ライフサイエンスコーパス: bioelectric

1 vestigate the interactions between redox and bioelectric activities during tail regeneration in Xenop

2 d control in liquids is widespread, spanning bioelectric activity in cells to electrical manipulation

3 Coherence between the bioelectric activity of sensorimotor cortex and contrala

4 n to regulate vascular function, no previous bioelectric analysis of pathological angiogenesis has be

5 tion of TNF-alpha, which in turn reduces the bioelectric barrier properties of the alveolar epitheliu

6 genous control of craniofacial patterning by bioelectric cell states.

7 Cracking the bioelectric code will have transformative implications f

8 provide an exciting opportunity to crack the bioelectric code, and learn to program cellular activity

9 The real-time dynamics of bioelectric communication among cells are not fully capt

10 in maize root caps were investigated using a bioelectric current as an indicator of gravity sensing.

11 Temporary modulation of regenerative bioelectric dynamics in amputated trunk fragments of pla

12 ded a new method to enhance DIET by means of bioelectric enrichment of Geobacter species.

13 Possible sources of the PERG bioelectric field are unmyelinated optic nerve axons adj

14 The PERG bioelectric field is consistent with a dipole model whos

15 PERG and FERG generate different bioelectric fields in the mouse.

16 e detection of local water movement and weak bioelectric fields.

17 ate hypoxia, raises the possibility that the bioelectric impact of neovascularization on vascular fun

18 d thickness) were conducted in both cohorts; bioelectric impedance analysis (BIA) was conducted only

19 mass index and the percentage of body fat by bioelectric impedance analysis and dual-energy X-ray abs

20 Fat mass was measured by using bioelectric impedance analysis in study 1 and deuterium

21 Body composition changes were assessed with bioelectric impedance analysis.

22 Fat mass was measured by bioelectric impedance analysis; fasting serum leptin con

23 phic LV mass to FFM and adipose body mass by bioelectric impedance and to anthropometric measurements

24 on (lean mass, fat mass) were estimated from bioelectric impedance by using population-specific predi

25 Doppler and 2D echocardiography and bioelectric impedance in 2744 Strong Heart Study partici

26 Standardized anthropometry and bioelectric impedance measurements were obtained at base

27 ed to investigate the properties of multiple bioelectric impedance signals recorded during congestive

28 Lean mass and fat mass were estimated from bioelectric impedance using population-specific predicti

29 follow-up, waist and hip circumferences and bioelectric impedance were measured.

30 x (BMI), body fat percentage (n = 400, using bioelectric impedance), dietary intake (n = 280, using a

31 Anthropometry, bioelectric impedance, dual-energy X-ray absorptiometry,

32 ass (FFM) and fat mass (FM) were measured by bioelectric impedance.

33 and percentage body fat (%BF) evaluated with bioelectric impedance] measurements were made, and lung

34 Learning to control bioelectric initiators of organogenesis offers significa

35 ructures to design a lipid-bilayer-supported bioelectric interface that is remotely controlled and te

36 Bioelectric measurements of NBC1-/- colons revealed incr

37 Growth, fat deposits, survival, and bioelectric measurements were analyzed.

38 ipulations in order to assess the utility of bioelectric modulation as a universal strategy for stem

39 In this study, we explored the bioelectric modulation of macrophage polarization by tar

40 We have studied the airway bioelectrics of neonatal mice homozygous for a null alle

41 a novel mechanism for regeneration via redox-bioelectric orchestration.

42 te many important and previously intractable bioelectric phenomena.

43 tudy of biomembrane electrostatics and other bioelectric phenomena.

44 -on-a-chip device engineering to analysis of bioelectric phenomena.

45 The bioelectric phenotype of these mice revealed organ-speci

46 without any improvement whatsoever in airway bioelectric phenotype.

47 any newly acquired hMSC population if their bioelectric properties are to be studied further.

48 Hence, bioelectric properties can stably override genome-defaul

49 We studied airway bioelectric properties in five CF patients with the rare

50 These findings suggest that control of bioelectric properties of macrophages could offer a prom

51 s clock genes, but little is known about the bioelectric properties of mouse MHb neurones and their p

52 the effects of recombinant TNF-alpha on the bioelectric properties of the alveolar epithelial parall

53 Are these altered bioelectric properties solely a result of electrical cou

54 eart, where illumination is used to elicit a bioelectric response in tissue modified to express photo

55 ing apoptotic remodeling as the link between bioelectric signaling and the establishment of organ siz

56 m, we report that membrane voltage-dependent bioelectric signaling determines both head size and orga

57 hese data identify a new functional role for bioelectric signaling in brain patterning, reveal intera

58 However, the data clearly indicate that bioelectric signaling is an autonomous layer of control

59 Bioelectric signaling is currently being explored as a n

60 e cellular functions, including development, bioelectric signaling, and amino acid and lipid metaboli

61 The genome is tightly linked to bioelectric signaling, via ion channel proteins that sha

62 review what is known about the chemical and bioelectric signals underlying this process and draw ana

63 tterning, which can be rescued by modulating bioelectric signals.

64 anatomical switch: experimental reversals of bioelectric state reset subsequent regenerative morpholo

65 nsduction machinery that converts changes in bioelectric state to second-messenger cascades.

66 iofacial development depends on a pattern of bioelectric states, not on ion- or channel-specific sign

67 pportunities in extracellular biomaterial or bioelectric systems.