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1 Additionally, we observed low bone volume density.
2 ult of a 1.6-fold reduction in mitochondrial volume density and altered substrate oxidation kinetics.
5 nsiveness of human liver cells to peroxisome volume density and in the activity of the beta-oxidation
7 or when normalising OXPHOS to mitochondrial volume density and muscle cristae surface area density.
8 ple permitted determination of mitochondrial volume density and the contribution of the loss of mitoc
9 cribed the relationship between podocyte GL3 volume density and the estimation error (R(2) =0.94) and
10 ups and UT when normalising to mitochondrial volume density and were lost when normalising to muscle
11 dicated by fractional anisotropy, streamline volume density, and mean diffusivity and evaluated withi
12 HOS enzyme activities, mitochondrial DNA and volume density, and mitochondria-specific respiratory ca
14 ximately 10(11) solar masses) of cool dense (volume density approximately 1 cm(-3)) gas, which is in
15 ated for osteocyte density (OD), bone vessel volume density (BVVD), and bone mineral density (BMD).
19 These differences paralleled cell number and volume density differences: 4-day limb buds had 2- to 2.
21 igh altitude (>5500 m), muscle mitochondrial volume density falls, with a particular loss of the subs
22 ies increased in both luminosity density and volume density from z approximately 10 to z approximatel
27 an increase in skeletal muscle mitochondrial volume density (Mito(VD)) over equivalent normoxic train
28 cle biopsies were analysed for mitochondrial volume density (Mito(VD)), capillarity, fibre types and
29 se, ultrastructural studies revealed reduced volume densities of myofibrils and higher densities of i
30 ge of Ca(2+) selectivities, depending on the volume density of carboxylate groups and the permittivit
32 er (i.e., "pore proper") contained a uniform volume density of fixed charge equivalent to that of one
33 ynapses made by single interneurones and the volume density of GABAergic synapses, it was calculated
34 hematoxlin & eosin-stained sections, the volume density of inflammatory cells (VvIC) and fibrobla
39 ic lung cancer transplantation models, tumor volume, density of vessels and pericytes, and functional
40 7.7) and micro-CT analysis (percentage bone volume density: test: 63.46 +/- 5.61; control: 51.20 +/-
41 RUN groups demonstrated higher mitochondrial volume density than the RA and UT groups while all activ
45 g and stained with Masson trichrome, and the volume density (Vv) of the gingival components was estim
46 onstrated that cardiac myocyte mitochondrial volume density was increased in insulin-resistant uncoup
50 tional areas, capillarity, and mitochondrial volume density were not different between the groups.
51 nge independently of shifts in mitochondrial volume density, which may be attributed to variations in