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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.
6      In addition, the oxidative capacity per mitochondrial volume (0.22 +/- 0.042 vs. 0.32 +/- 0.015
7           In 1alpha,25(OH)2D3-treated cells, mitochondrial volume and branching and expression of the
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
12 e (5HD) at 100 or 300 microM, also increased mitochondrial volume and inhibited respiration.
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
17 s conveyed by its individual fibers; and (4) mitochondrial volume/axon length rises >/=d(2).
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
21                                              Mitochondrial volume density and capillary density were
22                                              Mitochondrial volume density and capillary density were
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
26                                              Mitochondrial volume density was significantly lower in
27 iber cross-sectional areas, capillarity, and mitochondrial volume density were not different between
28                            DZX did not alter mitochondrial volume during CPG; however, it was associa
29                   5-Hydroxydecanoate reduced mitochondrial volume during exposure to both stresses wi
30 wever, it was associated with an increase in mitochondrial volume during MI.
31 itochondrial CO therapy, and connect cardiac mitochondrial volume expansion with the inducible networ
32                If, as found for optic nerve, mitochondrial volume fraction is constant with axon diam
33 stsynaptic density length and curvature, and mitochondrial volume fraction were similar for axosomati
34 lity of the synaptosomal preparations or the mitochondrial volume fraction.
35 f anions and is postulated to be involved in mitochondrial volume homeostasis in conjunction with the
36 el (IMAC) that is believed to be involved in mitochondrial volume homeostasis.
37       Early cure of infection also increased mitochondrial volume in Tmem compared with Teff, support
38                                              Mitochondrial volume in vastus lateralis biopsies increa
39                      We show that the axonal mitochondrial volume increase following acute demyelinat
40                            Both cellular and mitochondrial volume increased during exposure to MI and
41 ors are suppressed by control at two levels: Mitochondrial volume is actively distributed throughout
42  a constant fraction of axonal volume--thus, mitochondrial volumes rise as the diameter squared.
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
47                                              Mitochondrial volume was a strong predictor of bouton si
48                                              Mitochondrial volume was measured.

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