ライフサイエンスコーパス: commitment of @2 to

1 The commitment of a cell to a new fate corresponds to the di

2 Cell fate is determined when the commitment of cells to a particular fate is autonomously

3 The commitment of differentiating cells to a specialized fat

4 he mouse lose their capacity to instruct the commitment of hematopoietic precursors to a T cell fate,

5 y form a bistable loop that insures a robust commitment of R8 to a single fate, without allowing ambi

6 alone is available for liver bud growth and commitment of the endoderm to a hepatic cell fate.

7 f BMP-4 to regulate factors that control the commitment of adipocyte progenitors to an adipogenic pat

8 pear in embryogenesis, their origin reflects commitment of mesoderm to an hematopoietic fate and prov

9 havior can be attributed to an inappropriate commitment of these cells to an epithelial, rather than

10 Together, our findings suggest commitment of CML cells to apoptosis requires protracted

11 tensive treatment; it requires a substantial commitment of treatment resources to be effective.

12 measures are therefore needed to fulfil the commitment of organic farming to benefit farmland biodiv

13 e Runx2 transcription factor is required for commitment of mesenchymal cells to bone lineages and is

14 medical care, transparency of reporting, and commitment of fiscal resources to clinical care predicte

15 located predominantly in nuclei prior to the commitment of the ISMs to die and then accumulated to hi

16 Commitment of stem cells to different lineages is regula

17 d keratin 10, two keratins that indicate the commitment of keratinocytes to differentiate, were expre

18 nts displayed defects in Notch signaling and commitment of progenitors to differentiate.

19 Notch signaling promotes commitment of keratinocytes to differentiation and suppr

20 data uncover a unique mechanism whereby the commitment of stem cells to discrete lineages is coordin

21 icies, amid competing scholarly views on the commitment of states to environmental protection when en

22 ure of spores to nutrient germinants and the commitment of spores to germinate?

23 igher oil in rapeseed involves the concerted commitment of hexoses to glycolysis and eventual de novo

24 tional activity of RARs in EML cells and the commitment of these cells to granulocyte/monocyte progen

25 at Smad1 expression is sufficient to enhance commitment of mesoderm to hemangioblast fate.

26 With this approach, we demonstrate that commitment of embryonic cells to hematopoietic fates beg

27 er, these data indicate that RA inhibits the commitment of mesodermal cells to hematopoietic fates, f

28 Our analyses revealed that hematopoietic commitment of PSCs to hematopoietic precursors correlate

29 impact of SCD in young athletes warrants the commitment of additional resources to identify those at

30 The commitment of Plasmodium merozoites to invade red blood

31 cytes: inhibition of CaM KIV activity causes commitment of hematopoietic precursors to myeloid differ

32 ive activation of BMPs causes an increase in commitment of hematopoietic progenitors to myeloid diffe

33 vel of the NPM mRNA as well as promoting the commitment of muscle cells to myogenesis.

34 To identify genes involved in the commitment of MPCs to osteoblasts we examined the expres

35 Commitment of the VBI to primitive erythropoiesis and re

36 e and duration of TCR signaling required for commitment of T cells to proliferation.

37 sease control is driven by four factors: the commitment of pharmaceutical companies to provide free d

38 olving discipline, necessitating the ongoing commitment of various disciplines to pursue a greater un

39 The role of the T-cell receptor (TCR) in commitment of thymocytes to regulatory CD4(+)Foxp3(+) an

40 The commitment of cells to replicate and divide correlates w

41 Commitment of cells to senescence required continued p14

42 The commitment of cells to specific lineages during developm

43 s that regulate progenitor cell fate and the commitment of neurons to specific neurotransmitter pheno

44 of interactions involving p33 result in the commitment of p33 molecules to specific tasks.

