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1 eral, one-tenth to one-thirtieth of those in psoas.
2 ocalized with fatty infiltration but not the psoas.
3 nto single, permeabilized fibers from rabbit psoas.
4  scores) on the test data was the following: psoas: 0.85 +/- 0.12, quadratus lumborum: 0.72 +/- 0.14,
5  regional increases were in skeletal muscle (psoas, 142%) and the myocardium (64%).
6 ardia nova spondylodiscitis accompanied by a psoas abscess due to spread from pulmonary nocardiosis.
7   We review the literature for serovar Typhi psoas abscess in the absence of bacteremia and discuss t
8                             These included a psoas abscess secondary to Mycobacterium avium-intracell
9 steomyelitis (~4%), spinal epidural abscess, psoas abscess, splenic abscess, septic pulmonary emboli,
10 erica serotype Typhi presenting as a primary psoas abscess.
11  and subcutaneous adipose tissue, liver, and psoas and erector spinae muscle, based on quantitative c
12 re iliopsoas muscle volume (comprised of the psoas and iliacus muscles) using a convolutional neural
13                      Cross-sectional muscle (psoas and paraspinal) areas were measured on computed to
14 aining showed many lipid droplets within the psoas and quadriceps muscles of dysferlin-deficient A/J(
15 unction, and is determined radiologically by psoas and skeletal muscle measurement.
16 elationship between pre-operative CT-derived psoas and skeletal muscle parameters and outcomes in pat
17 s contrast with the effect of dATP in rabbit psoas and soleus fibers, where F(max) is unchanged even
18               For comparison, we also tested psoas and soleus muscle fibers.
19 f ROI area in normal control tissues (aorta, psoas) and in mathematical models (P < 0.01).
20 e, the signal-to-noise ratios at the kidney, psoas, and obturator levels were 30%, 23%, and 17% highe
21  performed at three anatomic levels (kidney, psoas, and obturator muscle).
22 eight squared were significant predictors of psoas area (P = .014 and P < .0001, respectively).
23 dated morphometric characteristics of aging (psoas area, psoas density, and abdominal aortic calcific
24 D]) and 4 scores based on muscle area (total psoas area, psoas muscle index, skeletal muscle area, an
25 he density indices PD and SMD (but not total psoas area, psoas muscle index, skeletal muscle area, or
26              The correlation between BMI and psoas attenuation was -0.321, between BMI and the densit
27 al paravertebral' vs. 'posterior approach', 'psoas compartment' vs. 'lumbar plexus block' vs. 'lumbar
28                        The height-normalized psoas cross-sectional area (PsoasL4-5) was measured on a
29  muscle scores, including 2 density indices (psoas density [PD] and skeletal muscle density [SMD]) an
30 metric characteristics of aging (psoas area, psoas density, and abdominal aortic calcification).
31  in soleus slow-twitch muscle fibers than in psoas fast-twitch muscle fibers.
32 n single skinned fibers isolated from rabbit psoas (fast) and soleus (slow) muscles.
33 relaxation from steady-state force in rabbit psoas fiber bundles was examined before and after phosph
34                    Actin filaments of rabbit psoas fiber were labeled with rhodamine-phalloidin.
35 ips in TnC((E59D,D75Y)) reconstituted rabbit psoas fibers and fluorescence spectroscopy of TnC((E59D,
36 a2+ activation in single glycerinated rabbit psoas fibers and skinned right ventricular trabeculae fr
37 he Ca2+ sensitivity of force in both skinned psoas fibers and trabeculae.
38                                   In skinned psoas fibers reconstituted with sTnC labeled at Cys 98 w
39 lculated internal [Pi] in contracting rabbit psoas fibers to < 5 microM.
40                   Active glycerinated rabbit psoas fibers were stretched at constant velocity (0.1-3.
41 ere compliance in single glycerinated rabbit psoas fibers, in the presence of ATP (5.0 mM), was measu
42                          However, in skinned psoas fibers, neither SL changes or force inhibition had
43 le, consistent with measurements from rabbit psoas fibers.
44 in, and introduced into permeabilized rabbit psoas fibers.
45 TPase assays and in troponin-replaced rabbit psoas fibers.
46 tion of cross-bridges of glycerinated rabbit psoas fibers.
47 s.e.m.) were imposed on permeabilised rabbit psoas fibre segments under sarcomere length control.
48 eclines was examined in demembranated rabbit psoas fibres and isolated myofibrils.
49 extracted from single, de-membranated rabbit psoas fibres and replaced by mixtures of purified rabbit
50 redevelopment (k(tr)) was examined in rabbit psoas fibres by substituting native TnC with either card
51 active tension depression induced by P(i) in psoas fibres is temperature sensitive, the depression be
52                                 In extracted psoas fibres that were reconstituted with fast sTnC the
53 lash photolysis of diazo-2 in rabbit skinned psoas fibres was investigated at 15 degrees C.
54 tion was increased in the cTnC-reconstituted psoas fibres.
