Energy turnover in relation to slowing of contractile properties during fatiguing contractions of the human anterior tibialis muscle.
about
Fatigue is a Brain-Derived Emotion that Regulates the Exercise Behavior to Ensure the Protection of Whole Body HomeostasisUnderstanding Muscle Dysfunction in Chronic Fatigue SyndromeBiomarkers of peripheral muscle fatigue during exercise.Potentiation and electrical stimulus frequency during self-paced exercise and recovery.Effect of temperature on crossbridge force changes during fatigue and recovery in intact mouse muscle fibers.Profiling of age-related changes in the tibialis anterior muscle proteome of the mdx mouse model of dystrophinopathyA motor unit-based model of muscle fatigue.Increasing temperature speeds intracellular PO2 kinetics during contractions in single Xenopus skeletal muscle fibersMotor unit number estimates and neuromuscular transmission in the tibialis anterior of master athletes: evidence that athletic older people are not spared from age-related motor unit remodeling.Changes in the force-velocity relationship of fatigued muscle: implications for power production and possible causes.The multiple roles of phosphate in muscle fatigue.Skeletal muscle fatigue.Ventilation and respiratory mechanics.Effects of low-load resistance exercise with blood flow restriction on high-energy phosphate metabolism and oxygenation level in skeletal muscle.Potassium dependent rescue of a myopathy with core-like structures in mouse.Force decline during fatigue is due to both a decrease in the force per individual cross-bridge and the number of cross-bridges.Phosphate increase during fatigue affects crossbridge kinetics in intact mouse muscle at physiological temperature.Failure to expand the motor unit size to compensate for declining motor unit numbers distinguishes sarcopenic from non-sarcopenic older men.Kinetic control of oxygen consumption during contractions in self-perfused skeletal muscle
P2860
Q21129258-F3114A40-D3D2-443F-8937-7757F7EBA4F1Q26753111-CAF82318-163F-4688-BB45-396CDE1300F8Q34470979-F266294E-5DB9-40A4-A5B5-6C59B8683B09Q34527755-932B33D1-A383-40F0-B403-97A4891572FFQ35023622-EFF0DC7E-B939-4DA2-9763-0706C920F48EQ36316393-A63ECC07-D01D-4F76-8BF5-9962BE382A8FQ36390726-1064DEE1-2E04-4D79-9772-92DE6880B2D1Q36527985-A4CE31D7-593F-452B-8612-BF0313E5E20DQ37339248-FA8FE76C-A7C9-4C37-AD89-5B6410097D99Q37765078-1E7857CE-0340-47A7-9354-3409F84007ECQ38068178-B95F72A7-DEFA-4AD8-BCCA-FF05ECC7EC14Q38116829-4DAA8ED7-5A08-4DE0-8144-7793E4574DA7Q38116832-5C159783-DE37-4158-BFEF-6E66EB37EB18Q41104838-C07BE073-C5E2-4515-975A-C79077D69DCBQ41955529-F3700217-C4E3-4109-8A06-E33E283D1F53Q45061670-F8DBCC37-51DD-4259-A2A4-68F3B3185821Q48044098-89225451-3734-42B7-8208-C14B3DA16DB7Q51741440-2301BFDA-487E-4480-BE8F-748FF6FF4604Q56550973-952DAF65-1D52-4DA4-869B-0F0C40C681ED
P2860
Energy turnover in relation to slowing of contractile properties during fatiguing contractions of the human anterior tibialis muscle.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Energy turnover in relation to ...... uman anterior tibialis muscle.
@en
Energy turnover in relation to ...... uman anterior tibialis muscle.
@nl
type
label
Energy turnover in relation to ...... uman anterior tibialis muscle.
@en
Energy turnover in relation to ...... uman anterior tibialis muscle.
@nl
prefLabel
Energy turnover in relation to ...... uman anterior tibialis muscle.
@en
Energy turnover in relation to ...... uman anterior tibialis muscle.
@nl
P2860
P1476
Energy turnover in relation to ...... uman anterior tibialis muscle.
@en
P2093
David A Jones
David B McIntyre
P2860
P304
P356
10.1113/JPHYSIOL.2009.175265
P407
P577
2009-07-13T00:00:00Z