ライフサイエンスコーパス: female germ cell

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

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

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

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

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

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

7 dentical subcellular distribution is seen in female germ cells.

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

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

10 eeper of meiotic initiation in both male and female germ cells.

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

12 required for survival and differentiation of female germ cells.

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

14 ession in sexually undifferentiated male and female germ cells.

15 atekeeper of meiotic onset, in both male and female germ cells.

16 onservation of this regulatory axis in human female germ cells.

17 cell-expressed genes briefly active in early female germ cells.

18 epressive modifications observed in male and female germ cells.

19 the single-cell RNA-sequencing data of human female germ cells.

20 derepression and dramatic loss of developing female germ cells.

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

22 creased expression of male-specific genes in female germ cells across generations and BaP doses.

23 ngle-cell RNA-sequencing on mouse and monkey female germ cells and downloaded the single-cell RNA-seq

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

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

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

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

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

29 the majority of genes under PHF7 control in female germ cells are not under PHF7 control in male ger

30 Male and female germ cells are usually produced during spermatoge

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

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

33 Female germ cells begin meiosis during embryogenesis.

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

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

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

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

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

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

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

41 revealed that this high MAX protein level in female germ cells declined significantly around physiolo

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

43 own to be biologically relevant for male and female germ cell development, respectively.

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

45 ation of cell cycle transitions may underlie female germ cell developmental allochrony between specie

46 nsights into the interspecies differences in female germ cell developmental time spans.

47 However, Max-null male and female germ cells did not complete the entire meiotic pr

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

49 the drastic increase in the ratio of male to female germ cell divisions after the onset of spermatoge

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

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

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

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

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

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

56 Male and female germ cells follow distinct developmental paths wi

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

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

59 For example, in Drosophila female germ cells, forced expression of the testis-speci

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

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

62 aled that sexually undifferentiated male and female germ cells had abundant MAX protein because of th

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

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

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

66 phf7 This study reveals that ectopic PHF7 in female germ cells leads to a loss of sexual identity and

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

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

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

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

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

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

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

74 s to meiosis results in heterogeneity in the female germ cell populations, which limits the studies o

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

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

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

78 The maturation of the female germ cell, the oocyte, requires the synthesis and

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

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

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

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

83 disrupted transcriptomic sexual identity of female germ cells transgenerationally.

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

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

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

87 e lacking transcription factors expressed in female germ cells, we analyzed global gene expression pr

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

89 o the transcriptome features of peri-meiotic female germ cells, which offers new information not only