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1 teal muscle but not of the severely affected 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 em to adult human skeletal muscle and rabbit 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
17 elvis along the anterolateral surface of the psoas muscle; and laterally, posterior to the descending
18 rtening of single skinned fibres from rabbit psoas muscle at 10 degrees C was measured using an NADH-
19 esolution x-ray patterns from relaxed rabbit psoas muscle at temperatures ranging from 1 degree C to
20                                              Psoas muscle attenuation (an indicator of fat infiltrati
21 ectron microscopy of 8-month-old A/J(dys-/-) psoas muscles confirmed lipid droplets within myofibers
22 5% of the myosin heads in the skinned rabbit psoas muscle contain the hydrolysis products.
23 n patterns were recorded from skinned rabbit psoas muscle fiber bundles stretched to non-overlap to a
24    The mechanical behavior of skinned rabbit psoas muscle fiber contractions and in vitro motility of
25       Exchange of G34DTnC(F29W) into skinned psoas muscle fibers decreased fiber calcium sensitivity
26 region, as previously demonstrated in rabbit psoas muscle fibers in rigor.
27 cytosolic proteins were obtained from rabbit psoas muscle fibers skinned in oil and transferred to ph
28              Contractility of skinned rabbit psoas muscle fibers was inhibited by treatment with 50 m
29 lcium (Ca) bound within sarcomeres of rabbit psoas muscle fibers were compared using electron probe x
30  permeabilized rabbit cardiac trabeculae and psoas muscle fibers were compared.
31 ion patterns from the relaxed skinned rabbit psoas muscle fibers where ATP hydrolysis was inhibited b
32 dogenous RLC was removed from skinned rabbit psoas muscle fibers, and replaced with either rat wildty
33 tramethylrhodamine and exchanged into rabbit psoas muscle fibers.
34  maximal calcium-activated tension of rabbit psoas muscle fibers.
35  (SH1) of the myosin head, in skinned rabbit psoas muscle fibers.
36 bunit, located in the myosin neck, in rabbit psoas muscle fibers.
37 nvestigated by sinusoidal analysis in rabbit psoas muscle fibers.
38  force redevelopment (ktr) in skinned rabbit psoas muscle fibers.
39 tivated contractions of demembranated rabbit psoas muscle fibers; the ATPase rate was either increase
40 5 % Brij), maximally Ca(2+)-activated rabbit psoas muscle fibres at 10 degrees C (ionic strength 200
41 T-jump) in maximally Ca(2+)-activated rabbit psoas muscle fibres at 8-9 degrees C (the fibre length (
42 loaded shortening velocity of skinned rabbit psoas muscle fibres is sensitive to [Ca2+].
43 C) in chemically skinned (0.5 % Brij) rabbit psoas muscle fibres.
44 in single, skinned muscle fibers from rabbit psoas muscle following either photolysis of caged nucleo
45 perties of skinned single fibres from rabbit psoas muscle have been correlated with biochemical steps
46 n by single permeabilised fibres from rabbit psoas muscle immersed in silicone oil was measured using
47 (Pi) and hence the ATPase activity of rabbit psoas muscle in single permeabilized muscle fibres initi
48  the helical order of myosin heads in rabbit psoas muscle in the presence of nonhydrolyzable ligands.
49 m; sarcomere length, 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mM, pH 7.1 and ionic stren
50 mm, sarcomere length 2.5 microm) from rabbit psoas muscle; [MgATP] was 4.6 mm, pH 7.1, ionic strength
51 (iv) metastasis site; and (v) entropy in the psoas muscle (reference tissue).
52 s (mean diameter, 71 microns) shed by rabbit psoas muscle swelling in 140 mM KC1 containing collagena
53                        In extracts of rabbit psoas muscle, the complete degradation of soluble protei
54 n patterns were obtained from skinned rabbit psoas muscle under relaxing and rigor conditions over a
55 pleen, kidney, small bowel, lumbar vertebra, psoas muscle, urinary bladder) as well as the noise-equi
56  in relaxed demembranated fibers from rabbit psoas muscle using fluorescence polarization from bifunc
57 mall-square to basketweave in relaxed rabbit psoas muscle varied with temperature, osmotic pressure,
58 hain (RLC) in demembranated fibers of rabbit psoas muscle was determined by polarized fluorescence.
59  chemically permeabilized fibres from rabbit psoas muscle were activated maximally at 5-6 degrees C a
60 trast signal intensities between lesions and psoas muscle were evaluated.
61           Single, skinned fibers from rabbit psoas muscle were used to test this hypothesis.
62  Small bundles of fibers from rabbit skinned psoas muscles were loaded with Ca2+ fluorophore (Fluo-3)
63 nd exchanged into skinned fibers from rabbit psoas muscle without significant effect of the tension t
64 hanged into demembranated fibres from rabbit psoas muscle without significant effect on active force

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