ライフサイエンスコーパス: ontogenesis

1 ac1 signaling results in abnormal cerebellar ontogenesis.

2 changes in size and shape of the body during ontogenesis.

3 e parallel but independent programs of human ontogenesis.

4 a functional role of Notch signaling in LCH ontogenesis.

5 ost fundamental processes of higher organism ontogenesis.

6 ithin plant mesophyll cells during haustoria ontogenesis.

7 determination during early embryogenesis and ontogenesis.

8 ized that PPARdelta might regulate epidermal ontogenesis.

9 dicating only a transient delay in epidermal ontogenesis.

10 del systems for the earliest stages of human ontogenesis.

11 ere progressively increased during epidermal ontogenesis.

12 ed by incorporating knowledge about atypical ontogenesis.

13 CSTase and SSase activities during in vitro ontogenesis.

14 Pyramidal cell ontogenesis and basilar dendritic differentiation were e

15 factor ER81 has been shown to be involved in ontogenesis and breast tumor formation.

16 Programs important in both normal ontogenesis and cancer progression broadly fall into thr

17 sustain ecological adaptations by modulating ontogenesis and development.

18 oupled CXCR4 regulates cell migration during ontogenesis and disease states including cancer and infl

19 a key survival pathway during normal B-cell ontogenesis and in a subset of diffuse large B-cell lymp

20 tor expression is critical for physiological ontogenesis and its expression is restricted postnatally

21 12 plays an essential role during epidermal ontogenesis and normal hair follicle cycling and that it

22 n vivo under physiological conditions (e.g., ontogenesis and pregnancy) and in pathology (allergic an

23 To examine the role of PTEN in ontogenesis and tumour suppression, we disrupted mouse P

24 e hand, on the anamnestic retention of their ontogenesis and, on the other, on the emergence of novel

25 mouse somatic growth and maintenance during ontogenesis, and IGF-I pathway is likely to be a target

26 pecific events in the brain during postnatal ontogenesis--are altered in autism.

27 ors accelerate not only permeability barrier ontogenesis, but also the expression of structural prote

28 eceptor family regulate permeability barrier ontogenesis by stimulating lipid metabolism and the form

29 Moreover, hormones that accelerate barrier ontogenesis (e.g. glucocorticoids, thyroid hormone, and

30 Somatic stem cells contribute to tissue ontogenesis, homeostasis, and regeneration through seque

31 was to develop an in vitro model of barrier ontogenesis in order to identify those factors critical

32 cholesterol sulfate cycle enzymes during SC ontogenesis is a component of the fetal epidermal differ

33 Since ontogenesis is a dynamic process in both space and time,

34 The regulation of epidermal ontogenesis is poorly understood, but nuclear hormone re

35 Our current understanding of retina ontogenesis is primarily based on animal models having n

36 The goal of epidermal ontogenesis is to form a stratum corneum (SC), which is

37 extent of L1-driven mosaicism arising during ontogenesis is unclear.

38 During inner ear ontogenesis, it is present in both sensory ganglion neur

39 tion of crucial neurotrophic pathways during ontogenesis, leading to aberrant parasympathetic innerva

40 able as a valuable resource for studying the ontogenesis, morphogenesis and function of the mammalian

41 e representative of the very early stages of ontogenesis, namely stem cells.

42 Specifically, postnatal ontogenesis of cerebellum and hippocampus was normal.

43 evelopment, we examined the distribution and ontogenesis of expression of prolactin receptors (PRLRs)

44 ly understandings provide a platform for the ontogenesis of further, deeper achievements in the human

45 undamental shift in our understanding of the ontogenesis of hemispheric asymmetries in humans.

46 that VentX expression is up-regulated during ontogenesis of human hematopoietic cells.

47 ry component may therefore contribute to the ontogenesis of hypertension in the pre-hypertensive SH r

48 omptly, corroborating its involvement in the ontogenesis of hypertension.

49 The present study examined the ontogenesis of LHRH neurons in early human embryos and f

50 d in identifying a gene that is critical for ontogenesis of multiple ectodermal tissues.

51 t a direct or indirect role for PROP1 in the ontogenesis of pituitary gonadotropes, as well as somato

52 complete understanding of the evolution and ontogenesis of primate handedness.

53 the silencing of which is a key event in the ontogenesis of senescent T cells.

54 CSTase and SSase activities during in vitro ontogenesis precisely mirrored those obtained in utero.

55 However, during hepatic ontogenesis the cyclin G2 expression level decreased wit

56 During ontogenesis, the chick oculomotor complex (OMN) is regul

57 effects of air exposure on epidermal barrier ontogenesis, we compared the activities of several key e

58 her these enzymes are induced during barrier ontogenesis, we examined their activity in epidermis of