Proton nuclear magnetic resonance (NMR) relaxation measurements are reported for frog muscle as a function of temperature and Larmor frequency. Each T1ρ, T2, and T1 measurement covered a time domain sufficient to identify the average relaxation time for most intracellular water. Using regression analysis the data were fit with a model where intracellular water molecules are exchanging between a large compartment in which mobility is similar to ordinary water and a small compartment in which motion is restricted. The regression results suggest that: the restricted compartment exhibits a distribution of motions skewed toward that of free water; the residence time of water molecules in the restricted compartment is approximately 1 ms; and, the...
Abstract1H NMR spectra of intact frog, and chicken skeletal muscles, were recorded at 470 MHz with t...
The electric quadrupole moment of the deuterium nucleus provides a nuclear magnetic resonance (NMR) ...
The anisotropy of the spin-lattice relaxation time (T1) and the spin-spin relaxation times (T2) of w...
Whole frog sartorius and gastrocnemius muscles were incubated in Ringer's solutions, either unenrich...
Whole gastrocnemius muscles were incubated in Ringer's solution enriched with H2–17O; the paired con...
The nuclear magnetic resonance (NMR) of water protons in live and glycerinated muscle, suspensions o...
The nuclear magnetic reasonance (NMR) relaxation times of protons in toad muscle water have been mea...
The observation of the spin-echo decay in a long time domain has revealed that there exist at least ...
The origin of the nonexponentiality of proton spin echoes of skeletal muscle has been carefully exam...
The spin-lattice relaxation time (T1) of water protons in mouse muscle was studied from 10(4) to 10(...
Whole striated muscles from the frog Rana esculenta were bathed in Ringer's solution enriched with H...
Nuclear magnetic resonance (NMR), and in particular transverse relaxation (T2), has been used to cha...
Spin-lattice relaxation times (T1's) of 13C-enriched glycine accumulated in frog muscles were determ...
The anisotropy of the spin-diffusion coefficient Ds of water protons in skeletal muscle has been stu...
Nuclear magnetic resonance (NMR) measurements provide both structural and dynamical information abou...
Abstract1H NMR spectra of intact frog, and chicken skeletal muscles, were recorded at 470 MHz with t...
The electric quadrupole moment of the deuterium nucleus provides a nuclear magnetic resonance (NMR) ...
The anisotropy of the spin-lattice relaxation time (T1) and the spin-spin relaxation times (T2) of w...
Whole frog sartorius and gastrocnemius muscles were incubated in Ringer's solutions, either unenrich...
Whole gastrocnemius muscles were incubated in Ringer's solution enriched with H2–17O; the paired con...
The nuclear magnetic resonance (NMR) of water protons in live and glycerinated muscle, suspensions o...
The nuclear magnetic reasonance (NMR) relaxation times of protons in toad muscle water have been mea...
The observation of the spin-echo decay in a long time domain has revealed that there exist at least ...
The origin of the nonexponentiality of proton spin echoes of skeletal muscle has been carefully exam...
The spin-lattice relaxation time (T1) of water protons in mouse muscle was studied from 10(4) to 10(...
Whole striated muscles from the frog Rana esculenta were bathed in Ringer's solution enriched with H...
Nuclear magnetic resonance (NMR), and in particular transverse relaxation (T2), has been used to cha...
Spin-lattice relaxation times (T1's) of 13C-enriched glycine accumulated in frog muscles were determ...
The anisotropy of the spin-diffusion coefficient Ds of water protons in skeletal muscle has been stu...
Nuclear magnetic resonance (NMR) measurements provide both structural and dynamical information abou...
Abstract1H NMR spectra of intact frog, and chicken skeletal muscles, were recorded at 470 MHz with t...
The electric quadrupole moment of the deuterium nucleus provides a nuclear magnetic resonance (NMR) ...
The anisotropy of the spin-lattice relaxation time (T1) and the spin-spin relaxation times (T2) of w...