scholarly article | Q13442814 |
P50 | author | Klaus Schulten | Q19665429 |
P2093 | author name string | Zhe Wu | |
Thomas J McIntosh | |||
Jihong Tong | |||
Margaret M Briggs | |||
P2860 | cites work | Effect of chain length and unsaturation on elasticity of lipid bilayers | Q24537369 |
Molecular characterization of an aquaporin cDNA from brain: candidate osmoreceptor and regulator of water balance | Q24563954 | ||
Optimizing water permeability through the hourglass shape of aquaporins | Q24607996 | ||
Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductance | Q24648744 | ||
Mechanical properties of lipid bilayers and regulation of mechanosensitive function: from biological to biomimetic channels | Q26864371 | ||
Control of the selectivity of the aquaporin water channel family by global orientational tuning | Q27638881 | ||
Mechanism of aquaporin-4's fast and highly selective water conduction and proton exclusion | Q27655332 | ||
All-atom empirical potential for molecular modeling and dynamics studies of proteins | Q27860468 | ||
Scalable molecular dynamics with NAMD | Q27860718 | ||
GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation | Q27860944 | ||
Purification and functional characterization of aquaporin-8. | Q27919674 | ||
Water permeability and characterization of aquaporin-11. | Q28000039 | ||
Cellular and molecular biology of the aquaporin water channels | Q28139434 | ||
Physical principles underlying the transduction of bilayer deformation forces during mechanosensitive channel gating | Q28217366 | ||
Update of the CHARMM all-atom additive force field for lipids: validation on six lipid types | Q29616710 | ||
Functional expression and characterization of an archaeal aquaporin. AqpM from methanothermobacter marburgensis. | Q30332388 | ||
Computational analysis of local membrane properties | Q30562222 | ||
The preference of tryptophan for membrane interfaces. | Q31997161 | ||
Regulation of ion channel function by the host lipid bilayer examined by a stopped-flow spectrofluorometric assay | Q33634122 | ||
Preparative scale production of functional mouse aquaporin 4 using different cell-free expression modes | Q33707547 | ||
Molecular basis of mechanotransduction in living cells. | Q33939989 | ||
The role of aquaporin-4 in cerebral water transport and edema. | Q34004991 | ||
Aquaporins in the brain: from aqueduct to "multi-duct". | Q34005760 | ||
The pore dimensions of gramicidin A. | Q34020191 | ||
Gramicidin A channels switch between stretch activation and stretch inactivation depending on bilayer thickness | Q34047621 | ||
Lipid bilayer thickness varies linearly with acyl chain length in fluid phosphatidylcholine vesicles | Q34056527 | ||
Elastic deformation and failure of lipid bilayer membranes containing cholesterol | Q34126582 | ||
Theory and simulation of water permeation in aquaporin-1. | Q34184380 | ||
Mattress model of lipid-protein interactions in membranes | Q34261688 | ||
Aquaporin water channels: molecular mechanisms for human diseases | Q34278132 | ||
Bilayer-dependent inhibition of mechanosensitive channels by neuroactive peptide enantiomers. | Q34331994 | ||
The dynamics and energetics of water permeation and proton exclusion in aquaporins | Q34412160 | ||
Three distinct roles of aquaporin-4 in brain function revealed by knockout mice | Q34505493 | ||
Roles of bilayer material properties in function and distribution of membrane proteins | Q34524435 | ||
An aquaporin-4/transient receptor potential vanilloid 4 (AQP4/TRPV4) complex is essential for cell-volume control in astrocytes | Q34572856 | ||
Aquaglyceroporin AQP9: solute permeation and metabolic control of expression in liver | Q34809159 | ||
Temporary loss of perivascular aquaporin-4 in neocortex after transient middle cerebral artery occlusion in mice | Q35011844 | ||
Multilevel summation method for electrostatic force evaluation | Q35076380 | ||
Emerging roles for lipids in shaping membrane-protein function. | Q35203586 | ||
The mobility of single-file water molecules is governed by the number of H-bonds they may form with channel-lining residues. | Q35833596 | ||
Importance of aquaporins in the physiopathology of brain edema | Q35849604 | ||
Computational studies of membrane channels | Q35856914 | ||
Influence of hydrophobic mismatch on structures and dynamics of gramicidin a and lipid bilayers | Q35866803 | ||
From structure to disease: the evolving tale of aquaporin biology | Q35875999 | ||
New insights into water transport and edema in the central nervous system from phenotype analysis of aquaporin-4 null mice. | Q35961506 | ||
Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity | Q36379107 | ||
Lipid bilayer-mediated regulation of ion channel function by amphiphilic drugs | Q36593666 | ||
Elasticity, strength, and water permeability of bilayers that contain raft microdomain-forming lipids | Q36678233 | ||
Bilayer thickness and membrane protein function: an energetic perspective. | Q36722414 | ||
Single-molecule methods for monitoring changes in bilayer elastic properties | Q36977298 | ||
Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice | Q37089696 | ||
Initial response of the potassium channel voltage sensor to a transmembrane potential | Q37156485 | ||
The water permeability of lens aquaporin-0 depends on its lipid bilayer environment | Q37166334 | ||
Sorting of lens aquaporins and connexins into raft and nonraft bilayers: role of protein homo-oligomerization | Q37405988 | ||
The channel architecture of aquaporin 0 at a 2.2-A resolution | Q37557408 | ||
Lipid bilayer modules as determinants of K+ channel gating | Q37583526 | ||
Brain volume regulation: osmolytes and aquaporin perspectives | Q37652042 | ||
Cholesterol and ion channels | Q37705156 | ||
Gating and conductance changes in BK(Ca) channels in bilayers are reciprocal | Q40139197 | ||
New possible roles for aquaporin-4 in astrocytes: cell cytoskeleton and functional relationship with connexin43. | Q40384671 | ||
Large-scale purification of functional recombinant human aquaporin-2. | Q40782806 | ||
Very high single channel water permeability of aquaporin-4 in baculovirus-infected insect cells and liposomes reconstituted with purified aquaporin-4. | Q41104307 | ||
Hydrophobic coupling of lipid bilayer energetics to channel function. | Q41881613 | ||
New insights of membrane environment effects on MscL channel mechanics from theoretical approaches. | Q42637082 | ||
Differential water permeability and regulation of three aquaporin 4 isoforms | Q43219898 | ||
Clinical features of opticospinal multiple sclerosis with anti-aquaporin 4 antibody. | Q44982007 | ||
Capsaicin regulates voltage-dependent sodium channels by altering lipid bilayer elasticity. | Q46557816 | ||
X-ray diffraction to determine the thickness of raft and nonraft bilayers | Q46795598 | ||
Mercury chloride decreases the water permeability of aquaporin-4-reconstituted proteoliposomes | Q46826906 | ||
Physiological importance of aquaporin water channels | Q46830033 | ||
Regulation of the gating of BKCa channel by lipid bilayer thickness | Q48316596 | ||
Lipid membranes with a majority of cholesterol: applications to the ocular lens and aquaporin 0. | Q53426607 | ||
Functional reconstitution and characterization of AqpZ, the E. coli water channel protein. | Q54076183 | ||
Membrane Thickness Changes Ion-Selectivity of Channel-Proteins | Q57374787 | ||
Scattering Density Profile Model of POPG Bilayers As Determined by Molecular Dynamics Simulations and Small-Angle Neutron and X-ray Scattering Experiments | Q61850940 | ||
Pore Formation Coupled to Ion Transport through Lipid Membranes as Induced by Transmembrane Ionic Charge Imbalance: Atomistic Molecular Dynamics Study | Q61875087 | ||
Serial permeability barriers to water transport in human placental vesicles | Q68989053 | ||
The effect of bilayer thickness on the activity of (Na+ + K+)-ATPase | Q72462043 | ||
The effects of bilayer thickness and tension on gramicidin single-channel lifetime | Q72714026 | ||
The conformational preference of gramicidin channels is a function of lipid bilayer thickness | Q73588301 | ||
CHARMM-GUI: a web-based graphical user interface for CHARMM | Q80900573 | ||
Structure of fully hydrated fluid phase lipid bilayers with monounsaturated chains | Q83129856 | ||
Differential expression of aquaporin-4 isoforms localizes with neuromyelitis optica disease activity | Q83186656 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 90-99 | |
P577 | publication date | 2016-07-01 | |
P1433 | published in | Biophysical Journal | Q2032955 |
P1476 | title | The Water Permeability and Pore Entrance Structure of Aquaporin-4 Depend on Lipid Bilayer Thickness | |
P478 | volume | 111 |
Q59811213 | Aquaporins: More Than Functional Monomers in a Tetrameric Arrangement |
Q93054243 | Characterization of Lipid-Protein Interactions and Lipid-Mediated Modulation of Membrane Protein Function through Molecular Simulation |
Q48507949 | Computing osmotic permeabilities of aquaporins AQP4, AQP5, and GlpF from near-equilibrium simulations |
Q59885157 | Microscopic view of lipids and their diverse biological functions |
Search more.