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1          Our findings demonstrate nerve- and bioelectric(9)-dependent intestinal regeneration and adv
2 vestigate the interactions between redox and bioelectric activities during tail regeneration in Xenop
3 d control in liquids is widespread, spanning bioelectric activity in cells to electrical manipulation
4                        Coherence between the bioelectric activity of sensorimotor cortex and contrala
5 n to regulate vascular function, no previous bioelectric analysis of pathological angiogenesis has be
6 channels and nutrient transporters integrate bioelectric and biochemical signals from the environment
7 nhancer regulation, immune-tissue crosstalk, bioelectric and metabolic cues and quantitative modellin
8                   Here we discuss the latest bioelectric and optogenetic advancements in ENS research
9 tion of TNF-alpha, which in turn reduces the bioelectric barrier properties of the alveolar epitheliu
10 has not been shown whether or how non-neural bioelectric cell networks can support computation.
11 genous control of craniofacial patterning by bioelectric cell states.
12  and computational modeling of developmental bioelectric circuits and channelopathies reveals how cel
13                                 Cracking the bioelectric code will have transformative implications f
14 provide an exciting opportunity to crack the bioelectric code, and learn to program cellular activity
15                    The real-time dynamics of bioelectric communication among cells are not fully capt
16 y of cardiomyocytes, studying heterocellular bioelectric coupling in vitro.
17 nserved, non-canonical signaling integrating bioelectric cues and amino acid transport in the establi
18    Altogether, our findings demonstrate that bioelectric cues contribute to S. Typhimurium targeting
19                 Here, I review evidence that bioelectric cues play defined instructional roles in orc
20 in maize root caps were investigated using a bioelectric current as an indicator of gravity sensing.
21 re vital for regulating ion movements (i.e., bioelectric currents) that control epithelial absorption
22 ng reduced survival, intestinal obstruction, bioelectric defects in the nasal epithelium, histopathol
23 ial of pai-conjugated polymers for advancing bioelectric detection technologies.
24 ance to the frequency parameter selection of bioelectric devices.
25         Temporary modulation of regenerative bioelectric dynamics in amputated trunk fragments of pla
26 ded a new method to enhance DIET by means of bioelectric enrichment of Geobacter species.
27             It is increasingly realized that bioelectric events in nonneural cells are critical for p
28                 Possible sources of the PERG bioelectric field are unmyelinated optic nerve axons adj
29                                     The PERG bioelectric field is consistent with a dipole model whos
30             PERG and FERG generate different bioelectric fields in the mouse.
31 cations in chronic diseases, where disrupted bioelectric fields may promote bacterial invasion and pa
32 e detection of local water movement and weak bioelectric fields.
33                            We found that the bioelectric gradient formed downstream of mechanical str
34 echanotransduction triggers the formation of bioelectric gradients across a tissue, which are further
35 s of mechanical stress and the generation of bioelectric gradients in mammary epithelial tissues.
36 ate hypoxia, raises the possibility that the bioelectric impact of neovascularization on vascular fun
37 d thickness) were conducted in both cohorts; bioelectric impedance analysis (BIA) was conducted only
38 mass index and the percentage of body fat by bioelectric impedance analysis and dual-energy X-ray abs
39               Fat mass was measured by using bioelectric impedance analysis in study 1 and deuterium
40  Body composition changes were assessed with bioelectric impedance analysis.
41                     Fat mass was measured by bioelectric impedance analysis; fasting serum leptin con
42 phic LV mass to FFM and adipose body mass by bioelectric impedance and to anthropometric measurements
43 on (lean mass, fat mass) were estimated from bioelectric impedance by using population-specific predi
44          Doppler and 2D echocardiography and bioelectric impedance in 2744 Strong Heart Study partici
45               Standardized anthropometry and bioelectric impedance measurements were obtained at base
46 ed to investigate the properties of multiple bioelectric impedance signals recorded during congestive
47   Lean mass and fat mass were estimated from bioelectric impedance using population-specific predicti
48  follow-up, waist and hip circumferences and bioelectric impedance were measured.
49 x (BMI), body fat percentage (n = 400, using bioelectric impedance), dietary intake (n = 280, using a
50                               Anthropometry, bioelectric impedance, dual-energy X-ray absorptiometry,
51 ass (FFM) and fat mass (FM) were measured by bioelectric impedance.
52 and percentage body fat (%BF) evaluated with bioelectric impedance] measurements were made, and lung
53                          Learning to control bioelectric initiators of organogenesis offers significa
54 ructures to design a lipid-bilayer-supported bioelectric interface that is remotely controlled and te
55 or the formation of well-defined, functional bioelectric interfaces at the biomolecular level to the
56 framework we then review the fundamentals of bioelectric interfaces with semiconductor nanowires and
57 ocus Review, we first discuss the history of bioelectric interfaces with semiconductor nanowires.
