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1 atriuretic peptide expression, and sustained capillarization.
2 phosphorylation of Akt and increased muscle capillarization.
3 escence, and whether this effect was lost in capillarization.
4 an important determinant of skeletal muscle capillarization.
5 ed to overall measures of peripheral villous capillarization.
6 cle fiber type distribution, fiber size, and capillarization.
7 differences are associated with increases in capillarization.
9 hanisms for retinal oxygen supply, including capillarization and acid-induced haemoglobin oxygen unlo
11 animal models, inhibitory effects of FZHY on capillarization and angiogenesis were further confirmed
12 vestigated the effects of FZHY on sinusoidal capillarization and angiogenesis with mice challenged fo
14 ipheral factors (skeletal muscle fibre type, capillarization and concentration of mitochondrial DNA [
15 combinant Emc10 enhanced infarct border-zone capillarization and exerted a sustained beneficial effec
17 Kupffer cells are responsible for sinusoidal capillarization and perisinusoidal matrix deposition, im
18 le vascular beds, promoting liver sinusoidal capillarization and portal hypertension, ischemic heart
20 oximity to liver sinusoidal endothelial cell capillarization and stellate cell activation demonstrate
21 hat a Nox2-based oxidase is required for SEC capillarization and that it may play a central role in v
22 nvestigate if AMPK regulates skeletal muscle capillarization and the angiogenic responses to exercise
23 ationship was observed between type II fiber capillarization and the change in type II-fiber CSA with
25 date the nature of and mechanisms leading to capillarization and to determine how LSECs promote HSC q
27 Vegfa from HS, enhanced infarct border-zone capillarization, and exerted sustained beneficial effect
29 proliferation, metabolic zonation, sinusoid capillarization, and hepatic stellate cell activation we
30 raining program improves muscle performance, capillarization, and mitochondrial content in both asymp
31 meliorated CCl(4) and DMN-induced sinusoidal capillarization, angiogenesis and expression of angiogen
32 correlations between VEGF protein and muscle capillarization are consistent with VEGF being an import
33 ion of both angiogenesis and pathogenic LSEC capillarization, as well as demonstrating a role for S1P
34 mentation and high-throughput, high-accuracy capillarization assessment in basement-membrane-immunost
36 (4) AMPK regulates basal VEGF expression and capillarization, but is not necessary for exercise-induc
38 unofluorescence was used to determine muscle capillarization, fiber size, SC content, and activity.
39 es proliferation, contributing to sinusoidal capillarization, impaired endothelial regeneration, and
41 ce, muscle mitochondrial function, and fiber capillarization in symptomatic and asymptomatic statin u
42 cells (SECs), including SEC defenestration, capillarization, increased junctional PECAM-1 expression
43 bryonic hepatic hemorrhage and microvascular capillarization induced by Smad6 deletion in endothelial
46 toration, portal inflammation and sinusoidal capillarization may not regress after viral eradication.
49 that affect liver function such as sinusoid capillarization or loss of metabolic zonation are common
50 ance to fatigue (P = 0.01), and muscle fiber capillarization (P < 0.01), with no differences between
53 ural demonstration of SEC defenestration and capillarization, quantitative immunofluorescence analysi
55 60-2770 accelerated the complete reversal of capillarization (restored differentiation of LSECs) with
57 onal changes in SEC signaling for sinusoidal capillarization that may be initial events in pathogenic
58 signaling for angiogenesis or liver sinusoid capillarization, the mechanism for initiating these effe
60 increased sinusoidal endothelial cell (SEC) capillarization, vascularization of the peribiliary vasc
62 marrow (BM) endothelial progenitor cells to capillarization was identified using rats transplanted w
65 etraining, at a time point long after muscle capillarization was observed to be similar to pre-traini
68 ) mice revealed a special form of sinusoidal capillarization, with effacement of endothelial zonation