55 d contraction in single demembranated rabbit psoas fibres.
56 actin in activating thin filaments of rabbit psoas fibres.
57 - 51 (abdominal wall muscle), and 59 +/- 35 (psoas) for the printed coil, as compared with 64 +/- 55,
58 ependent properties in skinned soleus (SSM), psoas (FSM) and ventricular trabeculae (CM) of the rat u
59 and ureteral reimplantation with and without psoas hitch.
60 ebral osteomyelitis with associated epidural/psoas/iliacus abscesses) were characterized, using molec
61 8 times and K1a is 2.2 times those in rabbit psoas, indicating that nucleotides bind to cross-bridges
62  infraspinatus (IF), longissimus dorsi (LD), psoas major (PM) and supraspinatus (SS) were obtained fr
63 mics profiling of longissimus dorsi (LD) and psoas major (PM) muscles in pigs from two different prod
64  segment the multifidus, erector spinae, and psoas major muscles (left and right segmented separately
65  CI = < 0.001 to < 0.001) of the multifidus, psoas major TCSA (OR = < 0.001, 95% CI = < 0.001 to < 0.
66 strophin protein abundance in the diaphragm, psoas major, and longissimus lumborum and a 5-fold incre
67 abdominal fat (VF), external muscle (EM) and psoas muscle (PM) were evaluated using 15 convolutional
68 (iv) metastasis site; and (v) entropy in the psoas muscle (reference tissue).
69 ded adjacent vertebral body destruction with psoas muscle abscess (n = 1, 4%), kidney infarct (n = 1,
70 s of choroid, renal tubules, glomerulus, and psoas muscle all showed similar lateral spacings at appr
71 se correlations between VAT and densities of psoas muscle and cortical and trabecular bone were -0.46
72 (total, subcutaneous, visceral fat area, and psoas muscle area at the L3-L4 level) were determined fo
73 n the duration of mTOR inhibitor therapy and psoas muscle area on multiple linear mixed-effect modeli
74  significantly associated with a decrease in psoas muscle area, suggesting that chronic mTOR inhibiti
75 rtening of single skinned fibres from rabbit psoas muscle at 10 degrees C was measured using an NADH-
76 esolution x-ray patterns from relaxed rabbit psoas muscle at temperatures ranging from 1 degree C to
77                                              Psoas muscle attenuation (an indicator of fat infiltrati
78 5% of the myosin heads in the skinned rabbit psoas muscle contain the hydrolysis products.
79  -13.4 to -5.2; P < .001) over 24 weeks, but psoas muscle fat did not significantly change (-0.42%; 9
80 n patterns were recorded from skinned rabbit psoas muscle fiber bundles stretched to non-overlap to a
81    The mechanical behavior of skinned rabbit psoas muscle fiber contractions and in vitro motility of
82       Exchange of G34DTnC(F29W) into skinned psoas muscle fibers decreased fiber calcium sensitivity
83 region, as previously demonstrated in rabbit psoas muscle fibers in rigor.
84 cytosolic proteins were obtained from rabbit psoas muscle fibers skinned in oil and transferred to ph
85              Contractility of skinned rabbit psoas muscle fibers was inhibited by treatment with 50 m
86 lcium (Ca) bound within sarcomeres of rabbit psoas muscle fibers were compared using electron probe x
87  permeabilized rabbit cardiac trabeculae and psoas muscle fibers were compared.
88 ion patterns from the relaxed skinned rabbit psoas muscle fibers where ATP hydrolysis was inhibited b
89 dogenous RLC was removed from skinned rabbit psoas muscle fibers, and replaced with either rat wildty
90  maximal calcium-activated tension of rabbit psoas muscle fibers.
91  (SH1) of the myosin head, in skinned rabbit psoas muscle fibers.
92 bunit, located in the myosin neck, in rabbit psoas muscle fibers.
93 nvestigated by sinusoidal analysis in rabbit psoas muscle fibers.
94  force redevelopment (ktr) in skinned rabbit psoas muscle fibers.
95 tramethylrhodamine and exchanged into rabbit psoas muscle fibers.
96 tivated contractions of demembranated rabbit psoas muscle fibers; the ATPase rate was either increase
97 5 % Brij), maximally Ca(2+)-activated rabbit psoas muscle fibres at 10 degrees C (ionic strength 200
98 T-jump) in maximally Ca(2+)-activated rabbit psoas muscle fibres at 8-9 degrees C (the fibre length (
99 loaded shortening velocity of skinned rabbit psoas muscle fibres is sensitive to [Ca2+].
100 C) in chemically skinned (0.5 % Brij) rabbit psoas muscle fibres.
101 in single, skinned muscle fibers from rabbit psoas muscle following either photolysis of caged nucleo
102 perties of skinned single fibres from rabbit psoas muscle have been correlated with biochemical steps
103 n by single permeabilised fibres from rabbit psoas muscle immersed in silicone oil was measured using
104 (Pi) and hence the ATPase activity of rabbit psoas muscle in single permeabilized muscle fibres initi
105  the helical order of myosin heads in rabbit psoas muscle in the presence of nonhydrolyzable ligands.
