sperm nuclei followed by nuclear transplantation into un

18 ea urchin eggs form nuclear envelopes around sperm nuclei following GTP hydrolysis in the presence of

19 enopus liver nuclei also inhibited growth of sperm nuclei formed in egg extracts.

20 nd centromeres were observed to aggregate in sperm nuclei, forming an average of 20 and 7 clusters, r

21 Egg and sperm nuclei fuse to form the embryo.

22 Egg and sperm nuclei fuse to form the embryo.

23 The organization of chromosomes in sperm nuclei has been proposed to possess a unique "hair

24 xtracts requires preincubating the substrate sperm nuclei in an extract under low ATP conditions.

25 Notably, sperm nuclei in mutants of either rrf-3 or another compo

26 Plasmids are introduced into decondensed sperm nuclei in vitro using restriction enzyme-mediated

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

30 Compared to sperm nuclei, nuclei from adult somatic cells replicate

31 to centrosomes and its activation by either sperm nuclei or anti-AurA antibody (alphaAurA)-induced d

32 stribution of replication origins in Xenopus sperm nuclei replicating in Xenopus egg extract.

33 ly reduces the number of replication foci in sperm nuclei supports this view.

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

36 During fertilization, sperm nuclei undergo a dramatic conversion from a heavil

37 In egg cytoplasm, histone H1 protects sperm nuclei undergoing genome-wide decondensation and c

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

42 Just prior to double fertilization, sperm nuclei within embryo sacs contain the 2C quantity

43 DNA packing by lysine rich peptides in sperm nuclei would allow much greater accessibility to s

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