45 The mechanisms underlying the commitment of telencephalic cells to specific regional i

46 ht control and, where required, irreversible commitment of the cell to specific developmental pathway

47 a histidine protein kinase that controls the commitment of this organism to sporulate in response to

48 p63 is essential for both commitment of ectoderm to stratified epithelia and for t

49 outline a novel genetic pathway that forces commitment of CTLs to terminal differentiation, thereby

50 y mechanism underlies the intrinsically high commitment of embryonic keratinocytes to terminal differ

51 Notch1 target, accounts in part for the high commitment of embryonic keratinocytes to terminal differ

52 uncover an early role for RBP-J and Notch in commitment of epidermal cells to terminally differentiat

53 hip between poly(A) signal extrusion and the commitment of the polymerase to terminate.

54 As part of the ongoing commitment of ASCO to the future of cancer care, the Lea

55 age cells, and/or a requirement for IL-7R in commitment of cells to the gamma/delta lineage.

56 imp1 expression in the epiblast mediates the commitment of cells to the germ line.

57 Furthermore, commitment of cells to the osteoblastic or chondrocytic

58 ced bias for monocular connectivity, and (2) commitment of connections to the same CO-compartment as

59 the presence of Nkx2.5, indicating that the commitment of CSCs to the myocyte lineage is regulated b

60 Foxp3 is essential for the commitment of differentiating thymocytes to the regulato

61 icted TCR-transgenic model, we show that the commitment of DP precursors to the CD8 T cell lineage is

62 nactive either in potentiating IL-3-mediated commitment of EML cells to the granulocyte lineage or in

63 le potentiating interleukin-3 (IL-3)-induced commitment of EML cells to the granulocyte/monocyte line

64 Commitment of hematopoietic cells to the erythroid linea

65 he identities of the regulators that mediate commitment of hematopoietic precursors to the T lymphocy

66 opoietic cells are cytokines, which regulate commitment of hematopoietic progenitors to the different

67 Commitment of hematopoietic progenitors to the T cell li

68 ctivator of NF-kappaB ligand (RANKL)-induced commitment of hemopoietic precursors to the osteoclastic

69 defects, suggesting a specific role in early commitment of lateral mesoderm to the endothelial linage

70 e transcriptional circuitry required for the commitment of lymphoid progenitors to the ILC lineage.

71 rs to a congenic host induces a preferential commitment of lymphoid progenitors to the T lineage and

72 hairpin RNA-mediated MYB knockdown promoted commitment of MEPs to the Mk lineage, further defining i

73 ating that Nurr1 is essential for specifying commitment of mesencephalic precursors to the full dopam

74 st two distinct mechanisms: facilitating the commitment of mesenchymal progenitors to the osteoblast

75 Thus, in zebrafish, commitment of mesoderm to the haematopoietic lineage occ

76 ich contains cell populations undergoing the commitment of mesoderm to the hematopoietic and endothel

77 tor of critical checkpoints that dictate the commitment of multipotent precursors to the T cell linea

78 expression of C/EBPalpha initiates with the commitment of multipotential precursors to the myeloid l

79 G-CSFR or IL-6 signals are required for the commitment of multipotential progenitors to the myeloid

80 Retention of the commitment of PGCs to the germ line after extended perio

81 g by increases in Numb expression led to the commitment of progenitor cells to the myoblast cell fate

82 The transcriptional events that regulate commitment of progenitors to the adipose lineage are poo

83 tion of Notch1 in infarcted mice impairs the commitment of resident CPCs to the myocyte lineage oppos

84 ovel activity is presumably important in the commitment of the translocon to the Sec-dependent pathwa

85 at the neural plate stage (E7.5), indicating commitment of these cells to the erythroid lineage befor

86 The data show that commitment of thymic precursors to the DN TCRalphabeta(+

87 8 and PROX1 expression, leading to increased commitment of venous ECs to the lymphatic fate.

88 and in this regard we provide evidence that commitments of CLP/CMP to the DC lineage strictly depend

89 on with what works begs questions about the commitment of decision-makers to this goal.

90 Although Foxp3 expression marks the commitment of progenitors to Treg cell lineage, how Treg

91 le in steroid-induced apoptosis prior to the commitment of the cells to undergo apoptosis; and (b) re

92 stage causes a dose-dependent suppression of commitment of cells to vegetal fates and ectoderm differ