ライフサイエンスコーパス: regional identity

1 ural stem cell self-renewal while preserving regional identity.

2 pecifying ventricular and suppressing atrial regional identity.

3 Hox transcription factors regulate to confer regional identity.

4 icient to induce progenitors to change their regional identity.

5 ure to active FGF and WNT signaling controls regional identity.

6 t cause transformation to a specific cell or regional identity.

7 rs in neural progenitor cells with different regional identity.

8 in LAD architecture that correspond to their regional identity.

9 analyses to identify putative regulators of regional identity.

10 ot lineage committed and retain rhombomere 1 regional identity.

11 ways generate diverse cell types with varied regional identities.

12 ox genes is crucial for the establishment of regional identities.

13 enitor cells, regardless of their lineage or regional identities.

14 ggest that they are not sufficient to bestow regional identities.

15 ating morphogenetic pathways that direct the regional identity and anteroposterior character of hindb

16 atterns the placode territory by influencing regional identity and by segregating inner ear and trige

17 Stem cell lines that faithfully maintain the regional identity and developmental potency of progenito

18 aded levels by progenitors, determines their regional identity and fate decisions to generate neocort

19 plants, revealing that oligodendrocytes have regional identity and generate different sheath lengths

20 d without Pbx2(+/-) sensitization, regulates regional identity and laminar patterning of the developi

21 dual transcription factors in control of the regional identity and neural differentiation within the

22 ndbrain even though the midbrain retains its regional identity and these neuronal precursors are rost

23 and orthologous neuronal subtypes as well as regional identity and transcriptomic heterogeneity withi

24 icular-subventricular zone (V-SVZ) exhibit a regional identity and, depending on their location, gene

25 ce, the NKX2-1 transcription factor controls regional identity and, with LHX6, is necessary to specif

26 study of the interplay between regeneration, regional identity, and hormonal plasticity in a vertebra

27 are required for proper segregation of early regional identities anterior and posterior to the mid-hi

28 ose that hindbrain progenitors have acquired regional identity as a group at 80% epiboly even before

29 eflect known genetic-ancestry relationships, regional identities, as well as inter-regional correlati

30 Thus, regional identity can, although rarely, override cell-ty

31 Several of these genes regulate regional identity, consistent with muscle harboring posi

32 oids and ileum-like organoids retained their regional identity, demonstrating that regional identity

33 Hox genes specify cell fate and regional identity during animal development.

34 an adhesion molecule involved in specifying regional identity during development, and it is enriched

35 Hox genes control regional identity during segmentation of the vertebrate

36 However, mechanisms that propagate regional identity from VZ progenitors to cortical plate

37 ommitment of telencephalic cells to specific regional identities have been examined through recent tr

38 d a collective of HD factors associated with regional identities in the face and limb.

39 Among insects, the genetic regulation of regional identities in the postoral head or gnathal segm

40 In animals, Hox transcription factors define regional identity in distinct anatomical domains.

41 The processes that specify early regional identity in dorsal and lateral regions of the m

42 he data suggest that ETT functions to impart regional identity in floral meristems that affects peria

43 by Shh, establishing aspects of hypothalamic regional identity in late-differentiating/postmitotic ce

44 Given that Hox genes regulate regional identity in organisms as diverse as mice and fl

45 These results suggest that restoration of regional identity in regeneration involves the interpret

46 ays that are required for establishing early regional identity in the GI tract.

47 nce that Hox genes determine oligodendrocyte regional identity in the mammalian brain.

48 e mechanisms that control the development of regional identity in the mammalian telencephalon.

49 ion at different ages could be used to shift regional identity in the subplate and cortical plate eit

50 dult intestine are known, but how intestinal regional identity is established during development is a

51 ontrols of neuronal production, the distinct regional identities of adult NSCs, and the epigenetic me

52 conserved transcription factors that control regional identities of cells and tissues along the devel

53 ntify a new role of Twist1 in patterning the regional identities of the CNCC-derived facial mesenchym

54 at identifies the developmental maturity and regional identity of in vitro models.

55 cytes in different regions of the brain, the regional identity of in vitro-derived astrocytes is ofte

56 f intrinsic molecular cues in specifying the regional identity of mammalian neocortex.

57 e from naive epiblast, nor can it change the regional identity of neural tissue.

58 their regional identity, demonstrating that regional identity of organoids is stable after initial p

59 a2 plays an important role in regulating the regional identity of rhombomere 2 (r2) and is the only H

60 e functions of the endoderm in growth versus regional identity of skeletal precursors have remained u

61 d the roles of beta-catenin signaling in the regional identity of thalamic progenitor cells.

62 addition, FoxI1e is required to maintain the regional identity of the animal cells of the blastula, t

63 Shh signalling from the ZLI confers regional identity of the flanking subregions of the ZLI,

64 distinct classes: (1) egl-5 is required for regional identity of the tail; (2) sem-4 is required for

65 importance of microbial populations for the regional identity of wine, and potentially extend to oth

66 he expression of leg 'gap' genes that confer regional identity on the developing leg.

67 connections are shaped by sequential maps of regional identity, propagated by the Pax6 --> Eomes -->

68 ons, we demonstrate here that cell-intrinsic regional identity provides differential responsiveness t

69 ), and CP contain distinct molecular maps of regional identity, reflecting different gene expression

70 capture interactions among three components: regional identities, regionalizing morphogens, and polar

71 myocardial differentiation (Isl1, Fgf8) and regional identity (Tbx2, Tbx3, Tbx20, Tgfb2).

72 r/posterior axis, whereas HOM-C genes confer regional identities to cells along the axis.

73 nes that provide rigidity, permeability, and regional identity to membranes.

74 mbination with other factors begin to impart regional identity to placode progenitors.

75 The Hox genes are implicated in conferring regional identity to the anteroposterior axis of the dev

76 The segregation of cells with distinct regional identity underlies formation of a sharp border,

77 in cells are coordinated across tissues) and regional (identities vary spatially across tissues) pola

78 To further investigate its regional identity, we conducted a cross-species transcri

79 he duodenal HIOs and human tissues had mixed regional identity, with gastric and ileal features.

80 expression of a number of genes that specify regional identity within the heart, thereby coordinating

81 a role for the Hoxd-10 gene in establishing regional identity within the spinal cord and imply that