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1  and endothelial function determined by wire myography.
2 y artery endothelial function by pressurized myography.
3 ndings, Western blot results, and results of myography.
4 nd vascular function was assessed using wire myography.
5 omic force microscopy, and wire and pressure myography.
6  contraction was measured using small vessel myography.
7  and on arterial constriction using pressure myography.
8 ries taken from animals at 24 hrs using wire myography.
9 tein-restricted pregnant rat dams using wire myography.
10 lung tissue and studied with the use of wire myography.
11 0-300 microm) was studied using small vessel myography.
12 iffness as demonstrated by wire and pressure myography.
13 d vascular reactivity was measured with wire myography.
14 tility of bladder strips was quantified with myography.
15 rfan mouse aorta using ex vivo small chamber myography.
16 valuated with magnetic resonance imaging and myography.
17 oglobin complex was evaluated using pressure myography.
18 ated and functional studies were assessed by myography.
19 ereas arterial function was assessed by wire myography.
20 nd dilator reactivity was determined by wire myography.
21 ck-out (KO) mice were examined with pressure myography.
22 stic tomography for non-invasive and in vivo myography.
23 oscopy, and ex vivo, using advanced pressure myography.
24 trol, n = 6) following (T/HS) using pressure myography.
25 senteric arteries from Adipo-MROE mice using myography and in cultured adipocytes.
26 he dysregulation of blood pressure, pressure myography and in vivo intravital microscopy were conduct
27                                              Myography and magnetic resonance imaging during dobutami
28  in aortic and mesenteric vessels using wire myography and membrane potential measurements.
29  mesenteric lymphatic vessels using pressure myography and protocols that imposed forward flow, eleva
30                                 We have used myography and the patch-clamp recording technique to com
31 anoscopy, proximity ligation assay, pressure myography, and laser speckle imaging to test premises in
32 ty ligation assay, calcium imaging' pressure myography, and Laser Speckle imaging was implemented to
33 rebral arteries using isobaric and isometric myography, and patch clamp.
34 , as well as traction force microscopy, wire myography, and patch-clamp techniques in human cells and
35 ile function was examined in vitro with wire myography, and perivascular adipose tissue (PVAT) morpho
36 , perfused, and ventilated mouse lungs, wire myography, and proliferation assays.
37 of mesenteric small arteries was assessed by myography, and responses to electrical field stimulation
38                           Using small-vessel myography, aorta from these mice exhibited endothelial d
39 ance methods, including electrical impedance myography, are increasingly being used as biomarkers of
40                                Bladder strip myography, assessment of bladder wall mechanics, and his
41                                     However, myography can only be performed on ex vivo sections of i
42                                 Our pressure myography data demonstrated that neflamapimod produced a
43                                Force-tension myography demonstrates that vessels from Opn4(-/-) mice
44 y, we evaluated whether electrical impedance myography (EIM) could serve this purpose.
45 n-invasive technique of electrical impedance myography (EIM) has shown potential as an outcome measur
46                         Electrical impedance myography (EIM) is a non-invasive, portable method that
47 ioning of electrodes in electrical impedance myography (EIM) is critical for accurately assessing dis
48 ed noninvasive, surface electrical impedance myography (EIM) methodology to SOD1(G93A) zebrafish and
49 ethod to detect ACS via electrical impedance myography (EIM), where a weak, high-frequency alternatin
50  color-word Stroop task by combining electro-myography (EMG) and event-related brain potentials (ERPs
51                                   Using wire myography, ex vivo vasoreactivity studies were conducted
52                                         Wire myography examined the functional effect of prorenin.
53 bit KCa channels acutely in ex vivo isobaric myography experiments and intracellular membrane potenti
54                                  In pressure myography experiments on isolated mouse ductus arteriosu
55                                 Further wire myography experiments showed that pre-incubation with re
56 ity of the NO storage materials is proved in myography experiments showing that the NO-releasing MOFs
57 , cellular, and biochemical analyses, and in myography experiments, as well.
58                                           In myography experiments, the Epac-selective cAMP analogue
59 ated diameter tracking software and low-cost myography hardware components.
60 t 12 months, tissues were collected for wire myography, histology and molecular analyses.
61 try during inhalation challenges and by wire myography in airways isolated from human and mouse lungs
62  KCNQ-dependent vasorelaxants, quantified by myography in rat mesenteric arteries.
63 ral artery reactivity was determined by wire myography in wild type (WT) and R6/2 mice at 12 and 16 w
64 sequencing) and vasodilator reactivity (wire myography) in the presence and absence of NAC treatment.
65 essure-induced tone, measured using isobaric myography, in isolated pressurized cerebral arteries was
66                                              Myography indicated reduced contractility of Nt5eKO BSM.
67 h muscle function was determined with tissue myography, intracellular calcium measurements, and regul
68                     Placental perfusions and myography investigated the effect of TC on vasculature.
69                                       Vessel myography is used to determine the functional mechanisms
70 c K+-induced force, measured using isometric myography, is supported by voltage-gated Ca2+ entry.
71 physiology, and ex vivo arteriolar-capillary myography of mice with conditional mural cell knockout o
72                                 In isometric myography on porcine coronary arteries, RA-2 inhibited b
73 nd function assessments via ex vivo pressure myography, or immunohistochemical analyses.
74  dilatation (EDD) to acetylcholine; pressure myography] progressively declined with age in control mi
75                                      Electro myography revealed a myopathic pattern associated with a
76 s at different oestrous stages, we performed myography, RT-qPCR, immunocytochemistry, and western blo
77 FoxO inhibitor and conducted ex vivo two-pin myography studies.
78                   Here we demonstrate, using myography, that activation of P2Y6 by either UDP or a sp
79                  Here, we demonstrate, using myography, that ADP and ADPbetaS dose-dependently induce
80                   Here we have used pressure myography to assess the contribution of noradrenaline an
81 els were studied through the use of pressure myography to determine vascular morphology, mechanics, a
82 s of phosphate on endothelial function using myography to study rat and human blood vessels.
83                               Using pressure myography to study rat isolated first-order cremaster mu
84       Vascular reactivity studies using wire myography uncovered impaired vasoconstriction and vasodi
85                                     Pressure myography using mesenteric arteries demonstrated that re
86 ated with citrullinated histone H3, and wire myography was performed to evaluate EC function.
87                         Pressurized arterial myography was performed using RMCAs exposed to intravasc
88 tion and expression were sought, and ex vivo myography was undertaken to measure bladder function.
89                                         Wire myography was used to assess vascular function in third-
90                            Small vessel wire myography was used to measure isometric tension develope
91                                   Using wire myography we demonstrate that endothelial-specific Nox4
92            Here, using electrophysiology and myography, we discovered that the KCNQ5 voltage-gated po
93                       Using ex vivo pressure myography, we found that loss of this critical signaling
94 maging, custom automated image analysis, and myography, we show that the swine coronary artery endoth
95 light transmittance experiments and pressure myography were also used to further examine the results
96 e (WT) (C57BL/6J) mice, assessed by pressure myography, were very sensitive to inhibition by the SUR2
97 liabilities are typically assayed using wire myography, which is limited by its high cost and low thr