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1 ult of a 1.6-fold reduction in mitochondrial volume density and altered substrate oxidation kinetics.
4 nsiveness of human liver cells to peroxisome volume density and in the activity of the beta-oxidation
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).
12 These differences paralleled cell number and volume density differences: 4-day limb buds had 2- to 2.
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
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
30 7.7) and micro-CT analysis (percentage bone volume density: test: 63.46 +/- 5.61; control: 51.20 +/-
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
39 tional areas, capillarity, and mitochondrial volume density were not different between the groups.
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