Quantification of Age-Related Changes in the Lateral Organization of the Lipid Portion of the Intact Membranes Isolated from the Left and Right Eye Lenses of the Same Human Donor
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[1] M. Pasenkiewicz-Gierula,et al. Molecular oxygen as a probe molecule in EPR spin-labeling studies of membrane structure and dynamics , 2022, Oxygen.
[2] R. Truscott,et al. Molecular Processes Implicated in Human Age-Related Nuclear Cataract , 2019, Investigative ophthalmology & visual science.
[3] James E. Hall,et al. BFSP1 C-terminal domains released by post-translational processing events can alter significantly the calcium regulation of AQP0 water permeability , 2019, Experimental eye research.
[4] W. Subczynski,et al. Detection of cholesterol bilayer domains in intact biological membranes: Methodology development and its application to studies of eye lens fiber cell plasma membranes , 2019, Experimental eye research.
[5] J. S. Hyde,et al. Saturation Recovery EPR Spin-Labeling Method for Quantification of Lipids in Biological Membrane Domains , 2017, Applied magnetic resonance.
[6] W. Subczynski,et al. Cholesterol Bilayer Domains in the Eye Lens Health: A Review , 2017, Cell Biochemistry and Biophysics.
[7] W. Subczynski,et al. Changes in the Properties and Organization of Human Lens Lipid Membranes Occurring with Age , 2017, Current eye research.
[8] W. Subczynski,et al. Organization of lipids in fiber-cell plasma membranes of the eye lens. , 2017, Experimental eye research.
[9] Saul Bellow,et al. Nobel Lecture , 2018, Green Planet Blues.
[10] W. Subczynski,et al. Amounts of phospholipids and cholesterol in lipid domains formed in intact lens membranes: Methodology development and its application to studies of porcine lens membranes. , 2015, Experimental eye research.
[11] W. Subczynski,et al. Lipid domains in intact fiber-cell plasma membranes isolated from cortical and nuclear regions of human eye lenses of donors from different age groups. , 2015, Experimental eye research.
[12] W. Subczynski,et al. Properties of membranes derived from the total lipids extracted from clear and cataractous lenses of 61–70-year-old human donors , 2015, European Biophysics Journal.
[13] W. Subczynski,et al. Lipid-protein interactions in plasma membranes of fiber cells isolated from the human eye lens. , 2014, Experimental eye research.
[14] W. Subczynski,et al. Properties of membranes derived from the total lipids extracted from the human lens cortex and nucleus. , 2013, Biochimica et biophysica acta.
[15] W. Subczynski,et al. Properties of fiber cell plasma membranes isolated from the cortex and nucleus of the porcine eye lens. , 2012, Experimental eye research.
[16] W. Subczynski,et al. Using spin-label electron paramagnetic resonance (EPR) to discriminate and characterize the cholesterol bilayer domain. , 2011, Chemistry and physics of lipids.
[17] P. Sens,et al. Eye lens membrane junctional microdomains: a comparison between healthy and pathological cases , 2011 .
[18] S. Bassnett,et al. Biological glass: structural determinants of eye lens transparency , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.
[19] W. Subczynski,et al. The immiscible cholesterol bilayer domain exists as an integral part of phospholipid bilayer membranes. , 2011, Biochimica et biophysica acta.
[20] Frederick A. Heberle,et al. Phase separation in lipid membranes. , 2011, Cold Spring Harbor perspectives in biology.
[21] W. Subczynski,et al. Functions of Cholesterol and the Cholesterol Bilayer Domain Specific to the Fiber-Cell Plasma Membrane of the Eye Lens , 2011, The Journal of Membrane Biology.
[22] Jean X. Jiang,et al. Gap junctions are selectively associated with interlocking ball-and-sockets but not protrusions in the lens , 2010, Molecular vision.
[23] T. W. White,et al. Lens gap junctions in growth, differentiation, and homeostasis. , 2010, Physiological reviews.
[24] T. Gonen,et al. Lipid-protein interactions probed by electron crystallography. , 2009, Current opinion in structural biology.
[25] Jean X. Jiang,et al. Gap junction remodeling associated with cholesterol redistribution during fiber cell maturation in the adult chicken lens , 2009, Molecular vision.
[26] W. Subczynski,et al. Physical properties of the lipid bilayer membrane made of cortical and nuclear bovine lens lipids: EPR spin-labeling studies. , 2009, Biochimica et biophysica acta.
[27] S. Blanksby,et al. Human lens lipids differ markedly from those of commonly used experimental animals. , 2008, Biochimica et biophysica acta.
[28] W. Subczynski,et al. Characterization of lipid domains in reconstituted porcine lens membranes using EPR spin-labeling approaches. , 2008, Biochimica et biophysica acta.
[29] W. Subczynski,et al. Oxygen permeability of the lipid bilayer membrane made of calf lens lipids. , 2007, Biochimica et biophysica acta.
[30] W. Subczynski,et al. Physical properties of the lipid bilayer membrane made of calf lens lipids: EPR spin labeling studies. , 2007, Biochimica et biophysica acta.
[31] S. Biswas,et al. Gap junctions contain different amounts of cholesterol which undergo unique sequestering processes during fiber cell differentiation in the embryonic chicken lens , 2007, Molecular vision.
[32] J. Kuszak,et al. Transgenic overexpression of connexin50 induces cataracts. , 2007, Experimental eye research.
