ライフサイエンスコーパス: male pronucleus

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1 arance of a low level de novo H3K9me2 in the male pronucleus.

2 h that propels the anterior migration of the male pronucleus.

3 We show here it also positions the male pronucleus.

4 i with a single centrosome detached from the male pronucleus.

5 inct mechanisms that regulate H3K9me2 in the male pronucleus.

6 we find replication of DNA derived from the male pronucleus.

7 c spindle that forms in association with the male pronucleus.

8 during the early stages of migration by the male pronucleus.

9 r the conversion of the sperm nucleus into a male pronucleus.

10 is established around the metaphase-arrested male pronucleus.

11 These events precede the development of the male pronucleus.

12 leus is not inherently less than that of the male pronucleus.

13 ion, a sperm nucleus reorganizes to become a male pronucleus.

14 d reformation of the nuclear envelope of the male pronucleus.

15 ch the female pronucleus migrates toward the male pronucleus.

16 If GNU eggs are inseminated, however, the male pronucleus also undergoes DNA replication.

17 initial position of centrosomes, between the male pronucleus and cell cortex at the embryo posterior,

18 e association must be maintained between the male pronucleus and the centrosomes during pronuclear mi

19 propose that robust MT nucleation pushes the male pronucleus anteriorly to join the female pronucleus

20 This finding shows that Wolbachia impair the male pronucleus but no extranuclear component of the spe

21 id eggs whose normal development requires no male pronucleus but still depends on extranuclear patern

22 le cycle (fue) is required in the zygote for male pronucleus-centrosome attachment and female pronucl

23 protein 1 beta (HP1beta) is abundant in the male pronucleus, despite the absence of di- and trimethy

24 ion, thus ensuring the formation of a viable male pronucleus during early embryonic development.

25 Wolbachia-induced sperm modification is the male pronucleus (e.g., DNA or pronuclear proteins) or so

26 Male pronucleus formation is inhibited upon deletion of

27 h the sperm entry site and trajectory of the male pronucleus in a significant majority of eggs.

28 om delayed nuclear envelope breakdown of the male pronucleus in Nasonia vitripennis.

29 null females show defective formation of the male pronucleus in vivo.

30 In this model, a centrosome pair at the male pronucleus initiates stochastic microtubule (MT) gr

31 Incorporation by the male pronucleus is always about four to five times great

32 rsion of the sperm nucleus into a functional male pronucleus is compromised in sarah mutant eggs, ind

33 ine specific H3 methylation reveals that the male pronucleus is negative for di- and trimethyl H3-K9

34 yos defective for the function of either the male pronucleus (mh, K81, and pal or both pronuclei (gnu

35 ation is also observed on the surface of the male pronucleus (MPN) in vivo during NE formation.

36 hat induced the appearance of H3K9me2 in the male pronucleus of the zygote treated with cycloheximide

37 go nuclear decondensation, form a functional male pronucleus, or initiate mitotic divisions in the eg

38 yos abolishes incorporation of H3.3 into the male pronucleus, renders the paternal genome unable to p

39 d that recruitment of lamina proteins to the male pronucleus requires, and probably accompanies, reor

40 t mediate nucleosome assembly in the nascent male pronucleus, the machinery for protamine removal rem

41 In one-cell embryos the migration of the male pronucleus to meet the female pronucleus after fert

42 ecruitment of nuclear lamina proteins to the male pronucleus, we examined the subcellular localizatio

43 us studies emphasizing pulling forces on the male pronucleus, we propose that robust MT nucleation pu

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