ライフサイエンスコーパス: myography

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1 y artery endothelial function by pressurized myography.

2 omic force microscopy, and wire and pressure myography.

3 contraction was measured using small vessel myography.

4 and on arterial constriction using pressure myography.

5 ries taken from animals at 24 hrs using wire myography.

6 tein-restricted pregnant rat dams using wire myography.

7 lung tissue and studied with the use of wire myography.

8 0-300 microm) was studied using small vessel myography.

9 ndings, Western blot results, and results of myography.

10 senteric arteries from Adipo-MROE mice using myography and in cultured adipocytes.

11 We have used myography and the patch-clamp recording technique to com

12 rebral arteries using isobaric and isometric myography, and patch clamp.

13 ile function was examined in vitro with wire myography, and perivascular adipose tissue (PVAT) morpho

14 of mesenteric small arteries was assessed by myography, and responses to electrical field stimulation

15 Using small-vessel myography, aorta from these mice exhibited endothelial d

16 Force-tension myography demonstrates that vessels from Opn4(-/-) mice

17 y, we evaluated whether electrical impedance myography (EIM) could serve this purpose.

18 ioning of electrodes in electrical impedance myography (EIM) is critical for accurately assessing dis

19 color-word Stroop task by combining electro-myography (EMG) and event-related brain potentials (ERPs

20 ity of the NO storage materials is proved in myography experiments showing that the NO-releasing MOFs

21 In myography experiments, the Epac-selective cAMP analogue

22 ral artery reactivity was determined by wire myography in wild type (WT) and R6/2 mice at 12 and 16 w

23 essure-induced tone, measured using isobaric myography, in isolated pressurized cerebral arteries was

24 h muscle function was determined with tissue myography, intracellular calcium measurements, and regul

25 c K+-induced force, measured using isometric myography, is supported by voltage-gated Ca2+ entry.

26 In isometric myography on porcine coronary arteries, RA-2 inhibited b

27 nd function assessments via ex vivo pressure myography, or immunohistochemical analyses.

28 Electro myography revealed a myopathic pattern associated with a

29 Here we demonstrate, using myography, that activation of P2Y6 by either UDP or a sp

30 Here, we demonstrate, using myography, that ADP and ADPbetaS dose-dependently induce

31 Here we have used pressure myography to assess the contribution of noradrenaline an

32 els were studied through the use of pressure myography to determine vascular morphology, mechanics, a

33 s of phosphate on endothelial function using myography to study rat and human blood vessels.

34 Using pressure myography to study rat isolated first-order cremaster mu

35 Pressure myography using mesenteric arteries demonstrated that re

36 Pressurized arterial myography was performed using RMCAs exposed to intravasc

37 Small vessel wire myography was used to measure isometric tension develope

38 Using wire myography we demonstrate that endothelial-specific Nox4

39 maging, custom automated image analysis, and myography, we show that the swine coronary artery endoth

40 liabilities are typically assayed using wire myography, which is limited by its high cost and low thr

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