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1 letes have an increased ratio of surface per mitochondrial volume.
2 or of maximal oxygen uptake rate than muscle mitochondrial volume.
3 ss, this study examined the effect of DZX on mitochondrial volume.
4 ) and Bmal1(-/-) mice had a 40% reduction in mitochondrial volume.
5 might increase its sensitivity to changes in mitochondrial volume.
8 in, porin, nNOS, p-nNOS, and Tfam as well as mitochondrial volume and cristae abundance were signific
9 ose of this study was to define the roles of mitochondrial volume and distribution in axonal degenera
10 uilibrate just before division, and that the mitochondrial volume and DNA-containing nucleoids instea
11 present a mechanism by which variability in mitochondrial volume and functionality, along with cell
13 ial morphology and physiology, a decrease in mitochondrial volume, and a severe suppression of cellul
14 ochondrial "membrane mass," has no effect on mitochondrial volume, and does not affect the permeabili
15 d significantly increased calcium, increased mitochondrial volume, and increased numbers of synaptic
16 d of transported tracer label showed reduced mitochondrial volumes as well as decreased active zone n
18 e demonstrate an increase in skeletal muscle mitochondrial volume density (Mito(VD)) over equivalent
19 Skeletal muscle biopsies were analysed for mitochondrial volume density (Mito(VD)), capillarity, fi
20 ch was the result of a 1.6-fold reduction in mitochondrial volume density and altered substrate oxida
23 cle biopsy sample permitted determination of mitochondrial volume density and the contribution of the
24 e to extreme high altitude (>5500 m), muscle mitochondrial volume density falls, with a particular lo
25 c analyses demonstrated that cardiac myocyte mitochondrial volume density was increased in insulin-re
27 iber cross-sectional areas, capillarity, and mitochondrial volume density were not different between
31 itochondrial CO therapy, and connect cardiac mitochondrial volume expansion with the inducible networ
33 stsynaptic density length and curvature, and mitochondrial volume fraction were similar for axosomati
35 f anions and is postulated to be involved in mitochondrial volume homeostasis in conjunction with the
41 ors are suppressed by control at two levels: Mitochondrial volume is actively distributed throughout
43 because of a reduction in the total cellular mitochondrial volume, suggesting that intermitochondrial
44 ddition of DZX did not alter the response of mitochondrial volume to CPG (P=0.912) but increased swel
45 mPT onset was assessed by measuring in situ mitochondrial volume using the 'thinness ratio' and the
46 strate that Letm1 is involved in maintaining mitochondrial volume via potassium/proton exchange acros
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