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 We propose that this regulative ability requires extensive and continuous sho

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28 However, the regulative mechanism of PHB during adipogenesis remains

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

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

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

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

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

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

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

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

37 The regulative potential of the cardiogenic mesoderm was exa

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

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

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

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

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

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

44 howing that this embryo also has significant regulative properties.

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

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

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

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

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