ライフサイエンスコーパス: regulative

1 ould enable early mouse development to be so regulative.

2 opment; however, the cellular basis of these regulative abilities has not been established.

3 tor concentration, providing a basis for the regulative abilities of the early mammalian embryo where

4 We propose that this regulative ability requires extensive and continuous sho

5 Here, we focus on one striking example of regulative activation of the skeletogenic GRN; the trans

6 t in vivo evidence illustrating how a highly regulative and interleaved communication between cell ad

7 They suggest this regulative behavior depends on a complex interplay betwe

8 r ablation, raising the possibility that the regulative behavior of distinct, MRF-expressing populati

9 egration hypothesis or the hypothesis of the regulative benefits of religion.

10 The regulative capability of single cells to give rise to al

11 To examine the regulative capacity of this structure, pieces of the arc

12 racic leg disc fragments possess exceptional regulative capacity, highlighted by the ability of anter

13 owever, in the absence of a noggin gradient, regulative cell-cell interactions can also pattern the t

14 nt of noggin protein within the explant, and regulative cell-cell interactions.

15 hat the regeneration of adult axons is under regulative control, very little is known about the signa

16 Earlier work showed that the regulative deployment of the GRN, unlike its deployment

17 chanism underlying a specific example of the regulative development for which the sea urchin embryo h

18 The underlying mechanisms enabling such regulative development have long been a topic of study.

19 hasizes cleavage parsimony, radial cleavage, regulative development, and enterocely are ancestral wit

20 Regulative development, demonstrated by many animal embr

21 ream regulation of the GRN during normal and regulative development.

22 t inputs activate this GRN during normal and regulative development.

23 s a paradigm of tissue self-organization and regulative development; however, the cellular basis of t

24 The possible regulative effects of Pura on AD-related genes consist i

25 , DLL1, DLL4, Notch1, Notch3, and Notch4.The regulative effects of TRIM28 on these angiogenic factors

26 implication of this model is that mosaic and regulative embryos are distinct merely by virtue of the

27 cy refers to the capacity of single cells in regulative embryos to engender all somatic and germline

28 ion, we systematically employed mutations in regulative epigenetic pathways suggested to be major pla

29 However, regulative eye development may occur if the precursors o

30 ld and/or dehydration stress, and a negative regulative function in dehydration tolerance was observe

31 We suggest that the regulative functions of the MSC may serve quality contro

32 The development of apoptosis, regulative gene expression, and viral clearance were sim

33 ults show ascidian notochord formation to be regulative in a fashion and to a degree never before app

34 xpressed in ccRCC, is involved in a positive-regulative loop with HIF-1alpha, and has a major action

35 Thus, a FMRP and SHP2 MAPK/ERK regulative mechanism controls basal and activity-depende

36 However, the regulative mechanism of PHB during adipogenesis remains

37 cluding mice, germ cells form in response to regulative mechanisms during development.

38 eural inducing strength of the node and that regulative mechanisms exist which mask the early phenoty

39 tudy sheds novel lights on the catalytic and regulative mechanisms of bacterial DMSP demethylation, l

40 howed that CML36 interacts directly with the regulative N terminus of the Arabidopsis plasma membrane

41 nt that accommodates these findings with the regulative nature of mouse embryos.

42 A-MATER complex localization may reflect the regulative nature of preimplantation mouse development.

43 of the self-organizing principles behind the regulative nature of the early mammalian embryo.

44 ere able to develop to term, emphasizing the regulative nature of their development.

45 PMC lineage, plays an essential role in the regulative pathway both in NSM cells and in animal blast

46 er stages of development, however, through a regulative pathway of skeletogenesis that is responsive

47 odels by extracting insightful gene-specific regulative patterns, and we analyse them for the specifi

48 The regulative potential of the cardiogenic mesoderm was exa

49 llaboration; (2) joint commitment; (3) "self-regulative pressure from 'we'"; and (4) the sense of int

50 teoarthritis (OA), and so recognition of the regulative processes during chondrogenesis can lead to a

51 at may act as the platform for catalysis and regulative processing of various degrees of H3K4 methyla

52 The mechanisms underlying the regulative properties are, however, poorly understood an

53 hether this process relies only on intrinsic regulative properties of regenerating tissues or whether

54 imb size and provides a mechanism explaining regulative properties of the limb bud.

55 chanisms that regulate the determinative and regulative properties of the P. hawaiensis embryo.

56 The well-known regulative properties of the sea urchin embryo, coupled

57 howing that this embryo also has significant regulative properties.

58 This indicates that the embryo's regulative response to germ layer founder loss, in the f

59 Ser(193) was demonstrated to have a regulative role during catalysis and is likely to be inv

60 These findings raise the possibility of a regulative role of these sRNAs during fruit onset and ma

61 They play important regulative roles in different biological processes as th

62 Although mouse development is regulative, the cleavage pattern of the embryo is not ra

63 Development in Dictyostelium is highly regulative, with cells within the prestalk and prespore