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1 em to adult human skeletal muscle and rabbit psoas muscle.
2 on passive fiber bundles from rabbit skinned psoas muscle.
3 terized in single skinned fibres from rabbit psoas muscle.
4 ge of [Ca(2+)] in skinned fibers from rabbit psoas muscle.
5 izzard and soleus muscles, but a decrease in psoas muscle.
6 of permeabilized fibres isolated from rabbit psoas muscle.
7 onstituted single skinned fibers from rabbit psoas muscle.
8 us RLC in single, skinned fibers from rabbit psoas muscle.
9 pCa units in fast-twitch fibres from rabbit psoas muscle.
10 n skinned single skeletal fibers from rabbit psoas muscle.
11 ndles of two to three myofibrils from rabbit psoas muscle.
12 teal muscle but not of the severely affected psoas muscle.
13 ded adjacent vertebral body destruction with psoas muscle abscess (n = 1, 4%), kidney infarct (n = 1,
14 s of choroid, renal tubules, glomerulus, and psoas muscle all showed similar lateral spacings at appr
15 se correlations between VAT and densities of psoas muscle and cortical and trabecular bone were -0.46
16 to active skinned single fibres from rabbit psoas muscle, and observed the effect on the slowest pha
18 elvis along the anterolateral surface of the psoas muscle; and laterally, posterior to the descending
19 (total, subcutaneous, visceral fat area, and psoas muscle area at the L3-L4 level) were determined fo
20 n the duration of mTOR inhibitor therapy and psoas muscle area on multiple linear mixed-effect modeli
21 significantly associated with a decrease in psoas muscle area, suggesting that chronic mTOR inhibiti
22 rtening of single skinned fibres from rabbit psoas muscle at 10 degrees C was measured using an NADH-
23 esolution x-ray patterns from relaxed rabbit psoas muscle at temperatures ranging from 1 degree C to
24 One reviewer drew regions of interest around psoas muscles at L3 to measure cross-sectional area.
26 ectron microscopy of 8-month-old A/J(dys-/-) psoas muscles confirmed lipid droplets within myofibers
28 -13.4 to -5.2; P < .001) over 24 weeks, but psoas muscle fat did not significantly change (-0.42%; 9
29 n patterns were recorded from skinned rabbit psoas muscle fiber bundles stretched to non-overlap to a
30 The mechanical behavior of skinned rabbit psoas muscle fiber contractions and in vitro motility of
33 cytosolic proteins were obtained from rabbit psoas muscle fibers skinned in oil and transferred to ph
35 lcium (Ca) bound within sarcomeres of rabbit psoas muscle fibers were compared using electron probe x
37 ion patterns from the relaxed skinned rabbit psoas muscle fibers where ATP hydrolysis was inhibited b
38 dogenous RLC was removed from skinned rabbit psoas muscle fibers, and replaced with either rat wildty
45 tivated contractions of demembranated rabbit psoas muscle fibers; the ATPase rate was either increase
46 5 % Brij), maximally Ca(2+)-activated rabbit psoas muscle fibres at 10 degrees C (ionic strength 200
47 T-jump) in maximally Ca(2+)-activated rabbit psoas muscle fibres at 8-9 degrees C (the fibre length (
50 in single, skinned muscle fibers from rabbit psoas muscle following either photolysis of caged nucleo
51 perties of skinned single fibres from rabbit psoas muscle have been correlated with biochemical steps
52 n by single permeabilised fibres from rabbit psoas muscle immersed in silicone oil was measured using
53 (Pi) and hence the ATPase activity of rabbit psoas muscle in single permeabilized muscle fibres initi
54 the helical order of myosin heads in rabbit psoas muscle in the presence of nonhydrolyzable ligands.
56 ores based on muscle area (total psoas area, psoas muscle index, skeletal muscle area, and skeletal m
57 ndices PD and SMD (but not total psoas area, psoas muscle index, skeletal muscle area, or skeletal mu
59 m; sarcomere length, 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mM, pH 7.1 and ionic stren
60 mm, sarcomere length 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mm, pH 7.1, ionic strength
61 d the effects of increasing [P(i)] on rabbit psoas muscle myosin's ability to generate force against
62 parameters, and the remaining nine reporting psoas muscle parameters, which were used for meta-analys
63 abdominal fat (VF), external muscle (EM) and psoas muscle (PM) were evaluated using 15 convolutional
65 s (mean diameter, 71 microns) shed by rabbit psoas muscle swelling in 140 mM KC1 containing collagena
66 d signal intensity (SI) ratio (SI(nodule)/SI(psoas muscle)), T2-weighted histogram features, and chem
68 n patterns were obtained from skinned rabbit psoas muscle under relaxing and rigor conditions over a
69 pleen, kidney, small bowel, lumbar vertebra, psoas muscle, urinary bladder) as well as the noise-equi
70 in relaxed demembranated fibers from rabbit psoas muscle using fluorescence polarization from bifunc
71 mall-square to basketweave in relaxed rabbit psoas muscle varied with temperature, osmotic pressure,
73 ing semaglutide for MASLD, despite decreased psoas muscle volume, there was no significant change in
74 hain (RLC) in demembranated fibers of rabbit psoas muscle was determined by polarized fluorescence.
76 chemically permeabilized fibres from rabbit psoas muscle were activated maximally at 5-6 degrees C a
79 Small bundles of fibers from rabbit skinned psoas muscles were loaded with Ca2+ fluorophore (Fluo-3)
80 nd exchanged into skinned fibers from rabbit psoas muscle without significant effect of the tension t
81 hanged into demembranated fibres from rabbit psoas muscle without significant effect on active force