ライフサイエンスコーパス: female germ cell

1 t1 in meiosis and meiotic gene activation in female germ cells.

2 nuage have not been identified in mammalian female germ cells.

3 gen-producing adrenal-like cells and loss of female germ cells.

4 genous nos transcript and exclusively in the female germ cells.

5 ivate aspects of male germ cell behaviour in female germ cells.

6 dentical subcellular distribution is seen in female germ cells.

7 velopment and at different times in male and female germ cells.

8 chanism that regulates the early survival of female germ cells.

9 and spermatogonia; DAZL also is expressed in female germ cells.

10 required for survival and differentiation of female germ cells.

11 the limiting factor for fusome maturation in female germ cells.

12 s required for this process in both male and female germ cells.

13 esis in males, whereas ectopic expression in female germ cells ablates the germline.

14 the WNT signalling pathway are expressed in female germ cells and embryos.

15 role in inhibiting methylation of the ICR in female germ cells and in somatic cells and, therefore, i

16 his dynamic expression pattern is limited to female germ cells and is under Sxl control.

17 unction is linked to inherited aneuploidy in female germ cells and may contribute to the maternal age

18 exes, GPBOX transcripts accumulate faster in female germ cells and peak at E12.5 when they are presen

19 Male and female germ cells are usually produced during spermatoge

20 tions of Ercc1 are required in both male and female germ cells at all stages of their maturation.

21 ons, not for initiating the first meiosis in female germ cells at the SD stage.

22 Female germ cells begin meiosis during embryogenesis.

23 nerstone of DNA methylation establishment in female germ cells, but also provides an important resour

24 indicate that L1 RNA transcribed in male or female germ cells can be carried over through fertilizat

25 Male and female germ cells can transmit genetic defects that lead

26 e CGFD-inducing activity was not specific to female germ cell chromatin and was heat stable but sensi

27 copies of a hotspot from the DNA of male and female germ cells, cloning the products into Escherichia

28 Oocytes, the female germ cells, contain all the messenger RNAs necess

29 he force driving the age-related increase in female germ cell death is multifactorial, but changes in

30 he initial stages of gametogenesis, male and female germ cells develop in full synchrony as a syncyti

31 demonstrate is an early molecular marker of female germ cell development.

32 Male germ cells arrest mitotically, while female germ cells directly enter meiotic prophase I.

33 and RNA-seq analysis on flow-sorted male and female germ cells during embryogenesis at three time poi

34 ylation imprints are established in male and female germ cells during gametogenesis, and the de novo

35 Ap63 isoform, is constitutively expressed in female germ cells during meiotic arrest and is essential

36 rous germline phenotype in which presumptive female germ cells exit the meiotic pathway and return to

37 hormone receptor complexes in male, but not female, germ cell extracts purified from fetuses at a de

38 e of its constituent molecules in regulating female germ cell fate, that this review will focus.

39 Male and female germ cells follow distinct developmental paths wi

40 s the generation of a large supply of mature female germ cells for future treatment of infertile wome

41 This data suggests that GP130 is required in female germ cells for their normal function, but is disp

42 used to differentially regulate the male and female germ cell genomes to allow for these distinct out

43 ibits very different effects on the male and female germ cell genomes.

44 rammed cell death is the most common fate of female germ cells in Drosophila and many animals.

45 In female germ cells, in which both X chromosomes are activ

46 uring the same developmental period in which female germ cells initiate meiosis and male germ cells e

47 e transcription of these repeats in male and female germ cells may facilitate the homologous recombin

48 y sex-specific methylation in either male or female germ cells, must escape these dynamic changes and

49 Tet1 deficiency significantly reduces female germ-cell numbers and fertility.

50 establishes the correct imprint in male and female germ cells of AS mice, homologous association and

51 int kinase gene, Bub1, induces aneuploidy in female germ cells of mice and that the effect increases

52 ne is specifically expressed in the male and female germ cells of the mouse and other vertebrates.

53 ependent acceleration of apoptosis occurs in female germ cells (oocytes), and this requires communica

54 germ cells mostly undergo apoptosis, whereas female germ cells preferentially arrest in early meiosis

55 In mammalian females, germ cells remain arrested as primordial follic

56 yonic gonads in organ culture causes male-to-female germ cell sex reversal.

57 It is also required in female germ cells to control mitosis and meiotic recombi

58 Sterility is due to failure of both male and female germ cells to progress past the first meiotic met

59 dial germ cells (PGCs) give rise to male and female germ cells to transmit the genome from generation

60 ted successfully with diplo-X (chromosomally female) germ cells to make functional eggs.

61 hat Dazla protein is cytoplasmic in male and female germ cells, unlike the nuclear RBM protein.

62 The persistence of GPBOX transcripts in female germ cells until E15.5 and their virtual disappea

63 e, we conditionally ablated Calr in male and female germ cells using Stra8 (mcKO) and Zp3 (fcKO) prom

64 distributed in the cytoplasm of the male and female germ cells, whereas these proteins are translocat