ライフサイエンスコーパス: gonadogenesis

1 s derive from a common precursor pool during gonadogenesis.

2 ng that lines represses hub cell fate during gonadogenesis.

3 nd identified twenty-four genes required for gonadogenesis.

4 t for testis differentiation at the onset of gonadogenesis.

5 that is required for Sox9 expression during gonadogenesis.

6 lineages and have distinct roles in somatic gonadogenesis.

7 rphic and initiates sex-specific programs of gonadogenesis.

8 howed that C. elegans gon-14 is required for gonadogenesis.

9 plays several distinct roles during somatic gonadogenesis.

10 b on a Numbl mutant background just prior to gonadogenesis.

11 primary focus has been the role of hnd-1 in gonadogenesis.

12 ate morphogenic processes are at work during gonadogenesis.

13 well as their migration and guidance during gonadogenesis.

14 ut does not appear to have any role in later gonadogenesis.

15 ng functions with hnd-1 in embryogenesis and gonadogenesis.

16 partially penetrant defects in viability and gonadogenesis.

17 with FOG co-factors exhibit abnormalities in gonadogenesis.

18 on-4 in an attempt to learn how it regulates gonadogenesis.

19 he regulation of both hermaphrodite and male gonadogenesis.

20 1 to early L2 stage hermaphrodites to permit gonadogenesis.

21 ee posterior parasegments at early stages in gonadogenesis.

22 tic vpr-1 expression is sufficient to induce gonadogenesis and fertility.

23 e ubiquitously expressed HDA-1 in C. elegans gonadogenesis and place hda-1 in the Notch signaling pat

24 r findings shed light on the complexities of gonadogenesis and the genetic regulation required for pr

25 e that the lag-2 gene, which plays a role in gonadogenesis and vulval development and encodes a Notch

26 results in specific postembryonic defects in gonadogenesis and vulval development.

27 ay in which germ cell pressure may influence gonadogenesis, and also predicts that adult germ cells m

28 Although embryonic gonadogenesis appeared normal, primordial follicles were

29 the C. elegans gonad is defined during early gonadogenesis by two somatic gonadal precursor cells, Z1

30 we describe a novel regulator of Drosophila gonadogenesis, clift, mutations in which abolish gonad f

31 (q645) allele is fully penetrant for the Sys gonadogenesis defect in hermaphrodites, but affects male

32 ch has also been called a gon-10 mutant (for gonadogenesis defective 10) and show that loss of HDA-1

33 We find that sys-1 is haplo-insufficient for gonadogenesis defects and that sys-1 and pop-1 mutants d

34 Inactivation of gem-1 enhances the gonadogenesis defects of gon-2 hypomorphic mutations, su

35 In this article, we demonstrate that the gonadogenesis defects of gon-2 loss-of-function mutants

36 pression is sufficient to prevent the severe gonadogenesis defects.

37 are maternal effect sterile due to arrested gonadogenesis following embryo hatching.

38 nimals, GSCs are established during preadult gonadogenesis following the proliferation and migration

39 We conclude that fkh-6 regulates gonadogenesis in both sexes, but is male specific in est

40 is of distal tip cell (DTC) migration during gonadogenesis in Caenorhabditis elegans has revealed the

41 blish a link between ribosome biogenesis and gonadogenesis in Caenorhabditis elegans that affects ger

42 racellular matrix component fibulin-1 rescue gonadogenesis in the absence of these proteases.

43 Gonadogenesis in the Drosophila embryo is a complex proc

44 The gon-4 gene is required for gonadogenesis in the nematode Caenorhabditis elegans.

45 Neuronal vpr-1 expression is sufficient for gonadogenesis induction during a limited time period sho

46 Instead, global gonadogenesis is mildly delayed relative to development

47 In gon-2 mutants, gonadogenesis is severely impaired; in some animals, non

48 of Pitx2 on the right side before and during gonadogenesis is sufficient to transform the right gonad

49 or 1 (Sf1), a nuclear receptor essential for gonadogenesis, is reduced to minimal levels in the Lhx9-

50 ing other genes that mediate early stages of gonadogenesis, Lhx9 mutants do not exhibit additional ma

51 cell (LC), a migratory cell crucial for male gonadogenesis of C. elegans.

52 or 1 (WT1) genes are essential for mammalian gonadogenesis prior to sexual differentiation.

53 to the seminiferous tubules of the testis as gonadogenesis proceeds, and both Sertoli cells and germ

54 During early gonadogenesis, proliferating cells in the coelomic epith

55 of these male-biased genes were involved in gonadogenesis, spermatogenesis, testicular determination

56 determination system, but genes involved in gonadogenesis, spermatogenesis, testicular determination

57 antagonistic effect on fkh-6 expression and gonadogenesis, which is relieved by cyclin D activity.