ライフサイエンスコーパス: developmental programming

1 gene methylation patterns and contribute to developmental programming.

2 d the kinetics of immune responses is set by developmental programming.

3 c mechanisms may be at the roots of adaptive developmental programming.

4 e malnourished embryonic kidney from adverse developmental programming.

5 emerging areas of pregnancy biology such as developmental programming.

6 pigenetic toxicant and could influence fetal developmental programming.

7 avioral changes were due to altered neuronal developmental programming.

8 as a novel mechanism of BPA-induced altered developmental programming.

9 sults reveal an NOD genetic defect in T cell developmental programming and checkpoint control that pe

10 rnal high-fat diet (HFD) alters hypothalamic developmental programming and disrupts offspring energy

11 the first time how early-life stress drives developmental programming and transgenerational effects

12 nse mechanisms activated by changes in plant developmental programming and/or stresses imposed during

13 Thus, the terms 'developmental programming' and the 'Developmental Origin

14 verse outcomes (growth, gestational age, and developmental programming); and infant adverse outcomes.

15 identify Grb10 as a key genetic component of developmental programming, and highlight the need for a

16 uences mRNA stability and cell-type-specific developmental programming, and is highly abundant in the

17 Aging and developmental programming are both associated with oxida

18 owever, molecular mechanisms underlying such developmental programming are not well characterized, an

19 d variation among different species in their developmental programming are poorly defined due to the

20 Developmental programming by early choline nutrition may

21 The observation that developmental programming can be reversed has been demon

22 ls are also unusually flexible in their late developmental programming, demonstrating substantial ove

23 in offspring adipose tissue, demonstrating a developmental programming effect.

24 ve helped to unravel distinctive elements of developmental programming for Tfh cells and unique effec

25 These studies demonstrate that the developmental programming in NK cells is not fixed, and

26 guishable function, migratory properties and developmental programming in vivo.

27 behavior, suggesting impact of this drug on developmental programming in zebrafish.

28 Developmental programming is defined as the process by w

29 An interesting aspect of developmental programming is the existence of transgener

30 Developmental programming links growth in early life wit

31 In an intergenerational developmental programming model affecting F2 mouse metab

32 suggests that maternal nutrition can induce developmental programming of adult hypertension in offsp

33 Our data suggest that developmental programming of aging importantly contribut

34 abnormalities may partly arise from altered developmental programming of beta-cells.

35 r results define the role of the fetal PT in developmental programming of brain function by maternal

36 pathways mediating cardiovascular aging and developmental programming of cardiovascular disease, and

37 pathways mediating cardiovascular aging and developmental programming of cardiovascular disease.

38 help identify modifiable targets to prevent developmental programming of common diseases.

39 r of discrete genetic mechanisms that govern developmental programming of cotton fiber morphogenesis

40 oglycan-deficient myofibers leads to altered developmental programming of developing and regenerating

41 Developmental programming of diabetes in these mice was

42 ion, embryonic stem (ES) cells can erase the developmental programming of differentiated cell nuclei

43 se activity but had no significant affect on developmental programming of dissacharidases.

44 sue (SAT) is suggested to play a role in the developmental programming of dysmetabolism based on stud

45 BPA selectively altered the normal developmental programming of estrogen-responsive genes v

46 s persistent long-term protective effects on developmental programming of hepatic lipotoxicity and in

47 actation, protects offspring from WD-induced developmental programming of hepatic lipotoxicity and ma

48 Does developmental programming of human body weight regulatio

49 , two common adverse conditions in utero, to developmental programming of insulin resistance remain u

50 target for clinical intervention against the developmental programming of metabolic disease resulting

51 ) in metabolic tissues is fundamental to the developmental programming of metabolic syndrome, but und

52 Using an in vivo - in vitro model of developmental programming of neuroinflammation induced b

53 or identifying the mechanisms underlying the developmental programming of offspring phenotype by subo

54 retinal and visual function, likely through developmental programming of retinal dopamine.

55 Recent studies suggest that developmental programming of the carotid body response t

56 arly prior stress history, contribute to the developmental programming of the hypothalamic-pituitary-

57 Further evidence for developmental programming of the metabolic syndrome has

58 to explain the lifelong persistence of such "developmental programming" of energy balance.

59 The influence of developmental programming on bronchial hyperreactivity i

60 sion after drug challenge, metabolic stress, developmental programming or other perturbation represen

61 Our results illustrate how developmental programming predisposes to beta-cell dysfu

62 The epigenetic mechanisms of developmental programming revealed here are likely to re

63 Cross-fostering is widely used in developmental programming studies to determine the relat

64 al transfer of this antidepressant, disrupts developmental programming using zebrafish (Danio rerio)