Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channel
about
Diversity of Cl(-) channelsA synthetic chloride channel restores chloride conductance in human cystic fibrosis epithelial cellsStructural and functional characterization of transmembrane segment IX of the NHE1 isoform of the Na+/H+ exchangerStructural and Functional Analysis of Transmembrane XI of the NHE1 Isoform of the Na+/H+ ExchangerStructural and Functional Analysis of Transmembrane Segment VI of the NHE1 Isoform of the Na+/H+ ExchangerStrategies for dealing with conformational sampling in structural calculations of flexible or kinked transmembrane peptides.Membrane-inserted conformation of transmembrane domain 4 of divalent-metal transporter.Aqueous solubilization of transmembrane peptide sequences with retention of membrane insertion and functionStructure and function of the cystic fibrosis transmembrane conductance regulator.Structural and biophysical properties of a synthetic channel-forming peptide: designing a clinically relevant anion selective pore.Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.Structural and functional analysis of the Na+/H+ exchangerChannel formation by antiapoptotic protein Bcl-2.Effect of diaminopropionic acid (Dap) on the biophysical properties of a modified synthetic channel-forming peptide.Diverse Applications of Nanomedicine.Influence of B-ring modifications on proton affinity, transmembrane anion transport and anti-cancer properties of synthetic prodigiosenes.Structural and functional characterization of transmembrane segment VII of the Na+/H+ exchanger isoform 1.Functional dissection of the R domain of cystic fibrosis transmembrane conductance regulator.Peptide models for membrane channels.Rectification of whole cell cystic fibrosis transmembrane conductance regulator chloride current.Cystic fibrosis transmembrane conductance regulator. Permeant ions find the pore.Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator.A synthetic S6 segment derived from KvAP channel self-assembles, permeabilizes lipid vesicles, and exhibits ion channel activity in bilayer lipid membrane.Interhelical packing in detergent micelles. Folding of a cystic fibrosis transmembrane conductance regulator construct.Hydrophobicity and helicity of membrane-interactive peptides containing peptoid residues.Second transmembrane domain of human uncoupling protein 2 is essential for its anion channel formation.Destabilization of the transmembrane domain induces misfolding in a phenotypic mutant of cystic fibrosis transmembrane conductance regulator.Guidelines for membrane protein engineering derived from de novo designed model peptides.Cystic fibrosis transmembrane conductance regulator: expression and helicity of a double membrane-spanning segment.
P2860
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P2860
Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channel
description
1994 nî lūn-bûn
@nan
1994 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Identification of an ion chann ...... stic fibrosis chloride channel
@ast
Identification of an ion chann ...... stic fibrosis chloride channel
@en
type
label
Identification of an ion chann ...... stic fibrosis chloride channel
@ast
Identification of an ion chann ...... stic fibrosis chloride channel
@en
prefLabel
Identification of an ion chann ...... stic fibrosis chloride channel
@ast
Identification of an ion chann ...... stic fibrosis chloride channel
@en
P2093
P2860
P356
P1476
Identification of an ion chann ...... stic fibrosis chloride channel
@en
P2093
J M Tomich
M Oblatt-Montal
P2860
P304
P356
10.1073/PNAS.91.4.1495
P407
P577
1994-02-01T00:00:00Z