The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein.

This publication has 49 references indexed in Scilit:

• Altered protein folding may be the molecular basis of most cases of cystic fibrosis
  FEBS Letters, 1992
• A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene
  Human Molecular Genetics, 1992
• Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity
  Science, 1991
• Dimerization of the P-glycoprotein in membranes
  Biochimica et Biophysica Acta (BBA) - Biomembranes, 1990
• An Escherichia coli vector to express and purify foreign proteins by fusion to and separation from maltose-binding protein
  Gene, 1988
• Vectors that facilitate the expression and purification of foreign peptides in Escherichia coli by fusion to maltose-binding protein
  Gene, 1988
• Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectors
  Gene, 1985
• Biological activities and spectroscopic properties of chromophoric and fluorescent analogs of adenine nucleoside and nucleotides, 2′,3′-O-(2,4,6-trinitrocyclohexadienylidene) adenosine derivatives
  Biochimica et Biophysica Acta (BBA) - General Subjects, 1982
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
  Analytical Biochemistry, 1976
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970