58 es, we investigated the relationship between bioelectric ion channel activity and calcium, finding th
59                                              Bioelectric measurements of NBC1-/- colons revealed incr
60          Growth, fat deposits, survival, and bioelectric measurements were analyzed.
61  in recent years become a popular target for bioelectric medicine due to its direct access to neuromo
62 ipulations in order to assess the utility of bioelectric modulation as a universal strategy for stem
63               In this study, we explored the bioelectric modulation of macrophage polarization by tar
64 es, passive filters, topological insulators, bioelectric networks and even, quantum computation, so t
65 ration and coupling with genetic mechanisms, bioelectric networks of potentials influence biological
66                   We have studied the airway bioelectrics of neonatal mice homozygous for a null alle
67 a novel mechanism for regeneration via redox-bioelectric orchestration.
68  V(m) using a suite of tools, we establish a bioelectric pathway that regulates pluripotency in verte
69 -on-a-chip device engineering to analysis of bioelectric phenomena.
70 te many important and previously intractable bioelectric phenomena.
71 tudy of biomembrane electrostatics and other bioelectric phenomena.
72 uble helical DNA is a very well investigated bioelectric phenomenon.
73 e animals.Measurements and Main Results: The bioelectric phenotype of the epithelia recapitulates the
74                                          The bioelectric phenotype of these mice revealed organ-speci
75 without any improvement whatsoever in airway bioelectric phenotype.
76 ghest electrochromic sensitivity for optical bioelectric potential detection.
77  any newly acquired hMSC population if their bioelectric properties are to be studied further.
78                                       Hence, bioelectric properties can stably override genome-defaul
79                            We studied airway bioelectric properties in five CF patients with the rare
80       These findings suggest that control of bioelectric properties of macrophages could offer a prom
81 s clock genes, but little is known about the bioelectric properties of mouse MHb neurones and their p
82                       In two recent studies, bioelectric properties of progenitors and migrating neur
83  the effects of recombinant TNF-alpha on the bioelectric properties of the alveolar epithelial parall
84                            Are these altered bioelectric properties solely a result of electrical cou
85 lating ion channel kinetics and thus of cell bioelectric properties, which is promising for oncologic
86 nserved proliferative responses triggered by bioelectric regulators.
87 eart, where illumination is used to elicit a bioelectric response in tissue modified to express photo
88 l multipolar iEBS research, we developed the Bioelectric Router for Adaptive Isochronous Neuro Stimul
89 ing apoptotic remodeling as the link between bioelectric signaling and the establishment of organ siz
90                           Here, we show that bioelectric signaling at 3 h is crucial for the formatio
91       Gap junction (GJ) channels can mediate bioelectric signaling by creating a fast, direct pathway
92 m, we report that membrane voltage-dependent bioelectric signaling determines both head size and orga
93 tal role of GJ communication in coordinating bioelectric signaling during development.
94 se advances suggest a roadmap for exploiting bioelectric signaling for interventions addressing devel
95 hese data identify a new functional role for bioelectric signaling in brain patterning, reveal intera
96 uscle cells and reveals how perturbations to bioelectric signaling in the neuromuscular system may co
97      However, the data clearly indicate that bioelectric signaling is an autonomous layer of control
98                                              Bioelectric signaling is currently being explored as a n
99 ch encodes the Cx46.8 protein, that mediates bioelectric signaling required for slow muscle developme
100            These direct measurements confirm bioelectric signaling that previous work has hypothesize
101 ns evolved from ancient cell types that used bioelectric signaling to perform computation.
102 liferation will advance our understanding of bioelectric signaling within development and disease sta
103 e cellular functions, including development, bioelectric signaling, and amino acid and lipid metaboli
104                                              Bioelectric signaling, intercellular communication facil
105              The genome is tightly linked to bioelectric signaling, via ion channel proteins that sha
106               Generation and transmission of bioelectric signals are significantly influenced by the
107 echanical forces are converted into discrete bioelectric signals by an ATP-Ca(2+)-Nfatc1-mechanosensi
108  review what is known about the chemical and bioelectric signals underlying this process and draw ana
109 mers can be harnessed to transform miniscule bioelectric signals, such as neuronal action potentials,
110 nce linking the regulation of development to bioelectric signals.
111 iments that reveal instructive developmental bioelectric signals.
112 itable," nevertheless, exhibit regulation by bioelectric signals.
113 tterning, which can be rescued by modulating bioelectric signals.
114 lants that enable sensing and stimulation of bioelectric signals.
115          Briefly manipulating the endogenous bioelectric state by depolarizing the injured tissue dur
116 anatomical switch: experimental reversals of bioelectric state reset subsequent regenerative morpholo
117 nsduction machinery that converts changes in bioelectric state to second-messenger cascades.
118 iofacial development depends on a pattern of bioelectric states, not on ion- or channel-specific sign
119 ristics of ENS disorders and the benefits of bioelectric stimulation to overcome functional deficits.
120 rstanding of how biological cells respond to bioelectric stimulation.
121                                              Bioelectric studies demonstrated that Ca(2+)-activated C
122 tion with subcellular spatial resolution for bioelectric studies.
123 pportunities in extracellular biomaterial or bioelectric systems.
124                Excitable media, ranging from bioelectric tissues and chemical oscillators to forest f
125 s at the interface between two non-excitable bioelectric tissues.

 
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