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1 oenzyme A dehydrogenase enzyme activities in quadriceps muscle.
2 maximum voluntary contractions of the right quadriceps muscle.
3 splantation underwent muscle biopsy from the quadriceps muscle.
4 igns decrease the required dissection of the quadriceps muscle.
5 l titers in the spinal cord and the infected quadriceps muscle.
6 bserved a generalized training effect across quadriceps muscles.
7 nly for maximum standardized uptake value in quadriceps muscles.
8 le group involved in physical activity - the quadriceps muscles.
9 me-based resistance exercise focusing on the quadriceps muscles.
10 issues by analyzing covariation patterns in quadriceps muscle activity during locomotion in rats.
11 MRS) transmit-receive surface coil under the quadriceps muscle allowed estimation of [PCr]; .V(O2) wa
12 -receive surface coil placed under the right quadriceps muscle allowed estimation of intramuscular [P
14 y (wild-type, WT) and dystrophic (mdx) mouse quadriceps muscles and evaluated transcript levels of th
15 s, CP-640186 lowered hepatic, soleus muscle, quadriceps muscle, and cardiac muscle malonyl-CoA with E
16 onths of age, there was gross atrophy of the quadriceps muscle, and other hindlimb muscles were varia
17 and ear), heart (heart base and ventricle), quadriceps muscle, and the tibiotarsal joint at 1, 2, 4,
18 matically increased in 4-week-old dystrophic quadriceps muscles, and to a lesser extent in diaphragm
19 6 (0.82-0.99), respectively, for gluteal and quadriceps muscles, and WSCV for gluteal and quadriceps
22 patients receiving placebo exhibited greater quadriceps muscle atrophy, with a -14.3 +/- 3.6% change
23 d increase in UCP3 mRNA levels occurs in rat quadriceps muscle between 12 and 24 h of food removal.
25 n intravenously to human subjects and needle quadriceps muscle biopsies were taken to measure [13C]le
26 see text]o2max) and microcirculation loss on quadriceps muscle biopsy (in CD31(+) immunofluorescence
28 ial occlusion pressures; cardiac output; and quadriceps muscle blood flow and oxygen tension (PMo2).
29 ts in significant contractile fatigue of the quadriceps muscle but not of the diaphragm in healthy, r
32 ed significantly improved motor performance, quadriceps muscle contractility, and sciatic nerve condu
34 onymous recurrent inhibition during isolated quadriceps muscle contraction, but to a much lesser exte
36 easured by dual-energy x-ray absorptiometry, quadriceps muscle cross-sectional area measured by magne
40 a phosphorus magnetic resonance spectroscopy quadriceps muscle exercise-recovery study before and aft
41 y muscles (IRL) exacerbated exercise-induced quadriceps muscle fatigue (Q(tw) = -12 +/- 8% IRL-CTRL v
43 en fluorescent protein (EGFP) in transfected quadriceps muscle fibers in living mice subjected to con
46 ation (NMES), applied to the surgical limb's quadriceps muscle for the first 6 weeks following surger
50 he IC/MS assay was used to quantitate OAs in quadriceps muscle from sedentary mice compared to fatigu
53 ulate in obesity, we performed lipidomics on quadriceps muscles from obese mice with impaired glucose
56 describe the biomechanical properties of the quadriceps muscle in ICU survivors 12 months after ICU d
57 kinase activation) and GLUT4-GFP-transfected quadriceps muscle in living, anesthetized mice either mu
60 be more severely affected by weakness of the quadriceps muscles in individuals with knee OA who have
64 the gene signature inversely correlated with quadriceps muscle mass (r = -0.50, p-value = 0.011) in I
68 n, exercise training significantly increased quadriceps muscle mitochondrial capacity by 24% and VO2
70 tudy was to determine whether fatigue of the quadriceps muscle occurs after high intensity cycle exer
71 In conclusion, contractile fatigue of the quadriceps muscle occurs after high intensity cycle exer
72 d a large-scale gene expression profiling in quadriceps muscle of arctic ground squirrels, comparing
73 Muscle biopsy samples were obtained from the quadriceps muscle of both the control and exercised legs
75 Similarly, cCTTI of porcine thymus into the quadriceps muscle of thymectomized T cell-depleted pigs
76 findings, eosinophils were prominent in the quadriceps muscles of 4-wk-old male mdx mice but no prof
77 rotein expression and were injected into the quadriceps muscles of BALB/c mice to measure specific an
78 wed many lipid droplets within the psoas and quadriceps muscles of dysferlin-deficient A/J(dys-/-) mi
80 r 2 kinase than were observed in Mtm1 p.R69C quadriceps muscle or in muscles from wild-type littermat
81 etermined post-exercise recovery kinetics of quadriceps muscle oxygen uptake (m VO2 ) measured by nea
82 ange, minute ventilation, blood lactate, and quadriceps muscle pH and phosphorylation potential by 31
83 injection of pMCKhLPL into the peritoneum or quadriceps muscle results in plasma triglyceride reducti
87 ne of B. burgdorferi in the ear, heart base, quadriceps muscle, skin, and tibiotarsal joint tissue of
88 aximal exercise performance, respiratory and quadriceps muscle strength and endurance and quality-of-
90 exercise capacity (6-min walk distance), and quadriceps muscle strength corrected for body weight (QS
91 e measures included demographic information, quadriceps muscle strength, and QA using a burst-superim
92 2 physical functioning scores, hamstring and quadriceps muscle strength, the Western Ontario and McMa
94 idation in myocytes cultured from human male quadriceps muscle taken from subjects with varied BMI, f
96 .3 0.4%, 2.7 0.2%, and 2.0 0.4% decreases in quadriceps muscle volume (P < 0.05) of the immobilized l
97 is muscle biopsies were performed to measure quadriceps muscle volume and daily MyoPS rates, respecti
100 quadriceps muscles, and WSCV for gluteal and quadriceps muscles was 2.2% and 3.6%, respectively.
102 rmine the kinetics of IL-6 secretion, intact quadriceps muscles were transfected with enhanced green