ライフサイエンスコーパス: psoas

1 ocalized with fatty infiltration but not the psoas.

2 eral, one-tenth to one-thirtieth of those in psoas.

3 nto single, permeabilized fibers from rabbit psoas.

4 ardia nova spondylodiscitis accompanied by a psoas abscess due to spread from pulmonary nocardiosis.

5 We review the literature for serovar Typhi psoas abscess in the absence of bacteremia and discuss t

6 These included a psoas abscess secondary to Mycobacterium avium-intracell

7 erica serotype Typhi presenting as a primary psoas abscess.

8 aining showed many lipid droplets within the psoas and quadriceps muscles of dysferlin-deficient A/J(

9 s contrast with the effect of dATP in rabbit psoas and soleus fibers, where F(max) is unchanged even

10 For comparison, we also tested psoas and soleus muscle fibers.

11 f ROI area in normal control tissues (aorta, psoas) and in mathematical models (P < 0.01).

12 dated morphometric characteristics of aging (psoas area, psoas density, and abdominal aortic calcific

13 The correlation between BMI and psoas attenuation was -0.321, between BMI and the densit

14 al paravertebral' vs. 'posterior approach', 'psoas compartment' vs. 'lumbar plexus block' vs. 'lumbar

15 The height-normalized psoas cross-sectional area (PsoasL4-5) was measured on a

16 metric characteristics of aging (psoas area, psoas density, and abdominal aortic calcification).

17 in soleus slow-twitch muscle fibers than in psoas fast-twitch muscle fibers.

18 n single skinned fibers isolated from rabbit psoas (fast) and soleus (slow) muscles.

19 relaxation from steady-state force in rabbit psoas fiber bundles was examined before and after phosph

20 Actin filaments of rabbit psoas fiber were labeled with rhodamine-phalloidin.

21 ips in TnC((E59D,D75Y)) reconstituted rabbit psoas fibers and fluorescence spectroscopy of TnC((E59D,

22 a2+ activation in single glycerinated rabbit psoas fibers and skinned right ventricular trabeculae fr

23 he Ca2+ sensitivity of force in both skinned psoas fibers and trabeculae.

24 In skinned psoas fibers reconstituted with sTnC labeled at Cys 98 w

25 lculated internal [Pi] in contracting rabbit psoas fibers to < 5 microM.

26 Active glycerinated rabbit psoas fibers were stretched at constant velocity (0.1-3.

27 ere compliance in single glycerinated rabbit psoas fibers, in the presence of ATP (5.0 mM), was measu

28 However, in skinned psoas fibers, neither SL changes or force inhibition had

29 le, consistent with measurements from rabbit psoas fibers.

30 in, and introduced into permeabilized rabbit psoas fibers.

31 TPase assays and in troponin-replaced rabbit psoas fibers.

32 tion of cross-bridges of glycerinated rabbit psoas fibers.

33 s.e.m.) were imposed on permeabilised rabbit psoas fibre segments under sarcomere length control.

34 eclines was examined in demembranated rabbit psoas fibres and isolated myofibrils.

35 extracted from single, de-membranated rabbit psoas fibres and replaced by mixtures of purified rabbit

36 redevelopment (k(tr)) was examined in rabbit psoas fibres by substituting native TnC with either card

37 active tension depression induced by P(i) in psoas fibres is temperature sensitive, the depression be

38 In extracted psoas fibres that were reconstituted with fast sTnC the

39 lash photolysis of diazo-2 in rabbit skinned psoas fibres was investigated at 15 degrees C.

40 tion was increased in the cTnC-reconstituted psoas fibres.

41 d contraction in single demembranated rabbit psoas fibres.

42 actin in activating thin filaments of rabbit psoas fibres.

43 ependent properties in skinned soleus (SSM), psoas (FSM) and ventricular trabeculae (CM) of the rat u

44 and ureteral reimplantation with and without psoas hitch.

45 ebral osteomyelitis with associated epidural/psoas/iliacus abscesses) were characterized, using molec

46 8 times and K1a is 2.2 times those in rabbit psoas, indicating that nucleotides bind to cross-bridges

47 strophin protein abundance in the diaphragm, psoas major, and longissimus lumborum and a 5-fold incre

48 (iv) metastasis site; and (v) entropy in the psoas muscle (reference tissue).

49 ded adjacent vertebral body destruction with psoas muscle abscess (n = 1, 4%), kidney infarct (n = 1,

50 s of choroid, renal tubules, glomerulus, and psoas muscle all showed similar lateral spacings at appr

51 se correlations between VAT and densities of psoas muscle and cortical and trabecular bone were -0.46

52 rtening of single skinned fibres from rabbit psoas muscle at 10 degrees C was measured using an NADH-

53 esolution x-ray patterns from relaxed rabbit psoas muscle at temperatures ranging from 1 degree C to

54 Psoas muscle attenuation (an indicator of fat infiltrati

55 5% of the myosin heads in the skinned rabbit psoas muscle contain the hydrolysis products.

56 n patterns were recorded from skinned rabbit psoas muscle fiber bundles stretched to non-overlap to a

57 The mechanical behavior of skinned rabbit psoas muscle fiber contractions and in vitro motility of

58 Exchange of G34DTnC(F29W) into skinned psoas muscle fibers decreased fiber calcium sensitivity

59 region, as previously demonstrated in rabbit psoas muscle fibers in rigor.

