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1 or low frequency (LFS; 3 h at 10 Hz to mimic endurance training).
2 me of the adaptations to exercise induced by endurance training.
3 testing and underwent 20 weeks of supervised endurance training.
4 ere measured before and after 5 and 10 wk of endurance training.
5  instead, exhibits plasticity with long-term endurance training.
6 tation on changes in VO2max during prolonged endurance training.
7 cise and facilitates molecular adaptation to endurance training.
8 events the adaptive intrinsic bradycardia of endurance training.
9 tal muscle and enhanced adaptive response to endurance training.
10 gnificantly with age, sex, body surface, and endurance training.
11 egulate hallmark adaptations associated with endurance training.
12 strated physiology characteristic of extreme endurance training.
13 s sex, race, and age in response to 20 wk of endurance training.
14 ance and molecular adaptations to subsequent endurance training.
15 mia in an experimental large animal model of endurance training.
16 egulate hallmark adaptations associated with endurance training.
17  mitochondrial haplotype in the responses to endurance training.
18 ges in athletes who participate in long-term endurance training.
19        The latter 3 groups performed 5 wk of endurance training 5 x/wk.
20 plementation neither enhances nor attenuates endurance training adaptations in young healthy men.
21 pha signaling pathway which may explain some endurance training adaptations.
22 d palmitate and linoleate kinetics but after endurance training, all were realigned with those of dec
23                          We also report that endurance training and a well-balanced diet activate the
24  rehabilitation, which includes strength and endurance training and educational, nutritional, and psy
25              This should have application in endurance training and future exercise industry.
26        These results show that low intensity endurance training and well-balanced diet activate the N
27 most mitochondrial adaptations to subsequent endurance training, but this effect may have been a resu
28 training and better performance after forced endurance training compared smtnl1(+/+) mice.
29 er." As a result, worldwide participation in endurance training, competitive long distance endurance
30 ty): seven participants performed 2 weeks of endurance training (cycling) and were tested pre-post in
31 he first 6 to 9 months after commencement of endurance training depending on the duration and intensi
32 rint interval training (SIT) and traditional endurance training elicit similar physiological adaptati
33 flavanone bioavailability.A 7-d cessation of endurance training enhanced, rather than reduced, the bi
34                  The novel methods show that endurance training (ET) and high intensity interval trai
35 iglyceride (IMTG) utilization is enhanced by endurance training (ET) and is linked to improved insuli
36  in peak oxygen uptake (V(O2peak)) following endurance training (ET) are primarily determined by cent
37  proposed as a time efficient alternative to endurance training (ET) for increasing skeletal muscle o
38 ecular adaptations to a subsequent period of endurance training (ET).
39  oxidation during exercise and the effect of endurance training, exercise intensity, and lipid supple
40 iovascular and haematological adaptations to endurance training facilitate greater maximal oxygen con
41 years; 6 male, 3 female) completed 1 year of endurance training followed by repeat measurements.
42     All group B patients underwent intensive endurance training for a median of 15 h/week (interquart
43 g volume, including decrements especially in endurance training frequency and volume.
44                                   High-level endurance training has been associated with right ventri
45                        Vigorous exertion and endurance training have been reported to increase atrial
46 solute intensity, persons who have undergone endurance training have greater fat oxidation during exe
47 on including inspiratory muscle training and endurance training have shown a promising effect post-Fo
48 ty power training (HIPT), and high-intensity endurance training (HIET)] on the resting concentration
49  type 2 diabetes and are decreased following endurance training in healthy young men and in rats.
50 ty and endurance performance during 10 wk of endurance training in healthy, young males.
51 nvestigated transcriptomic changes caused by endurance training in mice deficient in plakophilin-2 (P
52 physiological cardiac remodelling induced by endurance training in mice.
53 We hypothesized that prolonged and intensive endurance training in previously sedentary healthy young
54 inal study to assess the effects of one-year endurance training in the elderly.