[33] Thomas Walz,et al. The supramolecular architecture of junctional microdomains in native lens membranes , 2007, EMBO reports.
[34] Nalin M. Kumar,et al. Structural and immunocytochemical alterations in eye lens fiber cells from Cx46 and Cx50 knockout mice. , 2006, European journal of cell biology.
[35] Peter Agre,et al. Aquaporin Water Channels , 2004, Proceedings of the American Thoracic Society.
[36] S. Harrison,et al. Lipid–protein interactions in double-layered two-dimensional AQP0 crystals , 2005, Nature.
[37] D. Borchman,et al. Human lens phospholipid changes with age and cataract. , 2005, Investigative ophthalmology & visual science.
[38] J. Kuszak,et al. Development of lens sutures , 2004 .
[39] T. Gonen,et al. Aquaporin-0 membrane junctions form upon proteolytic cleavage. , 2004, Journal of molecular biology.
[40] Kai Simons,et al. Model systems, lipid rafts, and cell membranes. , 2004, Annual review of biophysics and biomolecular structure.
[41] R. Jacob,et al. Direct evidence for cholesterol crystalline domains in biological membranes: role in human pathobiology. , 2003, Biochimica et biophysica acta.
[42] James E. Hall,et al. Micro-domains of AQP0 in lens equatorial fibers. , 2002, Experimental eye research.
[43] J. S. Hyde,et al. Pulse EPR detection of lipid exchange between protein-rich raft and bulk domains in the membrane: methodology development and its application to studies of influenza viral membrane. , 2001, Biophysical journal.
[44] R. Truscott. Age-Related Nuclear Cataract: A Lens Transport Problem , 2000, Ophthalmic Research.
[45] H. Yin,et al. Membrane lipid alpha-crystallin interaction and membrane Ca2+ -ATPase activities. , 1999, Current eye research.
[46] D. Paul,et al. Targeted Ablation of Connexin50 in Mice Results in Microphthalmia and Zonular Pulverulent Cataracts , 1998, The Journal of cell biology.
[47] R. Truscott,et al. An impediment to glutathione diffusion in older normal human lenses: a possible precondition for nuclear cataract. , 1998, Experimental eye research.
[48] D. Marsh. Stoichiometry of lipid-protein interaction and integral membrane protein structure , 1997, European Biophysics Journal.
[49] M. Rosseneu,et al. Structural organization of lipid phase and protein-lipid interface in apolipoprotein-phospholipid recombinants: influence of cholesterol. , 1997, Biochimica et biophysica acta.
[50] D. Borchman,et al. Liquid chromatography/mass-spectrometric characterization of sphingomyelin and dihydrosphingomyelin of human lens membranes. , 1997, Ophthalmic research.
[51] Y. Ozaki,et al. Lipid-protein interactions in human and bovine lens membranes by Fourier transform Raman and infrared spectroscopies. , 1996, Experimental eye research.
[52] D. Borchman,et al. Separation and characterization of the unknown phospholipid in human lens membranes. , 1994, Investigative ophthalmology & visual science.
[53] J. S. Hyde,et al. Molecular organization and dynamics in bacteriorhodopsin-rich reconstituted membranes: discrimination of lipid environments by the oxygen transport parameter using a pulse ESR spin-labeling technique. , 1994, Biochemistry.
[54] C. Louis,et al. The distribution of the fiber cell intrinsic membrane proteins MP20 and connexin46 in the bovine lens. , 1992, Journal of cell science.
[55] J. D. Robertson,et al. Distribution of gap junctions and square array junctions in the mammalian lens. , 1989, Investigative ophthalmology & visual science.
[56] N. Ryba,et al. Molecular exchange at the lipid-rhodopsin interface: spin-label electron spin resonance studies of rhodopsin-dimyristoylphosphatidylcholine recombinants. , 1987, Biochemistry.
[57] D. Melville,et al. Exchange rates and numbers of annular lipids for the calcium and magnesium ion dependent adenosinetriphosphatase. , 1985, Biochemistry.
[58] J. B. Massey,et al. Thermodynamics of lipid-protein association. Enthalphy of association of apolipoprotein A-II with dimyristoylphosphatidylcholine-cholesterol mixtures. , 1984, Biochimica et biophysica acta.
[59] A. Tall,et al. Interaction of cholesterol, phospholipid and apoprotein in high density lipoprotein recombinants. , 1978, Biochimica et biophysica acta.
[60] P. Zelenka,et al. Phospholipid composition and metabolism in the embryonic chick lens. , 1978, Experimental eye research.
[61] B. Aloni,et al. The erythrocyte membrane site for the effect of temperature on osmotic fragility. , 1977, Biochimica et biophysica acta.
[62] W. J. Soeting,et al. Lipids in tissues of the eye. XV. Essential fatty acids in lens lipids. , 1976, Experimental eye research.
[63] D. Wallach,et al. Variations of lipid-protein interactions in erythrocyte ghosts as a function of temperature and pH in physiological and non-physiological ranges. A study using a paramagnetic quenching of protein fluorescence by nitroxide lipid analogues. , 1975, Biochimica et biophysica acta.
[64] M. Houslay,et al. Cholesterol is excluded from the phospholipid annulus surrounding an active calcium transport protein , 1975, Nature.
[65] G. Vanderkooi,et al. Evidence for boundary lipid in membranes. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[66] W. Hubbell,et al. Spin-label studies of the excitable membranes of nerve and muscle. , 1968, Proceedings of the National Academy of Sciences of the United States of America.