ライフサイエンスコーパス: female germ line

1 1 in the erasure of paternal imprints in the female germ line.

2 ransmitted to EE2 granddaughters through the female germ line.

3 me stability at key stages of meiosis in the female germ line.

4 regulatory ability when they pass through a female germ line.

5 ry and recapitulating the development of the female germ line.

6 w that RNAi is established in the Drosophila female germ line.

7 lly higher in the male germ line than in the female germ line.

8 may also be required for maintenance of the female germ line.

9 d reversibly silenced by passage through the female germ line.

10 ted cell and may require passage through the female germ line.

11 s of meiotic initiation used in the male and female germ lines?

12 nce occurs at A(vy); when passed through the female germ line, A(vy) epigenotype is not completely "r

13 to be maintained, Wolbachia must infect the female germ line after being acquired by horizontal tran

14 ir as a key quality control mechanism in the female germ line and a critical determinant of fertility

15 tion or gonadal disruption in roach down the female germ line and add to existing evidence that male

16 ts were tested for expression of mRNA in the female germ line and for repression of hybrid dysgenesis

17 into the communication between males and the female germ line and soma to regulate reproduction and l

18 complementing, overlapping functions in the female germ line and the early embryo.

19 Deletion of both gene products from the female germ line arrests germ-line development.

20 activity results in stem cell tumors in the female germ line as well as female-to-male somatic trans

21 We show that deletion of Mis18alpha in the female germ line at the time of birth has no impact on c

22 r introducing mtDNA mutations into the mouse female germ line by means of embryonic stem (ES) cell cy

23 ection for higher recombination rates in the female germ line by the elimination of aneuploid embryos

24 The 7.3-kb AaVgR mRNA is present only in female germ-line cells and is abundant in previtellogeni

25 sequences, and are specifically expressed in female germ-line cells.

26 The mammalian female germ line challenges this model because of the ce

27 A secondary genetic screen was to generate female germ-line clones of these potential cell division

28 e novo mtDNA mutations are suppressed in the female germ line; despite this, mtDNA heteroplasmy is re

29 These results suggest that, in the female germ line, diet-induced A(vy) hypermethylation oc

30 ic components between germ cells and, in the female germ line, enrich select cells in the cyst to bec

31 ere we comprehensively define the Drosophila female germ line epigenome throughout oogenesis and show

32 findings have implications for understanding female germ line fidelity, the regulation of fertility a

33 enesis, a manifestation of P activity in the female germ line; however, none had any effect on P-elem

34 is maternally loaded in embryos through the female germ line in D. virilis.

35 Our results thus suggest that the female germ line is able to recognize and select against

36 of mitochondrial units of segregation in the female germ line is relatively small in relation to the

37 strate that ectopic expression of PSI in the female germ line is sufficient to repress splicing of an

38 at differential methylation between male and female germ lines is a key determinant of the mutation r

39 mits the TEs in an active state, whereas the female germ line maintains repression of the TEs.

40 findings indicate that, in both the male and female germ lines, meiosis is initiated through retinoic

41 In the female germ line, mitotic nondisjunction ensures that th

42 alyze syntaxin1's role in early development, female germ line mosaics mutant for syntaxin1 expression

43 Meiosis in the female germ line of mammals is distinguished by a prolon

44 romosomal Cre-mediated recombinations in the female germ line of mice.

45 Here, we use female germ-line-specific depletion to study Piwi functi

46 In the female germ line the gamma mutant frequency induced by i

47 appear to be selectively eliminated from the female germ line, thereby minimizing their impact on pop

48 w that INX-14 and INX-22 are required in the female germ line to inhibit oocyte maturation, MAPK acti

49 Our analysis indicates that MSI in the female germ line was approximately 9%.

50 ated by transmission of RSVIgmyc through the female germ line, was also produced in founder transgeni

51 stinguish between these possibilities in the female germ line, we compared mouse oocyte development i

52 d process of monitoring the integrity of the female germ line, whereas the functions of p53 are restr