55 garding the long-term effects of high-volume endurance training, including potential maladaptation.
56 e-type specific in the posterior muscles and endurance training increased its content in type I muscl
57                                              Endurance training increased the basal mRNA level of hex
58 bility before and after exercise may augment endurance training-induced adaptations of human skeletal
59 idative and performance ability derived from endurance training-induced increases in muscle mitochond
60                                              Endurance training induces a partial fast-to-slow muscle
61                                  Conversely, endurance training induces eccentric hypertrophy and enh
62                                              Endurance training induces numerous cardiovascular and s
63 le-component modalities, that is, continuous endurance training, interval training, and resistance tr
64 rcise interventions consisting of continuous endurance training, interval training, resistance traini
65 pothesised that cardiovascular adaptation to endurance training is augmented following puberty.
66      Specifically, older adults who initiate endurance training later in life are unable to improve v
67          One year of prolonged and intensive endurance training leads to cardiac morphological adapta
68 iated with immune dysfunction, but long-term endurance training may confer protective effects on immu
69     Here, we analyze how sex differences and endurance training mediate changes in skeletal muscles,
70                                              Endurance training neither affected skeletal muscle FNDC
71 hanges are consistent with those elicited by endurance training of the limb muscles in normal subject
72 se, similar in extent to that achieved after endurance training of wild-type littermates.
73 ated in both LRT and HRT rats that underwent endurance training on a treadmill compared with those th
74                    The beneficial effects of endurance training on microvasculature are widely known.
75 y was, therefore, to determine the effect of endurance training on O2 saturation of Mb (SmbO2) and Pm
76 fatty acid (n-3 PUFA) supplementation during endurance training on tryptophan (Trp) metabolism and me
77 rs) were randomized to 4 weeks of supervised endurance training or to a control group.
78                                     Although endurance training preferentially induces PGC-1alpha1 ex
79 cardiovascular stiffening, whereas life-long endurance training preserves left ventricular (LV) compl
80                         Prolonged, sustained endurance training preserves ventricular compliance with
81 this study was to evaluate the effects of an endurance training program on microvasculature of skelet
82 sessed the age-dependent effects of a 4-week endurance training program on the catabolic-anabolic bal
83 ) followed a personalized moderate-intensity endurance training program, while the nontraining (n = 1
84  evaluated in mice after completing a 6-week endurance training program.
85 ring over 30 years was reversed by a 6-month endurance training program.
86 ise were assessed before and after a 6-month endurance training program.
87  women) aged 17-63 y participated in a 20-wk endurance training program.
88 6J mice were compared with or without a 5 wk endurance training protocol at rest or after an acute ex
89  diabetes after undergoing deconditioning or endurance training respectively.
90  acidity and can be evaluated for monitoring endurance, training routines, or athletic performance.
91 consisted primarily of four 30- to 40-minute endurance training sessions (low-impact aerobics; brisk
92                         Subjects performed 3 endurance training sessions per week for 10 wk.
93                                              Endurance training shifts fuel selection towards fats to
94 ifferences in aerosol particle emission, but endurance-training subjects emitted significantly more a
95 pair the metabolic adaptations to short-term endurance training, suggesting that the ills of inactivi
96 ith type 2 diabetes show reversibility after endurance training through increased contributions of th
97  tissue (AT) lipolysis becomes elevated upon endurance training to cope with enhanced energy demands.
98 f a combination of a human PKP2 mutation and endurance training to trigger an ARVC-like phenotype.
99  Age, sex, body surface area, and high-level endurance training were determinants of RA area.
100  biochemical responses to acute exercise and endurance training were investigated in female Fischer 3
101 In contrast, the right ventricle responds to endurance training with eccentric remodeling at all leve
102        We aim to investigate associations of endurance training with incidence of atrial fibrillation
103              We investigated associations of endurance training with incidence of bradycardia and pac

 
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