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1 ult of a 1.6-fold reduction in mitochondrial volume density and altered substrate oxidation kinetics.
2                                Mitochondrial volume density and capillary density were analyzed by st
3                                Mitochondrial volume density and capillary density were three times gr
4 nsiveness of human liver cells to peroxisome volume density and in the activity of the beta-oxidation
5                                           mt volume density and mtDNA copy number was increased by ap
6 ple permitted determination of mitochondrial volume density and the contribution of the loss of mitoc
7 ximately 10(11) solar masses) of cool dense (volume density approximately 1 cm(-3)) gas, which is in
8 ated for osteocyte density (OD), bone vessel volume density (BVVD), and bone mineral density (BMD).
9 d the kidney enlargement by 44% and the cyst volume density by 29% in Cy/+ rats.
10 ificant preservation of alveolar surface and volume density compared with wild-type littermates.
11                           Alterations in the volume, density, connectivity and functional activation
12 These differences paralleled cell number and volume density differences: 4-day limb buds had 2- to 2.
13  mean intercapillary distance and fibroblast volume density evident.
14 igh altitude (>5500 m), muscle mitochondrial volume density falls, with a particular loss of the subs
15 ies increased in both luminosity density and volume density from z approximately 10 to z approximatel
16             We measured alveolar surface and volume density in animals exposed to 14 days more of air
17 ic reticulum stress and a reduction in Golgi volume density in comparison to control.
18     Rapamycin significantly reduced the cyst volume density in Cy/+ rats by >40%.
19                                         Bone volume density increased significantly (P = 0.001) in bo
20 an increase in skeletal muscle mitochondrial volume density (Mito(VD)) over equivalent normoxic train
21 cle biopsies were analysed for mitochondrial volume density (Mito(VD)), capillarity, fibre types and
22 se, ultrastructural studies revealed reduced volume densities of myofibrils and higher densities of i
23 ge of Ca(2+) selectivities, depending on the volume density of carboxylate groups and the permittivit
24 er (i.e., "pore proper") contained a uniform volume density of fixed charge equivalent to that of one
25 ynapses made by single interneurones and the volume density of GABAergic synapses, it was calculated
26                               In PDCimG, the volume density of inflammatory cells and the RANKL/OPG r
27                                  The reduced volume density of myofibre (32%) in tailshaker muscle is
28                                 However, the volume density of photosensitive membrane (> or =60%) ex
29 6 in the 38-month-old as calculated from the volume density of these abnormalities.
30  7.7) and micro-CT analysis (percentage bone volume density: test: 63.46 +/- 5.61; control: 51.20 +/-
31           For the two measures of percentage volume density, the mean difference was 1.61 percentage
32      Morphometric analysis revealed that the volume density (V(v)) of MC was increased in silicotic l
33                               The normalized volume density (Vv) of IGF-I-positive (IGF-I+) interstit
34 g and stained with Masson trichrome, and the volume density (Vv) of the gingival components was estim
35 onstrated that cardiac myocyte mitochondrial volume density was increased in insulin-resistant uncoup
36                                Mitochondrial volume density was significantly lower in elderly compar
37                                   Arteriolar volume density was similar to that in the other groups.
38                 SR relative surface area and volume densities were reduced by 63% and 76%, indicating
39 tional areas, capillarity, and mitochondrial volume density were not different between the groups.

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