60 cytosolic proteins were obtained from rabbit psoas muscle fibers skinned in oil and transferred to ph

61 Contractility of skinned rabbit psoas muscle fibers was inhibited by treatment with 50 m

62 lcium (Ca) bound within sarcomeres of rabbit psoas muscle fibers were compared using electron probe x

63 permeabilized rabbit cardiac trabeculae and psoas muscle fibers were compared.

64 ion patterns from the relaxed skinned rabbit psoas muscle fibers where ATP hydrolysis was inhibited b

65 dogenous RLC was removed from skinned rabbit psoas muscle fibers, and replaced with either rat wildty

66 (SH1) of the myosin head, in skinned rabbit psoas muscle fibers.

67 bunit, located in the myosin neck, in rabbit psoas muscle fibers.

68 nvestigated by sinusoidal analysis in rabbit psoas muscle fibers.

69 force redevelopment (ktr) in skinned rabbit psoas muscle fibers.

70 tramethylrhodamine and exchanged into rabbit psoas muscle fibers.

71 maximal calcium-activated tension of rabbit psoas muscle fibers.

72 tivated contractions of demembranated rabbit psoas muscle fibers; the ATPase rate was either increase

73 5 % Brij), maximally Ca(2+)-activated rabbit psoas muscle fibres at 10 degrees C (ionic strength 200

74 T-jump) in maximally Ca(2+)-activated rabbit psoas muscle fibres at 8-9 degrees C (the fibre length (

75 loaded shortening velocity of skinned rabbit psoas muscle fibres is sensitive to [Ca2+].

76 C) in chemically skinned (0.5 % Brij) rabbit psoas muscle fibres.

77 in single, skinned muscle fibers from rabbit psoas muscle following either photolysis of caged nucleo

78 perties of skinned single fibres from rabbit psoas muscle have been correlated with biochemical steps

79 n by single permeabilised fibres from rabbit psoas muscle immersed in silicone oil was measured using

80 (Pi) and hence the ATPase activity of rabbit psoas muscle in single permeabilized muscle fibres initi

81 the helical order of myosin heads in rabbit psoas muscle in the presence of nonhydrolyzable ligands.

82 s (mean diameter, 71 microns) shed by rabbit psoas muscle swelling in 140 mM KC1 containing collagena

83 n patterns were obtained from skinned rabbit psoas muscle under relaxing and rigor conditions over a

84 in relaxed demembranated fibers from rabbit psoas muscle using fluorescence polarization from bifunc

85 mall-square to basketweave in relaxed rabbit psoas muscle varied with temperature, osmotic pressure,

86 hain (RLC) in demembranated fibers of rabbit psoas muscle was determined by polarized fluorescence.

87 chemically permeabilized fibres from rabbit psoas muscle were activated maximally at 5-6 degrees C a

88 trast signal intensities between lesions and psoas muscle were evaluated.

89 Single, skinned fibers from rabbit psoas muscle were used to test this hypothesis.

90 nd exchanged into skinned fibers from rabbit psoas muscle without significant effect of the tension t

91 hanged into demembranated fibres from rabbit psoas muscle without significant effect on active force

92 to active skinned single fibres from rabbit psoas muscle, and observed the effect on the slowest pha

93 In extracts of rabbit psoas muscle, the complete degradation of soluble protei

94 pleen, kidney, small bowel, lumbar vertebra, psoas muscle, urinary bladder) as well as the noise-equi

95 teal muscle but not of the severely affected psoas muscle.

96 ndles of two to three myofibrils from rabbit psoas muscle.

97 em to adult human skeletal muscle and rabbit psoas muscle.

98 on passive fiber bundles from rabbit skinned psoas muscle.

99 terized in single skinned fibres from rabbit psoas muscle.

100 ge of [Ca(2+)] in skinned fibers from rabbit psoas muscle.

101 izzard and soleus muscles, but a decrease in psoas muscle.

102 of permeabilized fibres isolated from rabbit psoas muscle.

103 onstituted single skinned fibers from rabbit psoas muscle.

104 us RLC in single, skinned fibers from rabbit psoas muscle.

105 pCa units in fast-twitch fibres from rabbit psoas muscle.

106 n skinned single skeletal fibers from rabbit psoas muscle.

107 m; sarcomere length, 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mM, pH 7.1 and ionic stren

108 mm, sarcomere length 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mm, pH 7.1, ionic strength

109 elvis along the anterolateral surface of the psoas muscle; and laterally, posterior to the descending

110 ectron microscopy of 8-month-old A/J(dys-/-) psoas muscles confirmed lipid droplets within myofibers

111 Small bundles of fibers from rabbit skinned psoas muscles were loaded with Ca2+ fluorophore (Fluo-3)

112 after incorporating the complex into rabbit psoas myofibrils.

113 The presence of a positive psoas sign, fever, or migratory pain to the right lower

114 onship were examined in slow soleus and fast psoas skeletal muscle fibers.

115 tutions on the mechanical behavior of rabbit psoas skeletal myofibrils by replacing endogenous Tm and

116 eriment is based on the facts that in rabbit psoas the thin filament (1.12 micrometer) is longer than

117 temperature sensitive in soleus STFs than in psoas, which are fast-twitch fibres.