Emerging drug treatments for cystic fibrosis.

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Macromolecular interactions and ion transport in cystic fibrosis.Cystic fibrosis transmembrane regulator missing the first four transmembrane segments increases wild type and DeltaF508 processing.Emerging drug treatments for cystic fibrosis

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P2860

Emerging drug treatments for cystic fibrosis.

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2003 nî lūn-bûn

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Emerging drug treatments for cystic fibrosis.

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Emerging drug treatments for cystic fibrosis.

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Emerging drug treatments for cystic fibrosis.

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Emerging drug treatments for cystic fibrosis.

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Emerging drug treatments for cystic fibrosis.

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Emerging drug treatments for cystic fibrosis.

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P1476

Emerging drug treatments for cystic fibrosis.

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P2093

Pamela L Zeitlin

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P2860

Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome

Recombinant human DNase I reduces the viscosity of cystic fibrosis sputum

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Molecular chaperones in the cytosol: from nascent chain to folded protein

Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis

Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy

Phenylacetylglutamine May Replace Urea as a Vehicle for Waste Nitrogen Excretion

Molecular chaperones in cellular protein folding

Degradation of CFTR by the ubiquitin-proteasome pathway

Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

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523-535

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scholarly article

review article

P356

10.1517/14728214.8.2.523

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English

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2003-11-01T00:00:00Z

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14662004

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P921

cystic fibrosis

Emerging drug treatments for cystic fibrosis.

about

P2860

P2860

Emerging drug treatments for cystic fibrosis.

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