194 related articles for article (PubMed ID: 3502025)
1. Cell volumes and water contents of frog muscles in solutions of permeant sugars and sugar alcohols.
Ling GN
Physiol Chem Phys Med NMR; 1987; 19(3):159-75. PubMed ID: 3502025
[TBL] [Abstract][Full Text] [Related]
2. Predictions of polarized multilayer theory of solute distribution confirmed from a study of the equilibrium distribution in frog muscle of twenty-one nonelectrolytes including five cryoprotectants.
Ling GN; Niu Z; Ochsenfeld M
Physiol Chem Phys Med NMR; 1993; 25(3):177-208. PubMed ID: 8115493
[TBL] [Abstract][Full Text] [Related]
3. Studies on the physical state of water in living cells and model systems. X. The dependence of the equilibrium distribution coefficient of a solute in polarized water on the molecular weights of the solute: experimental confirmation of the "size rule" in model studies.
Ling GN; Hu W
Physiol Chem Phys Med NMR; 1988; 20(4):293-307. PubMed ID: 3254539
[TBL] [Abstract][Full Text] [Related]
4. Studies on the physical state of water in living cells and model systems. XI. The equilibrium distribution coefficients of pentoses in muscle cell water: their dependence primarily on the molecular weights of the pentoses and lesser dependence on their stereospecificity.
Ling GN; Ochsenfeld MM
Physiol Chem Phys Med NMR; 1988; 20(4):309-17. PubMed ID: 3254540
[TBL] [Abstract][Full Text] [Related]
5. Studies on the physical state of water in living cells and model systems. VI. Concentration-dependent sustained volume changes of dialysis sacs containing aqueous solution of native and denatured protein, gelatin, and oxygen-containing polymers immersed in solutions of Na salt and of sugar and sugar alcohol.
Ling GN; Ochsenfeld MM
Physiol Chem Phys Med NMR; 1987; 19(3):177-92. PubMed ID: 3441519
[TBL] [Abstract][Full Text] [Related]
6. Studies on the physical state of water in living cells and model systems. VII. Exclusion of sugars and sugar alcohols from the water in sulfonate ion exchange resins: the "size rule".
Ling GN
Physiol Chem Phys Med NMR; 1987; 19(3):193-8. PubMed ID: 3441520
[TBL] [Abstract][Full Text] [Related]
7. A new theory of the water contents of living cells in solutions containing different concentrations of permeant solutes.
Ling GN
Physiol Chem Phys Med NMR; 1986; 18(2):131. PubMed ID: 3809260
[No Abstract] [Full Text] [Related]
8. A quantitative theory of solute distribution in cell water according to molecular size.
Ling GN
Physiol Chem Phys Med NMR; 1993; 25(3):145-75. PubMed ID: 8115492
[TBL] [Abstract][Full Text] [Related]
9. What determines the normal water content of a living cell?
Ling G
Physiol Chem Phys Med NMR; 2004; 36(1):1-19. PubMed ID: 15789970
[TBL] [Abstract][Full Text] [Related]
10. A physical theory of the living state: application to water and solute distribution.
Ling GN
Scanning Microsc; 1988 Jun; 2(2):899-913. PubMed ID: 3399856
[TBL] [Abstract][Full Text] [Related]
11. Sugars exert a major influence on the vitrification properties of ethylene glycol-based solutions and have low toxicity to embryos and oocytes.
Kuleshova LL; MacFarlane DR; Trounson AO; Shaw JM
Cryobiology; 1999 Mar; 38(2):119-30. PubMed ID: 10191035
[TBL] [Abstract][Full Text] [Related]
12. Studies on the physical state of water in living cells and model systems: IX. Theoretical significance of a straight line relationship between intracellular concentration of a partially excluded solute and its concentration in the bathing medium.
Ling GN
Physiol Chem Phys Med NMR; 1988; 20(4):281-92. PubMed ID: 3076014
[TBL] [Abstract][Full Text] [Related]
13. A unitary cause for the exclusion of Na+ and other solutes from living cells, suggested by effluxes of Na+, D-arabinose, and sucrose from normal, dying, and dead muscles.
Ling GN; Walton CL; Ochsenfeld MM
J Cell Physiol; 1981 Mar; 106(3):385-98. PubMed ID: 6971295
[TBL] [Abstract][Full Text] [Related]
14. The cell water problem posed by electron microscopic studies of ion binding in muscle.
Edelmann L
Scanning Microsc; 1988 Jun; 2(2):851-65. PubMed ID: 3399854
[TBL] [Abstract][Full Text] [Related]
15. Active solute transport across frog skin and epithelial cell systems according to the association-induction hypothesis.
Ling GN
Physiol Chem Phys; 1981; 13(4):356-82. PubMed ID: 7330099
[TBL] [Abstract][Full Text] [Related]
16. Solute exclusion by polymer and protein-dominated water: correlation with results of nuclear magnetic resonance (NMR) and calorimetric studies and their significance for the understanding of the physical state of water in living cells.
Ling GN
Scanning Microsc; 1988 Jun; 2(2):871-84. PubMed ID: 3041574
[TBL] [Abstract][Full Text] [Related]
17. Studies on the physical state of water in living cells and model systems. IV. Freezing and thawing point depression of water by gelatin, oxygen-containing polymers and urea-denatured proteins.
Ling GN; Zhang ZL
Physiol Chem Phys Med NMR; 1983; 15(5):391-406. PubMed ID: 6675032
[TBL] [Abstract][Full Text] [Related]
18. Cooperative interaction among cell surface sites: evidence in support of the surface adsorption theory of cellular electrical potentials.
Ling GN; Fisher A
Physiol Chem Phys Med NMR; 1983; 15(5):369-78. PubMed ID: 6609378
[TBL] [Abstract][Full Text] [Related]
19. Surfactant solutions and porous substrates: spreading and imbibition.
Starov VM
Adv Colloid Interface Sci; 2004 Nov; 111(1-2):3-27. PubMed ID: 15571660
[TBL] [Abstract][Full Text] [Related]
20. Quench-flow analysis reveals multiple phases of GluT1-mediated sugar transport.
Blodgett DM; Carruthers A
Biochemistry; 2005 Feb; 44(7):2650-60. PubMed ID: 15709778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]