106         After normalization for stature, the psoas muscle index was used to define sarcopenia.
107 ores based on muscle area (total psoas area, psoas muscle index, skeletal muscle area, and skeletal m
108 ndices PD and SMD (but not total psoas area, psoas muscle index, skeletal muscle area, or skeletal mu
109                                              Psoas muscle measurements are frequently used as markers
110 d the effects of increasing [P(i)] on rabbit psoas muscle myosin's ability to generate force against
111 parameters, and the remaining nine reporting psoas muscle parameters, which were used for meta-analys
112 s (mean diameter, 71 microns) shed by rabbit psoas muscle swelling in 140 mM KC1 containing collagena
113 n patterns were obtained from skinned rabbit psoas muscle under relaxing and rigor conditions over a
114  in relaxed demembranated fibers from rabbit psoas muscle using fluorescence polarization from bifunc
115 mall-square to basketweave in relaxed rabbit psoas muscle varied with temperature, osmotic pressure,
116                                              Psoas muscle volume decreased by 9.3% (95% confidence in
117 ing semaglutide for MASLD, despite decreased psoas muscle volume, there was no significant change in
118 hain (RLC) in demembranated fibers of rabbit psoas muscle was determined by polarized fluorescence.
119  in recipient heart, liver, lung, spleen, or psoas muscle was within background levels.
120  chemically permeabilized fibres from rabbit psoas muscle were activated maximally at 5-6 degrees C a
121 trast signal intensities between lesions and psoas muscle were evaluated.
122           Single, skinned fibers from rabbit psoas muscle were used to test this hypothesis.
123 nd exchanged into skinned fibers from rabbit psoas muscle without significant effect of the tension t
124 hanged into demembranated fibres from rabbit psoas muscle without significant effect on active force
125 d signal intensity (SI) ratio (SI(nodule)/SI(psoas muscle)), T2-weighted histogram features, and chem
126  to active skinned single fibres from rabbit psoas muscle, and observed the effect on the slowest pha
127 ne segments, subcutaneous fat, visceral fat, psoas muscle, and skeletal muscle.
128                        In extracts of rabbit psoas muscle, the complete degradation of soluble protei
129 pleen, kidney, small bowel, lumbar vertebra, psoas muscle, urinary bladder) as well as the noise-equi
130 us RLC in single, skinned fibers from rabbit psoas muscle.
131  pCa units in fast-twitch fibres from rabbit psoas muscle.
132 n skinned single skeletal fibers from rabbit psoas muscle.
133 ndles of two to three myofibrils from rabbit psoas muscle.
134 teal muscle but not of the severely affected psoas muscle.
135 em to adult human skeletal muscle and rabbit psoas muscle.
136 on passive fiber bundles from rabbit skinned psoas muscle.
137 terized in single skinned fibres from rabbit psoas muscle.
138 ge of [Ca(2+)] in skinned fibers from rabbit psoas muscle.
139 izzard and soleus muscles, but a decrease in psoas muscle.
140 of permeabilized fibres isolated from rabbit psoas muscle.
141 onstituted single skinned fibers from rabbit psoas muscle.
142 m; sarcomere length, 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mM, pH 7.1 and ionic stren
143 mm, sarcomere length 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mm, pH 7.1, ionic strength
144 elvis along the anterolateral surface of the psoas muscle; and laterally, posterior to the descending
145 One reviewer drew regions of interest around psoas muscles at L3 to measure cross-sectional area.
146 ectron microscopy of 8-month-old A/J(dys-/-) psoas muscles confirmed lipid droplets within myofibers
147  Small bundles of fibers from rabbit skinned psoas muscles were loaded with Ca2+ fluorophore (Fluo-3)
148  after incorporating the complex into rabbit psoas myofibrils.
149                Abscesses were located in the psoas (n = 25, 55.3%), renal-perirenal (n = 7, 14.8%), a
150           Radiological sarcopenia defined by psoas or skeletal muscle parameters was associated with
151 l muscle groups including the left and right psoas, quadratus lumborum, erector spinae, gluteus mediu
152                   The presence of a positive psoas sign, fever, or migratory pain to the right lower
153 onship were examined in slow soleus and fast psoas skeletal muscle fibers.
154 tutions on the mechanical behavior of rabbit psoas skeletal myofibrils by replacing endogenous Tm and
155 eriment is based on the facts that in rabbit psoas the thin filament (1.12 micrometer) is longer than
156                                              Psoas volume and fat fraction were assessed from liver m
157                                          The psoas was the first and most affected muscle in the lowe
158              Myofibrils isolated from rabbit psoas were activated and relaxed using a perfusion syste
159 temperature sensitive in soleus STFs than in psoas, which are fast-twitch fibres.

 
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