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Volumn 40, Issue 22, 2001, Pages 6620-6627
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Asymmetric structure of the cystic fibrosis transmembrane conductance regulator chloride channel pore suggested by mutagenesis of the twelfth transmembrane region
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Author keywords
[No Author keywords available]
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Indexed keywords
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR);
CELLS;
MUTAGENESIS;
NEGATIVE IONS;
PROTEINS;
STRUCTURE (COMPOSITION);
BIOLOGICAL MEMBRANES;
CHLORIDE CHANNEL;
MUTANT PROTEIN;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
ANIMAL CELL;
ARTICLE;
CARBOXY TERMINAL SEQUENCE;
CHLORIDE CONDUCTANCE;
CONTROLLED STUDY;
CYSTIC FIBROSIS;
NONHUMAN;
PATCH CLAMP;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
PROTEIN BINDING;
PROTEIN EXPRESSION;
PROTEIN STRUCTURE;
SITE DIRECTED MUTAGENESIS;
AMINO ACID SEQUENCE;
ANIMALS;
ANIONS;
CELL LINE;
CELL MEMBRANE PERMEABILITY;
CHLORIDES;
CHO CELLS;
CRICETINAE;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
ELECTRIC CONDUCTIVITY;
HUMANS;
MEMBRANE POTENTIALS;
MOLECULAR SEQUENCE DATA;
MUTAGENESIS, SITE-DIRECTED;
PATCH-CLAMP TECHNIQUES;
PEPTIDE FRAGMENTS;
PROTEIN STRUCTURE, TERTIARY;
THIOCYANATES;
TRANSFECTION;
ANIMALIA;
MAMMALIA;
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EID: 0035811064
PISSN: 00062960
EISSN: None
Source Type: Journal
DOI: 10.1021/bi002819v Document Type: Article |
Times cited : (37)
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References (49)
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